
doi: 10.1271/bbb.68.749
pmid: 15056913
Insulin microcrystals were encapsulated (microcrystal/PLGA) within poly(lactide-co-glycolide) (PLGA 50:50) by the multiple emulsification solvent evaporation technique and compared with insulin solution microspheres (solution/PLGA) in terms of their morphology, size distribution, drug content, encapsulation efficiency, and stability of insulin during release.
insulin, Polymers, Capsules, stability, microcrystal, Drug Delivery Systems, poly (lactide-<I>co</I>-glycolide) (PLGA), Polylactic Acid-Polyglycolic Acid Copolymer, microsphere, Microscopy, Electron, Scanning, Insulin, Lactic Acid, Polyglycolic Acid
insulin, Polymers, Capsules, stability, microcrystal, Drug Delivery Systems, poly (lactide-<I>co</I>-glycolide) (PLGA), Polylactic Acid-Polyglycolic Acid Copolymer, microsphere, Microscopy, Electron, Scanning, Insulin, Lactic Acid, Polyglycolic Acid
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