Search

CRISPR/Cas13a with precise and controllable programming of endonuclease activity has been served as powerful tool for RNA sensing. Although with high sensitivity, existing CRISPR/Cas13a-based biosensors need complex amplification procedure or special equipment that limited quantification capability. Here, Mn-doped NiCo 2 O 4 (Mn/NiCo 2 O 4 ) nanozyme with enhanced peroxidase activity was synthesized and combined with CRISPR/Cas13a-based reaction to develop a simple, sensitive and universal biosensor for RNA detection, which is achieved through target recognition that activates Cas enzymes to cleave RNA reporter for inhibiting Mn/NiCo 2 O 4 nanozyme to assemble on microplate. The Mn/NiCo 2 O 4 nanozyme assembled on microplate can be monitored through colorimetric and fluorometric approaches. On one hand, Mn/NiCo 2 O 4 nanozyme offers ideal peroxidase activity to catalyze colorimetric reaction, and as low as dozens of amol level of RNA target can be sensitively detected by naked eyes without any amplification procedures. On the other hand, Mn/NiCo 2 O 4 can be also served as a signal amplifier to produce large amount of Co 2+ , Mn 2+ and Ni 2+ to quench the fluorescence of calcein. The fluorescent approach can achieve higher sensitivity (about 40-fold) than colorimetric method. More importantly, the proposed biosensor can work well for multiple RNA detection in real biological samples, showing a great potential for monitoring non-coding RNA-related diseases., Competing Interests: Declaration of competing interest The authors declare no conflict of 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 © 2024 Elsevier B.V. All rights reserved.)

Water pollution caused by bisphenol A (BPA) has become the world problem. Designing and preparing cost-effective and biodegradable sorbents for the effectively adsorptive removal of bisphenol A from wastewater is of immense significance. Herein, a natural polysaccharide (chitin) was used as raw materials to be grafted with styrene (GS), then crosslinked with α,α'-dichloro-p-xylene (DCX) to form the hyper-crosslinked polymer (labeled as CGS@DCX). The CGS@DCX showed high adsorptive affinity for bisphenol A, with adsorption capacity of 441 mg g -1 . Various studies gave an insight into the adsorption process, demonstrating that the highly efficient adsorption of BPA by the CGS@DCX is mainly based on the π-π stacking, hydrogen-bond interaction, polar interaction and pore adsorption. Moreover, the CGS@DCX had high chemical stability, good reusability (9 cycles) and fast adsorption kinetics (10 min) for adsorption of BPA. This work provides a promising strategy for the design and synthesis of novel yet eco-friendly sorbents to solve environmental problems., Competing Interests: Declaration of competing interest The authors declare no conflict of 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 © 2024 Elsevier B.V. All rights reserved.)

Herein, a novel carboxyl-functionalized porous organic polymer (COOH-POP) was prepared as sorbent. Due to multiple hydrogen bonds and π-π interactions between COOH-POP and phenols, COOH-POP shows good enrichment ability and very fast adsorption rate for phenols. Then, an analytical method was developed for determination of five phenols (2-chlorophenol, bisphenol A, 2,6-dichlorophenol, 2,4-dichlorophenol and p-tert-butylphenol) in bottled water, lemon juice, peach juice and honey samples using COOH-POP as solid phase extraction sorbent in combination with high performance liquid chromatography. Under optimal conditions, the COOH-POP based method gave the detection limits (S/N = 3) of 0.02-0.10 ng mL -1 for bottled water, 0.03-0.12 ng mL -1 for lemon juice, 0.03-0.25 ng mL -1 for peach juice and 0.7-1.5 ng g -1 for honey samples. The recoveries for spiked samples ranged from 84.0 % to 119.0 % with relative standard deviation less than 7.6 %. This study provides a new yet effective method for enrichment of phenols by designing carboxyl-functionalized porous organic polymer as sorbent., 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 © 2023. Published by Elsevier B.V.)

Herein, two novel amino-functionalized triazine-based hyper-crosslinked porous polymer (NH 2 -HCPs) (named as DPT-BB, DPT-DX) were designed and synthesized by direct crosslinking of 2,4-diamino-6-phenyl-1,3,5-triazine (DPT) with 4,4'-bis(chloromethyl)-1,1'-biphenyl (BB) or α, α'-dichloro-p-xylene (DX). Thanks to the amino functional group and hyper-crosslinked porous structure, NH 2 -HCPs displayed remarkable adsorption ability for phenolic EDCs. The adsorption mechanism mainly involved hydrogen bond, π-π interaction, hydrophobic interaction and pore filling. Thus DPT-BB was applied as solid phase extraction sorbent to extract phenolic EDCs from water and orange juice samples prior to quantitative analysis by high performance liquid chromatography. Under the optimal conditions, detection limit as low as 0.07-0.2 ng mL -1 for water and 0.1-0.27 ng mL -1 for orange juice was achieved. Good recoveries spanned the range of 83.5%-114% were obtained for spiked samples, with relative standard deviations below 8.9%. The results demonstrated that the developed method displayed excellent practicability for sensitive analysis of EDCs., 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 © 2023 Elsevier B.V. All rights reserved.)

Aflatoxin B1 (AFB1) with tremendous toxic effects has caused a serious threat to food security. Accurate quantification of AFB1 in food can effectively prevent the risk of human intake of AFB1. Herein, a colorimetric and fluorescent dual-mode aptasensor for accurate and sensitive detection of AFB1 has been developed based on MnO 2 nanoflowers (MnO 2 NFs) for the first time. MnO 2 NFs could catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) into blue oxidation product (TMBox) by H 2 O 2 , which would be used for visible detection of AFB1. Simultaneously, MnO 2 NFs can be served as a signal amplifier and reduced by ascorbic acid to generate lots of Mn 2+ which would quench the fluorescence of calcein for fluorescent detection of AFB1. Both colorimetric and fluorescent methods have been successfully applied for determination of AFB1 in milk samples with satisfactory results. The proposed dual-mode detection method with high detection sensitivity and accuracy showed great promise for monitoring AFB1 in food., 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 © 2023 Elsevier B.V. All rights reserved.)

Endocrine disrupting chemicals (EDCs) pose a serious threat to human health even at extremely low concentration. Three carboxyl functionalized porous polymers (PDA-DPBP, PTCDA-DPBP and ODPA-DPBP) were synthesized for the first time and employed as solid-phase extraction sorbent to enrich phenolic EDCs at trace level. Compared with PTCDA-DPBP, ODPA-DPBP and corresponding carboxyl-free counterpart (PC-DPBP), PDA-DPBP delivered superior enrichment efficiency for the phenolic EDCs, which can be ascribed to the strong hydrogen bonding, pore filling, hydrophobic interaction and π-π interaction between PDA-DPBP and phenolic EDCs. Coupled with high performance liquid chromatography, phenolic EDC residues in bottled water, juice and milk samples were enriched and determined. At the optimum conditions, the PDA-DPBP based method provided a good linear response in the range of 0.04-100ng mL -1 for bottled water, 0.07-100ng mL -1 for juice and 0.15-500ng mL -1 for milk samples. The detection limits (S/N=3) were 0.01-0.04, 0.02-0.06 and 0.05-0.10ng mL -1 for bottled water, juice and milk, respectively. The method recoveries were in the range from 81.6% to 116%, with RSDs ≤ 7.7%. This work provides an attractive and reliable alternative method for sensitive determination of phenolic EDCs., 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 © 2023 Elsevier B.V. All rights reserved.)

There is an urgent need to prepare advanced functional materials for extraction and enrichment of trace organic pollutants from different samples. In this work, two novel phosphate-functionalized porous organic polymers (DBP-POP and DPP-POP) were synthesized for the first time. Compared with phosphate-free counterpart, both phosphate-functionalized POPs showed excellent adsorption performance for the neonicotinoids due to the hydrogen bonding, π-π interaction and hydrophobic interaction. For ease of separating the sorbent from solution, magnetic DBP-POP (M-DBP-POP) was further prepared as sorbent to extract neonicotinoids from environmental water and lemon juice samples prior to their determination by high performance liquid chromatography-ultraviolet detection. Under optimal conditions, the detection limits (S/N = 3) of the method were 0.01-0.08 ng mL -1 for water and 0.03-0.10 ng mL -1 for lemon juice. The recoveries were in the range of 80.0% to 113.0% with relative standard deviation less than 10.6%. This work demonstrated the feasibility of phosphate-functionalized POPs for adsorption applications., 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 © 2023 Elsevier B.V. All rights reserved.)

A MXene-based heterostructure (BiOI/Ti 3 C 2 T X ) was synthesized via simple hydrothermal synthesis strategy. The BiOI/Ti 3 C 2 T X exhibited distinctly enhanced photoelectrochemical (PEC) activity, excellent durability and high selectivity because the introduction of Ti 3 C 2 T X could facilitate the separation of photogenerated electron-hole pairs. Since the redox process of glucose resulted in a decreasing photocurrent of BiOI/Ti 3 C 2 T X , a BiOI/Ti 3 C 2 T X based signal-off PEC sensing platform was constructed to sensitively determine glucose for the first time. Under the optimal conditions, the BiOI/Ti 3 C 2 T X sensor displayed a good linearity ranging from 0.03 μΜ to 1500 μΜ with the limit of detection down to 0.02 μΜ. The sensor was successfully applied for the glucose detection in human urine with satisfactory accuracy and repeatability, confirming its practical applicability and good serviceability. Moreover, the BiOI/Ti 3 C 2 T X sensor also exhibited superb selectivity and stability, providing a great potential application in the development of glucose sensor., 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 Elsevier B.V. All rights reserved.)

Design and fabrication of functionalized hypercrosslinked polymers (HCPs) for enhancing their performance by using green renewable monomers has attracted considerable research interest. In this study, hydroxyl‑functional HCP (labeled as OHHCP) was prepared via the knitting method by applying natural naringenin as a monomer for the first time. Due to the good hydrophilicity and strong H-bonding ability, the OHHCP showed high extraction capacity for nitroimidazoles. Thus, it was successfully applied as a potent adsorbent for solid phase extraction of five nitroimidazoles in water, honey and chicken meat, followed by high-performance liquid chromatography-diode array detector analysis. At the optimized conditions, the limit of detections (S/N = 3) of the proposed method for water, honey and chicken samples were 0.02 - 0.06 ng mL -1 , 0.5 - 1.0 ng g - 1 and 0.8 - 1.0 ng g - 1 , respectively. The recoveries were 80.0 - 110%, and the relative standard deviations were below 10.0%. The OHHCP also displayed good application prospects for other organic compounds with H-bonding capability. This study highlights the facile preparation of OH-functionalized HCPs from renewable and natural resources as potent adsorbents for polar compounds., Competing Interests: Declaration of competing interest The authors declare no conflict of 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 Elsevier B.V. All rights reserved.)

In this study, a novel nitrogen-rich magnetic hypercrosslinked polymer (Fe 3 O 4 @Ph-HCP) was fabricated via a facile one-pot reaction of 1,3,5-triphenylbenzene, 2,4-dichloropyrimidine and phenyl-functionalized magnetic Fe 3 O 4 nanoparticles. The Fe 3 O 4 @Ph-HCP possessed high specific surface, abundant nanopores and good stability. Especially, Fe 3 O 4 @Ph-HCP exhibited excellent adsorption capability with fast adsorption rate to neonicotinoid insecticides. It was applied as a superior magnetic adsorbent for rapid enrichment and isolation of four neonicotinoid insecticides (thiamethoxam, imidacloprid, acetamiprid and thiacloprid) from honey, tomato, lettuce and Chinese cabbage samples prior to high performance liquid chromatography-diode array detection. Under the optimized conditions, the good linearity was obtained in the range of 1-1000 ng g -1 for honey, tomato, lettuce and Chinese cabbage samples, and the detection limits (S/N = 3) were 0.30-0.67 ng g -1 for honey, 1-1.5 ng g -1 for tomato, lettuce and Chinese cabbage. The spiked recoveries were 80.1-111%, and relative standard deviations were less than 10.0%. These results demonstrate that the developed method can be used as a good alternative method for sensitive determination of neonicotinoid insecticides in complex samples., Competing Interests: Declaration of Competing Interest The authors declare no conflict of 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.)

Food safety is a great concern of the general public. Chlorophenols (CPs) as organic pollutant can be found in drinking water and foods, causing serious harm to human health. Herein, imine-linked covalent organic frameworks (COFs), named as TAPT-AN-COF, was synthesized by aniline modulation strategy through condensation of 1,3,5-triformylphoroglucinol and 4,4',4''-(1,3,5-Triazine-2,4,6-triyl)trianiline with aniline as modulator. The prepared TAPT-AN-COF possesses good crystallinity and regular morphology, displaying excellent adsorption capability towards CPs pollutants. Thus, the TAPT-AN-COF was used as novel adsorbent for off-line solid-phase extraction of four CPs (2-CP, 3-CP, 2,3-CPs, 2,4-CPs) from bottled water, tea drink and honey samples before high performance liquid chromatography-ultraviolet detection. Under optimal conditions, wide linear range, low detection limits and satisfactory extraction recovery were gained. The π-stacking and hydrophobic interactions between the TAPT-AN-COF and the analytes played an important role in the adsorption. The established method has a great potential in determining other hydrophobic aromatic compounds., Competing Interests: Declaration of Competing Interest The authors declare no conflict of interest., (Copyright © 2021. Published by Elsevier B.V.)