Abstract
Alkaline phosphatase (ALP) was immobilized with cross-linking agents glutaraldehyde and cysteamine by forming a self-assembled monolayer on a screen printed gold electrode. ALP converts p-nitrophenyl phosphate to p-nitrophenol and phosphate. p-Nitrophenol loses H + ion and turns into the negatively charged compound p-nitrophenolate at medium pH. As a result, the unstable product formed is measured chronoamperometrically at an application potential of + 0.95 V. The biosensor response depends linearly on p-nitrophenyl phosphate concentration between 0.05 0.6 mM with a response time of 40 seconds. Detection limit of the biosensor is 0.033 mM. © 2011 Informa Healthcare USA, Inc.
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Yorganci, E., & Akyilmaz, E. (2011). Alkaline phosphatase based amperometric biosensor immobilized by cysteamine-glutaraldehyde modified self-assembled monolayer. Artificial Cells, Blood Substitutes, and Biotechnology, 39(5), 317–323. https://doi.org/10.3109/10731199.2011.563363
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