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Transition from passive to active targeting of oral insulin nanomedicines: Enhancement in bioavailability and glycemic control in diabetes

dc.contributor.authorKaklotar D.; Agrawal P.; Abdulla A.; Singh R.P.; Sonali; Mehata A.K.; Singh S.; Mishra B.; Pandey B.L.; Trigunayat A.; Muthu M.S.
dc.date.accessioned2025-05-24T09:27:15Z
dc.description.abstractOral insulin nanomedicines are effective tools for therapy and management of both Type I and Type II diabetes. This review summarizes the various nanocarriers developed so far in the literature for oral delivery of insulin. It includes lipid-based (i.e., solid lipid nanoparticles and liposomes) and polymeric-based insulin nanomedicines (i.e., chitosan nanoparticles, alginate nanoparticles, dextran nanoparticles and nanoparticles of synthetic polymers) for sustained, controlled and targeted oral delivery of insulin. Mainly, goblet cell-targeting, vitamin B12 receptor-targeting, folate receptor-targeting and transferrin receptor-targeting aspects were focused. Currently, passive and active targeting approaches of oral insulin nanomedicines have improved the oral absorption of insulin and its bioavailability (up to 14%) that produced effective glycaemic control in in vivo models. These results indicate a promising future of oral insulin nanomedicines for the treatment of diabetes. © 2016 Future Medicine Ltd.
dc.identifier.doihttps://doi.org/10.2217/nnm.16.43
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/16034
dc.relation.ispartofseriesNanomedicine
dc.titleTransition from passive to active targeting of oral insulin nanomedicines: Enhancement in bioavailability and glycemic control in diabetes

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