Preparation, characterization and in vitro release studies of insulin-loaded double-walled poly(lactide-co-glycolide) microspheres

The purpose of this study was to fabricate insulin-loaded double-walled and singlepolymer poly(lactide-co-glycolide) (PLGA) microspheres using a fast degrading glucose core, hydroxyl-terminated poly(lactide-co-glycolide) (Glu-PLGA) and a moderate degrading carboxyl-terminated PLGA polymers. A modifi...

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Bibliographic Details
Main Authors: Ansary, Md. Rezaul Haque, Rahman, Md. Mokhlesur, Awang, Mohamed, Katas, Haliza, Ab. Hadi, Hazrina, Abd Almonem, Doolaanea
Format: Article
Language:English
English
Published: Springer 2016
Subjects:
Online Access:http://irep.iium.edu.my/47774/1/Mokhles-DDTR-D-15-00072_R1.pdf
http://irep.iium.edu.my/47774/4/47774_Preparation%2C%20characterization_wos_scopus.pdf
http://irep.iium.edu.my/47774/
http://link.springer.com/article/10.1007%2Fs13346-016-0278-y
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Institution: Universiti Islam Antarabangsa Malaysia
Language: English
English
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Summary:The purpose of this study was to fabricate insulin-loaded double-walled and singlepolymer poly(lactide-co-glycolide) (PLGA) microspheres using a fast degrading glucose core, hydroxyl-terminated poly(lactide-co-glycolide) (Glu-PLGA) and a moderate degrading carboxyl-terminated PLGA polymers. A modified water-in-oil-in-oilin-water (w/o/o/w) emulsion solvent evaporation technique was employed to prepare double-walled microspheres, whereas single-polymer microspheres were fabricated by a conventional water-in-oil-in-water (w/o/w) emulsion solvent evaporation method. The effect of fabrication techniques and polymer characteristics on microspheres size,morphology, encapsulation efficiency, in vitro release and insulin stability were evaluated. The prepared double-walled microspheres were essentially non-porous,smooth surfaced, and spherical in shape, whereas single-polymer microspheres were highly porous. Double-walled microspheres exhibited a significantly reduced initial burst followed by sustained and almost complete release of insulin compared to singlepolymer microspheres. Initial burst release was further suppressed from double-walled microspheres when the mass ratio of the component polymers was increased. In conclusion, double-walled microspheres made of Glu-PLGA and PLGA can be a potential delivery system of therapeutic insulin.