1,229 results
Search Results
2. A Distance-Based Microfluidic Paper-Based Biosensor for Glucose Measurements in Tear Range
- Author
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Mohsen Rabbani and Samira Allameh
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Paper ,Materials science ,business.industry ,Microfluidics ,Glucose Measurement ,Bioengineering ,Biosensing Techniques ,General Medicine ,Microfluidic Analytical Techniques ,Applied Microbiology and Biotechnology ,Biochemistry ,Glucose Oxidase ,Paper based biosensor ,Glucose ,Range (statistics) ,Optoelectronics ,business ,Molecular Biology ,Horseradish Peroxidase ,Distance based ,Biotechnology - Abstract
The prevalence of diabetes has increased over the past years. Therefore, developing minimally invasive, user-friendly and cost-effective glucose biosensors is necessary especially in low-income and developing countries. Cellulose paper-based analytical devices have attracted the attention of many researchers due to affordability, not requiring trained personnel, and complex equipment. This paper describes a microfluidic paper-based analytical device for the detection of glucose in tear with the naked eye. The paper-based biosensor fabricated by laser CO2, and GOx/HRP enzymatic solution coupled with TMB was utilized as reagents. A sample volume of 10 µl was needed for the biosensor operation and the results were observable within 5 minutes. To evaluate the device performance, color intensity-based and distance-based results were analyzed by ImageJ and Tracker. Distance-based results showed a linear behavior in the range of 0.1–0.6 mM with an R2 = 0.967 and LOD of 0.2 mM. The results could be perceived by the naked eye without any need to further equipment or trained personnel in a relatively short time (3–5 minutes). Moreover, glucose concentration could be obtained non-invasively by tears collected by this µPAD.
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- 2022
3. Traffic light type paper-based analytical device for intuitive and semi-quantitative naked-eye signal readout
- Author
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Sera Ohta, Ryuya Hiraoka, Yuki Hiruta, and Daniel Citterio
- Subjects
Paper ,Point-of-Care Testing ,Lab-On-A-Chip Devices ,Biomedical Engineering ,Bioengineering ,Hydrogen Peroxide ,General Chemistry ,Microfluidic Analytical Techniques ,Biochemistry - Abstract
Microfluidic paper-based analytical devices (μPADs) have attracted great attention as potential candidates for point-of-care testing (POCT). Nevertheless, only a limited number of μPADs expected to satisfy the standard of Clinical Laboratory Improvement Amendments (CLIA) waived tests as issued by the US Food and Drug Administration (FDA) have been reported. This work introduces a "traffic light type μPAD", enabling highly intuitive semi-quantitative equipment-free naked-eye readout with no need for calibration, subjective interpretation or calculation. Assay results are displayed as traffic light colours reporting 5 analyte concentration levels (green/greenyellow/yellow/yellowred/red). The device has been designed to never display all three colours simultaneously, eliminating any risk for misinterpretation. The mechanism relies on the modulation of sample flow through a network of paperfluidic channels modified with a hydrophobic to hydrophilic phase-switching substance responsive to H
- Published
- 2022
4. Rapid and inexpensive process to fabricate paper based microfluidic devices using a cut and heat plastic lamination process
- Author
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Nityanand Kumawat, Soja Saghar Soman, Sanjairaj Vijayavenkataraman, and Sunil Kumar
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Paper ,Mice ,Hot Temperature ,Lab-On-A-Chip Devices ,Biomedical Engineering ,Animals ,Humans ,Bioengineering ,General Chemistry ,Microfluidic Analytical Techniques ,Hydrophobic and Hydrophilic Interactions ,Plastics ,Biochemistry - Abstract
Microfluidic paper-based analytical devices (microPADs) are emerging as simple-to-use, low-cost point-of-care testing platforms. Such devices are mostly fabricated at present by creating hydrophobic barriers using wax or photoresist patterning on porous paper sheets. Even though devices fabricated using these methods are used and tested with a wide variety of analytes, still they pose many serious practical limitations for low-cost automated mass fabrication for their widespread applicability. We present an affordable and simple two-step process - cut and heat (CH-microPADs) - for the selective fabrication of hydrophilic channels and reservoirs on a wide variety of porous media such as tissue/printing/filter paper and cloth types, such as cotton and polyester, by a lamination process. The technique presents many advantages as compared to existing commonly used methods. The devices possess excellent mechanical strength against bending, folding and twisting, making them virtually unbreakable. They are structurally flexible and show good chemical resistance to various solvents, acids and bases, presenting widespread applicability in areas such as clinical diagnostics, biological sensing applications, food processing, and the chemical industry. Fabricated paper media 96 well-plate CH-microPAD configurations were tested for cell culture applications using mice embryonic fibroblasts and detection of proteins and enzymes using ELISA. With a simple two-step process and minimal human intervention, the technique presents a promising step towards mass fabrication of inexpensive disposable diagnostic devices for both resource-limited and developed regions.
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- 2022
5. Effects of cellulose nanofibrils and starch compared with polyacrylamide on fundamental properties of pulp and paper
- Author
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Hossein Jalali Torshizi, Milad Tajik, Hossein Resalati, and Yahya Hamzeh
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Paper ,Chemical Phenomena ,Starch ,Polyacrylamide ,Acrylic Resins ,Nanofibers ,Bagasse pulp ,engineering.material ,Biochemistry ,chemistry.chemical_compound ,Biopolymers ,stomatognathic system ,Structural Biology ,Nano ,Cellulose ,Molecular Biology ,Mechanical Phenomena ,chemistry.chemical_classification ,Pulp (paper) ,Cationic polymerization ,General Medicine ,Polymer ,Chemical engineering ,chemistry ,engineering - Abstract
Bio-based additives received significant attention in pulp and paper properties improvement. For this, the most cited biochemical Cellulose Nano Fibrils (CNFs) and Cationic Starch (CS) were experimentally compared with the most declared synthetic chemical, Cationic Polyacrylamide (CPAM). SEM images showed better paper surface filling by the utilization of the chemicals. The three studied polymers, in solely or combination mechanism, improved mainly bagasse pulp and paper properties compared to the blank sample, except for pulp drainage, which decreased by CNFs to lower volumes presumably due to its intrinsic characteristics. Cationic polymers (CP) compared to CP/CNFs approaches increased pulp retention and drainage but decreased paper density and strengths. The best pulp retention and drainage achieved by CS followed by CPAM, while paper air persistency, density, and strength properties evaluated highest by CP/CNFs followed by CNFs. Generally, CS revealed a more significant improvement in pulp and paper properties than CPAM either with or without CNFs.
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- 2021
6. Sensitive electrochemical detection of cholesterol using a portable paper sensor based on the synergistic effect of cholesterol oxidase and nanoporous gold
- Author
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Keshuai Shang, Shuangjue Wang, Xia Wang, Siyu Chen, and Xinyu Gao
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Paper ,Spectrum analyzer ,Cholesterol oxidase ,Biosensing Techniques ,Electrochemical detection ,Biochemistry ,Nanopores ,chemistry.chemical_compound ,Structural Biology ,Humans ,Electrodes ,Molecular Biology ,Detection limit ,Chromatography ,Cholesterol Oxidase ,Chemistry ,Nanoporous ,Cholesterol ,Temperature ,Electrochemical Techniques ,General Medicine ,Hydrogen-Ion Concentration ,Pseudomonas aeruginosa ,lipids (amino acids, peptides, and proteins) ,Gold - Abstract
As a crucial biomarker for some diseases, the determination of cholesterol in human serum is of great significance for the diagnosis and prevention of these diseases. Hence, a portable cholesterol detection method is necessary for clinical and domestic applications. Here, a portable paper sensor was designed for cholesterol detection by modifying screen-printed electrode (SPE) with nanoporous gold (NPG). To achieve the reliable cholesterol detection, a synergistic strategy was proposed based on the oxidation of cholesterol by cholesterol oxidase (ChOx) and the reduction of oxidation product (H2O2) by NPG. Compared to existing electrochemical sensors, the resulting paper sensor exhibited a wider linear response in a range from 50 μM to 6 mM as well as a higher sensitivity of 32.68 μA mM−1 cm−2 with a lower detection limit of 8.36 μM. Moreover, the portable paper sensor presented strong anti-interference capability and stability in the detection of cholesterol in human serum, and the data detected by the portable paper sensor were consistent with that obtained by an automatic biochemical analyzer. These unique performances confirmed that the proposed paper sensor was a sensitive, reliable, and portable cholesterol detection method, making it a good choice for cholesterol detection.
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- 2021
7. Carbon fiber paper spray ionization mass spectrometry
- Author
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Shanshan Wang, Jiahui Bai, Kang Wang, and Yinlong Guo
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Paper ,Flavonoids ,Spectrometry, Mass, Electrospray Ionization ,Carbon Fiber ,Environmental Chemistry ,Humans ,Protons ,Polycyclic Aromatic Hydrocarbons ,Biochemistry ,Spectroscopy ,Mass Spectrometry ,Adenosine Monophosphate ,Analytical Chemistry - Abstract
Carbon fiber paper (CFP) is commonly used as a proton exchange membrane in fuel cells due to its prominent areal electrosorption capacity, exceptional conductivity and excellent chemical stability. In this paper, we first explored the feasibility of carbon fiber paper as a specific paper substrate in paper spray ionization mass spectrometry (PSI-MS). The results demonstrated that CFPSI-MS combines the merits of PSI and carbon fiber ionization (CFI) and exhibits better performance of various compound analyses than either of these techniques alone. The application of CFP can highly enhance the signal stability and detection sensitivity of a diverse array of analytes, especially in negative ionization mode. The ion intensity of target analytes such as saccharides and flavonoids was improved 2-90-fold. Many nonpolar/low-polarity analytes, such as polycyclic aromatic hydrocarbons, which are difficult to ionize by traditional PSI-MS, were successfully detected by CFPSI-MS with a 2.5 kV high voltage. Moreover, CFPSI-MS presents high sensitivity in semiquantitative analysis, and the limits of detection (LODs) of cyclic adenosine monophosphate (CAMP), naringin and tivantinib in whole blood were improved 2-100-fold compared to those in traditional PSI-MS. In real sample analysis, CFPSI-MS also exhibits excellent capability in human breath analysis and blood metabolomic profiling.
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- 2022
8. LC-HRMS screening of per- and polyfluorinated alkyl substances (PFAS) in impregnated paper samples and contaminated soils
- Author
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Christian Zwiener, Rebecca Bauer, Martin E. Maier, Florian Herrmann, and Boris Bugsel
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Paper ,010504 meteorology & atmospheric sciences ,Soil test ,PFAS ,HRMS ,010501 environmental sciences ,engineering.material ,01 natural sciences ,Biochemistry ,Perfluorinated carboxylic acids ,Analytical Chemistry ,Soil ,chemistry.chemical_compound ,Fluorotelomer ,Alkyl ,0105 earth and related environmental sciences ,chemistry.chemical_classification ,Chemistry ,Compost ,Contamination ,Phosphate ,Environmental chemistry ,Soil water ,engineering ,Soil horizon ,Research Paper - Abstract
High per- and polyfluorinated alkyl substance (PFAS) concentrations have been detected in agricultural soils in Southwest Germany. Discharges of PFAS-contaminated paper sludge and compost are suspected to be the cause of the contamination. Perfluorinated carboxylic acids (PFCAs) have been detected also in groundwater, drinking water, and plants in this area. Recently, previously unknown compounds have been identified by high-resolution mass spectrometry (HRMS). Major contaminants were polyfluorinated dialkylated phosphate esters (diPAPs) and N-ethyl perfluorooctane sulfonamide ethanol–based phosphate diester (diSAmPAP). In this study, HRMS screening for PFAS was applied to 14 soil samples from the contaminated area and 14 impregnated paper samples which were from a similar period than the contamination. The paper samples were characterized by diPAPs (from 4:2/6:2 to 12:2/12:2), fluorotelomer mercapto alkyl phosphates (FTMAPs; 6:2/6:2 to 10:2/10:2), and diSAmPAP. In soil samples, diPAPs and their transformation products (TPs) were the major contaminants, but also FTMAPs, diSAmPAP, and their TPs occurred. The distribution patterns of the carbon chain lengths of the precursor PFAS in soil samples were shown to resemble those in paper samples. This supports the hypothesis that paper sludge is a major source of contamination. The presence of major degradation products like PFCAs, FTSAs, or PFOS and their distribution of carbon chain lengths indicate the activity of biotic or abiotic degradation processes and selective leaching processes from the upper soil horizons. Graphical abstract Supplementary Information The online version contains supplementary material available at 10.1007/s00216-021-03463-9.
- Published
- 2021
9. REVEALR: A Multicomponent XNAzyme-Based Nucleic Acid Detection System for SARS-CoV-2
- Author
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John C. Chaput and Kefan Yang
- Subjects
Male ,Paper ,Analyte ,Loop-mediated isothermal amplification ,Computational biology ,010402 general chemistry ,Sensitivity and Specificity ,01 natural sciences ,Biochemistry ,Catalysis ,chemistry.chemical_compound ,Colloid and Surface Chemistry ,Limit of Detection ,Nasopharynx ,Chlorocebus aethiops ,Animals ,Humans ,CRISPR ,Vero Cells ,Detection limit ,SARS-CoV-2 ,COVID-19 ,RNA ,DNA, Catalytic ,General Chemistry ,Nucleic acid amplification technique ,0104 chemical sciences ,Oligodeoxyribonucleotides ,chemistry ,COVID-19 Nucleic Acid Testing ,Nucleic acid ,RNA, Viral ,Female ,Nucleic Acid Amplification Techniques ,DNA - Abstract
Isothermal amplification strategies capable of rapid, inexpensive, and accurate nucleic acid detection provide new options for large-scale pathogen detection, disease diagnosis, and genotyping. Here we report a highly sensitive multicomponent XNA-based nucleic acid detection platform that combines analyte preamplification with X10-23-mediated catalysis to detect the viral pathogen responsible for COVID-19. The platform, termed RNA-Encoded Viral Nucleic Acid Analyte Reporter (REVEALR), functions with a detection limit of ≤20 aM (∼10 copies/μL) using conventional fluorescence and paper-based lateral flow readout modalities. With a total assay time of 1 h, REVEALR provides a convenient nucleic acid alternative to equivalent CRISPR-based approaches, which have become popular methods for SARS-CoV-2 detection. The assay shows no cross-reactivity for other in vitro transcribed respiratory viral RNAs and functions with perfect accuracy against COVID-19 patient-derived clinical samples.
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- 2021
10. Surface hydrophobization of pulp fibers in paper sheets via gas phase reactions
- Author
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Stefan Spirk, Sarah Krainer, Carina Waldner, Ulrich Hirn, Eero Kontturi, Philipp Wulz, Graz University of Technology, Department of Bioproducts and Biosystems, Aalto-yliopisto, and Aalto University
- Subjects
Paper ,Materials science ,Spectrophotometry, Infrared ,Trimethylsilyl ,Silylation ,Fluoroacetates ,Acetic Anhydrides ,Palmitates ,Gas phase ,Hydrophobisation ,02 engineering and technology ,Biochemistry ,Contact angle ,03 medical and health sciences ,chemistry.chemical_compound ,Structural Biology ,Tensile Strength ,Ultimate tensile strength ,Organosilicon Compounds ,Fiber ,Cellulose ,Porosity ,Molecular Biology ,030304 developmental biology ,0303 health sciences ,Photoelectron Spectroscopy ,Water ,General Medicine ,021001 nanoscience & nanotechnology ,Fibers ,Acetic anhydride ,Ultrasonic Waves ,chemistry ,Chemical engineering ,Wettability ,Volatilization ,Trifluoroacetic anhydride ,0210 nano-technology - Abstract
Funding Information: The financial support of the Austrian Federal Ministry of Digital and Economic Affairs and the National Foundation for Research, Technology and Development , Austria, is gratefully acknowledged. We also thank the industrial partners Mondi, Canon Production Printing, Kelheim Fibres, and SIG Combibloc for their support. Publisher Copyright: © 2021 Copyright: Copyright 2021 Elsevier B.V., All rights reserved. Hydrophobization of cellulosic materials and particularly paper products is a commonly used procedure to render papers more resistant to water and moisture. Here, we explore the hydrophobization of unsized paper sheets via the gas phase. We employed three different compounds, namely palmitoyl chloride (PCl), trifluoroacetic anhydride/acetic anhydride (TFAA/Ac2O)) and hexamethyldisilazane (HMDS) which were vaporized and allowed to react with the paper sheets via the gas phase. All routes yielded hydrophobic papers with static water contact angles far above 90° and indicated the formation of covalent bonds. The PCl and TFAA approach negatively impacted the mechanical and optical properties of the paper leading to a decrease in tensile strength and yellowing of the sheets. The HMDS modified papers did not exhibit any differences regarding relevant paper technological parameters (mechanical properties, optical properties, porosity) compared to the non-modified sheets. XPS studies revealed that the HMDS modified samples have a rather low silicon content, pointing at the formation of submonolayers of trimethylsilyl groups on the fiber surfaces in the paper network. This was further investigated by penetration dynamic analysis using ultrasonication, which revealed that the whole fiber network has been homogeneously modified with the silyl groups and not only the very outer surface as for the PCl and the TFAA modified papers. This procedure yields a possibility to study the influence of hydrophobicity on paper sheets and their network properties without changing structural and mechanical paper parameters.
- Published
- 2021
11. Study of the metabolic alterations in patulin-induced neoplastic transformation in normal intestinal cells
- Author
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Neha Singh, Sanjeev K. Shukla, Gaurav Sharma, Indra Dev, and Kausar M. Ansari
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Paper ,0303 health sciences ,animal structures ,Cell growth ,Health, Toxicology and Mutagenesis ,Glyoxylate and dicarboxylate metabolism ,Metabolism ,Toxicology ,In vitro ,Patulin ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Metabolomics ,chemistry ,Biochemistry ,030220 oncology & carcinogenesis ,Cancer cell ,cardiovascular system ,Neoplastic transformation ,030304 developmental biology - Abstract
Several surveillance studies have reported significantly high level of patulin (PAT), mycotoxin in fruit juices suggesting the possible exposure to human. In vitro studies have showed that PAT can alter the permeability, ion transport and modulates tight junction of intestine. In real scenario, human can be exposed with low levels of PAT for longer duration through different fruits and their products. Hence, keeping this possibility in view, we conducted a study where normal intestinal cells were exposed with non-toxic levels of PAT for longer duration and found that PAT exposure causes cancer-like properties in normal intestinal cells. It is a well-known fact that cancer cells rewired their metabolism for cell growth and survival and metabolites closely depict the phenotypic properties of cells. Here, metabolomic study was performed in the PAT transformed and passage matched non-transformed cells using 1H HRMAS NMR. We have identified 12 significantly up-regulated metabolites, which, interestingly, were majorly amino acids, suggesting that PAT-induced pre-cancerous cells are involved in acquirement of nutrients for high protein turn-over. Furthermore, pathway analysis of metabolomics data indicated that aminoacyl tRNA biosynthesis, D-glutamate metabolism, glyoxylate and dicarboxylate metabolism and nitrogen metabolism were majorly hampered in PAT-induced pre-cancerous properties in normal intestinal cells.
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- 2021
12. Simple and Sensitive Detection of Bacterial Hydrogen Sulfide Production Using a Paper-Based Colorimetric Assay
- Author
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Byung-Ki Ahn, Yong-Jin Ahn, Young-Ju Lee, Yeon-Hee Lee, and Gi-Ja Lee
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Bacteria ,hydrogen sulfide ,bacteria ,paper ,colorimetric assay ,Colorimetry ,Hydrogen Sulfide ,Electrical and Electronic Engineering ,Sulfides ,Biochemistry ,Instrumentation ,Atomic and Molecular Physics, and Optics ,Analytical Chemistry ,Hydrogen - Abstract
Hydrogen sulfide (H2S) is known to participate in bacteria-induced inflammatory response in periodontal diseases. Therefore, it is necessary to quantify H2S produced by oral bacteria for diagnosis and treatment of oral diseases including halitosis and periodontal disease. In this study, we introduce a paper-based colorimetric assay for detecting bacterial H2S utilizing silver/Nafion/polyvinylpyrrolidone membrane and a 96-well microplate. This H2S-sensing paper showed a good sensitivity (8.27 blue channel intensity/μM H2S, R2 = 0.9996), which was higher than that of lead acetate paper (6.05 blue channel intensity/μM H2S, R2 = 0.9959). We analyzed the difference in H2S concentration released from four kinds of oral bacteria (Eikenella corrodens, Streptococcus sobrinus, Streptococcus mutans, and Lactobacillus casei). Finally, the H2S level in Eikenella corrodens while varying the concentration of cysteine and treatment time was quantified. This paper-based colorimetric assay can be utilized as a simple and effective tool for in vitro screening of H2S-producing ability of many bacteria as well as salivary H2S analysis.
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- 2022
13. Semi-enclosed paper sensor for highly sensitive and selective detection of proline
- Author
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Mallesh Santhosh and Tusan Park
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Isatin ,Paper ,Chitosan ,Proline ,Lab-On-A-Chip Devices ,Arabidopsis ,Environmental Chemistry ,Colorimetry ,Indicators and Reagents ,Biochemistry ,Spectroscopy ,Analytical Chemistry - Abstract
In the current study, we have utilized semi-enclosed, leak-proof, microfluidic paper-based analytical devices (μPAD's) modified with isatin conjugated chitosan as specific colorimetric reagent for the detection of proline. Proline is one of the globally accepted stress biomarker in plants and also one of the prominent amino acid present in wine and some processed food. Quantification of proline is regularly required in agriculture field, food and wine industries. Specific interaction of isatin with proline, uniform film forming ability of chitosan which results in uniform coloration and the presence of leak-proof layer which prevent the diffusion of colorimetric reagent deeper resulted in enhancement of color signal intensity at the reaction zone were utilized. Further, the images of the μPAD's were captured using smartphone with 3D printed imaging box which houses smartphone and μPAD's. This platform utilizes smartphone flash for uniform illumination and ensures constant positioning of μPAD's to capture images. This greatly enhances the sensitivity and accuracy of our platform. Compared to previously published highly sensitive multi-layer, paper-based platform for detection of proline, current method has enhanced detection range (∼7 fold) and has comparable limit of detection of 23.75 μM. Moreover, the developed μPAD's platform has reduced optimum reaction temperature and time compared to previous work. The developed paper based platform was utilized for evaluation of proline content in young Arabidopsis plants which are subjected to water stress for 5 days. The devised paper-based methods have the potential to be applicable for the on-site evaluation of various stresses in plants.
- Published
- 2022
14. Multicolorimetric ELISA biosensors on a paper/polymer hybrid analytical device for visual point-of-care detection of infection diseases
- Author
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Lei Ma, Yousef Abugalyon, and Xiujun Li
- Subjects
Paper ,Polymers ,Computer science ,Point-of-Care Systems ,Point-of-care detection ,Enzyme-Linked Immunosorbent Assay ,Biosensing Techniques ,02 engineering and technology ,Communicable Diseases ,Sensitivity and Specificity ,Multicolorimetric ELISA ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,Humans ,Disease biomarker ,Integrated processing ,Paper/polymer hybrid microfluidic device ,Horseradish Peroxidase ,High potential ,Point of care ,Detection limit ,Quantitative biomarker detection ,Infectious disease ,business.industry ,010401 analytical chemistry ,Hydrogen Peroxide ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Visual detection ,Embedded system ,Colorimetry ,Spectrophotometry, Ultraviolet ,Hepatitis C virus core Antigen ,0210 nano-technology ,business ,Biosensor ,Biomarkers ,Research Paper - Abstract
Graphical abstract Enzyme-linked immunosorbent assay (ELISA) is widely used for the detection of disease biomarkers. However, it utilizes time-consuming procedures and expensive instruments, making it infeasible for point-of-care (POC) analysis especially in resource-limited settings. In this work, a multicolorimetric ELISA biosensor integrated on a paper/polymer hybrid microfluidic device was developed for rapid visual detection of disease biomarkers at point of care, without using costly equipment. This multicolormetric ELISA platform was built on multiple distinct color variants resulted from the catalytic oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) and the etching of gold nanorods (AuNRs). The vivid color changes could be easily distinguished by the naked eye, and their red mean values allowed quantitative biomarker detection, without using any sophisticated instruments. When this multicolorimetric ELISA was integrated on a paper/polymer hybrid analytical device, it not only provided integrated processing and high portability but also enabled fast assays in about 50 min due to the unique advantages of paper/polymer hybrid devices. The limit of detection of 9.1 ng/μL of the hepatitis C virus core antigen, a biomarker for hepatitis C, was achieved using this multicolorimetric ELISA platform. This multicolor ELISA analytical device provides a new versatile, user-friendly, affordable, and portable immunosensing platform with high potential for on-site detections of various viruses, proteins, and biomarkers for low-resource settings such as at home, public venues, rural areas, and developing nations. Supplementary Information The online version contains supplementary material available at 10.1007/s00216-021-03359-8.
- Published
- 2021
15. Paper-Based Enzymatic Colorimetric Assay for Rapid Malathion Detection
- Author
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Xiao-Yan Zhang, Jian-Hui Li, Yunpeng Bai, Yu-Lian Zhao, and Xue-Lei Deng
- Subjects
Paper ,0106 biological sciences ,Analyte ,Immobilized enzyme ,Hydrolases ,Bioengineering ,Biosensing Techniques ,Poloxamer ,01 natural sciences ,Applied Microbiology and Biotechnology ,Biochemistry ,chemistry.chemical_compound ,010608 biotechnology ,Kinetic constant ,Molecular Biology ,Acrylic acid ,chemistry.chemical_classification ,Chromatography ,010405 organic chemistry ,Chemistry ,General Medicine ,Paper based ,Enzymes, Immobilized ,0104 chemical sciences ,Enzyme ,Malathion ,Colorimetry ,Biosensor ,Biotechnology - Abstract
Due to their unique properties, paper-based biosensors have attracted attention as inexpensive devices for on-site analysis. To achieve fast and sensitive detection of analytes, immobilization of enzymes with high apparent activities on paper is highly desirable; however, this is challenging. Herein, we report an improved approach to attach a malathion degrading enzyme, PoOPHM9, on paper via an interlocking network of Pluronic F127 (PF127)–poly(acrylic acid)–enzyme conjugates. The addition of PF127 improved retention of enzymatic activity as the apparent kinetic constant Vmax of the immobilized enzyme increased two-fold compared with the paper prepared without PF127. The PF127–poly(acrylic acid)–PoOPHM9 papers provided rapid colorimetric detection of malathion at 0.1–50 mM. The detection was completed within 5 min using a smartphone and image analysis software. As a proof-of-concept, malathion-contaminated water, plant, and apple samples were analyzed with the papers successfully. This material is promising for on-site rapid analysis of malathion-contaminated samples.
- Published
- 2021
16. Hydroquinone exposure accumulates neutral lipid by the activation of CDP-DAG pathway in Saccharomyces cerevisiae
- Author
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Vasanthi Nachiappan and Abhishek Raj
- Subjects
Paper ,chemistry.chemical_classification ,0303 health sciences ,Reactive oxygen species ,biology ,Chemistry ,Cellular respiration ,Health, Toxicology and Mutagenesis ,030302 biochemistry & molecular biology ,Saccharomyces cerevisiae ,Phospholipid ,Toxicology ,biology.organism_classification ,03 medical and health sciences ,chemistry.chemical_compound ,Biochemistry ,Apoptosis ,Lipid droplet ,Phosphatidylcholine ,Membrane biogenesis ,lipids (amino acids, peptides, and proteins) ,030304 developmental biology - Abstract
Benzene metabolites (HQ and BQ) are toxic compounds and their presence in human cause alteration in cellular respiration and kidney damage. In the current study, Saccharomyces cerevisiae has been used as a model organism and acute exposure of hydroquinone (HQ) decreased cell growth and increased reactive oxygen species (ROS). The expression of apoptosis regulatory genes (YCA1, NUC1, YSP1 and AIF1) were increased with HQ exposure in the wild-type cells. HQ exposure in the wild-type cells altered both the phospholipid and neutral lipid levels. Phosphatidylcholine is a vital membrane lipid that has a vital role in membrane biogenesis and was increased significantly with HQ. The neutral lipid results were supported with lipid droplets data and mRNA expression study. The phospholipid knockouts (Kennedy pathway) accumulated neutral lipids via the CDP-DAG (cytidine-diphosphate-diacylglycerol) pathway genes both in the presence and absence of HQ.
- Published
- 2021
17. Hypochlorous acid decreases antioxidant power, inhibits plasma membrane redox system and pathways of glucose metabolism in human red blood cells
- Author
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Asif Ali, Riaz Mahmood, and Irfan Qadir Tantry
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Paper ,chemistry.chemical_classification ,0303 health sciences ,Antioxidant ,biology ,Hypochlorous acid ,Health, Toxicology and Mutagenesis ,medicine.medical_treatment ,Inflammation ,Carbohydrate metabolism ,Toxicology ,Redox ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Enzyme ,Biochemistry ,chemistry ,030220 oncology & carcinogenesis ,Myeloperoxidase ,biology.protein ,medicine ,Glycolysis ,medicine.symptom ,030304 developmental biology - Abstract
Hypochlorous acid (HOCl) is generated at a high concentration by activated neutrophils at sites of inflammation in a myeloperoxidase catalyzed reaction. The increased and sustained production of HOCl at inflammatory sites may lead to tissue injury and this process is believed to play an important role in the progression of several diseases like chronic inflammation, atherosclerosis and some types of cancers. We have examined the effect of HOCl on human red blood cells (RBCs) under in vitro conditions. Treatment of RBC with different concentrations of HOCl (0.05–2.5 mM) at 37°C resulted in decreased activities of major antioxidant enzymes while the antioxidant power of RBC was weakened, as shown by lowered metal-reducing and free radical quenching ability of HOCl treated cells. RBC plasma membrane redox system was also inhibited suggesting membrane damage. The enzymes of glucose metabolism were inhibited indicating deranged energy metabolism. Electron microscopic images showed gross morphological changes in HOCl treated RBC. These results show that HOCl causes major alterations in the cellular antioxidant defense system and inhibition of glycolytic pathways, which increase the susceptibility of RBC to oxidative damage.
- Published
- 2021
18. Recent advances in lab-on-paper diagnostic devices using blood samples
- Author
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Hwee Yeong Ng, Wen-Chin Lee, Chien Te Lee, Chih-Yao Hou, and Lung-Ming Fu
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Paper ,Medical diagnostic ,medicine.medical_specialty ,Point-of-Care Systems ,Biomedical Engineering ,Bioengineering ,02 engineering and technology ,01 natural sciences ,Biochemistry ,Lab-On-A-Chip Devices ,Fabrication methods ,medicine ,Humans ,Medical physics ,Diabetes diagnosis ,business.industry ,010401 analytical chemistry ,General Chemistry ,Microfluidic Analytical Techniques ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Liver function ,Drug analysis ,0210 nano-technology ,business ,Capillary Action - Abstract
Lab-on-paper, or microfluidic paper-based analytical devices (μPADs), use paper as a substrate material, and are patterned with a system of microchannels, reaction zones and sensing elements to perform analysis and detection. The sample transfer in such devices is performed by capillary action. As a result, external driving forces are not required, and hence the size and cost of the device are significantly reduced. Lab-on-paper devices have thus attracted significant attention for point-of-care medical diagnostic purposes in recent years, particularly in less-developed regions of the world lacking medical resources and infrastructures. This review discusses the major advances in lab-on-paper technology for blood analysis and diagnosis in the past five years. The review focuses particularly on the many clinical applications of lab-on-paper devices, including diabetes diagnosis, acute myocardial infarction (AMI) detection, kidney function diagnosis, liver function diagnosis, cholesterol and triglyceride (TG) analysis, sickle-cell disease (SCD) and phenylketonuria (PKU) analysis, virus analysis, C-reactive protein (CRP) analysis, blood ion analysis, cancer factor analysis, and drug analysis. The review commences by introducing the basic transmission principles, fabrication methods, structural characteristics, detection techniques, and sample pretreatment process of modern lab-on-paper devices. A comprehensive review of the most recent applications of lab-on-paper devices to the diagnosis of common human diseases using blood samples is then presented. The review concludes with a brief summary of the main challenges and opportunities facing the lab-on-paper technology field in the coming years.
- Published
- 2021
19. An electricity- and instrument-free infectious disease sensor based on a 3D origami paper-based analytical device
- Author
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Chiao-Wen Chen, Wang-Huei Sheng, Chien-Fu Chen, Yuh-Shiuan Chien, Hao Yuan, and Chung-An Chen
- Subjects
Paper ,Computer science ,Real-time computing ,Biomedical Engineering ,Human immunodeficiency virus (HIV) ,Bioengineering ,02 engineering and technology ,medicine.disease_cause ,Communicable Diseases ,01 natural sciences ,Biochemistry ,Electricity ,Infectious disease diagnosis ,Lab-On-A-Chip Devices ,medicine ,Humans ,Instrumentation (computer programming) ,010401 analytical chemistry ,General Chemistry ,Paper based ,Microfluidic Analytical Techniques ,021001 nanoscience & nanotechnology ,Biocompatible material ,P24 antigen ,0104 chemical sciences ,Infectious disease (medical specialty) ,Timer ,0210 nano-technology - Abstract
Infectious diseases cause millions of deaths annually in the developing world. Recently, microfluidic paper-based analytical devices (μPADs) have been developed to diagnose such diseases, as these tests are low cost, biocompatible, and simple to fabricate. However, current μPADs are difficult to use in resource-limited areas due to their reliance on external instrumentation to measure and analyze the test results. In this work, we propose an electricity and external instrumentation-free μPAD sensor based on the colorimetric enzyme-linked immunosorbent assay (ELISA) for the diagnosis of infectious disease (3D-tPADs). Designed based on the principle of origami, the proposed μPAD enables the sequential steps of the colorimetric ELISA test to be completed in just ∼10 min. In addition, in order to obtain an accurate ELISA result without using any instrument, we have integrated an electricity-free "timer" within the μPAD that can be controlled by the buffer viscosity and fluid path volume to indicate the appropriate times for washing and color development steps, which can avoid false positive or false negative results caused by an extended or shortened amount of washing and development times. Due to the low background noise and high positive signal intensity of the μPAD, positive and negative detection results can be distinguished by just the naked eye. Furthermore, the ELISA result can be semi-quantified by comparing the results shown on the μPAD with a color chart diagram with a detection limit of HIV type 1(HIV-1) p24 antigen as low as 0.03 ng mL-1. These results demonstrate the proposed sensor can perform infectious disease diagnosis without external instrumentation or electricity, extending the application of the μPAD test for on-site detection and use in resource-limited settings.
- Published
- 2021
20. Detection of doxycycline hyclate and oxymetazoline hydrochloride in pharmaceutical preparations via spectrophotometry and microfluidic paper-based analytical device (μPADs)
- Author
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Jwan O. Abdulsattar, Alexander Iles, Nicole Pamme, Hind Hadi, and Samantha Richardson
- Subjects
Paper ,Microfluidics ,Oxymetazoline ,Excipient ,02 engineering and technology ,01 natural sciences ,Biochemistry ,Doxycycline Hyclate ,Analytical Chemistry ,Absorbance ,Spectrophotometry ,medicine ,Environmental Chemistry ,Oxymetazoline Hydrochloride ,Spectroscopy ,Detection limit ,Chromatography ,medicine.diagnostic_test ,Chemistry ,010401 analytical chemistry ,Microfluidic Analytical Techniques ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Nasal decongestant ,Pharmaceutical Preparations ,Doxycycline ,0210 nano-technology ,Colorimetric analysis ,medicine.drug - Abstract
There is growing demand for simple to operate, sensitive, on-site quantitative assays to investigate concentrations of drug molecules in pharmaceutical preparations for quality assurance. Here, we report on the development of two colorimetric analysis methods for the study the antibiotic doxycycline hyclate (DOX) and the nasal decongestant oxymetazoline hydrochloride (OXY), in solution as well as in their respective formulations. We compare a UV/vis spectrophotometry method with a color change recorded on a microfluidic paper-based analytical device (μPAD). Detection is based on the pharmaceutical compounds coupling with diazotized 4-aminoacetophenone (DAAP) under alkaline conditions to produce colored azo-dye products. These azo-compounds were monitored by absorbance at 425 nm for DOX and 521 nm for OXY, with linear calibration graphs in the concentration range of 0.5–35 mg L−1 (DOX) and 1.0–40 mg L−1 (OXY) and limits of detection of 0.24 mg L−1 (DOX) and 0.32 mg L−1 (OXY). For the μPAD method, color intensity was measured from photographs and a linear increase was observed at concentrations from above approximately 15 mg L−1 for both compounds and up to 35 mg L−1 for DOX and 40 mg L−1 for OXY. The developed methods were also applied to the formulated pharmaceuticals and no interference was found from the excipient. Thus, the paper-based device provides an inexpensive, simple alternative approach for use outside centralized laboratories with semi-quantitative capability.
- Published
- 2020
21. Starch-based nanospheres modified filter paper for o/w emulsions separation and contaminants removal
- Author
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Pixin Wang, Kun Xu, Ying Tan, Yungang Bai, Xiaopeng Pei, Baichao Zhang, Yinchuan Wang, Fan Zhang, Kankan Zhai, and Chao Wang
- Subjects
Paper ,Materials science ,Starch ,Portable water purification ,02 engineering and technology ,Substrate (printing) ,engineering.material ,Biochemistry ,Water Purification ,03 medical and health sciences ,chemistry.chemical_compound ,Coating ,Structural Biology ,Superhydrophilicity ,Molecular Biology ,030304 developmental biology ,0303 health sciences ,Filter paper ,General Medicine ,021001 nanoscience & nanotechnology ,Environmentally friendly ,Separation process ,chemistry ,Chemical engineering ,engineering ,Emulsions ,0210 nano-technology ,Filtration ,Nanospheres - Abstract
There is a pressing need around the world to develop novel functional biodegradable materials to separate oil/water mixtures and emulsions completely. Recently, superhydrophilicity and underwater superoleophobicity materials have been attracted attention due to their high efficiency in oil/water separation. However, it is still a challenge to prepare materials that combine oil/water separation and water purification in an environment-friendly way. In this work, biodegradable starch-based nanospheres (SNPs) coated filter paper was prepared in a low-cost, simple, and environmentally friendly manner. The SNPs coating could not only help to change the wettability of the substrate material but also build the hierarchical micro and nano structures which are conducive to separation and purification process. After modification by coating SNPs, the filter paper exhibited excellent performance in a wide range of oil/water mixtures or emulsions separation and the wettability of the filter paper could be regulated by adjusting the pH value. The modified filter paper presented good recyclability after several separation process. Furthermore, the as-prepared filter paper could also remove water-soluble contaminants during the oil/water separation process, thus realizing to combine separation and purification process in one single step. This biodegradable starch-based separating material with good separation performance, stability and recyclability has significant application potential in practical separation and purification process.
- Published
- 2020
22. Cellulosic paper with high antioxidative and barrier properties obtained through incorporation of tannin into kraft pulp fibers
- Author
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Yunzhong Ji, Liqiang Jin, Qinghua Xu, and Yingjuan Fu
- Subjects
Paper ,02 engineering and technology ,Biochemistry ,Antioxidants ,03 medical and health sciences ,chemistry.chemical_compound ,Structural Biology ,Tannin ,Cellulose ,Molecular Biology ,030304 developmental biology ,chemistry.chemical_classification ,0303 health sciences ,Papermaking ,Periodate ,General Medicine ,021001 nanoscience & nanotechnology ,Food packaging ,Cellulose fiber ,chemistry ,Kraft process ,Chemical engineering ,Cellulosic ethanol ,0210 nano-technology ,Tannins - Abstract
In this work, we prepared novel cellulosic paper by incorporating tannin into the kraft pulp for potential application in active food packaging. The kraft pulp fibers were firstly periodate oxidized to obtain the dialdehyde cellulosic fibers, and then reacted with varied dosages of tannin to incorporate them into the fibers by covalent bondings between aldehyde groups on cellulose and active hydrogen on tannin. Handsheets were prepared using the tannin incorporated fibers through papermaking process and the properties were characterized. The percentage of tannin in the paper increased with the increase of the tannin dosage. FT-IR spectra confirmed the successful incorporation of tannin into the cellulosic fibers. It was found that paper after incorporation of tannin turned to be surface hydrophobic with contact angles higher than 90°, which may probably due to the covalent bonds between tannin and cellulose. The handsheets show high antioxidative and UV-shielding properties, which both increased with the increase of the tannin percentage in the paper. Water vapor transmission rate (WVTR) decreased after the incorporation of tannin, and this could facilitate its application in food packaging. The breaking length of tannin incorporated paper decreased insignificantly, less than 10% with the tannin percentage as high as 45%.
- Published
- 2020
23. A review on cationic starch and nanocellulose as paper coating components
- Author
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Artur J.M. Valente, António P. Mendes de Sousa, Paulo Ferreira, Mohit Sharma, Roberto Aguado, and Dina Murtinho
- Subjects
Paper ,Flocculation ,Materials science ,Starch ,Context (language use) ,Nanotechnology ,02 engineering and technology ,engineering.material ,Biochemistry ,Nanocellulose ,03 medical and health sciences ,chemistry.chemical_compound ,Coating ,Structural Biology ,Cationic starch ,Cellulose ,Molecular Biology ,030304 developmental biology ,Paper coating ,0303 health sciences ,Printing quality ,Papermaking ,Cellulose nanocrystals ,Cationic polymerization ,General Medicine ,021001 nanoscience & nanotechnology ,Nanostructures ,chemistry ,engineering ,Cellulose nanofibrils ,0210 nano-technology - Abstract
Starch and derivatives thereof have proven their usefulness in paper coating processes. Among these derivatives, cationic starch has been widely used in the paper industry as a flocculation, dispersion and ink fixing agent. In another context, nanoscale cellulosic materials have been shown to improve the strength, retention of fillers, the barrier properties of packaging paper products, and printing qualities. This review summarizes the recent studies on the general components used in paper coating, describes the conventional and alternative synthetic processes of cationic starches and nanocellulose, and deals with their current and potential applications in papermaking, focusing primarily on surface treatments. Moreover, environmental applications have been considered to expand the understanding and usefulness of these materials. Further research on modified polysaccharides is encouraged to replace, in a feasible way, petro-based components of coating formulations, and to provide paper surfaces with new properties.
- Published
- 2020
24. Colorimetric Paper-Based Sensors against Cancer Biomarkers
- Author
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Mariana Carneiro, Maria Goreti Ferreira Sales, Ligia Rodrigues, Felismina Moreira, and Repositório Científico do Instituto Politécnico do Porto
- Subjects
Paper ,Point-of-Care Systems ,Cancer diagnosis ,Microfluidic Analytical Techniques ,Biochemistry ,Atomic and Molecular Physics, and Optics ,Analytical Chemistry ,Lab-On-A-Chip Devices ,Neoplasms ,Biomarkers, Tumor ,Colorimetry ,Paper-based devices ,Electrical and Electronic Engineering ,Instrumentation ,Colorimetric detection ,Biomarkers - Abstract
Cancer is a major cause of mortality and morbidity worldwide. Detection and quantification of cancer biomarkers plays a critical role in cancer early diagnosis, screening, and treatment. Clinicians, particularly in developing countries, deal with high costs and limited resources for diagnostic systems. Using low-cost substrates to develop sensor devices could be very helpful. The interest in paper-based sensors with colorimetric detection increased exponentially in the last decade as they meet the criteria for point-of-care (PoC) devices. Cellulose and different nanomaterials have been used as substrate and colorimetric probes, respectively, for these types of devices in their different designs as spot tests, lateral-flow assays, dipsticks, and microfluidic paper-based devices (μPADs), offering low-cost and disposable devices. However, the main challenge with these devices is their low sensitivity and lack of efficiency in performing quantitative measurements. This review includes an overview of the use of paper for the development of sensing devices focusing on colorimetric detection and their application to cancer biomarkers. We highlight recent works reporting the use of paper in the development of colorimetric sensors for cancer biomarkers, such as proteins, nucleic acids, and others. Finally, we discuss the main advantages of these types of devices and highlight their major pitfalls., This research was funded by Portuguese Foundation for Science and Technology (FCT), under the scope of the strategic funding of UIDB/04469/2020 unit and through Mariana Carneiro PhD grant reference SFRH/BD/131959/2017.
- Published
- 2022
25. Multimodal imaging of hemorrhagic transformation biomarkers in an ischemic stroke model
- Author
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M J Pushie, M Messmer, N J Sylvain, J Heppner, J M Newton, H Hou, M J Hackett, M E Kelly, and L Peeling
- Subjects
Paper ,Metals and Alloys ,Biophysics ,Hemorrhage ,Multimodal Imaging ,Biochemistry ,Brain Ischemia ,Stroke ,Biomaterials ,Chemistry (miscellaneous) ,Animals ,Humans ,Biomarkers ,Ischemic Stroke - Abstract
Hemorrhagic transformation of ischemic stroke has devastating consequences, with high mortality and poor functional outcomes. Animal models of ischemic stroke also demonstrate the potential for hemorrhagic transformation, which complicates biochemical characterization, treatment studies, and hinders poststroke functional outcomes in affected subjects. The incidence of hemorrhagic transformation of ischemic stroke in animal model research is not commonly reported. The postmortem brain of such cases presents a complex milieu of biomarkers due to the presence of healthy cells, regions of varying degrees of ischemia, dead and dying cells, dysregulated metabolites, and blood components (especially reactive Fe species released from lysed erythrocytes). To improve the characterization of hemorrhage biomarkers on an ischemic stroke background, we have employed a combination of histology, X-ray fluorescence imaging (XFI), and Fourier transform infrared (FTIR) spectroscopic imaging to assess 122 photothrombotic (ischemic) stroke brains. Rapid freezing preserves brain biomarkers in situ and minimizes metabolic artifacts due to postmortem ischemia. Analysis revealed that 25% of the photothrombotic models had clear signs of hemorrhagic transformation. The XFI and FTIR metabolites provided a quantitative method to differentiate key metabolic regions in these models. Across all hemorrhage cases, it was possible to consistently differentiate otherwise healthy tissue from other metabolically distinct regions, including the ischemic infarct, the ischemic penumbra, blood vessels, sites of hemorrhage, and a region surrounding the hemorrhage core that contained elevated lipid oxidation. Chemical speciation of deposited Fe demonstrates the presence of heme-Fe and accumulation of ferritin.
- Published
- 2022
26. Rapid segmentation and sensitive analysis of CRP with paper-based microfluidic device using machine learning
- Author
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Qihong Ning, Wei Zheng, Hao Xu, Armando Zhu, Tangan Li, Yuemeng Cheng, Shaoqing Feng, Li Wang, Daxiang Cui, and Kan Wang
- Subjects
Machine Learning ,Paper ,C-Reactive Protein ,Lab-On-A-Chip Devices ,Microfluidic Analytical Techniques ,Biochemistry ,Analytical Chemistry - Abstract
Microfluidic paper-based analytical devices (μPADs) have been widely used in point-of-care testing owing to their simple operation, low volume of the sample required, and the lack of the need for an external force. To obtain accurate semi-quantitative or quantitative results, μPADs need to respond to the challenges posed by differences in reaction conditions. In this paper, multi-layer μPADs are fabricated by the imprinting method for the colorimetric detection of C-reactive protein (CRP). Different lighting conditions and shooting angles of scenes are simulated in image acquisition, and the detection-related performance of μPADs is improved by using a machine learning algorithm. The You Only Look Once (YOLO) model is used to identify the areas of reaction in μPADs. This model can observe an image only once to predict the objects present in it and their locations. The YOLO model trained in this study was able to identify all the reaction areas quickly without incurring any error. These reaction areas were categorized by classification algorithms to determine the risk level of CRP concentration. Multi-layer perceptron, convolutional neural network, and residual network algorithms were used for the classification tasks, where the latter yielded the highest accuracy of 96%. It has a promising application prospect in fast recognition and analysis of μPADs.
- Published
- 2022
27. Rapid determination and continuous monitoring of propofol in microliter whole blood sample during anesthesia by paper spray ionization-mass spectrometry
- Author
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Ying-Lin Zhou, Ying Liu, Xin-Xiang Zhang, Wei-Dong Mi, Chang-Sheng Zhang, and Xiao-Hui Zhang
- Subjects
Paper ,Calibration curve ,Sedation ,02 engineering and technology ,Mass spectrometry ,01 natural sciences ,Biochemistry ,Mass Spectrometry ,Analytical Chemistry ,Limit of Detection ,medicine ,Humans ,Protein precipitation ,Propofol ,Monitoring, Physiologic ,Whole blood ,Detection limit ,Chemistry ,010401 analytical chemistry ,Continuous monitoring ,Reproducibility of Results ,Reference Standards ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Anesthesia ,medicine.symptom ,0210 nano-technology ,Anesthetics, Intravenous ,medicine.drug - Abstract
Propofol is a widely used intravenous anesthetic agent in sedation and general anesthesia. To improve the safety and maintain the depth of anesthesia, it is important to develop a rapid, sensitive, and reliable method to monitor the concentration of propofol in blood during anesthesia continuously. Here, we present a novel strategy based on paper spray ionization-mass spectrometry (PSI-MS) to detect propofol. Samples (in 10 μL) were mixed with methanol as protein precipitation solvent and 2,6-dimethylphenol as internal standard. Protein micro-precipitation was achieved with methanol by vortexing and centrifuging for 5 s each, and propofol was extracted to the supernatant. PSI-MS was performed in negative ionization mode, and MS signal lasted for 1 min. The analysis of a single sample was completed within 2 min. The area ratios of propofol to internal standard were calculated for quantification. Limit of detection of 5.5 ng mL−1 and limit of quantification of 18.2 ng mL−1 were achieved for propofol in whole blood. Calibration curve was linear in the range of 0.02–10 μg mL−1. The developed method was used successfully in monitoring the propofol concentration in 3 patients’ whole blood during anesthesia, showing its further application in controlling and feeding-back target concentration infusion.
- Published
- 2020
28. Inhibition of rat brain and human red cell acetylcholinesterase by thiocarbamate herbicides
- Author
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Edward A. Lock
- Subjects
Paper ,chemistry.chemical_classification ,biology ,Paraoxon ,Health, Toxicology and Mutagenesis ,Glutathione ,Toxicology ,Acetylcholinesterase ,Enzyme assay ,Thiocarbamate ,chemistry.chemical_compound ,Enzyme ,chemistry ,Biochemistry ,biology.protein ,medicine ,Thiocarbamates ,IC50 ,medicine.drug - Abstract
Thiocarbamates are a major class of herbicides that were used extensively in the agricultural industry. Toxicological evaluation showed molinate caused reproductive impairment in male rats, whilst others produced behavioural effects at high doses. Rats dosed with molinate either as a single large oral dose of 100 mg/kg or as multiple doses of 50 mg/kg for 7 days produced inhibition of brain acetylcholinesterase (AChE). Molinate and other thiocarbamate herbicides undergo metabolism to form sulphoxides that can carbamoylate thiol’s such as glutathione and proteins. We have chemically synthesised the sulphoxide and sulphone metabolites of six thiocarbamate herbicides and examined their ability to inhibit rat brain and human red cell AChE in vitro. Parent thiocarbamates were inactive, whilst the sulphoxides produced inhibition with IC50’s in the 1–10 mM range, the sulphone metabolites were the most active with IC50’s for molinate, pebulate, EPTC and vernolate in the μM range. Inhibition was both time- and dose-dependent with biomolecular rate constants for the inhibition of the human red cell enzyme of 0.3 × 102 and 2.0 × 102 M−1 min−1 for molinate sulphoxide and sulphone, respectively. No recovery of enzyme activity, with either enzyme, was seen following dilution of the inhibitor to a concentration that does not inhibit the enzyme for up to 24 h at 25°C at pH 7.4. The metabolites of these thiocarbamate herbicides are rather poor inhibitors of AChE when compared to the organophosphorus ester, paraoxon or the monomethylcarbamate, eserine. Unlike eserine the inhibition produced by the thiocarbamates is irreversible.
- Published
- 2020
29. Non-targeted detection and differentiation of agonists versus antagonists, directly in bioprofiles of everyday products
- Author
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Gertrud E. Morlock, Nele Hockamp, and Ines Klingelhöfer
- Subjects
Paper ,Bioanalysis ,medicine.drug_class ,Cosmetics ,Saccharomyces cerevisiae ,Endocrine Disruptors ,Proof of Concept Study ,Biochemistry ,Analytical Chemistry ,chemistry.chemical_compound ,Phenols ,Trenbolone ,Limit of Detection ,Androgen Receptor Antagonists ,medicine ,Humans ,Environmental Chemistry ,Bioassay ,Benzhydryl Compounds ,Spectroscopy ,Fluorescent Dyes ,Chromatography, Reverse-Phase ,Chromatography ,Chemistry ,Galactosides ,beta-Galactosidase ,Androgen ,Aliivibrio fischeri ,Bioactive compound ,Anti-Bacterial Agents ,Androgen receptor ,Receptors, Androgen ,Nandrolone ,Dihydrotestosterone ,Androgens ,Biological Assay ,Chromatography, Thin Layer ,Hymecromone ,medicine.drug - Abstract
Xenoestrogens exert antiandrogenic effects on the human androgen receptor. In the analytical field, such antagonists block the detection of testosterone and falsify results obtained by sum parameter assays. Currently, such agonistic versus antagonistic effects are not differentiated in complex mixtures. Oppositely acting hormonal effects present in products of everyday use can only be differentiated after tedious fractionation and isolation of the individual compounds along with subjection of each fraction/compound to the status quo bioassay testing. However, such long-lasting procedures are not suited for routine. Hence, we developed a fast bioanalytical tool that figures out agonists versus antagonists directly in complex mixtures. Exemplarily, 8 cosmetics and 15 thermal papers were analyzed. The determined antagonistic potentials of active compounds found were comparable to the ones of known antagonists (in reference shown for bisphenol A, 4-n-nonylphenol and four parabens). Relevant biological/chromatographic parameters such as cell viability, culture conditions, dose response curves, limits of biological detection/quantification and working range (shown for testosterone, dihydrotestosterone, nandrolone and trenbolone) were investigated to obtain the best sensitivity of the biological detection. The developed and validated method was newly termed reversed phase high-performance thin-layer chromatography planar yeast ant-/agonistic androgen screen (RP-HPTLC-pYAAS bioassay). Results were also compared with the RP-HPTLC-Aliivibrio fischeri bioassay (applied on RP plates for the first time). As proof-of-concept, the transfer to another bioassay (RP-HPTLC-pYES) was successfully demonstrated, analogously termed RP-HPTLC-pYAES bioassay detecting anti-/estrogens (exemplarily shown for evaluation of 4 pharmaceuticals used in breast cancer treatment). The new imaging concept provides (1) detection and differentiation of individual agonistic versus antagonistic effects in the bioprofiles, (2) bioanalytical quantification of their activity potential by scanning densitometry and (3) characterization of unknown bioactive compound zones by hyphenation to high-resolution mass spectrometry. Depending on the hormonal bioassay, 15 samples were analyzed in parallel within 5 h or 6 h (calculated as 20 or 24 min per sample). For the first time, piezoelectric spraying of the yeast cells was successfully demonstrated for the planar yeast–based bioassays.
- Published
- 2020
30. Microfluidic Paper-Based Analytical Device for Histidine Determination
- Author
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Yu Takano, Yasuhisa Nakano, Z. Hugh Fan, Toshikazu Nishida, Akimitsu Kugimiya, Jiro Kohda, Xiao Jiang, and Akane Fujikawa
- Subjects
Paper ,0106 biological sciences ,Fabrication ,Materials science ,Cost-Benefit Analysis ,Microfluidics ,Bioengineering ,01 natural sciences ,Applied Microbiology and Biotechnology ,Biochemistry ,Chemistry Techniques, Analytical ,law.invention ,Molybdenum blue ,Limit of Detection ,law ,Lab-On-A-Chip Devices ,010608 biotechnology ,Histidine ,Molecular Biology ,Filtration ,Chromatography ,010405 organic chemistry ,General Medicine ,Paper based ,0104 chemical sciences ,Biosensor ,Biotechnology - Abstract
A laminated paper-based analytical device (LPAD) for histidine detection was fabricated from a chromatography filtration paper and laminate films. Histidine recognition was effected by histidyl-tRNA synthetase (HisRS), and its detection was signaled colorimetrically based on the molybdenum blue reaction. The analytical conditions and detectable concentration range of histidine were examined. The method provided selective quantification from 1 to 100 μM histidine. LPAD fabrication is considerably simple, involving only the craft-cutting of the chromatography filtration paper and laminate film, and is cost-effective.
- Published
- 2020
31. Bladder cancer hunting: A microfluidic paper‐based analytical device
- Author
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Bo Liu, Tingting Han, Qingyun Jiang, Aziz Ur Rehman Aziz, Na Li, Haijun Ren, Zhengyao Zhang, and Hangyu Zhang
- Subjects
Paper ,medicine.medical_specialty ,Clinical Biochemistry ,Urology ,02 engineering and technology ,Urine ,Malignancy ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,Antigens, Neoplasm ,Lab-On-A-Chip Devices ,Biomarkers, Tumor ,Drug response ,Humans ,Medicine ,Bladder cancer ,medicine.diagnostic_test ,business.industry ,010401 analytical chemistry ,Nuclear Proteins ,Cancer ,Equipment Design ,Cystoscopy ,Paper based ,021001 nanoscience & nanotechnology ,medicine.disease ,0104 chemical sciences ,Urinary Bladder Neoplasms ,0210 nano-technology ,business - Abstract
Bladder cancer is the fourth most common cancer in men, and it is becoming a prevalent malignancy. Most of the regular clinical examinations are prompt evaluations with cystoscopy, renal function testing, which require high-precision instrument, well-trained operators, and high cost. In this study, a microfluidic paper-based analytical device (μPAD) was fabricated to detect nuclear matrix protein 22 (NMP22) and bladder cancer antigen (BTA) from the urine samples. Urine samples were collected from 11 bladder cancer patients and 10 well-beings as experiment and control groups, respectively, to verify the working efficiency of μPAD. A remarkable checkout efficiency of up to 90.91% was found from the results. Meanwhile, this method is feasible for home-based self-detection from urine samples within 10 min for the total process, which provides a new way for quick, economical, and convenient tumor diagnosis, prognosis evaluation, and drug response.
- Published
- 2020
32. The preparation of graphene ink from the exfoliation of graphite in pullulan, chitosan and alginate for strain-sensitive paper
- Author
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Kamal Yusoh, Nurul Farhana Abu Kasim, Wan Farhana W Idris, Abu Hannifa Abdullah, and Zulhelmi Ismail
- Subjects
Paper ,Materials science ,Alginates ,Sonication ,02 engineering and technology ,Biochemistry ,law.invention ,Chitosan ,03 medical and health sciences ,chemistry.chemical_compound ,Adsorption ,Structural Biology ,law ,Conductive ink ,Electric Impedance ,Graphite ,Glucans ,Molecular Biology ,030304 developmental biology ,0303 health sciences ,Graphene ,Pullulan ,General Medicine ,021001 nanoscience & nanotechnology ,Exfoliation joint ,chemistry ,Chemical engineering ,Ink ,Stress, Mechanical ,0210 nano-technology - Abstract
A sonication of graphite in polysaccharide (pullulan, chitosan and alginate) is one of the viable methods for the preparation of few-layer graphene. However, the effect of these adsorbed polysaccharides on the electrical performance of the produced graphene so far is not yet clear. In order to investigate the present effect of pullulan, chitosan and alginate on the electrical characteristic of resulted graphene, we have produced few-layer graphene using bath sonication of graphite in pullulan, chitosan and alginate medium for the application as electrical conductive ink in strain-sensitive. Data from the TEM reveals the appearance of folded few-layer graphene flakes after sonication for 150 min while the XPS data shows that the chitosan-based graphene possesses the highest carbon-oxygen ratio of 7.2 as compared to that of the pullulan and alginate-based graphene. By subjecting the produced graphene as the ink for paper-based strain sensor, we have discovered that the chitosan-graphene has the best resistivity value (1.66 × 10-3 Ω⋅cm) and demonstrate the highest sensitivity towards strain (GF: 18.6). This result interestingly implies the potential of the reported chitosan-based conductive ink as a strain-sensitive material for future food packaging.
- Published
- 2020
33. Paper-based colorimetric sensor for easy and simple detection of polygalacturonase activity aiming for diagnosis of Allium white rot disease
- Author
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Mi Rha Lee, Young-Soo Choi, Kwang-Yeol Yang, Cheol Soo Kim, and Kyeong-Hwan Lee
- Subjects
Paper ,02 engineering and technology ,Polygalacturonase activity ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,Colorimetric sensor ,Ascomycota ,Limit of Detection ,Spectrophotometry ,medicine ,Environmental Chemistry ,Pectinase ,Spectroscopy ,Plant Diseases ,Detection limit ,Chromatography ,medicine.diagnostic_test ,biology ,Chemistry ,010401 analytical chemistry ,021001 nanoscience & nanotechnology ,biology.organism_classification ,Plant disease ,0104 chemical sciences ,Polygalacturonase ,Allium ,Colorimetry ,0210 nano-technology ,Quantitative analysis (chemistry) - Abstract
Polygalacturonase (PG) activity in plants can serve as an important index for plant disease. However, the conventional method to detect PG activity is a complex process and requires a skilled technician and expensive analytical equipment. In this study, a paper-based colorimetric sensor was developed based on the principle of the ruthenium red (RR) dye method for easy and simple measurement of PG activity. The proposed paper-based sensor has a three-layer structure for detection of PG activity in samples. The sensor sensitivity was enhanced by optimizing the pH of the sodium acetate buffer used in polygalacturonic acid (PGA)-RR complex formation and the reaction temperature for PG and the PGA-RR complex. Further, for quantitative analysis of PG activity, Delta RGB analysis was conducted to detect color changes in the sensing window of the sensor. Results presented that the linear measurement range of the paper sensor was 0.02-0.1 unit with the limit of detection of 0.02 unit, which showed a similar detection range, but a lower detection limit, compared to the spectrophotometry. Furthermore, PG activity based on culture condition was measured using samples from Sclerotium cepivorum to verify the potential application of the developed paper-based sensor in the field. The measured activity showed no statistically significant difference from the values obtained from the spectrophotometry at 95% confidence level. Therefore, the paper-based colorimetric sensor can be used to predict plant diseases in Allium crops during the stage of pathogen invasion, potentially contributing to the improvement of crop production.
- Published
- 2020
34. High-strength paper enhanced by chitin nanowhiskers and its potential bioassay applications
- Author
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Congcan Shi, Junfei Tian, Jing Wu, Tang Hua, Minghui He, Guangxue Chen, and Li Dongjian
- Subjects
Paper ,Materials science ,Surface Properties ,Chitin ,02 engineering and technology ,Biochemistry ,Nanomaterials ,03 medical and health sciences ,chemistry.chemical_compound ,Structural Biology ,Wet strength ,Bioassay ,Surface charge ,Cellulose ,Molecular Biology ,030304 developmental biology ,0303 health sciences ,Temperature ,General Medicine ,021001 nanoscience & nanotechnology ,Nanostructures ,Cellulose fiber ,Chemical engineering ,chemistry ,Biological Assay ,0210 nano-technology - Abstract
In this paper, nanochitin was used as an alternative natural nanomaterial to combine with cellulose fibers for fabricating high-strength paper. Two typical chitin nanowhiskers having contrasting sign of surface charge were compared to evaluate the enhancement performance on paper in details. The results show that nanochitin with positive charges on the surface has a significant effect on the strength properties of the prepared paper, especially on wet strength. When the dosage of chitin nanowhiskers was 2%, the wet strength index was increased to 2.48 N·m/g, which is important for paper-based analytical devices with the common use in liquid analysis. Typical colorimetric glucose assays were successfully performed, suggesting the improved analytical performance on these prepared paper.
- Published
- 2020
35. Fast screening method for molecular recognition of islet amyloid polypeptide from whole blood samples collected from diabetic patients with disposable stochastic sensors obtained by nanolayer, and nanolayer by nanolayer deposition using cold plasma
- Author
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Ioana Popa-Tudor, A. Anghel, Raluca-Ioana Stefan-van Staden, and Marius Badulescu
- Subjects
Paper ,Silver ,Time Factors ,Materials science ,Plasma Gases ,Amyloid ,Early detection ,02 engineering and technology ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,Molecular recognition ,Limit of Detection ,Screening method ,Humans ,Deposition (phase transition) ,Whole blood ,geography ,Chromatography ,geography.geographical_feature_category ,010401 analytical chemistry ,Electrochemical Techniques ,Equipment Design ,Plasma ,021001 nanoscience & nanotechnology ,Islet ,Islet Amyloid Polypeptide ,Nanostructures ,0104 chemical sciences ,Diabetes Mellitus, Type 1 ,Diabetes Mellitus, Type 2 ,0210 nano-technology ,Porosity - Abstract
Nanolayer and nanolayer by nanolayer deposition of nanofilms of Ag and C using cold plasma in sequences (Ag, Ag-C, Ag-Ag-C), on porous paper, were used to design three disposable stochastic sensors for the assay of amyloid polypeptide from whole blood. The nanofilms were modified with α-cyclodextrin. The test developed using the nanofilm-based disposable stochastic sensors is used for early detection of diabetes. The wider linear concentration range (1.00 × 10−6–1.00 ng mL−1) and the lower limit of quantification (1.00 × 10−6ng mL−1) were obtained using the disposable stochastic sensors based on Ag-C and Ag-Ag-C, while the highest sensitivity (3.19 × 104 s−1/μg mL−1) was recorded using the disposable stochastic sensor based on Ag-Ag-C. The screening methods were fully validated using whole blood samples from confirmed patients, when the recovery of the islet amyloid polypeptide was higher than 98.00%.
- Published
- 2020
36. Comprehensive model of electromigrative transport in microfluidic paper based analytical devices
- Author
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Federico Schaumburg, Pablo A. Kler, and Claudio Luis Alberto Berli
- Subjects
Electrophoresis ,Paper ,Materials science ,Otras Ingenierías y Tecnologías ,Differential equation ,Capillary action ,Clinical Biochemistry ,Microfluidics ,INGENIERÍAS Y TECNOLOGÍAS ,02 engineering and technology ,ELECTROPHORESIS ,01 natural sciences ,Biochemistry ,Electromigration ,Analytical Chemistry ,Diffusion ,ELECTROOSMOTIC FLOW ,PAPER-BASED MICROFLUIDICS ,Diffusion (business) ,010401 analytical chemistry ,Electric Conductivity ,TRANSPORT PHENOMENA ,Mechanics ,Microfluidic Analytical Techniques ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Models, Chemical ,MATHEMATICAL MODELING ,Electric potential ,0210 nano-technology ,Transport phenomena ,Porous medium - Abstract
A complete mathematical model for electromigration in paper-based analytical devices is derived, based on differential equations describing the motion of fluids by pressure sources and EOF, the transport of charged chemical species, and the electric potential distribution. The porous medium created by the cellulose fibers is considered like a network of tortuous capillaries and represented by macroscopic parameters following an effective medium approach. The equations are obtained starting from their open-channel counterparts, applying scaling laws and, where necessary, including additional terms. With this approach, effective parameters are derived, describing diffusion, mobility, and conductivity for porous media. While the foundations of these phenomena can be found in previous reports, here, all the contributions are analyzed systematically and provided in a comprehensive way. Moreover, a novel electrophoretically driven dispersive transport mechanism in porous materials is proposed. Results of the numerical implementation of the mathematical model are compared with experimental data, showing good agreement and supporting the validity of the proposed model. Finally, the model succeeds in simulating a challenging case of free-flow electrophoresis in paper, involving capillary flow and electrophoretic transport developed in a 2D geometry. Fil: Schaumburg, Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina Fil: Kler, Pablo Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Centro de Investigaciones en Métodos Computacionales. Universidad Nacional del Litoral. Centro de Investigaciones en Métodos Computacionales; Argentina Fil: Berli, Claudio Luis Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina
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- 2020
37. USB powered microfluidic paper‐based analytical devices
- Author
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Cody S. Carrell, Pablo A. Kler, Charles S. Henry, Claudio Luis Alberto Berli, and Federico Schaumburg
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Paper ,Computer science ,Clinical Biochemistry ,Microfluidics ,INGENIERÍAS Y TECNOLOGÍAS ,02 engineering and technology ,USB ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,law.invention ,Electrolytes ,Electric Power Supplies ,law ,Separation zone ,PAPER-BASED MICROFLUIDICS ,Tecnología de Laboratorios Médicos ,Sensitivity (control systems) ,Electronics ,NUMERICAL PROTOTYPING ,Ingeniería Médica ,Isotachophoresis ,business.industry ,UNIVERSAL SERIAL BUS ,010401 analytical chemistry ,Equipment Design ,Paper based ,Microfluidic Analytical Techniques ,021001 nanoscience & nanotechnology ,Sample (graphics) ,0104 chemical sciences ,ISOTACHOPHORESIS ,0210 nano-technology ,business ,Computer hardware ,Communication channel - Abstract
Microfluidic paper-based analytical devices (μPADs) allow user-friendly and portable chemical determinations, although they provide limited applicability due to insufficient sensitivity. Several approaches have been proposed to address poor sensitivity in μPADs, but they frequently require bulky equipment for power and/or read-outs. Universal serial buses (USB) are an attractive alternative to less portable power sources and are currently available in many common electronic devices. Here, USB-powered μPADs (USB μPADs) are proposed as a fusion of both technologies to improve performance without adding instrumental complexity. Two ITP USB μPADs were developed, both powered by a 5 V potential provided through standard USB ports. The first device was fabricated using the origami approach. Its operation was analyzed experimentally and numerically, yielding a two-order-of-magnitude sample focusing in 15 min. The second ITP USB μPAD is a novel design, which was numerically prototyped with the aim of handling larger sample volumes. The reservoirs were moved away from the ITP channel and capillary action was used to drive the sample and electrolytes to the separation zone, predicting 25-fold sample focusing in 10 min. USB μPADs are expected to be adopted by minimally-trained personnel in sensitive areas like resource-limited settings, the point-of-care and in emergencies. Fil: Schaumburg, Federico. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina Fil: Kler, Pablo Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Centro de Investigaciones en Métodos Computacionales. Universidad Nacional del Litoral. Centro de Investigaciones en Métodos Computacionales; Argentina Fil: Carrell, Cody S.. State University of Colorado - Fort Collins; Estados Unidos Fil: Berli, Claudio Luis Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina Fil: Henry, Charles S.. State University of Colorado - Fort Collins; Estados Unidos
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- 2020
38. Preparation of cellulose nanocrystals based on waste paper via different systems
- Author
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Yi Jing, Xinyue Xing, Ying Han, and Qiwen Jiang
- Subjects
Paper ,Materials science ,Scanning electron microscope ,02 engineering and technology ,Biochemistry ,03 medical and health sciences ,chemistry.chemical_compound ,Hydrolysis ,Crystallinity ,X-Ray Diffraction ,Structural Biology ,Spectroscopy, Fourier Transform Infrared ,Thermal stability ,Fiber ,Cellulose ,Molecular Biology ,030304 developmental biology ,Waste Products ,0303 health sciences ,Sulfuric acid ,General Medicine ,Sulfuric Acids ,021001 nanoscience & nanotechnology ,chemistry ,Chemical engineering ,Ammonium Sulfate ,Thermogravimetry ,Nanoparticles ,Ammonium persulfate ,0210 nano-technology ,Oxidation-Reduction - Abstract
China, a big paper-making country, produced hundreds of millions of tons of waste paper which contain a lot of fiber every year. Cellulose nanocrystals were extracted from recycled waste paper which can be a high value utilization of secondary fiber. In this paper, cellulose nanocrystals were successfully extracted from waste paper fibers via two different systems, sulfuric acid hydrolysis (SCNCs) and one-step ammonium persulfate (APS) oxidation (OCNCs). This not only broadened the methods of extracting CNCs from waste paper, but also improved the dispersion and reactivity of CNCs. The CNCs products were investigated by FT-IR spectroscopy for functional group structure, X-ray diffraction for crystal structure, TG-DTG for thermal stability and scanning electron microscope, transmission electron microscope for morphology. The results showed that both OCNCs and SCNCs were a rod-like structure. The crystallinity of OCNCs and SCNCs increased to 72.45 and 77.56, but with a low yield of 22.42% and 41.22%, respectively. The result also suggested H2O2 formed by decomposition of APS, selectively oxidized the hydroxyl on the C6 in cellulose to carboxyl, introduced 0.57 mmol/g carboxyl. Successful preparation of CNCs extracted from waste paper can effectively utilize the fiber resources in waste paper, thus transforming into higher economic benefits.
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- 2020
39. A novel trimodal system on a paper-based microfluidic device for on-site detection of the date rape drug 'ketamine'
- Author
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Mahmoud A. Tantawy, Ali M. Yehia, and Mohamed A. Farag
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Paper ,Microfluidics ,Potentiometric titration ,Poison control ,Nanotechnology ,Biosensing Techniques ,02 engineering and technology ,USB ,Sensitivity and Specificity ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,law.invention ,Beverages ,chemistry.chemical_compound ,law ,Lab-On-A-Chip Devices ,Microchip Analytical Procedures ,Polyaniline ,Humans ,Environmental Chemistry ,Figure of merit ,Spectroscopy ,Optical Imaging ,010401 analytical chemistry ,Ketamine hydrochloride ,Reproducibility of Results ,Electrochemical Techniques ,021001 nanoscience & nanotechnology ,Chip ,0104 chemical sciences ,chemistry ,Rape ,Calibration ,Potentiometry ,Ketamine ,0210 nano-technology - Abstract
Paper-based microfluidic device was designed with wax-printing to combine potentiometric, fluorimetric and colorimetric detection zones. This newly developed trimodal paper chip has been used for on-site determination of ketamine hydrochloride (KET) as a date rape drug in beverages. The device employed polyaniline nano-dispersion as conducting polymer in ion sensing paper electrodes designed to fit USB plug connector. Carbon dots-gold nanoparticles and cobalt thiocyanate were used in fluorescence and color detection zones, respectively. Cellular phone's camera facilitated the on-site fluorimetric and color detection. The implemented trimodal detection system exhibited specificity for KET detection in the presence of several other beverage interferences i.e., biogenic amines. This innovative sensor brings together analytical figures of merit for effective KET detection in single aliquot of spiked beverages. The proposed paper-based chip also fulfils WHO criteria for point-of-care devices posing the proposed trimodal paper device as an active part for rapid, on-site drug diagnostics and to be applied further for other similar drugs.
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- 2020
40. Highly sensitive enclosed multilayer paper-based microfluidic sensor for quantifying proline in plants
- Author
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Cheol Soo Kim, Min Kyu Im, Mi Rha Lee, Young-Soo Choi, and Kyeong-Hwan Lee
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Paper ,Proline ,Surface Properties ,Microfluidics ,Arabidopsis ,Evaporation ,02 engineering and technology ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,chemistry.chemical_compound ,Environmental Chemistry ,Particle Size ,Spectroscopy ,Detection limit ,Wax ,Molecular Structure ,Chemistry ,fungi ,010401 analytical chemistry ,Ninhydrin ,food and beverages ,Microfluidic Analytical Techniques ,Contamination ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,visual_art ,visual_art.visual_art_medium ,Indicators and Reagents ,0210 nano-technology ,Biological system ,Quantitative analysis (chemistry) - Abstract
Free proline, termed proline, is a biomarker used for diagnosing drought stress in plants. A previously developed proline–ninhydrin reaction-based paper sensor could quickly and easily detect proline, but it was limited by low sensitivity. In this study, we developed an enclosed multilayer paper-based microfluidic sensor with high sensitivity for the quantitative detection of proline in plants. The multilayer paper-based sensor was manufactured using simple wax printing and origami methods, and contained an internal mixing channel to allow good mixing of the proline with ninhydrin, increasing the proline–ninhydrin reactivity and providing accurate and sensitive proline detection. By preloading ninhydrin onto the sample loading area, uniform coloration of the sensing window was achieved, allowing quantitative analysis of various proline concentrations using a constant reaction time. Only the sensing window and sample loading area were exposed to limit sample evaporation and contamination from the external environment. The LOD of the fabricated sensor was 23 μM, which is approximately 29-fold lower than that of the previously proposed paper sensor (657 μM). Samples were extracted from A. thaliana plants subjected to drought stress for proline detection. The proline concentrations measured using the developed paper sensor and a spectrophotometric method were not statistically significant at a confidence level of 95%. Therefore, the developed sensor can be applied to measure proline concentrations precisely in the field with a low detection limit. The developed paper-based sensor can be used to detect the early stages of drought in plants and thus improve crop productivity.
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- 2020
41. In Vitro Selection of a DNA Aptamer Targeting Degraded Protein Fragments for Biosensing
- Author
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John D. Brennan, Qiang Zhang, Yingfu Li, Meng Liu, Yangyang Chang, Dingran Chang, Christy Y. Hui, and Jiayi Wang
- Subjects
Paper ,Aptamer ,Clostridium difficile toxin B ,Biosensing Techniques ,Protein degradation ,010402 general chemistry ,01 natural sciences ,Catalysis ,law.invention ,Feces ,law ,Humans ,A-DNA ,Toxins, Biological ,010405 organic chemistry ,Chemistry ,General Medicine ,General Chemistry ,Aptamers, Nucleotide ,Clostridium difficile ,Peptide Fragments ,In vitro ,3. Good health ,0104 chemical sciences ,Biochemistry ,Proteolysis ,Recombinant DNA ,Biosensor - Abstract
Protein biomarkers often exist as degradation fragments in biological samples, and affinity agents derived using a purified protein may not recognize them, limiting their value for clinical diagnosis. Herein, we present a method to overcome this issue, by selecting aptamers against a degraded form of the toxin B protein, which is a marker for diagnosing toxigenic Clostridium difficile infections. This approach has led to isolation of a DNA aptamer that recognizes degraded toxin B, fresh toxin B, and toxin B spiked into human stool samples. DNA aptamers selected using intact recombinant toxin B failed to recognize degraded toxin B, which is the form present in stored stool samples. Using this new aptamer, we produced a simple paper-based analytical device for colorimetric detection of toxin B in stool samples, or in the NAP1 strain of Clostridium difficile. The combined aptamer-selection and paper-sensing strategy can expand the practical utility of DNA aptamers in clinical diagnosis.
- Published
- 2020
42. Paper-based nuclease protection assay with on-chip sample pretreatment for point-of-need nucleic acid detection
- Author
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Eka Noviana, Josephine Hofstetter, David S. Dandy, Sidhartha Jain, Charles S. Henry, and Brian J. Geiss
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Paper ,Point-of-Care Systems ,Sample (material) ,02 engineering and technology ,Computational biology ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,Nucleic acid thermodynamics ,chemistry.chemical_compound ,Limit of Detection ,Lab-On-A-Chip Devices ,Nucleic Acids ,Nucleic Acid Amplification Tests ,Oligonucleotide Array Sequence Analysis ,Chemistry ,010401 analytical chemistry ,Nuclease protection assay ,DNA ,Paper based ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Nucleic acid ,0210 nano-technology ,Nucleic acid detection - Abstract
Pathogen detection is crucial for human, animal, and environmental health; crop protection; and biosafety. Current culture-based methods have long turnaround times and lack sensitivity. Nucleic acid amplification tests offer high specificity and sensitivity. However, their cost and complexity remain a significant hurdle to their applications in resource-limited settings. Thus, point-of-need molecular diagnostic platforms that can be used by minimally trained personnel are needed. The nuclease protection assay (NPA) is a nucleic acid hybridization-based technique that does not rely on amplification, can be paired with other methods to improve specificity, and has the potential to be developed into a point-of-need device. In traditional NPAs, hybridization of an anti-sense probe to the target sequence is followed by single-strand nuclease digestion. The double-stranded target-probe hybrids are protected from nuclease digestion, precipitated, and visualized using autoradiography or other methods. We have developed a paper-based nuclease protection assay (PB-NPA) that can be implemented in field settings as the detection approach requires limited equipment and technical expertise. The PB-NPA uses a lateral flow format to capture the labeled target-probe hybrids onto a nitrocellulose membrane modified with an anti-label antibody. A colorimetric enzyme-substrate pair is used for signal visualization, producing a test line. The nuclease digestion of non-target and mismatched DNA provides high specificity while signal amplification with the reporter enzyme-substrate provides high sensitivity. We have also developed an on-chip sample pretreatment step utilizing chitosan-modified paper to eliminate possible interferents from the reaction and preconcentrate nucleic acids, thereby significantly reducing the need for auxiliary equipment. Graphical abstract.
- Published
- 2020
43. A facile microfluidic paper-based analytical device for acetylcholinesterase inhibition assay utilizing organic solvent extraction in rapid detection of pesticide residues in food
- Author
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Chen Wang, Qinqin Zheng, Jin Lili, Chengyin Lu, Xin Liu, Li Zhu, Zhenxia Hao, and Hongping Chen
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Paper ,Food Contamination ,02 engineering and technology ,01 natural sciences ,Biochemistry ,Analytical Chemistry ,chemistry.chemical_compound ,Carbaryl ,Phoxim ,Environmental Chemistry ,Acetonitrile ,Spectroscopy ,Chromatography ,Pesticide residue ,010401 analytical chemistry ,Extraction (chemistry) ,Organophosphate ,Pesticide Residues ,Microfluidic Analytical Techniques ,Pesticide ,021001 nanoscience & nanotechnology ,Acetylcholinesterase ,Organophosphates ,0104 chemical sciences ,Fruit and Vegetable Juices ,chemistry ,Malus ,Carbamates ,Cholinesterase Inhibitors ,Volatilization ,0210 nano-technology ,Food Analysis ,Water Pollutants, Chemical - Abstract
The incompatibility of most organic solvents with acetylcholinesterase (AChE) inhibition assay normally limits pesticide extraction efficiency in sample pretreatment, which might cause false negatives in real world sample assessment. Herein, a novel method has been developed for an improved AChE inhibition assay via organic solvent extraction combined spontaneous in situ solvent evaporation on microfluidic paper-based analytical devices. Enzyme pre-immobilization procedure was spared and AChE was added to the system after sampling step until a complete in-situ solvent evaporation process was performed on chip. IC50 levels of the six investigated organophosphate and carbamate pesticides indicated a completely eliminated influence of solvents on AChE behavior with the new method. Most importantly, analytical performances were significantly improved in food sample measurements. Reduction in matrix effect was observed when acetonitrile was adopted for lettuce sample pretreatment instead of water. Studies on different pesticides suggested a remarkably decreased discrimination effect on recoveries from sample pretreatment with the new developed method. The recovery level for phoxim spiked head lettuce samples reached (107.5 ± 14.2) %, in comparison with that of (18.6 ± 1.4) % from water-based extraction. Spiked water and apple juice samples with carbaryl concentration of as low as 0.02 mg L−1 were also successfully recognized with the present method by visual detection. This is the first report on direct sampling of organic extracts for AChE inhibition assay on-chip and it might provide a new perspective for real world sample assessments involving bio-reagents.
- Published
- 2020
44. An LC-MS/MS method for comparing the stability of ethanol's non-oxidative metabolites in dried blood spots during 90 days
- Author
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Hao Wang, Jing Chang, Jiaolun Li, Chengqiang Zhang, Zebin Lin, Yunfeng Zhang, Jingru Wang, Xinyu Zhang, Yulan Rao, Yi Zhang, and Zhibin Huang
- Subjects
Paper ,Time Factors ,Health (social science) ,Alcohol Drinking ,Glucuronates ,Alcohol ,Glycerophospholipids ,Sulfuric Acid Esters ,Toxicology ,Biochemistry ,Ethyl sulfate ,03 medical and health sciences ,Behavioral Neuroscience ,chemistry.chemical_compound ,0302 clinical medicine ,Ethyl glucuronide ,Drug Stability ,Tandem Mass Spectrometry ,Liquid chromatography–mass spectrometry ,Humans ,Desiccation ,Whole blood ,Detection limit ,Chromatography ,Ethanol ,Filter paper ,Fatty Acids ,General Medicine ,030227 psychiatry ,Neurology ,chemistry ,Oxidation-Reduction ,Biomarkers ,030217 neurology & neurosurgery ,Chromatography, Liquid - Abstract
Problems of stability were found for biomarkers of alcohol consumption: ethyl glucuronide (EtG), ethyl sulfate (EtS), phosphatidylethanols (PEths), and fatty acid ethyl esters (FAEEs) in whole blood. The purpose of this study was to establish a method for the determination of these four kinds of ethanol's non-oxidative metabolites in dried blood spots (DBS) by liquid chromatography tandem mass spectrometry (LC-MS/MS), and to evaluate their stability. In this method, 50 μL of human blood was spotted onto a filter paper for DBS analysis. Samples were extracted by methanol, reconstituted by 2-propanol, and injected into the LC-MS/MS system. Limits of detection were among 0.5–50 ng/mL, and deviations in accuracy and precision were all lower than 15% at three quality control levels. The stability of the four kinds of ethanol non-oxidative metabolites in DBS was investigated during a 90-day range under three temperatures, −20 °C, 4 °C, and 25 °C. EtG and EtS showed a high level of stability in DBS in the 90-day range, regardless of the temperature. FAEEs were unstable after three days. PEths showed stability within 15 days in postmortem DBS and 60 days in antemortem DBS, respectively, at all temperatures.
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- 2020
45. Paper-based colorimetric biosensor of blood alcohol with in-situ headspace separation of ethanol from whole blood
- Author
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Duangjai Nacapricha, Saranya Auparakkitanon, Thitaporn Sonsa-ard, Yanisa Thepchuay, Jirayu Sitanurak, and Nuanlaor Ratanawimarnwong
- Subjects
Paper ,Biosensing Techniques ,02 engineering and technology ,01 natural sciences ,Biochemistry ,Horseradish peroxidase ,Armoracia ,Analytical Chemistry ,Mice ,chemistry.chemical_compound ,Animals ,Environmental Chemistry ,Benzothiazoles ,Horseradish Peroxidase ,Spectroscopy ,Whole blood ,Chromatography ,Ethanol ,biology ,Filter paper ,Chemistry ,Chromogenic ,010401 analytical chemistry ,Reproducibility of Results ,021001 nanoscience & nanotechnology ,0104 chemical sciences ,Alcohol oxidase ,Alcohol Oxidoreductases ,Reagent ,biology.protein ,Colorimetry ,Indicators and Reagents ,Sulfonic Acids ,0210 nano-technology ,Biosensor - Abstract
This work presents a novel development that exploits the concept of in-situ gas-separation together with a specific enzymatic colorimetric detection to produce a portable biosensor called “Blood Alcohol Micro-pad” for direct quantitation of ethanol in whole blood. The thin square device (25 mm × 25 mm × 1.8 mm) comprises two layers of patterned filter paper held together with a double-sided mounting tape with an 8-mm circular hole (the headspace). In operation, the reagent is deposited on one layer and covered with sticky tape. Then 8 μL of a blood sample is dispensed onto the opposite layer and covered with sticky tape. Diffusion of ethanol across the 1.6 mm narrow headspace permits selective detection of ethanol by the enzymatic reagents deposited on the opposite layer. This reagent zone contains alcohol oxidase, horseradish peroxidase and 2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt, as the chromogenic reagent. The color intensity, measured from the recorded digital image, resulting from the enzymatic assay of ethanol, correlates with the concentration of blood alcohol. The results obtained with spiked mice and sheep blood samples, using an external calibration in the range of 1–120 mg dL−1ethanol, gave recoveries of 93.2–104.4% (n = 12). The “Blood Alcohol Micro-pad” gave good precision with %RSD
- Published
- 2020
46. Paper-based sol-gel thin films immobilized cytochrome P450 for enzyme activity measurement
- Author
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Nantana Nuchtavorn, Leena Suntornsuk, Mirek Macka, and Jiraporn Leanpolchareanchai
- Subjects
Paper ,Immobilized enzyme ,02 engineering and technology ,Catechu ,01 natural sciences ,Biochemistry ,Michaelis–Menten kinetics ,Analytical Chemistry ,Cytochrome P-450 Enzyme System ,Oxazines ,Benzene Derivatives ,Humans ,Environmental Chemistry ,Spectroscopy ,Eclipta prostrata ,chemistry.chemical_classification ,Detection limit ,Chromatography ,Molecular Structure ,biology ,010401 analytical chemistry ,Substrate (chemistry) ,Enzymes, Immobilized ,021001 nanoscience & nanotechnology ,biology.organism_classification ,Enzyme assay ,0104 chemical sciences ,Enzyme Activation ,Enzyme ,chemistry ,biology.protein ,0210 nano-technology ,Gels ,Ethers - Abstract
Cytochrome P450 (CYP450), and in particular CYP3A4, is the most abundantly expressed CYP450 isozyme implicated in many drug-drug and medicinal plant-drug interactions. Therefore, incorporation of CYP3A4 enzyme screening at an early stage of drug discovery is preferable in order to avoid enzymatic interactions. Here we present for the first time a paper-based CYP3A4 immobilized sol-gel-derived a platform using resorufin benzyl ether as a fluorogenic enzyme substrate used to investigate enzyme activity. The fluorescence intensity of the product can be simply quantified by using a handheld digital microscope and an image analysis software. The limit of quantitation was 0.35 μM with good precision (RSDs 0.05), while offering simplicity and lower cost. Kinetic parameters of the immobilized CYP3A4 in sol-gel coated paper were calculated from the Lineweaver-Burk plot, including Michaelis constant (Km) and maximum velocity (Vmax), which were 2.71 ± 0.35 μM and 0.43 ± 0.05 μM/min, respectively. Moreover, a functional test of these devices was conducted by assessments of known CYP3A4 inhibitors (i.e. ketoconazole, itraconazole) and inducers (i.e. phenytoin, carbamazepine). To further demonstrate the broad range of uses, the devices were utilized to assay plant extracts i.e. Areca catechu seeds, Camellia sinensis leaves, Eclipta prostrata aerial part, providing results in good agreement with previous studies. Furthermore, the sol-gel immobilized enzyme stored at 4 °C can increase storage stability, offering the activity of 86.3 ± 0.4% after 3-weeks storage, equivalent to the activity of the free enzyme solution after 1-week storage. The developed paper-based devices offer versatility, portability and low-cost.
- Published
- 2020
47. Evaluation of the fibrillation method on lignocellulosic nanofibers production from eucalyptus sawdust: A comparative study between high-pressure homogenization and grinding
- Author
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M. Àngels Pèlach, Helena Oliver-Ortega, Pere Mutjé, Sami Boufi, Marc Delgado-Aguilar, and Quim Tarrés
- Subjects
Paper ,Materials science ,Nanofibers ,02 engineering and technology ,Raw material ,Lignin ,Biochemistry ,Homogenization (chemistry) ,03 medical and health sciences ,chemistry.chemical_compound ,Structural Biology ,Homogenizer ,Recycling ,Cellulose ,Molecular Biology ,030304 developmental biology ,Eucalyptus ,0303 health sciences ,General Medicine ,021001 nanoscience & nanotechnology ,Pulp and paper industry ,Wood ,Grinding ,chemistry ,Nanofiber ,visual_art ,Pulverizer ,visual_art.visual_art_medium ,Sawdust ,0210 nano-technology - Abstract
The production of cellulose nanofibers (CNF) usually consist of two different phases. First of all, lignocellulosic fibers need to be treated by means of either chemical, enzymatic or mechanical treatments. Then, in the second phase, the treated lignocellulosic fibers need to be submitted to mechanical fibrillation. This last treatment is usually critical in terms of energy consumption, as well as for providing the appropriate characteristics to the resulting CNF. In the present work, we have investigated the effect of fibrillating lignocellulosic nanofibers (LCNF) made from eucalyptus sawdust by means of high-pressure homogenization and grinding. The obtained results showed that, to achieve the same property level of LCNF, the grinder consumed 12.86 kWh/kg, while the homogenizer, 19.07 kWh/kg, bringing to the light the suitability of grinding for LCNF production. Overall, the present work shows the feasibility of using eucalyptus sawdust, which is a residue from the pulp and paper industry, as raw material for LCNF production, at the same time that brings to the light the relevance of the fibrillation equipment in terms of energy efficiency, approaching the production of LCNF to the industry.
- Published
- 2020
48. A novel 3D paper-based microfluidic electrochemical glucose biosensor based on rGO-TEPA/PB sensitive film
- Author
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Guo-Cheng Han, Zhencheng Chen, Cheng Fang, Haolin Xiao, and Liangli Cao
- Subjects
Blood Glucose ,Paper ,Working electrode ,Biosensing Techniques ,Biochemistry ,Reference electrode ,Analytical Chemistry ,Glucose Oxidase ,Limit of Detection ,Humans ,Environmental Chemistry ,Glucose oxidase ,Sweat ,Spectroscopy ,Detection limit ,biology ,Chemistry ,Glucose meter ,Electrochemical Techniques ,Equipment Design ,Hydrogen Peroxide ,Microfluidic Analytical Techniques ,Enzymes, Immobilized ,Ethylenediamines ,Glucose ,Linear range ,Chemical engineering ,Printing, Three-Dimensional ,Electrode ,biology.protein ,Graphite ,Oxidation-Reduction ,Biosensor - Abstract
A novel 3D paper-based microfluidic screen-printed electrode (SPE) composed of two layers was constructed by photolithography and screen-printing technology. Aldehyde functionalized hydrophilic zone of the counter and reference electrodes layer was prepared for glucose oxidase immobilization. Highly conductive Prussian blue deposited reduced graphene oxide-tetraethylene pentamine (rGO-TEPA/PB) modified paper working electrode layer can be used as an electrochemical sensitive membrane for quantitative detection of hydrogen peroxide (H2O2), which was the enzyme-catalyzed reaction product. Therefore, this 3D paper-based microfluidic electrochemical biosensor can be used for quantitative detection of glucose. Under optimum conditions, the proposed biosensor can be used for quantitative determination of glucose over a wide linear range of 0.1 mM∼25 mM with detection limit of 25 μM. Finally, the 3D paper-based microfluidic electrochemical biosensor was applied to determine glucose in human sweat and blood, and the obtained results were in good consistency with values measured by Roche's blood glucose meter. In addition, the proposed 3D paper-based electrochemical device showed good repeatability, stability, and anti-interference, which would be of great potential to monitor glucose in complex biological fluids.
- Published
- 2020
49. Smartphone coupled with paper-based chemical sensor for on-site determination of iron(III) in environmental and biological samples
- Author
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Ramsingh Kurrey, Monisha, Indrapal Karbhal, Shamsh Pervez, Deepak Sinha, Goutam K. Patra, Bhuneshwari Sahu, Kamlesh Shrivas, Tushar Kant, and Manas Kanti Deb
- Subjects
Paper ,Analyte ,Materials science ,Iron ,010401 analytical chemistry ,Water ,Substrate (chemistry) ,02 engineering and technology ,021001 nanoscience & nanotechnology ,01 natural sciences ,Biochemistry ,Silver nanoparticle ,0104 chemical sciences ,Analytical Chemistry ,chemistry.chemical_compound ,Electron transfer ,chemistry ,Linear range ,Limit of Detection ,Bromide ,Deposition (phase transition) ,Smartphone ,0210 nano-technology ,Selectivity ,Nuclear chemistry - Abstract
We report a smartphone–paper-based sensor impregnated with cetyltrimethylammonium bromide modified silver nanoparticles (AgNPs/CTAB) for determination of Fe3+ in water and blood plasma samples. The methodology for determination of Fe3+ is based on the change in signal intensity of AgNPs/CTAB fabricated on a paper substrate after the deposition of analyte, using a smartphone followed by processing with ImageJ software. The mechanism of sensing for detection and determination of Fe3+ is based on the discoloration of AgNPs which impregnated the paper substrate. The discoloration is attributed to the electron transfer reaction taking place on the surface of NPs in the presence of CTAB. Fe3+ was determined when the paper was impregnated with 1 mM AgNPs for 5 min of reaction time and the substrate was kept under acidic conditions. The linear range for determination of total iron in terms of Fe3+ was 50–900 μg L−1 with a limit of determination (LOD) of 20 μg L−1 and coefficient of variation (CV) of 3.2%. The good relative recovery of 91.3–95.0% and interference studies showed the selectivity of the method for determination of total iron in water and blood plasma samples. Smartphone–paper-based sensors have advantages of simplicity, rapidity, user-friendliness, low cost, and miniaturization of the method for on-site determination of total iron compared to methods that require sophisticated analytical instruments.
- Published
- 2020
50. Paper-based electrodes modified with cobalt phthalocyanine colloid for the determination of hydrogen peroxide and glucose
- Author
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María Carmen Blanco-López, Agustín Costa-García, and A. Sánchez-Calvo
- Subjects
Paper ,Indoles ,Inorganic chemistry ,chemistry.chemical_element ,Biosensing Techniques ,Biochemistry ,Analytical Chemistry ,Catalysis ,Nanomaterials ,Glucose Oxidase ,chemistry.chemical_compound ,Organometallic Compounds ,Electrochemistry ,Environmental Chemistry ,Glucose oxidase ,Colloids ,Hydrogen peroxide ,Electrodes ,Spectroscopy ,biology ,Cellulose electrode ,Reproducibility of Results ,Electrochemical Techniques ,Hydrogen Peroxide ,Enzymes, Immobilized ,Fruit and Vegetable Juices ,Glucose ,chemistry ,Electrode ,Phthalocyanine ,biology.protein ,Nanoparticles ,Cobalt - Abstract
Cobalt(ii) phthalocyanine (CoPc) was suspended in aqueous medium and the colloidal system was used as catalyst for the electrochemical determination of hydrogen peroxide on paper-based electrodes modified with carbon nanomaterials. H2O2 was oxidised at 0.275 V vs. Ag pseudoreference electrode. This system was adapted to develop a glucose sensor with glucose oxidase immobilized on the cellulose electrode. CoPc suspended nanoparticles acted as nanoenzyme mimicking peroxidase activity and were combined with different carbon nanomaterials to form hybrids with optimised catalytic performance. GO-CoPc paper-based electrodes yielded the best results with a linear range of ∼12 μM to 49 mM for H2O2 and 0.1 mM to 1 mM for glucose. Glucose was determined in physiological serum and juice samples with recoveries of 93.3 and 94.2% respectively. CoPc could replace HRP for the catalytic sensing of H2O2, without the need to be dissolved. This material can be used in situ in a simple protocol with other nanomaterials for electrode modification. The sensor described has the advantage of easy preparation, using the catalyst in colloidal form, long term stability, and versatility to be adapted to other low cost and disposable enzymatic systems.
- Published
- 2020
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