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A sensor for non-enzymatic hydrogen peroxide (HO) detection was developed based on silicon quantum dots (SiQDs). The fluorescent SiQDs were synthesized using a one-pot hydrothermal method. The SiQDs were made water-soluble and pH-stable by covering their surfaces with amino and hydroxyl groups. Additionally, the prepared SiQDs had a large Stokes shift (131 nm), excellent photostability (442 min), and hypotoxicity (, 99% cell viability was retained after a 24 h-treatment at 8.0 mg mL of SiQDs). The dynamic quenching effect induced by HO effectively suppresses the blue fluorescence of SiQDs. Under the optimum conditions, the SiQD-based HO sensor exhibited a wide linear range (10-1000 μM), high sensitivity and selectivity, and good anti-interference ability. The detection limit and relative standard deviation were 1.7 μM and 4.5% ( = 20 μM, = 7), respectively. Accordingly, a simple, enzyme-free, and highly efficient method was established for detecting HO in aqueous solutions. Moreover, this eco-friendly fluorescent sensor successfully determined the HO concentration in human serum samples with 92.0-102.4% recoveries.
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http://dx.doi.org/10.1039/d5ay00038f | DOI Listing |
Anal Methods
April 2025
College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang, 438000, China.
A sensor for non-enzymatic hydrogen peroxide (HO) detection was developed based on silicon quantum dots (SiQDs). The fluorescent SiQDs were synthesized using a one-pot hydrothermal method. The SiQDs were made water-soluble and pH-stable by covering their surfaces with amino and hydroxyl groups.
View Article and Find Full Text PDFFood Chem
December 2021
School of Food Science and Technology, Dalian Polytechnic University, No. 1, Qinggongyuan, Ganjingzi District, Dalian, Liaoning 116034, People's Republic of China; Liaoning Key Lab for Aquatic Processing Quality and Safety, No. 1, Qinggongyuan, Ganjingzi District, Dalian, Liaoning 116034, People's R
Active food packaging materials containing procyanidins (PC) exhibits outstanding antimicrobial activity, but PC is easy to be hydrolyzed by acid. A novel water-soluble chitosan (CS)-based copolymer was prepared to be used as a carrier to provide a pH-stable environment for loading PC. CS was copolymerized with polyvinyl alcohol (PVA) via a coupling reagent-mediated approach.
View Article and Find Full Text PDFJ Drug Deliv Sci Technol
December 2020
College of Pharmacy, Koneru Lakshmaiah Education Foundation, Vaddeswaram, AP, 522502, India.
Polyvinylpyrrolidone (PVP) is a water-soluble polymer obtained by polymerization of monomer -vinylpyrrolidone. PVP is an inert, non-toxic, temperature-resistant, pH-stable, biocompatible, biodegradable polymer that helps to encapsulate and cater both hydrophilic and lipophilic drugs. These advantages enable PVP a versatile excipient in the formulation development of broad conventional to novel controlled delivery systems.
View Article and Find Full Text PDFACS Appl Mater Interfaces
May 2015
†Department of Mechanical Engineering, The University of Hong Kong, Hong Kong Special Administrative Region, China.
Polyelectrolyte complexes formed between chitosan (CS) and anionic polymers have attracted increasing interest in drug delivery. In this study, CS is copolymerized with hypromellose via a coupling reagent-mediated approach to form a water-soluble, nontoxic CS derivative, namely hypromellose-graft-CS (HC), which is subsequently complexed with carboxymethylcellulose (CMC) to generate a polyampholytic hydrogel. When compared with conventional CS, HC is highly water-soluble across a wide pH range, and has a substantially higher pH buffering capacity to provide a pH-stable environment for delivery of drugs.
View Article and Find Full Text PDFToxicology
April 2011
Department of Biomedical Engineering, Key Laboratory of Biomedical Engineering of Ministry of Education, Zhejiang University, Zheda Road 38, Hangzhou 310027, China.
Quantum dots (QDs), as novel bioimaging and drug delivery agents, are generally introduced into vascular system by injection, and thus directly exposed to vascular endothelial cells (ECs). However, the adverse effects of QDs on ECs are poorly understood. In this study, employing human umbilical vein ECs (HUVECs), we investigated the potential vascular endothelial toxicity of mercaptosuccinic acid (MSA)-capped CdTe QDs in vitro.
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