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In vivo study found improved fasting blood glucose levels with nano-metformin, suggesting enhanced binding affinities.
The particle size of the antihyperglycemic drug metformin has been reduced to the nano range. The structural and microstructural characterizations of pure metformin and nano-metformin have been carried out by the Rietveld refinement of the XRD patterns and by analyzing UV-Vis absorption spectra. A docking study has also been performed to calculate the binding affinities of pure metformin and nano-metformin. To confirm the theoretical result of the docking study, an in vivo study has also been performed by administering both pure metformin and nano-metformin to 18-h-fasted normal mice. It has been confirmed that the FBGLs (fasting blood glucose levels) of mice have been reduced more in the case of nano-metformin compared to that of pure metformin. This in vivo result is in good agreement with the molecular docking result, which confirmed the higher binding efficacy of nano-metformin than that of pure metformin. This study proposes a new route to enhance the efficacy of a drug solely by reducing its particle size to the nanoscale without using any external agents.
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Ghosh et al. (2026) studied this question.
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