Development of a polypyrrole-based amperometric phosphate biosensor

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Abstract

A biosensor is developed by co-entrapment of Purin Nucleoside Phosphorylase (PNP) and xanthine oxidase (XOD) and potassium ferrocyanide (K4Fe(CN)6 into a polypyrrole (PPy) film via., galvanostatic polymerisation of pyrrole. The optimum conditions for formation of the Ppy-PNP-XOD-Fe(CN)64- film are 0.3 M pynole. 6.2 UmL-1 XOD, 49 UmL-1 PNP, 40 mM K4Fe (CN)6, polymerisation period of 200 sec and an applied current density of 0.5 mA cm-2. The optimum potential for the amperometric biosensing of phosphate was 200 mV vs. Ag/AgCl (3 M KCl) in 0.05 M barbitone buffer. The achievable linear concentration range was between 0.1 and 1 mM, while the minimum detectable amount was 10 μM. © 2009 Asian Network for Scientific Information.

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APA

Lawal, A. T., & Adeloju, S. B. (2009). Development of a polypyrrole-based amperometric phosphate biosensor. Journal of Applied Sciences, 9(10), 1907–1914. https://doi.org/10.3923/jas.2009.1907.1914

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