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A pyrophosphatase biosensor with photocurrent analysis
摘要： A light-induced photochemical biosensor was developed for the analysis of inorganic pyrophosphatase (PPase). PPase hydrolyzes pyrophosphate (PPi) into two independent o-phosphate ions. Two PPi units can chelate a copper ion (Cu2+), forming a PPi–Cu2+–PPi complex and preventing the Cu2+ triggers other reactions. A transparent indium tin oxide (ITO) electrode was coated with a layer of CdS quantum dots (QDs), and then 3,4-diaminobenzoic acid (DBA) was deposited as the anchor. A solution of the PPi–Cu2+–PPi complex and o-phenylenediamine (OPD) was mixed with the analytical sample and then a drop of the mixture was placed on the modified ITO electrode. In the absence of PPase, no reaction occurred between OPD and DBA. A photocurrent was obtained upon excitation of the CdS QDs under light. In the presence of PPase, Cu2+ was released from the complex, triggering the reaction of OPD with DBA on the electrode surface, thereby shielding the CdS QDs from excitation by the light. The observed photocurrent decreased. The difference in the two measured photocurrents corresponded to the activity of PPase. This photochemical biosensor had excellent sensitivity for PPase in the range from 0.8 to 5000 mU, with a limit of detection of 0.41 mU.
关键词： Quantum dots,Biosensor,o-Phenylenediamine,Photocurrent,PPase
更新于2025-09-23 15:23:52
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Non-oxidation reduction strategy for highly selective detection of ascorbic acid with dual-ratio fluorescence and colorimetric signals
摘要： Ascorbic acid (AA), one of the most important vitamins, acts a critical role in various physiological reactions and is involved in many diseases. Thus, the development of highly selectivity methods for detecting AA level with the presence of different reducing substances is of great significance in complicated serum matrix. In this paper, a non-oxidation reduction regulation (NRR) strategy was designed to construct a novel dual-ratio fluorescence and colorimetric dual-readout assay for highly selective detection of AA. The strategy involves three processes: Ag+ oxidated o-phenylenediamine (OPD) to 2,3-diaminophenazine (OPDox), AA inhibited the generation of OPDox and the AA was oxidized to dehydroascorbic acid (DHAA). The specific performance of DHAA NRR, due to the condensation reaction between dicarbonyl group of DHAA and diamine group of OPD, that is confirmed by ESI-MS and 1H NMR spectra analysis, can remarkably enhance the selectivity of AA detection. Additionally, the proposed method based on NRR strategy not only provides a sensing platform for probing AA but also shows promising outlook in biomedical studies.
关键词： O-phenylenediamine,Non-oxidation reduction regulation,Ascorbic acid,Dual-ratio,Dual-readout
更新于2025-09-23 15:21:21
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Polymeric Ionic Liquid-Based Fluorescent Amphiphilic Block Copolymer Micelle for Selective and Sensitive Detection of p-Phenylenediamine
摘要： Highly sensitive and selective detection of p-phenylenediamine (PPD) is achieved by a fluorescence sensor, which is constructed by encapsulating the hydrophobic fluorescent 1-pyrenecarboxaldehyde (Py-CHO) into the polymeric ionic liquid (PIL)-based amphiphilic block copolymers (BCPs) micelle. Amine-aldehyde condensation reaction between PPD and Py-CHO leads to the fluorescence quenching of Py-CHO, giving rise to the basis for quantitative detection of PPD. The core cavity of micelle formed by the self-assembly of PIL provides excellent hydrophobic environment for the accommodation of fluorescent Py-CHO, offering the significant improved sensitivity and selectivity on PPD detection. The amount of PIL in fabricating amphiphilic block copolymer micelle, the BCPs-Py-CHO micelle concentration and the detection pH condition are investigated to obtain the best performance of this sensor. Accurate detection of PPD is achieved in the range of 0.02-10 μmol L-1 under optimal conditions, and the detection limit is 0.007 μmol L-1 (3σ/s). The developed sensor is successfully applied to the determination of PPD contents in hair dyes, spiked water and urine samples.
关键词： Amphiphilic block copolymer micelle,p-Phenylenediamine,Fluorescence sensor,Polymeric ionic liquid,1-Pyrenecarboxaldehydes
更新于2025-09-10 09:29:36
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Fast electron transfer and enhanced visible light photocatalytic activity by using poly-o-phenylenediamine modified AgCl/g-C3N4 nanosheets
摘要： Exfoliation of bulk graphitic carbon nitride (g-C3N4) into two-dimensional (2D) nanosheets is one of the effective strategies to improve its photocatalytic properties so that the 2D g-C3N4 nanosheets (CN) have larger specific surface areas and more reaction sites. In addition, poly-o-phenylenediamine (PoPD) can improve the electrical conductivity and photocatalytic activity of semiconductor materials. Here, the novel efficient composite PoPD/AgCl/g-C3N4 nanosheets was first synthesized by a precipitation reaction and the photoinitiated polymerization approach. The obtained photocatalysts have larger specific surface areas and could achieve better visible-light response. However, silver chloride (AgCl) is susceptible to agglomeration and photocorrosion. The PoPD/AgCl/CN composite exhibits an extremely high photocurrent density, which is three times that of CN. Obviously enhanced photocatalytic activities of PoPD/AgCl/g-C3N4 are revealed through the photodegradation of tetracycline. The stability of PoPD/AgCl/CN is demonstrated based on four cycles of experiments that reveal that the degradation rate only decreases slightly. Furthermore, ?O2? and h+ are the main active species, which are confirmed through a trapping experiment and ESR spin-trap technique. Therefore, the prepared PoPD/AgCl/CN can be considered as a stable photocatalyst, in which PoPD is added as a charge carrier and acts a photosensitive protective layer on the surface of the AgCl particles. This provides a new technology for preparing highly stable composite photocatalysts that can effectively deal with environmental issues.
关键词： AgCl,Visible light irradiation,Poly-o-phenylenediamine,g-C3N4 nanosheets,Photocatalytic
更新于2025-09-09 09:28:46
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Effect of Amino Anilines on the Fluorescence of Coumarin Derivative
摘要： The effect of stereo electronic factors of amino anilines such as ortho-phenylenediamine (OPD) and para-phenylenediamine (PPD) on the fluorescence of 5,6-benzo-4-azidomethyl coumarin (5BAMC) in polar aprotic and polar protic solvents has been studied. From UV absorption and 1 H NMR studies, observed blue shift in the presence of PPD is due to H-bonding with 5BAMC. Fluorescence quenching studies indicate the role of static and dynamic quenching mechanisms for both the quenchers and larger quenching efficiency of PPD than OPD. The sphere of action static quenching and finite sink approximation models reveal static effect in the excited state and diffusion limited bimolecular quenching reactions. Electrochemical analysis indicates that quenching efficiency of PPD is more than OPD based on the magnitudes of free energy change for electron transfer. Binding equilibria analysis confirms that the magnitude of binding between PPD and 5BAMC is stronger compared to OPD. It is also noticed that the binding between PPD and 5BAMC in polar protic solvents is stronger than that in aprotic solvents. Lastly, from the magnitudes of thermodynamic parameters, interaction between PPD and 5BAMC is hydrophobic and spontaneous. Thus from the present investigation, it is concluded that the separation between two –NH2 groups in amino anilines plays role in their interaction with coumarin derivative 5BAMC.
关键词： hydrophobic interaction,H-bonding,para-phenylenediamine,binding sites,ortho-phenylenediamine
更新于2025-09-04 15:30:14