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Accelerating protein release from microparticles for regenerative medicine applications
There is a need to control the spatio-temporal release kinetics of growth factors in order to mitigate current usage of high doses. A novel delivery system, capable of providing both structural support and controlled release kinetics, has been developed from PLGA microparticles. The inclusion of a h...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654200/ https://www.ncbi.nlm.nih.gov/pubmed/23623071 http://dx.doi.org/10.1016/j.msec.2013.02.020 |
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author | White, Lisa J. Kirby, Giles T.S. Cox, Helen C. Qodratnama, Roozbeh Qutachi, Omar Rose, Felicity R.A.J. Shakesheff, Kevin M. |
author_facet | White, Lisa J. Kirby, Giles T.S. Cox, Helen C. Qodratnama, Roozbeh Qutachi, Omar Rose, Felicity R.A.J. Shakesheff, Kevin M. |
author_sort | White, Lisa J. |
collection | PubMed |
description | There is a need to control the spatio-temporal release kinetics of growth factors in order to mitigate current usage of high doses. A novel delivery system, capable of providing both structural support and controlled release kinetics, has been developed from PLGA microparticles. The inclusion of a hydrophilic PLGA–PEG–PLGA triblock copolymer altered release kinetics such that they were decoupled from polymer degradation. A quasi zero order release profile over four weeks was produced using 10% w/w PLGA–PEG–PLGA with 50:50 PLGA whereas complete and sustained release was achieved over ten days using 30% w/w PLGA–PEG–PLGA with 85:15 PLGA and over four days using 30% w/w PLGA–PEG–PLGA with 50:50 PLGA. These three formulations are promising candidates for delivery of growth factors such as BMP-2, PDGF and VEGF. Release profiles were also modified by mixing microparticles of two different formulations providing another route, not previously reported, for controlling release kinetics. This system provides customisable, localised and controlled delivery with adjustable release profiles, which will improve the efficacy and safety of recombinant growth factor delivery. |
format | Online Article Text |
id | pubmed-3654200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-36542002013-07-01 Accelerating protein release from microparticles for regenerative medicine applications White, Lisa J. Kirby, Giles T.S. Cox, Helen C. Qodratnama, Roozbeh Qutachi, Omar Rose, Felicity R.A.J. Shakesheff, Kevin M. Mater Sci Eng C Mater Biol Appl Article There is a need to control the spatio-temporal release kinetics of growth factors in order to mitigate current usage of high doses. A novel delivery system, capable of providing both structural support and controlled release kinetics, has been developed from PLGA microparticles. The inclusion of a hydrophilic PLGA–PEG–PLGA triblock copolymer altered release kinetics such that they were decoupled from polymer degradation. A quasi zero order release profile over four weeks was produced using 10% w/w PLGA–PEG–PLGA with 50:50 PLGA whereas complete and sustained release was achieved over ten days using 30% w/w PLGA–PEG–PLGA with 85:15 PLGA and over four days using 30% w/w PLGA–PEG–PLGA with 50:50 PLGA. These three formulations are promising candidates for delivery of growth factors such as BMP-2, PDGF and VEGF. Release profiles were also modified by mixing microparticles of two different formulations providing another route, not previously reported, for controlling release kinetics. This system provides customisable, localised and controlled delivery with adjustable release profiles, which will improve the efficacy and safety of recombinant growth factor delivery. Elsevier 2013-07-01 /pmc/articles/PMC3654200/ /pubmed/23623071 http://dx.doi.org/10.1016/j.msec.2013.02.020 Text en © 2013 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article White, Lisa J. Kirby, Giles T.S. Cox, Helen C. Qodratnama, Roozbeh Qutachi, Omar Rose, Felicity R.A.J. Shakesheff, Kevin M. Accelerating protein release from microparticles for regenerative medicine applications |
title | Accelerating protein release from microparticles for regenerative medicine applications |
title_full | Accelerating protein release from microparticles for regenerative medicine applications |
title_fullStr | Accelerating protein release from microparticles for regenerative medicine applications |
title_full_unstemmed | Accelerating protein release from microparticles for regenerative medicine applications |
title_short | Accelerating protein release from microparticles for regenerative medicine applications |
title_sort | accelerating protein release from microparticles for regenerative medicine applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3654200/ https://www.ncbi.nlm.nih.gov/pubmed/23623071 http://dx.doi.org/10.1016/j.msec.2013.02.020 |
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