| Literature DB >> 23648263 |
Suchanda Banerjee1, Priyabrata Sarkar, Anthony P F Turner.
Abstract
Glucose-6-phosphate (G6P) plays an important role in carbohydrate metabolism of all living organisms. Compared with the conventional analytical methods available for estimation of G6P, the biosensors having relative simplicity, specificity, low cost, and fast response time are a promising alternative. We have reported a G6P biosensor based on screen-printed electrode using Prussian Blue (PB) nanoparticles and enzymes, glucose-6-phosphate dehydrogenase, and glutathione reductase. The PB nanoparticles acted as a mediator and thereby enhanced the rate of electron transfer in a bienzymatic reaction. The Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy study confirmed the formation of PB, whereas atomic force microscopy revealed that PB nanoparticles were approximately 25 to 30 nm in diameter. Various optimization studies, such as pH, enzyme, and cofactor loading, were conducted to obtain maximum amperometric responses for G6P measurement. The developed G6P biosensor showed a broad linear response in the range of 0.01 to 1.25 mM, with a detection limit of 2.3 μM and sensitivity of 63.3 μA/mM at a signal-to-noise ratio of 3 within 15s at an applied working potential of -100 mV. The proposed G6P biosensor also exhibited good stability and excellent anti-interference ability, and it worked well for serum samples.Entities:
Keywords: Amperometry; Glucose-6-phosphate; Prussian Blue nanoparticles; Screen-printed electrode
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Year: 2013 PMID: 23648263 DOI: 10.1016/j.ab.2013.04.025
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365