4.5 Article

CdSeTe@CdS@ZnS Quantum-Dot-Sensitized Macroporous Tio2 Film: A Multisignal-Amplified Photoelectrochemical Platform

Journal

CHEMPHYSCHEM
Volume 16, Issue 13, Pages 2826-2835

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.201500489

Keywords

apoptosis; biosensors; microporous materials; quantum dots; semiconductors

Funding

  1. National Basic Research Program of China [2011CB933502]
  2. National Natural Science Foundation of China [21335004, 21475057]
  3. Program for New Century Excellent Talents in University [NCET-12-0256]
  4. Scientific Research Foundation of Graduate School of Nanjing University [2013 CL11]

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A macroporous TiO2 film (M-TiO2), which was prepared by burning off the polystyrene microsphere (PS) template from a PS/TiO2 composite film, can provide a large active surface, improve electron-transport performance, and increase the photocurrent. Furthermore, core-shell-shell CdSeTe@CdS@ZnS quantum dots (QDs) were introduced to sensitize the M-TiO2 film, which can efficiently broaden the absorption spectra range, separate and transfer charge carriers, reduce recombination loss, and improve photovoltaic response, with a sensitization shell of CdS and a passivation shell of ZnS. A multisignal-amplified photoelectrochemical platform was fabricated by further modifying this film with a combination of biotin-DEVD-peptide (Biotin-Gly-Asp-Gly-Asp-Glu-Val-Asp-Gly-Cys) (which is specifically cleaved by caspase-3) and streptavidin-labeled alkaline phosphatase (SA-ALP). Under the enzymatic catalysis of ALP with the substrate 2-phospho-L-ascorbic acid trisodium salt (AAP), ascorbic acid (AA) was generated as a better electron donor, leading to increased photocurrent output. The activity of caspase-3, which depends on the amount of residual peptide on the electrode, was inversely proportional to the amount of AA. By monitoring the variation of photocurrent caused by AA, caspase-3 activity and the therapeutic effect of nilotinib (a special medicine of chronic myeloid leukemia, CML) were indirectly detected and evaluated. The photoelectrochemical platform can be used as a potential evaluation system for monitoring caspase-3 activity and drug effects.

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