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Original Article

In vitro Ciprofloxacin release from poly(lactide-co-glycolide) microspheres

, , , &
Pages 155-161 | Received 01 Sep 1995, Accepted 10 Oct 1995, Published online: 26 Jun 2009
 

Abstract

Biodegradable microspheres of PLGA (75:25 and 50:50) containing Ciprofloxacin (CIPRO) were prepared by two different procedures based on: (i) solvent-evaporation, and (ii) evaporation-extraction of the organic phase. The encapsulation rates from the different formulations were quite variable, as well the release patterns of the drug from the microspheres. The evaporation-extraction method seems to be more efficient for the CIPRO encapsulation compared with the solvent evaporation method. The 50:50 PLGA composition released the drug faster and showed degradation signs after incubation in aqueous medium in both manufacturing methodologies.

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