کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5521601 | 1545310 | 2017 | 9 صفحه PDF | دانلود رایگان |
This study aimed to assess the biodistribution of antihyperglycemic insulin-loaded alginate/dextran sulfate-based nanoparticles dual coated with chitosan and technetium-99m-albumin (99mTc-BSA) after oral administration.The oral administration of 50Â IU/kg insulin-loaded nanoparticles to type 1 diabetic rats showed prolonged antihyperglycemic effects up to 12Â h and relative pharmacological availability of 5.04% comparing to the subcutaneous administration. The oral antihyperglycemic effect was further compared between type 1 and type 2 diabetic models by the intraperitoneal glucose tolerance test, revealing that the effect lasted longer in the type 1 diabetic model. 99mTc-BSA revealed to be a good nanoparticles' tracer since there was no systemic absorption and 99mTc-BSA-nanoparticles were capable of increasing their residence time in the intestinal epithelium of balb-c mice when compared with 99mTc-BSA biodistribution. Thus, this biopolymeric-based delivery nanoparticulate system is a promising tool for the therapy of type 1 and type 2 diabetic individuals and prevention of T1D.
Biodistribution of insulin-loaded alginate/dextran sulfate-based nanoparticles dual coated with chitosan and 99mTc-albumin after oral administration. The comparison of the oral antihyperglycemic effect between type 1 and type 2 diabetic models after the intraperitoneal glucose tolerance test revealed that the effect lasted longer in the type 1 model and that the glycemia increased to a greater extend in the type 2 model.137
Journal: European Journal of Pharmaceutics and Biopharmaceutics - Volume 113, April 2017, Pages 88-96