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A macroporous TiO 2 film (M‐TiO 2 ), which was prepared by burning off the polystyrene microsphere (PS) template from a PS/TiO 2 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‐TiO 2 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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Zhou et al. (2015) studied this question.
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