Hydrophilic poly (ethylene glycol) capped poly (lactic-co-glycolic) acid nanoparticles for subcutaneous delivery of insulin in diabetic rats

[Display omitted] •Low molecular weight PLGA copolymers were synthesized by melt polycondensation.•The insulin loaded PEG capped PLGA NPs (ISPPLG NPs) were synthesized by water-oil-water emulsion solvent evaporation method.•The in-vivo studies of ISPPLG NPs carried out in diabetic rats by subcutaneo...

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Published inInternational journal of biological macromolecules Vol. 95; pp. 1190 - 1198
Main Authors S, Saravanan, S, Malathi, P S L, Sesh, S, Selvasubramanian, S, Balasubramanian, V, Pandiyan
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.02.2017
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Summary:[Display omitted] •Low molecular weight PLGA copolymers were synthesized by melt polycondensation.•The insulin loaded PEG capped PLGA NPs (ISPPLG NPs) were synthesized by water-oil-water emulsion solvent evaporation method.•The in-vivo studies of ISPPLG NPs carried out in diabetic rats by subcutaneous administration show considerable reduction in serum glucose level.•Histopathological studies reveal that ISPPLG NPs could restore the damages caused by oxidants during hyperglycaemia.•Synthesis of PEG capped PLGA Nps by water-oil-water emulsion solvent evaporation method. The aim of the present study is to evaluate the effect of insulin loaded poly(ethylene glycol) capped poly(lactic-co-glycolic)acid nanoparticles (ISPPLG NPs) by subcutaneous administration in diabetic rats. A series of biodegradable low molecular weight PLGA [90/10 (PLG2) and 80/20 (PLG4)] copolymers were synthesized by melt polycondensation and their ISPPLG NPs were synthesized by water-oil-water (W/O/W) emulsion solvent evaporation method. The PLGA copolymers and their nanoparticles were characterized. The maximum encapsulation efficiency of ISPPLG4 NPs is 66% and the diameter of the nanoparticles is about 140nm. The in-vivo studies of ISPPLG NPs carried out in diabetic rats by subcutaneous administration show considerable reduction in serum glucose level along with partial restoration of tissue defense systems. Histopathological studies reveal that ISPPLG NPs could restore the damages caused by oxidants during hyperglycaemia. The subcutaneous administration of ISPPLG4 NPs is thus an effective method of reducing hyperglycaemia associated complications.
ISSN:0141-8130
1879-0003
DOI:10.1016/j.ijbiomac.2016.11.009