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Coronavirus disease 2019 (COVID-19) has affected not only individual lives but also the world and global systems, both natural and human-made. Besides millions of deaths and environmental challenges, the rapid spread of the infection and its very high socioeconomic impact have affected healthcare, economic status and wealth, and mental health across the globe. To better appreciate the pandemic's influence, multidisciplinary and interdisciplinary approaches are needed. In this chapter, world-leading scientists from different backgrounds share collectively their views about the pandemic's footprint and discuss challenges that face the international community., (© 2024. The Author(s), under exclusive license to Springer Nature Switzerland AG.)

Under alkaline treatment, zirconyl chloride (ZrOCl 2 .8H 2 O) became a zirconia gel and formed a stable complex with beta-cyclodextrin (βCD). This complex was highly active in reactive oxygen species (ROS) formation via H 2 O 2 decomposition. Its surface with numerous hydroxyl groups acts as an ionic sponge to capture the charged reaction intermediates, including superoxide (O 2 -• ) and the hydroxyl radical ( • OH). ROS, especially • OH radicals, are harmful to living microorganisms because of their kinetic instability, high oxidation potential, and chemical nonselectivity. Therefore, • OH radicals can engage in fast reactions with virtually any adjacent biomolecule. With H 2 O 2 , the complex with cationic and hydrophobic moieties interacted with the anionic bacterial membrane of two Gram-positive ( Staphylococcus aureus and S. epidermidis ) and two Gram-negative ( Escherichia coli and Klebsiella pneumoniae ) strains. The Zr-βCD-H 2 O 2 also eradicated more than 99% of the biofilm of these four pathogens. Considering the difficult acquisition of resistance to the oxidation of • OH, the results suggested that this βCD-based nanomaterial might be a promising agent to target both drug-resistant pathogens with no cytotoxicity and exceptional antimicrobial activity.

Perchlorate, ClO 4 - , with diverse applications, has become one of the major contaminants in surface and groundwater sources. This highly soluble and stable anion poses a considerable threat to human health given that it contaminates drinking water, vegetables, milk, and other contaminated food products. ClO 4 - can impair the thyroid function; thus, drinking water with high levels of this anion is a severe problem worldwide. However, due to the high solubility, stability, and mobility of ClO 4 - , its remediation and monitoring remain a major challenge. Considering the various analytical methods, including electrochemistry, each method has advantages and disadvantages in terms of detection sensitivity, selectivity, analysis time, and cost. Also, sample preconcentration and clean-up must be performed for the analysis of more complex matrices such as food and biological samples to ensure a low detection limit and selectivity. Both ion chromatography (IC) and capillary electrophoresis (CE) coupled with electrochemical detection, in addition to liquid chromatography (LC)-mass spectrometry (MS), are expected to play key roles due to their lower detection limit with excellent sensitivities and selectivity. Herein, we also discuss the perspective on various electrode materials for the detection of ClO 4 - regarding whether ClO 4 - can be measured at the lowest levels with the highest selectivity.

Under ultrasonication, cuprous oxide (Cu 2 O) microparticles (<5 µm) were fragmented into nanoparticles (NPs, ranging from 10 to 30 nm in diameter), and interacted strongly with alkali lignin (Mw = 10 kDa) to form a nanocomposite. The ultrasonic wave generates strong binding interaction between lignin and Cu 2 O. The L-Cu nanocomposite exhibited synergistic effects with enhanced antibiofilm activities against E. coli, multidrug-resistant (MDR) E. coli, S. aureus (SA), methicillin-resistant SA, and P. aeruginosa (PA). The lignin-Cu 2 O (L-Cu) nanocomposite also imparted notable eradication of such bacterial biofilms. Experimental evidence unraveled the destruction of bacterial cell walls by L-Cu, which interacted strongly with the bacterial membrane. After exposure to L-Cu, the bacterial cells lost the integrated structural morphology. The estimated MIC for biofilm inhibition for the five tested pathogens was 1 mg/mL L-Cu (92 % lignin and 8 % Cu 2 ONPs, w/w %). The MIC for bacterial eradication was noticeably lower; 0.3 mg/mL (87 % lignin + 13 % Cu 2 ONPs, w/w %) for PA and SA, whereas this value was appreciably higher for MDR E. coli (0.56 mg/mL, 86 % lignin and 14 % Cu 2 O NPs). Such results highlighted the potential of L-Cu as an alternative to neutralize MDR pathogens., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022. Published by Elsevier B.V.)

Carbon dots (CDs) were simply prepared from charcoal by hydrothermal processing at 180 °C for 15 h without any chemicals. The as-prepared CDs with an average diameter of 5 ± 6 nm exhibited a predominant absorption peak at 290 nm, corresponding to the n to π* transition of the oxygen functional groups (C═O) and the free amine functional groups (-NH 2 ). The resulting CDs were then incorporated into cotton and polyester by facile ultrasonication for 1 h. The obtained CD-coated fabrics were first evaluated for their UV-blocking capability and then for their antibacterial properties against two model pathogens: Gram-negative E. coli and Gram-positive S. aureus . Both cotton and polyester showed no UV protection at 280 or 380 nm; conversely, cotton or polyester decorated with CDs exhibited a UV blocking ratio of 82-98%. The CD-coated fabrics showed 100% antibacterial activities against E. coli and S. aureus, whereas the pristine fabrics showed no effect. The CDs/fabrics could adsorb Hg 2+ and Fe 3+ , resulting in a drastic fluorescence quenching. As such, this distinct feature was exploited for the removal and detection of these two ions with the limits of detection of 55and 72 μM, respectively.

Numerous epithelial cells and sometimes leukocytes release AMPs as their first line of defense. AMPs encompass cationic histatins, defensins, and cathelicidin to encounter oral pathogens with minimal resistance. However, their concentrations are significantly below the effective levels and AMPs are unstable under physiological conditions due to proteolysis, acid hydrolysis, and salt effects. In parallel to a search for more effective AMPs from natural sources, considerable efforts have focused on synthetic stable and low-cytotoxicy AMPs with significant activities against microorganisms. Using natural AMP templates, various attempts have been used to synthesize sAMPs with different charges, hydrophobicity, chain length, amino acid sequence, and amphipathicity. Thus far, sAMPs have been designed to target Streptococcus mutans and other common oral pathogens. Apart from sAMPs with antifungal activities against Candida albicans , future endeavors should focus on sAMPs with capabilities to promote remineralization and antibacterial adhesion. Delivery systems using nanomaterials and biomolecules are promising to stabilize, reduce cytotoxicity, and improve the antimicrobial activities of AMPs against oral pathogens. Nanostructured AMPs will soon become a viable alternative to antibiotics due to their antimicrobial mechanisms, broad-spectrum antimicrobial activity, low drug residue, and ease of synthesis and modification.

Considering the global spread of bacterial infections, the development of anti-biofilm surfaces with high antimicrobial activities is highly desired. This work unraveled a simple, sonochemical method for coating Cu 2 O nanoparticles (NPs) on three different flexible substrates: polyester (PE), nylon 2 (N2), and polyethylene (PEL). The introduction of Cu 2 O NPs on these substrates enhanced their surface hydrophobicity, induced ROS generation, and completely inhibited the growth of sensitive ( Escherichia coli and Staphyloccocus aureus ) and drug-resistant (MDR E. coli and MRSA) planktonic and biofilm. The experimental results confirmed that Cu 2 O-PE exhibited complete biofilm mass reduction ability for all four strains, whereas Cu 2 O-N2 showed more than 99% biomass inhibition against both drug-resistant and sensitive pathogens in 6 h. Moreover, Cu 2 O-PEL also indicated a 99.95, 97.73, 98.00, and 99.20% biomass reduction of MRSA, MDR E. coli , E. coli , and S. aureus , respectively. All substrates were investigated for time-dependent inhibitions, and the associated biofilm mass and log reduction were evaluated. The mechanisms of Cu 2 O NP action against the mature biofilms include the generation of reactive oxygen species (ROS) as well as electrostatic interaction between Cu 2 O NPs and bacterial membranes. The current study could pave the way for the commercialization of sonochemically coated Cu 2 O NP flexible substrates for the prevention of microbial contamination in hospitals and industrial environments.

The growth of industrialization and the population has increased the usage of fossil fuels, resulting in the emission of large amounts of CO 2. This serious environmental issue can be abated by using sustainable and environmentally friendly materials with promising novel and superior performance as an alternative to petroleum-based plastics. Emerging nanomaterials derived from abundant natural resources have received considerable attention as candidates to replace petroleum-based synthetic polymers. As renewable materials from biomass, cellulose nanocrystals (CNCs) nanomaterials exhibit unique physicochemical properties, low cost, biocompatibility and biodegradability. Among a plethora of applications, CNCs have become proven nanomaterials for energy applications encompassing energy storage devices and supercapacitors. This review highlights the recent research contribution on novel CNC-conductive materials and CNCs-based nanocomposites, focusing on their synthesis, surface functionalization and potential applications as supercapacitors (SCs). The synthesis of CNCs encompasses various pretreatment steps including acid hydrolysis, mechanical exfoliation and enzymatic and combination processes from renewable carbon sources. For the widespread applications of CNCs, their derivatives such as carboxylated CNCs, aldehyde-CNCs, hydride-CNCs and sulfonated CNC-based materials are more pertinent. The potential applications of CNCs-conductive hybrid composites as SCs, critical technical issues and the future feasibility of this endeavor are highlighted. Discussion is also extended to the transformation of renewable and low-attractive CNCs to conductive nanocomposites using green approaches. This review also addresses the key scientific achievements and industrial uses of nanoscale materials and composites for energy conversion and storage applications.

Carbon dots (CDs) and their doped counterparts including nitrogen-doped CDs (N@CDs) have been synthesized by bottom-up or top-down approaches from different precursors. The attractiveness of such emerging 2D‑carbon-based nanosized materials is attributed to their excellent biocompatibility, preparation, aqueous dispersibility, and functionality. The antimicrobial, optical, and electrochemical properties of CDs have been advocated for two important biotechnological applications: bacterial eradication and sensing/biosensing. CDs as well as N@CDs act as antimicrobial agents as their surfaces encompass functional hydroxyl, carboxyl, and amino groups that generate free radicals. As a new class of photoluminescent nanomaterials, CDs can be employed in diversified analytics. CDs with surface carboxyl or amino groups form nanocomposites with nanomaterials or be conjugated with biorecognition molecules toward the development of sensors/biosensors. The deployment of conductive CDs in electrochemical sensing has also increased significantly because of their quantum size, excellent biocompatibility, enzyme-mimicking activity, and high surface area. The review also addresses the ongoing challenges and promises of CDs in pathogenesis and analytics. Perspectives on the future possibilities include the use of CDs in microbial viability assay, wound healing, antiviral therapy, and medical devices., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Rapid detection of human coronavirus disease 2019, termed as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) or COVID-19 infection, is urgently needed for containment strategy owing to its unprecedented spreading. Novel biosensors can be deployed in remote clinical settings without central facilities for infection screening. Electrochemical biosensors serve as analytical tools for rapid detection of viral structure proteins, mainly spike (S) and nucleocapsid (N) proteins, human immune responses, reactive oxygen species, viral ribonucleic acid, polymerase chain reaction by-products, and other potential biomarkers. The development of point-of-care testing devices is challenging due to the requirement of extensive validation, a time-consuming and expensive step. Together with specific biorecognition molecules, nanomaterial-based biosensors have emerged for the fast detection of early viral infections., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this article., (© 2021 Elsevier B.V. All rights reserved.)

Rapid and simple electroanalysis of acrylamide (ACR) was feasible by a gold electrode modified with gold nanoparticles (AuNPs) and dithiothreitol (DTT) with enhanced detection sensitivity and selectivity. The roughness of bare gold (Au) increased from 0.03 μm to 0.04 μm when it was decorated with AuNPs. The self-assembly between DTT and AuNPs resulted in a surface roughness of 0.09 μm. The DTT oxidation occurred at +0.92 V. The Au/AuNPs/DTT surface exhibited a surface roughness of 0.24 μm after its exposure to ACR with repeated analysis. SEM imaging illustrated the formation of a polymer layer on the Au/AuNPs/DTT surface. Surface plasmon resonance analysis confirmed the presence of AuNPs and DTT on the gold electrode and the binding of ACR to the electrode's active surface area. The peak area obtained by differential pulse voltammetry was inversely proportional to the ACR concentrations. The limit of detection (LOD) and the limit of quantitation (LOQ) were estimated to be 3.11 × 10 -9 M and 1 × 10 -8 M, respectively, with wide linearity ranging from 1 × 10 -8 M to 1 × 10 -3 M. The estimated levels of ACR in potato chips and coffee samples by the sensor were in agreement with those of high-performance liquid chromatography.

Polypyrrole (PPY) spherical particles synthesized using carbon dots as an efficient catalyst were strongly embedded on fluorinated nonwoven fabric by ultrasonication to form a membrane with high hydrophilicity. An optimal amount of PPY adhered to the membrane after 30 min of sonication enhanced the overall membrane area with high hydrophilicity. Oil with high hydrophobicity was repelled by the resulting membrane, whereas water was freely penetrated and diffused from the membrane. The membrane exhibited good reusability and efficiency for the recovery of oil from a cooking oil-water mixture within 30 s. The incorporation of PPY in the fluorinated fabric imparts significant antibacterial properties against two common pathogens, Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive). The anti-biofouling membrane could pave the way for its potential application to separate spilled oil from contaminated waters, comprising different microorganisms and living species. The novelty of this manuscript is described in a new system, the fabrication of PPY membranes with two important properties: biocidal and oil/water separation., (Copyright © 2021. Published by Elsevier B.V.)

Molecular diagnostics has been the front runner in the world's response to the COVID-19 pandemic. Particularly, reverse transcriptase-polymerase chain reaction (RT-PCR) and the quantitative variant (qRT-PCR) have been the gold standard for COVID-19 diagnosis. However, faster antigen tests and other point-of-care (POC) devices have also played a significant role in containing the spread of SARS-CoV-2 by facilitating mass screening and delivering results in less time. Thus, despite the higher sensitivity and specificity of the RT-PCR assays, the impact of POC tests cannot be ignored. As a consequence, there has been an increased interest in the development of miniaturized, high-throughput, and automated PCR systems, many of which can be used at point-of-care. This review summarizes the recent advances in the development of miniaturized PCR systems with an emphasis on COVID-19 detection. The distinct features of digital PCR and electrochemical PCR are detailed along with the challenges. The potential of CRISPR/Cas technology for POC diagnostics is also highlighted. Commercial RT-PCR POC systems approved by various agencies for COVID-19 detection are discussed.

Nitrogen-doped carbon nanodots (N@CDs) were prepared by hydrothermal processing of bovine serum albumin (Mw: 69,324 with 607 amino acids). A polyaniline (PANI-N@CDs) nanocomposite was then synthesized by ultrasonication and used to degrade Congo red (CR), methylene blue (MB), Rhodamine B (RhB), and crystal violet (CV) four common organic dyes. The PANI-N@CD nanocomposite simultaneously adsorbed and concentrated the dye from the bulk solution and degraded the adsorbed dye, resulting in a high rate of dye degradation. The combination of holes (h+), hydroxyl (OH • ), and O 2 •- was involved in the N@CD-mediated photocatalytic degradation of the dyes. Under visible light illumination at neutral pH, the PANI-N@CDs were proven as an efficient adsorbent and photocatalyst for the complete degradation of CR within 20 min. MB and RhB were also degraded but required longer treatment times. These findings supported the design of remediation processes for such dyes and predicted their fate in the environment. The nanocomposite also exhibited antimicrobial activities against Gram-negative bacterium E. coli and Gram-positive bacterium S. aureus .

Carbon dots (CDs) were obtained from medicinal turmeric leaves ( Curcuma longa ) by a facile one-step hydrothermal method and evaluated for their bactericidal activities against two gram-negative; Escherichia coli , Klebsiella pneumoniae , and two gram-positive counterparts; Staphylococcus aureus , S. epidermidis . The CDs exhibited spherical shapes with a mean size of 2.6 nm. The fluorescence spectra of CDs revealed intense fluorescence at λ ex / em = 362/429 nm with a bright blue color in an aqueous solution. The CDs showed strong photostability under various environmental conditions (pH, salt, and UV-radiation). The complete bactericidal potency of CDs was 0.25 mg/mL for E.coli and S. aureus after 8 h of exposure, while for K. pneumoniae , and S. epidermidis , the CDs at 0.5 mg/mL good antibacterial effect within 8 h and complete eradication after 24 h of exposure is observed. The release of reactive oxygen species played a crucial role in the death of the bacterial cell. The present study provides a strategy for the preparation of CDs from a medicinal plant and their potential antibacterial activities against four common contagious pathogens.

The synthesis of nitrogen-doped carbon dots (N@CDs) was accomplished by a hydrothermal process using meta - phenylenediamine as a source of carbon and nitrogen. As prepared N@CDs exhibited bright blue color fluorescence emission (λ ex = 340 nm and λ em = 420 nm) with a quantum yield of 12%. Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus were eradicated by N@CDs with a minimum inhibition concentration (MIC) of 1 and 0.75 mg/mL, respectively. The N@CDs were also proven as nanovesicles for drug molecules where the drug release displayed a sustained time-dependent profile at the physiological condition. The release of ciprofloxacin as a model drug was governed by the Korsmeyer-Peppas model, indicating ∼60% of its release from the N@CD conjugated drug system at the physiological pH. Selective analysis of trinitrophenol (TNP), a popular explosive, was achieved by fluorescence quenching of N@CDs, compared favorably with other nitrophenols. An estimated detection limit of TNP was 2.45 μM with a linear response spanning from 1 to 75 μM.

Conducting polymers (CPs) have been at the center of research owing to their metal-like electrochemical properties and polymer-like dispersion nature. CPs and their composites serve as ideal functional materials for diversified biomedical applications like drug delivery, tissue engineering, and diagnostics. There have also been numerous biosensing platforms based on polyaniline (PANI), polypyrrole (PPY), polythiophene (PTP), and their composites. Based on their unique properties and extensive use in biosensing matrices, updated information on novel CPs and their role is appealing. This review focuses on the properties and performance of biosensing matrices based on CPs reported in the last three years. The salient features of CPs like PANI, PPY, PTP, and their composites with nanoparticles, carbon materials, etc. are outlined along with respective examples. A description of mediator conjugated biosensor designs and enzymeless CPs based glucose sensing has also been included. The future research trends with required improvements to improve the analytical performance of CP-biosensing devices have also been addressed., Competing Interests: The authors declare no conflict of interest.

Polypyrrole grafted with chitosan (PPy-g-CS) and poly (pyrrole-N-(1-naphthyl) ethylenediamine, a copolymer, (COP) have been synthesized by a one-step microwave procedure with carbon dots(C-Dots) as initiators. The electrostatic interaction between the positively charged polymers and negatively charged microbial cell membranes is widely anticipated to be responsible for cellular lysis. However, Escherichia coli exposed to PPy-g-CS (zeta potential = +46.9 mV) was completely perished after 3 h while COP (zeta potential = +64.1 mV) exhibited no antimicrobial effect. The two polymers were capable of eradicating Staphylococcus aureus, implying the charged effect is the main mechanism of cell death. The two polymers could also chelate calcium and other nutrients as well as form an external barrier to suppress the penetration of essential nutrients to support microbial survival and proliferation. In particular, pyrrole grafted chitosan was reasoned to stack onto the bacterial surface to impede the mass transfer and suppress the bacterial metabolic activity. The binding of chitosan to teichoic acids, essential acids of Gram-positive bacteria, would provoke a sequence of events and lead to bacterial death., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

CuO, TiO 2, or SiO 2 was decorated on polyaniline (PANI) by a sonochemical method, and their antimicrobial properties were investigated for two common Gram-negative pathogens: Pseudomonas aeruginosa (PA) and Klebsiella pneumoniae (KP). Without PANI, CuO, TiO 2 , or SiO 2 with a concentration of 220 µg/mL exhibited no antimicrobial activities. In contrast, PANI-CuO and PANI-TiO 2 (1 mg/mL, each) completely suppressed the PA growth after 6 h of exposure, compared to 12 h for the PANI-SiO 2 at the same concentration. The damage caused by PANI-SiO 2 to KP was less effective, compared to that of PANI-TiO 2 with the eradication time of 12 h versus 6 h, respectively. This bacterium was not affected by PANI-CuO. All the composites bind tightly to the negative groups of bacteria cell walls to compromise their regular activities, leading to the damage of the cell wall envelope and eventual cell lysis.

A nanocomposite comprising Ag nanoparticles on AgCl/Ag 2 S nanoparticles was decorated on multi-walled carbon nanotubes and used to modify a glassy carbon electrode. Chitosan was also formulated in the nanocomposite to stabilize Ag 2 S nanoparticles and interact strongly with the glucose moiety of arbutin (AR) and ascorbyl glucoside (AA2G), two important ingredients in whitening lotion products. The modified electrode was characterized by Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) and cyclic voltammetry and used for the simultaneous analysis of hydroquinone (HQ), AR, and AA2G. The electrode showed excellent electrocatalysis towards the analytes by shifting the anodic peak potential to a negative direction with ≈5-fold higher current. The sensor displayed a linearity of 0.91-27.2 μM for HQ, 0.73-14.7 μM for AR, and 1.18-11.8 μM for AA2G, without cross-interference. A detection limit was 0.4 μM for HQ, 0.1 μM for AR, and 0.25 μM for AA2G. The sensor was applied to determine HQ, AR, and AA2G spiked in the whitening lotion sample with excellent recovery. The measured concentration of each analyte was comparable to that of the high performance liquid chromatographic (HPLC) method.

Polyaniline (PANI) and polypyrrole (PPY) were synthesized by carbon dots (CDs) under UV irradiation and then sonicated together with zinc acetate and copper acetate to form the PANI-Zn@CuO and PPY-Zn@Cu composites. The former consisted of agglomerated spherical particles with diameters of 1-5 µm, whereas the latter displayed irregular stick shapes with similar diameters. The bacterial potency of the composites against Escherichia coli and Staphylococcus aureus was enhanced remarkably with Zn doping in the CuO matrix, designated as Zn 0.11 Cu 0.89 O, at 0.144 mg/mL. The cell death was mainly attributed to the release of reactive oxygen species (ROS) that would severely damage DNA, proteins, and lipids. Bacteria could adhere to neutral surfaces of the composites by van der Waals attractive forces. The binding event disrupted the native surface charge of bacterial cells to induce cell lysis and result in eventual cell death.

Two crystalline and five amorphous benzimidazole polymers (BINP) were synthesized and conjugated to porous silica via amine and aldehyde-based materials by a simple reflux procedure. The resulting polymers were subject to thermal analysis for monitoring and quantification of the adsorption and desorption of CO 2 . All the polymers were capable of adsorbing CO 2 from a flowing stream of only 80 mL/min at 25 °C. The adsorbed CO 2 onto the polymers were effectively desorbed at room temperature, illustrating the potential application of such polymers for repeated adsorption/desorption of CO 2 . The CO 2 adsorption capacities of these polymers were dependent upon their nitrogen content, specific surface area, and pore size. The available nitrogen atoms for binding to the carbon of CO 2 via tetrel bonds also plays an important role in the capture of this gas. Minimal and much lower CO 2 adsorption was also noted with two crystalline polymers, compared to the five amorphous counterparts. Intermolecular hydrogen bonding and π-π interaction effectively prevented the polymer N sites of the crystalline polymers from interacting with polarized CO 2 molecules.

Polyaniline (PANI) synthesized by simple CDs (carbon dots) initiated polymerization has formed a composite with TiO 2 and SiO 2 , respectively via a sonochemical method. These PANI@TiO 2 and PANI@SiO 2 composites were proven as effective adsorbent materials to rapidly adsorb the anionic and cationic dyes from wastewater at neutral pH and ambient temperature. Selected popular cationic and anionic organic dyes consisted of methylene blue (MB), brilliant blue (BB), Evans blue (EB), crystal violet (CV), Congo red (CR), rhodamine B (RB), and rhodamine 6G (R6G). The adsorption equilibria were governed by Langmuir and Freundlich isotherms. The kinetic results revealed that the PANI@TiO 2 and PANI@SiO 2 composite materials synthesized via the sonochemical method are efficient adsorbents compared to other adsorbent materials for the removal of organic dyes from the water. The adsorbed dyes were effectively desorbed from the composites, rendering the reusability of PANI@TiO 2 and PANI@SiO 2 . The estimated adsorption capacities of PANI@TiO 2 and PANI@SiO 2 composites were 89, 93, 80, 94 and 74, 71, 61, 61 mg/g for MB, CR, CV, and R6G, respectively., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2019 Elsevier B.V. All rights reserved.)

A high-performance liquid chromatography (HPLC) method equipped with a boron-doped diamond (BDD) electrode was established for the simultaneous determination of phenol, 4-ethylphenol (4-EP), guaiacol, 4-ethylguaiacol (4-EG), 4-vinylguaiacol (4-VG), eugenol, and o-, m- and p-cresol. The separation was performed on a reversed-phase HALO C 18 core-shell column (3.0 × 50 mm, 2.7 µm) with a mobile phase comprising 10 mM formate, pH 3, and 15% acetonitrile (ACN) (v/v), a flow rate of 1.5 mL/min, corresponding to a total run time of 9 min. The electrochemical detection (ECD) was set at +1.5 V vs. Pd/H 2 in oxidative mode. Under optimized operating conditions, good linearity was obtained for the nine phenolics with corresponding coefficients of determination (R 2 ) above 0.998. The limits of detection (LODs, S/N = 3) were 10 nM-1 µM, with an 80-fold increase in sensitivity for guaiacol achieved with ECD over ultraviolet (UV) detection. The sensitive and selective HPLC-ECD method was successfully applied for the identification and quantification of the nine phenolics in Islay, Irish, Scotch, and Highland whiskey samples, with significantly higher concentrations of the flavorings determined in Islay whiskey., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Overconsumption of biotin (5-100 mg daily) as a supplement by the general population poses a significant problem for clinical immunoassays (IAs) based on biotin-streptavidin (SA) interactions. This affinity pair has been exploited in immunoassays because of its avidity, sensitivity, specificity, and stability. The elevated biotin level in plasma varies from patient to patient, and its severe interference cannot easily be predicted and quantified. Thus, immunoassay manufacturers must investigate the biotin interference in the developed immunoassays to satisfy the threshold of 3510 ng/mL (14 367 nM), as stipulated by the FDA. There is no concrete solution to circumvent the biotin interference without extra costs and technical difficulties, albeit different strategies have been attempted. They include the IA format with biotinylated reagents prebound to streptavidin, the removal of biotin from the specimen, sample treatment, and biotin interference-free assays. The general public has been instructed to stop taking biotin supplements for 48 h or even weeks before the test, depending on the specific test, dose, and frequency of biotin uptake. As lab-based techniques cannot accommodate an enormous number of public samples, a rapid analytical procedure for biotin is urgently needed to quantify for its interference in immunoassays., Competing Interests: The authors declare no competing financial interest., (Copyright © 2019 American Chemical Society.)

A simple one-step process for the polymerization of dopamine has been developed using nitrogen-doped carbon dots (N@C-dots) as the sole initiator. The synthesized amorphous polydopamine (PDA)-doped N@C-dots (PDA-N@C-dots composite) exhibited a negative charge of -39 mV with particle sizes ranging from 200 to 1700 nm. The stable colloidal solution was active against methicillin-resistant Staphylococcus aureus (MRSA), a Gram-negative bacterium. The strong adhesion of the polymer to the bacterial membrane resulted in a limited diffusion of nutrients and wastes in and out of the cell cytosol, which is a generic mechanism to trigger cell death. Another possible route is the autoxidation of the catechol moiety of PDA to form quinone and release reactive oxygen species (ROS) such as superoxide radicle and hydrogen peroxide, two well-known ROS with antimicrobial properties against both Gram-negative and Gram-positive bacteria., Competing Interests: The authors declare no conflicts of interest.

A glassy carbon electrode (GCE) was modified with a nanocomposite consisting of multiwalled carbon nanotubes (MWCNTs) loaded with silver-argentous oxide nanoparticles (Ag-Ag 2 O). The electrode is shown as a viable tool for sensing histamine using differential pulse voltammetry (DPV). The modified GCE, best operated at a potential of 0.97 V (vs. Ag/AgCl) shows higher electrocatalytic activity compared to GCEs modified with MWCNTs or Ag-Ag 2 O only. Under the optimum conditions, the detection limit is 2 μg⋅L -1 (0.18 μM) and the response is linear in the 5 mg⋅L -1 to 200 mg⋅L -1 histamine concentration range. Sodium chloride, putrescine and cadaverine, commonly present in biological samples and foods, do not interfere. Other performance features include good recoveries, fabrication reproducibility and operational/storage stability. The modified GCE was applied for determination of histamine in fish sauce samples. Graphical abstract A glassy carbon modified with a thin Ag-Ag 2 O layer decorated on MWCNTs exhibits an enhanced surface area, increasing catalyst interface, and reduced overpotential towards histamine.

Biotinylated antibodies/antigens are currently used in many immunoassay formats in clinical settings for diversified analytes and biomarkers to offer high detection selectivity and sensitivity. Biotin cannot be synthesized by mammals and must be taken as an essential supplement. Normal intake of biotin from various foods and milk causes no effect on the streptavidin/biotin-based immunoassays. However, overconsumption of biotin (daily doses 100-300 mg) poses a significant problem for immunoassays using the biotin-strept(avidin) pair. Biotin interferences are noted in immunoassays of thyroid markers, drugs, hormones, cancer markers, the biomarker for cardiac function (β-human chorionic gonadotropin), etc. The biotin level required for serious interference in test results varies significantly from test to test and cannot easily be predicted. Immunoassay manufacturers with technologies based on strept(avidin)-biotin binding must investigate the interference from biotin (up to at least 1200 ng/mL or 4.9 μM of biotin) in various formats. There is no concrete solution to circumvent the biotin interference encountered in blood samples, short of biotin removal. Considering the short half-life of biotin in the human body, patients must stop taking biotin supplements for >48 h before the test. However, this scenario is not considered for patients in emergency situations or those with biotinidase deficiency, mitochondrial metabolic disorders or multiple sclerosis. Apparently, a rapid analytical procedure for biotin is urgently needed to quantify for its interference in immunoassays using strep(avidin)-biotin chemistry. To date, there is no quick and reliable procedure for the detection of biotin at below nanomolar levels in blood and biological samples. Traditional lab-based techniques including HPLC/MS-MS cannot process an enormous number of public samples. Biosensors with high detection sensitivity, miniaturization, low cost, and multiplexing have the potential to address this issue., (Copyright © 2019 Elsevier Inc. All rights reserved.)

Captavidin, a nitrated avidin with moderate affinity with biotin, irreversibly adsorbs on carboxymethylcellulose to form a regenerable biorecognition element for biotin. This layer was retained and stabilized on a boron-doped diamond electrode by a Nafion film for repeated impedance analyses of biotin down to below 1 nM. The labeless electrochemical sensing scheme was then demonstrated for the analysis of biotin in blood plasma. The incorporation of captavidin confers detection specificity and regenerability, whereas the Nafion and carboxymethylcellulose layers circumvent the diffusion of endogenous electroactive species. The biosensing layer is simply regenerated by applying oxidation of +2 V for 1 min instead of its submersion in carbonate buffer for 10 min., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Nafion formed on the surface of a boron-doped diamond electrode allows for a chemosensing system for biotin. The modified electrode is capable of oxidizing biotin and offers a detection limit of 5 nM, the average normal level of biotin in blood plasma. The developed method was successfully applied to determine biotin in human plasma samples and a popular health product as two popular models., Competing Interests: The authors declare no competing financial interest.

This work unraveled kinetics, isotherm, and thermodynamic properties of methylene blue (MB) adsorbed on polyaniline (PANI) and polypyrrole (PPY). The two polymers, PANI and PPY, synthesized by a facile C-dot (CD)-initiated polymerization method have been proven as the effective adsorbent materials to remove MB from wastewater. This dye model is also generally employed as a redox indicator in analytical chemistry and exhibits blue in an oxidizing environment, but it is colorless when exposed to a reducing agent. The effects of temperature, adsorbent amount contact time, and dye concentration were consistently examined. The adsorption capacity of the polymers at 28 °C could reach 19.2 mg/g. The adsorption equilibrium of the dye was attained after 90 and 120 min of contact time with PANI and PPY, respectively. The equilibrium details were well described by Freundlich and Langmuir isotherms. Results showed that PANI and PPY prepared using CD-initiated polymerization are better adsorbents compared to the commercial PANI powder for the removal of MB from water., Competing Interests: The authors declare no competing financial interest.

Silver-doped CdS quantum dots capped with mercaptoacetic acid were incorporated into a chitosan-coated filter paper to fabricate a colorimetric test stripe for mercury. Chitosan assisted in the stabilization of CdSAg QDs on cellulose and enhanced the analyte diffusion in the test stripe. Hg(II) ions were captured by mercaptoacetic acid on CdSAg, resulting in a visualized color change from yellow to deep brown. For enhanced sensitivity and quantitation with good reproducibility, the color intensity was recorded, transmitted to a smartphone camera and computed by the ImageJ software to provide a digital readout. The assay was rapid, simple, and selective for mercury as several potential interfering species provoked no signal response. The applicability of the sensing approach was demonstrated for the analysis of spiked Hg(II) ions in cosmetic cream with a detection limit of 124 μM. Graphical abstract Schematic of a colorimetric test stripe consisting of silver-doped CdS quantum dots coated withmercaptoacetic acid and embedded into a chitosan matrix on paper. It enables mercury(II) to be visuallyquantified even in complex matrices such as cosmetics.

As the leading cause of morbidity and mortality of cystic fibrosis (CF) patients, early detection of Pseudomonas aeruginosa (PA) is critical in the clinical management of this pathogen. Herein, we describe rapid and sensitive electroanalytical methods using differential pulse voltammetry (DPV) at a boron-doped diamond (BDD) electrode for the detection of PA signaling biomolecules. Monitoring the production of key signaling molecules in bacterial cultures of P. aeruginosa PA14 over 8 h is described, involving sample pretreatment by liquid-liquid and solid-phase extraction. In addition, direct electrochemical detection approach of PA signaling molecules is also reported in conjunction with hexadecyltrimethylammonium bromide (CTAB) to disrupt the bacterial membrane.

A sensitive and rapid sandwich immunoassay (IA) was developed for human lipocalin-2 (LCN2) by functionalizing a KOH-treated polystyrene microtiter plate with multiwalled carbon nanotubes (MWCNTs) dispersed in 3-aminoproyltriethoxysilane (APTES). The significantly increased surface area due to the presence of MWCNTs led to a high immobilization density of 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) activated anti-LCN2 capture antibodies (Ab). The anti-LCN2 Ab-bound MTPs were stable for 6 weeks when stored in 0.1M PBS, pH 7.4 at 4°C. The IA detects LCN2 from 0.6 to 5120pgmL -1 with a limit of detection (LOD) and limit of quantification (LOQ) of 0.9pgmL -1 and 6pgmL -1 , respectively. The assay offered a ~50-fold lower LOD and ~3-fold faster IA, compared to a commercial sandwich enzyme-linked immunosorbent assay kit., (Copyright © 2016 Elsevier B.V. All rights reserved.)

Human fetuin A (HFA) plays a prominent pathophysiological role in numerous diseases and pathophysiological conditions with considerable biomedical significance; one example is the formation of calciprotein particles in osteoporosis and impaired calcium metabolisms. With impressive advances in in vitro diagnostic assays during the last decade, ELISAs have become a workhorse in routine clinical diagnostics. Recent diagnostic formats involve high-sensitivity immunoassay procedures, surface plasmon resonance, rapid immunoassay chemistries, signal enhancement, and smartphone detection. The current trend is toward fully integrated lab-on-chip platforms with smartphone readouts, enabling health-care practitioners and even patients to monitor pathological changes in biomarker levels. This review provides a critical analysis of advances made in HFA assays along with the challenges and future prospects., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Two-dimensional (2D) graphene, sp 2 -hybridized carbon, and its two major derivatives, graphene oxide (GO) and reduced graphene oxide (rGO) have played an important role in immunoassays (IAs) and immunosensing (IMS) platforms for the detection of carcinoembryonic antigen (CEA), an implicated tumor biomarker found in several types of cancer. The graphene family with high surface area is functionalized to form stable nanocomposites with gold nanoparticles (AuNPs) and electron mediators. The capture anti-CEA antibody (Ab) with high density can be anchored on AuNPs of such composites to provide remarkable detection sensitivity, significantly below the level found in normal subjects and cancer patients. Electrochemical and fluorescence/chemiluminescence-quenching properties of graphene-based nanocomposites are exploited in various detection schemes. Future endeavors are envisioned for the development of an array platform with high-throughput for CEA together with other tumor biomarkers and C-reactive protein, a universal biomarker for infection and inflammation. The ongoing efforts dedicated to the replacement of a lab-based detector by a cellphone with smart applications will further enable cost-effective and frequent monitoring of CEA in order to establish its clinical relevance and provide tools for real-time monitoring of patients during chemotherapy., (Copyright © 2015 Elsevier B.V. All rights reserved.)

A global upsurge in antibiotic resistance has led to research in metal-based antimicrobial therapy. Nonetheless, the clinical translation of metal oxides is often hampered by their poor aqueous solubility. This work unravels the surfactant-free synthesis of a water-soluble PEGylated nanographene oxide/zinc-doped copper oxide complex (NGO-PEG-Zn-CuO) with superior antibacterial activity. We uncover its mechanism of bacterial cell death over E. coli and S. aureus associated with oxidative stress and high production of reactive oxygen species (ROS) compared to NGO-ZnCuO, ZnCuO and NGO-PEG. A simple, one-step sonochemical technique is employed to deposit the Zn-CuO nanoparticles (NPs) on NGO-PEG. This complex demonstrates excellent aqueous solubility in different physiological solutions, including serum. Moreover, it exhibits excellent stability in water for a period of more than two months with almost no cytotoxicity effect on HeLa cells. Taken together, these results display the superior potency of the NGO-PEG-ZnCuO complex as a soluble and non-toxic compound with enhanced antibacterial properties.

Considerable advances in point-of-care testing (POCT) devices stem from innovations in cellphone (CP)-based technologies, paper-based assays (PBAs), lab-on-a-chip (LOC) platforms, novel assay formats, and strategies for long-term reagent storage. Various commercial CP platforms have emerged to provide cost-effective mobile health care and personalized medicine. Such assay formats, as well as low-cost PBAs and LOC-based assays, are paving the way to robust, automated, simplified, and cost-effective POCT. Strategies have also been devised to stabilize reagent storage and usage at ambient temperature. Nevertheless, successful commercialization and widespread implementation of such clinically viable technologies remain subject to several challenges and pending issues., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

Pseudomonas aeruginosa uses a hierarchical cell-cell communication system consisting of a number of regulatory elements to coordinate the expression of bacterial virulence genes. Sensitive detection of quorum sensing (QS) molecules has the potential for early identification of P. aeruginosa facilitating early medical intervention. A recently isolated cell-cell communication molecule, a thiazole termed IQS, can bypass the las QS system of P. aeruginosa under times of stress, activating a subset of QS-controlled genes. This compound offers a new target for pathogen detection and has been prepared in a one step protocol. A simple electrochemical strategy was employed for its sensitive detection using boron-doped diamond and glassy carbon electrodes by cyclic voltammetry and amperometry., (Copyright © 2014 Elsevier Ltd. All rights reserved.)

: A simple procedure was developed for the fabrication of electrochemical glucose biosensors using glucose oxidase (GOx), with graphene or multi-walled carbon nanotubes (MWCNTs). Graphene and MWCNTs were dispersed in 0.25% 3-aminopropyltriethoxysilane (APTES) and drop cast on 1% KOH-pre-treated glassy carbon electrodes (GCEs). The EDC (1-ethyl-(3-dimethylaminopropyl) carbodiimide)-activated GOx was then bound covalently on the graphene- or MWCNT-modified GCE. Both the graphene- and MWCNT-based biosensors detected the entire pathophysiological range of blood glucose in humans, 1.4-27.9 mM. However, the direct electron transfer (DET) between GOx and the modified GCE's surface was only observed for the MWCNT-based biosensor. The MWCNT-based glucose biosensor also provided over a four-fold higher current signal than its graphene counterpart. Several interfering substances, including drug metabolites, provoked negligible interference at pathological levels for both the MWCNT- and graphene-based biosensors. However, the former was more prone to interfering substances and drug metabolites at extremely pathological concentrations than its graphene counterpart.

Coated capillary electrophoresis equipped with a boron doped diamond (BDD) electrode was developed for analysis of chemically synthesised 2-heptyl-3-hydroxy-4-quinolone (HHQ), 2-heptyl-3-hydroxy-4-quinolone (PQS), and 2-methyl analogues. Detection was then extended to biological samples. PQS and its biological precursor, HHQ, are two key regulators of bacterial cooperative behaviour known as quorum sensing in the nosocomial pathogen Pseudomonas aeruginosa. The fused silica capillary was coated with a thin layer of poly (diallyldimethylammonium) chloride to reverse the electroosmosis, allowing fast migration of PQS and HHQ with improved selectivity. The four model compounds were baseline resolved using a 50 mM H(3)PO(4)-Tris, pH 2.0 buffer with 20% (v/v) acetonitrile as buffer additive. With an injection time of 3 s, the detection limits of four analytes ranging from 60 to 100 nM (S/N=3) were observed when the BDD electrode was poised at +1.5 V vs. 3 M Ag/AgCl. As expected, no PQS or HHQ was detected from the supernatant of the P. aeruginosa (pqsA) mutant. A concentration of HHQ of 247 μM was detected from the supernatant of the pqsH mutant, which catalyses the conversion of HHQ to PQS in the presence of molecular oxygen by monooxygenase. The separation and detection scheme was applicable to follow the conversion of HHQ to PQS in P. aeruginosa when entering the stationary phase of growth. The results obtained by coated capillary electrophoresis with BDD detection were validated and compared well with LC-MS data., (Copyright © 2012 Elsevier B.V. All rights reserved.)