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Stereocomplexes based on poly(lactic acid) and insulin: formulation and release studies
Diastereoisomeric complexes of insulin with d-poly(lactic acid) ( d-PLA) or stereocomplexes of d- and l-PLA entrapping insulin were discovered. The complexes were spontaneously formed when insulin and d-PLA were mixed together in acetonitrile solution. Complexes of insulin– d-PLA formed a microparti...
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Published in: | Biomaterials 2002-11, Vol.23 (22), p.4389-4396 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Diastereoisomeric complexes of insulin with
d-poly(lactic acid) (
d-PLA) or stereocomplexes of
d- and
l-PLA entrapping insulin were discovered. The complexes were spontaneously formed when insulin and
d-PLA were mixed together in acetonitrile solution. Complexes of insulin–
d-PLA formed a microparticulate precipitate after a few hours in the solution. The porous 1–3
μm precipitate, which contained both insulin and
d-PLA, was insoluble in solvents that dissolve isotactic PLA, and had an additional transition temperature at 169°C. When suspending these particles in buffer solution of pH 7.4, 37°C, insulin was constantly released for a few weeks.
l-PLA or
d,
l-PLA did not form a precipitate with insulin, which indicates stereospecificity to the complex formation. Microparticulates were also obtained when
l-PLA was added to the
d-PLA–insulin solution. In this case two types of complexes,
d-PLA–insulin and
d-PLA–
l-PLA complexes, were formed. These macromolecular stereocomplexes may form the onset of the development of a new generation of controlled release systems for peptides and proteins, by molecular complexation with enantiomeric polymers. |
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ISSN: | 0142-9612 1878-5905 |
DOI: | 10.1016/S0142-9612(02)00179-5 |