Use of Surfactants in Polylactic Acid Protein Microspheres
- 1 January 1995
- journal article
- research article
- Published by Taylor & Francis in Drug Development and Industrial Pharmacy
- Vol. 21 (5) , 549-558
- https://doi.org/10.3109/03639049509048122
Abstract
This paper describes the effect on the in vitro release profile of poly(D,L-lactic) acid (DL-PLA), and poly(D,L-lactic-co-glycolic) acid (D,L-PLGA), microspheres containing BSA as a model protein prepared by the double emulsion technique, due to the addition of surfactant agents in the first emulsion (W/O) made using two type of homogenizer. In the first stage D,L-PLA microspheres were prepared with a mixture of Span-40® and Tween-80® to get HLB 6 and 7, W/O ratio in the first emulsion 1:3 and two types of homogenizers (High pressure homogenizer and Sonicator) against microspheres without surfactants. The microspheres made with high pressure homogenizer presented less BSA trapping efficiency and higher burst effect than those made with sonicator which showed a very slow release rate. In the second stage D,L-PLA and D,L-PLGA microspheres with and without surfactant agents and using sonicator were compared. The BSA release from D,L-PLGA microspheres was continuous, but batches with HLB 6 and without surfactant presented a initial release of 55% of the incorporated BSA while batch with HLB 7 showed less burst effect and slower release rate. The D,L-PLA microspheres released a percentage of incorporated drug at the beginning of the in vitro assay and then stopped.Keywords
This publication has 13 references indexed in Scilit:
- Effects of polymerization variables on PLGA properties: molecular weight, composition and chain structureInternational Journal of Pharmaceutics, 1993
- Evaluation of a Microreservoir-Type Biodegradable Microcapsule for Controlled Release of ProteinsDrug Development and Industrial Pharmacy, 1993
- In Vitro and In Vivo Release of Poly(DL-Lactic Acid) Microspheres Containing Neurotensin Analogue Prepared by Novel Oil-in-Water Solvent Evaporation MethodJournal of Pharmaceutical Sciences, 1992
- A biodegradable delivery system for peptides: preclinical experience with the gonadotrophin-releasing hormone agonist ZoladexJournal of Controlled Release, 1992
- Factors influencing the release of peptides and proteins from biodegradable parenteral depot systemsJournal of Controlled Release, 1992
- Release of peptides from sustained delivery systems (microcapsules and microparticles) in vivoInternational Journal of Peptide and Protein Research, 1990
- Controlled-release of leuprolide acetate from polylactic acid or copoly(lactic/glycolic) acid microcapsules: Influence of molecular weight and copolymer ratio of polymer.CHEMICAL & PHARMACEUTICAL BULLETIN, 1988
- In vivo release profiles of leuprolide acetate from microcapsules prepared with polylactic acids or copoly(lactic/glycolic) acids and in vivo degradation of these polymers.CHEMICAL & PHARMACEUTICAL BULLETIN, 1988
- A new technique to efficiently entrap leuprolide acetate into microcapsules of polylactic acid or copoly(lactic/glycolic) acid.CHEMICAL & PHARMACEUTICAL BULLETIN, 1988
- Controlled Release of a Luteinizing Hormone-Releasing Hormone Analogue from Poly(d,l-lactide—co-glycolide) MicrospheresJournal of Pharmaceutical Sciences, 1984