Assessment of Biotransformed Silica Nanoparticle on Blood Glucose Level in Human: An In Vitro Investigation.

Indian J Clin Biochem

Formerly: Environmental Biochemistry and Molecular Biology Laboratory, Department of Biochemistry, University College of Medical Sciences and GTB Hospital, University of Delhi, Dilshad Garden, Delhi, 110095 India.

Published: January 2024

Diabetes has affected nearly half a billion people worldwide. According to current guidelines, glycemic control is essential to mitigate diabetic complications. The antihyperglycemic effects of various chemically synthesized nanoparticles have been reported in animal models. However, their impact on humans has not been previously reported. This study was conducted to biosynthesize and assess the antihyperglycemic property of silica nanoparticles (SiO-NPs) since they are non-toxic and biocompatible. SiO-NPs biosynthesized using the endophytic fungus . In this collaborative study, 26 people, either hyperglycemic or euglycemic, diagnosed at the Endocrinology Outpatients, according to the American Diabetes Association, USA, were recruited. Silica nanoparticles were characterized and assessed for in vitro antihyperglycemic property using blood samples. Particle size distribution based on TEM images confirms that the average size of silica nanoparticle is 25 nm and is monodispersed in nature. The XRD pattern shows that only one broad peak at 2θ = 220 corresponds to the plane (101) of silica nanoparticles. UV Visible spectra show the λ at 270 nm, peaks in FTIR at 1536 cm, 1640 cm, and 3420 cm for the protein cap. The mean blood glucose was 120.2 mg/dL in the 'SiO-NP untreated' group and decreased to 97.24 mg/dL in the 'SiO-NP treated' group. A paired t-test (P-value < 0.0001) indicates a strong relationship between antihyperglycemia and silica NP. In our study, it has been observed that the biosynthesized silica nanoparticles using the endophytic fungus show antihyperglycemic property in vitro.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10784254PMC
http://dx.doi.org/10.1007/s12291-022-01084-2DOI Listing

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