Low-Potential Photoelectrochemical Biosensing Using Porphyrin-Functionalized TiO2 Nanoparticles

A novel photoelectrochemical biosensing platform for the detection of biomolecules at relatively low applied potentials was constructed using porphyrin-functionalized TiO2 nanoparticles. The functional TiO2 nanoparticles were prepared by dentate binding of TiO2 with sulfonic groups of water-soluble...

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Veröffentlicht in:Analytical chemistry (Washington) 2010-10, Vol.82 (20), p.8711-8716
Hauptverfasser: Tu, Wenwen, Dong, Yitong, Lei, Jianping, Ju, Huangxian
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Sprache:eng
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Zusammenfassung:A novel photoelectrochemical biosensing platform for the detection of biomolecules at relatively low applied potentials was constructed using porphyrin-functionalized TiO2 nanoparticles. The functional TiO2 nanoparticles were prepared by dentate binding of TiO2 with sulfonic groups of water-soluble [meso-tetrakis(4-sulfonatophenyl)porphyrin] iron(III) monochloride (FeTPPS) and characterized by transmission electron microscopy; contact angle measurement; and Raman, X-ray photoelectron, and ultraviolet−visible absorption spectroscopies. The functional nanoparticles showed good dispersion in water and on indium tin oxide (ITO) surface. The resulting FeTPPS-TiO2-modified ITO electrode showed a photocurrent response at +0.2 V to a light excitation at 380 nm, which could be further sensitized through an oxidation process of biomolecules by the hole-injected FeTPPS. Using glutathione as a model, a methodology for sensitive photoelectrochemical biosensing at low potential was thus developed. Under optimal conditions, the proposed photoelectrochemical method could detect glutathione ranging from 0.05 to 2.4 mmol L−1 with a detection limit of 0.03 mmol L−1 at a signal-to-noise ratio of 3. The photoelectrochemical biosensor had an excellent specificity against anticancer drugs and could be successfully applied to the detection of reduced glutathione in gluthion injection, showing a promising application in photoelectrochemical biosensing.
ISSN:0003-2700
1520-6882
DOI:10.1021/ac102070f