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Jagriti Narang,1 Nitesh Malhotra,2 Chaitali Singhal,1 Gajendra Singh,3 Chandra Shekhar Pundir4 1Amity Institute of Nanotechnology, 2Amity Institute of Physiotherapy, Amity University, Noida, Uttar Pradesh, 3Department of Pharmacy, University of Health Sciences, 4Department of Biochemistry, M. D. University, Rohtak, Haryana, India Abstract: This paper reports the fabrication of highly sensitive metformin sensor based on Prussian blue (PB) nanocubes/carbon nanosphere (CNS) heterostructures composed of a perfect cube and spherical composite on a fluorine-doped tin oxide surface. Due to the excellent biocompatibility of PB nanocubes the PB/CNS based Mf sensor exhibited a wide linear range of 0.001–10mM with a response duration of less than 5s and a detection limit (based on signal to noise ratio) of 0.1µM. Keywords: metformin, PB nanocubes, carbon nanospheres, sensor, FTO electrode

The Structure of Rottlerin Part III

Background & objectives: The use of epoxy resin membrane as a support for immobilization of enzyme has resulted into improved sensitivity and stability of biosensors for uric acid, ascorbic acid and polyphenols. The present work was aimed to prepare an improved amperometric biosensor for determination of serum cholesterol required in the diagnostics and management of certain pathological conditions. Methods: Epoxy resin membrane with immobilized cholesterol oxidase was mounted on the cleaned platinum (Pt) electrode with a parafilm to construct a working electrode. This working electrode along with Ag/AgCl as reference and Ag wire as an auxiliary electrode were connected through a three terminal electrometer to construct a cholesterol biosensor. Results: The sensor showed optimum response within 25 sec at pH 7.0 and 45°C. The linear working range of biosensor was 1.0 to 8.0 mM cholesterol. Km and Imax for cholesterol were 5.0 mM and 9.09 μA, respectively. The biosensor measured serum cholesterol. The minimum detection limit of the sensor was 1.0 mM. The mean analytical recoveries of added cholesterol in serum (2.84 and 4.13 mM) were 91.4±2.8 and 92.3±3.1 per cent (n=6), respectively. Within and between assay coefficient of variation (CV) were