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- 实验方案
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Photo-Sensitive Pb5S2I6 Crystal Incorporated Polydopamine Biointerface Coated on Nanoporous TiO2 as an Efficient Signal-on Photoelectrochemical Bioassay for Ultrasensitive Detection of Cr(VI) ions
摘要： An ultrasensitive Visible light-triggered photoelectrochemical (PEC) sensor was designed based on ideal photoactive lead sulfoiodide (Pb5S2I6) as low band gap crystal, which hydrothermally synthesized rapidly at low temperature (160°C) in hydrochloride acid media followed by its incorporation into polydopamine as reactive photo-biointerface, through a facile in situ electropolymerization method, coated on nanoporous TiO2 grown by anodization on Ti foil. The structure of as-prepared samples and their photoelectrochemical properties were fully characterized. This unique photo-sensitive Pb5S2I6 catalyst-based PEC bioassay was constructed for the detection of low-abundant Cr(VI) ion in real samples. Applying central composite design, individual and mutual interaction effects were evaluated to obtain optimized solution pH, applied potential and radiant light wavelength as operational factors influencing the PEC efficiency for Cr(VI) detection. At optimal condition, the proposed sensor due to effective suppress in electron–hole recombinations showed a very low detection limit of 3.0 nM, over a broad linear concentration range of 0.01 μM-80 μM in addition to high sensitivity versus 1.9 μA/μM Cr(VI). Proposed PEC sensor displayed high selectivity, reproducibility and stability as well as improved excitation conversion efficiency, which make it highly applicable using solar energy. The potential applicability of the designed sensor was evaluated in water, tomato juice and hair color.
关键词： Photoelectrochemical biosensor,Nanoporous TiO2,Cr(VI) ions,Visible light excitation.,Pb5S2I6 crystal
更新于2025-11-21 11:01:37
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Photoelectrochemical Biosensor Based on Co3O4 Nanoenzyme Coupled with PbS Quantum Dots for Hydrogen Peroxide Detection
摘要： A novel kind of hydrogen peroxide (H2O2) photoelectrochemical (PEC) sensor was constructed based on Co3O4 and PbS nanomaterials modified indium tin oxide (ITO) photoelectrode. The Co3O4 nanoparticles, as mimic enzyme of catalase (CAT), can catalyze H2O2 to generate oxygen (O2) in suit. Then the electron acceptor of O2 enhances the cathodic photocurrent of the photoelectrode. The PEC sensor exhibited high sensitivity because of the formation of p-p type heterostructure between PbS and Co3O4 semiconductors. The photocurrent enhancement can be used to detect concentration of H2O2. The calibration plot was linear in the range from 5 to 250 μM and the detection limit was estimated to be 1.2 μM. The results demonstrated the possibility of nanozyme application in PEC biosensors and the substitution of Co3O4 nanozyme for the natural enzyme.
关键词： hydrogen peroxide,PbS,nanozyme,photoelectrochemical biosensor,Co3O4
更新于2025-11-19 16:56:42
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Photoelectrochemical biosensor for microRNA detection based on a MoS2/g-C3N4/black TiO2 heterojunction with Histostar@AuNPs for signal amplification
摘要： Herein, a novel photoelectrochemical (PEC) biosensor was developed for the ultrasensitive detection of microRNA-396a based on a MoS2/g-C3N4/black TiO2 heterojunction as the photoactive material and gold nanoparticles carrying Histostar antibodies (Histostar@AuNPs) for signal amplification. Briefly, MoS2/g-C3N4/black TiO2 was deposited on an indium tin oxide (ITO) electrode surface, after which gold nanoparticles (AuNPs) and probe DNA were assembled on the modified electrode. Hybridization with miRNA-396a resulted in a rigid DNA:RNA hybrid being formed, which was recognized by the S9.6 antibody. The captured antibody can further conjugate with the secondary IgG antibodies of Histostar@AuNPs, thereby leading to the immobilization of horse radish peroxidase (HRP). In the presence of HRP, the oxidation of 4-chloro-1-naphthol (4-CN) by H2O2 was accelerated, producing the insoluble product benzo-4-chlorohexadienone on the electrode surface and causing a significant decrease in the photocurrent. The developed biosensor could detect miRNA-396a at concentrations from 0.5 fM to 5000 fM, with a detection limit of 0.13 fM. Further, the proposed method can also be used to investigate the effect of heavy metal ions on the expression level of miRNAs. Results suggest that the biosensor developed herein offers a promising platform for the ultrasensitive detection of miRNA.
关键词： S9.6 antibody,Histostar@AuNPs,MicroRNA detection,MoS2/g-C3N4/black TiO2 heterojunction,Photoelectrochemical biosensor
更新于2025-11-14 17:04:02
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Highly Sensitive Photoelectrochemical Biosensor Based on Quantum Dots Sensitizing Bi <sub/>2</sub> Te <sub/>3</sub> Nanosheets and DNA-Amplifying Strategies
摘要： In this work, the Bi2Te3 nanosheets treated by N-vinyl-Pyrrolidinone (NVP) showed the highly sufficient and stable photocurrent for being served as novel photoactive material. Accordingly, with CdTe quantum dots (QDs) sensitizing the Bi2Te3 nanosheets, a photoelectrochemical (PEC) biosensor coupling of DNA amplifying strategies was constructed for sensitive miRNA-21 detection. Initially, the Bi2Te3 nanosheets on electrode have conductive surface states with dissipationless electronic property, thus providing a highly stable photocurrent as well as large surface-to-volume ratio. Then, with the participation of target miRNA-21 and auxiliary DNA, the strand displacement amplification (SDA) took place, thereby opening substantial DNA hairpins for triggering next hybridization chain reaction (HCR). Through the HCR, long DNA tails decorated with CdTe QDs could thus be assembled on electrode for enhancing the photocurrent of Bi2Te3 nanosheets. As a result, the proposed PEC biosensor showed a wide detection range from 10 fM to 100 pM with a detection limit (LOD) of 3.3 fM, displaying a promising avenue to construct simply, ultrasensitive and stable analytical techniques and a tremendous potential in bioanalysis and early clinical diagnosis.
关键词： DNA amplifying strategies,Bi2Te3 nanosheets,sensitive detection,CdTe quantum dots,photoelectrochemical biosensor
更新于2025-09-23 15:19:57
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Photoelectrochemical biosensor for hydroxymethylated DNA detection and T4-β-glucosyltransferase activity assay based on WS2 nanosheets and carbon dots
摘要： 5-Hydroxymethylcytosine (5hmC) plays an important role in switching genes on and off in mammals, and it is implicated in both embryonic development and cancer progression. Herein, a novel photoelectrochemical (PEC) biosensor was developed for 5hmC detection based on WS2 nanosheets as the photoactive material and boronic acid functionalized carbon dots (B-CDs) for signal amplification unit. This biosensor can also be used for T4-β-glucosyltransferase (β-GT) activity assessment. Firstly, WS2 nanosheets and gold nanoparticles (AuNPs) were immobilized on an ITO electrode surface. Then probe DNA was immobilized on this electrode surface via Au-S bond. Afterwards, the complementary DNA containing 5hmC was then captured on the modified electrode surface by hybridization. Subsequently, β-GT transferred glucose from uridine diphosphoglucose to the hydroxyl groups of the 5hmC residues. After glycosylation, B-CDs could further be immobilized on the modified electrode surface resulting in a strong photocurrent. The PEC biosensor afforded high selectivity, excellent sensitivity and good reproducibility, with detection limits of 0.0034 nM and 0.028 unit/mL for 5hmC and β-GT, respectively. Results demonstrate that the photoelectrochemical strategy introduced here based on WS2 nanosheets and B-CDs offers a versatile platform for hydroxymethylated DNA detection, β-GT activity assessment and β-GT inhibitor screening.
关键词： Photoelectrochemical biosensor,DNA hydroxymethylation,β-Glucosyltransferase,WS2 nanosheets,carbon dots
更新于2025-09-09 09:28:46
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A TiO2/g-C3N4/CdS Nanocomposite-Based Photoelectrochemical Biosensor for Ultrasensitive Evaluation of T4 Polynucleotide Kinase Activity
摘要： Herein, an efficient photoelectrochemical (PEC) platform was constructed by a co-sensitization strategy with a cascade energy level arrangement for the ultrasensitive evaluation of T4 polynucleotide kinase (T4 PNK). Based on CdSe quantum dots (QDs) with an extremely narrow bandgap, this co-sensitization strategy offered a highly efficient sensitizer with a matching band-edge level of a ternary TiO2/g-C3N4/CdS nanocomposite. In this protocol, the ternary nanocomposite was first prepared to serve as the matrix to construct the PEC sensing platform. On the other hand, a well-designed hairpin DNA1 probe with 5’-hydroxyl termini was specifically phosphorylated by T4 PNK which would be selectively cleaved with lambda exonuclease (λ-Exo) outputting 3’-thiol end ssDNA2. After tagged with CdSe QDs, ssDNA2 was captured by the complementary capture DNA3 on the electrode surface. As a result, CdSe QDs were in close contact with the ternary nanocomposite matrix, leading to an enhanced photocurrent response. Therefore, this proposed PEC platform displayed an analytical performance with a wide linear range from 0.0001 to 0.02 U mL-1 and a low detection limit down to 6.9 × 10-5 U mL-1. Moreover, this ternary nanocomposite-based platform exhibited excellent selectivity, good reproducibility, and remarkable storage stability, which shows the great potential for the T4 PNK detection and inhibitor screening.
关键词： CdSe quantum dots,T4 polynucleotide kinase,ternary nanocomposite,co-sensitization strategy,photoelectrochemical biosensor
更新于2025-09-04 15:30:14
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Dual-Channel Photoelectrochemical Ratiometric Aptasensor with Up-converting Nanocrystals Using Spatial-Resolved Technique on Homemade 3D Printed Device
摘要： A near-infrared light (NIRL)-activated ratiometric photoelectrochemical (PEC) aptasensor was fabricated for detection of carcinoembryonic antigen (CEA) coupling with upconversion nanoparticles (UCNPs)-semiconductor nanocrystals-based spatial-resolved technique on a homemade 3D printing device in which a self-regulating integrated electrode was designed for dual signal readout. The as-prepared NaYF4:Yb, Er UCNPs@CdTe nanocrystals were initially assembled on two adjacent photoelectrodes, then CEA aptamer 1 (A1) and capture DNA (CA) were modified onto two working photoelectrodes (WP1 and WP2) through covalent binding, respectively, and then gold nanoparticle-labeled CEA aptamer 2 (Au NP-A2) were immobilized on the surface of functional WP2 for the formation of double-stranded DNA. Upon target CEA introduction, the various concentrations of CEA were captured on the WP1, whereas the binding of the CEA with Au NP-A2 could be released from the WP2 thanks to the highly affinity of CEA toward A2. The dual signal readout with the 'signal-off' of WP1 and 'signal-on' of WP2 were employed for the spatial-resolved PEC (SR-PEC) strategy to detect CEA as an analytical model. Combining NaYF4:Yb, Er UCNPs@CdTe nanocrystals with spatial-resolved model on 3D printing device, the PEC ratiometric aptasensor based on steric hindrance effect and exciton-plasmon interactions (EPI) exhibited a linear range from 10.0 pg mL-1 to 5.0 ng mL-1 with a limit of detection of 4.8 pg mL-1 under 980 nm illumination. The SR-PEC ratiometric strategy showed acceptable stability and reproducibility with a superior anti-interference ability. This approach can provide the guidance for the design of ratiometric, multiplexed and point-of-care biosensors.
关键词： 3D printing device,upconversion nanoparticles,Photoelectrochemical biosensor,ratiometric,spatial-resolved technique,carcinoembryonic antigen
更新于2025-09-04 15:30:14