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ACS Appl Mater Interfaces. 2017 Jan 11;9(1):136-144. doi: 10.1021/acsami.6b12434. Epub 2016 Dec 22.

Fluorescent Biosensor for Phosphate Determination Based on Immobilized Polyfluorene-Liposomal Nanoparticles Coupled with Alkaline Phosphatase.

Author information

1
Instituto de Biología Molecular y Celular, Universidad Miguel Hernández , 03202, Elche, Alicante, Spain.

Abstract

This work describes the development of a novel fluorescent biosensor based on the inhibition of alkaline phosphatase (ALP). The biosensor is composed of the enzyme ALP and the conjugated cationic polyfluorene HTMA-PFP. The working principle of the biosensor is based on the fluorescence quenching of this polyelectrolyte by p-nitrophenol (PNP), a product of the hydrolysis reaction of p-nitrophenyl phosphate (PNPP) catalyzed by ALP. Because HTMA-PFP forms unstable aggregates in buffer, with low fluorescence efficiency, previous stabilization of the polyelectrolyte was required before the development of the biosensor. HTMA-PFP was stabilized through its interaction with lipid vesicles to obtain stable blue-emitting nanoparticles (NPs). Fluorescent NPs were characterized, and the ability to be quenched by PNP was evaluated. These nanoparticles were coupled to ALP and entrapped in a sol-gel matrix to produce a biosensor that can serve as a screening platform to identify ALP inhibitors. The components of the biosensor were examined before and after sol-gel entrapment, and the biosensor was optimized to allow the determination of phosphate ion in aqueous medium.

KEYWORDS:

alkaline phosphatase inhibitors; biosensor; conjugated polyelectrolytes; fluorescent nanoparticles; lipid vesicles; p-nitrophenol; phosphate ion

PMID:
27966351
DOI:
10.1021/acsami.6b12434
[Indexed for MEDLINE]

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