Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers
The purpose of the is study is to examine the hydrolytic degradation of irradiated crosslinked poly(L-lactide) (PLLA-ir) and poly(lactide-co-glycolide) (PLGA-ir). It was observed that upon crosslinking, the samples demonstrated enhanced mechanical properties and thermal stability. They also exhibite...
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sg-ntu-dr.10356-153092023-03-04T15:41:18Z Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers Han, Sheng Chou. Loo Say Chye Joachim School of Materials Science and Engineering Pan Jie DRNTU::Engineering::Materials::Biomaterials The purpose of the is study is to examine the hydrolytic degradation of irradiated crosslinked poly(L-lactide) (PLLA-ir) and poly(lactide-co-glycolide) (PLGA-ir). It was observed that upon crosslinking, the samples demonstrated enhanced mechanical properties and thermal stability. They also exhibited very insignificant mass loss and water uptake over a degradation period of 12 weeks. There was notable loss in the gel fraction formed, although it was not enough to affect the physical state of the polymers. The polymers were able to retain its geometrical structure post-degradation. PLLA-ir and PLGA-ir were also observed to be able to retain much of their mechanical properties (yield strength, Young’s modulus and strain at yield) after hydrolysis, although the polymers were more brittle than before irradiation. There was also no observable change in the thermal stability of the polymers as they were degraded. Given its superior resistance to hydrolytic degradation, crosslinked PLLA-ir and PLGA-ir could potentially be ideal choices for biomedical applications like fixation or load bearing devices, over an implantation period of 3 to 6 months. Bachelor of Engineering (Materials Engineering) 2009-04-27T07:19:16Z 2009-04-27T07:19:16Z 2009 2009 Final Year Project (FYP) http://hdl.handle.net/10356/15309 en Nanyang Technological University 43 p. application/pdf |
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DRNTU::Engineering::Materials::Biomaterials Han, Sheng Chou. Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers |
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The purpose of the is study is to examine the hydrolytic degradation of irradiated crosslinked poly(L-lactide) (PLLA-ir) and poly(lactide-co-glycolide) (PLGA-ir). It was observed that upon crosslinking, the samples demonstrated enhanced mechanical properties and thermal stability. They also exhibited very insignificant mass loss and water uptake over a degradation period of 12 weeks. There was notable loss in the gel fraction formed, although it was not enough to affect the physical state of the polymers. The polymers were able to retain its geometrical structure post-degradation. PLLA-ir and PLGA-ir were also observed to be able to retain much of their mechanical properties (yield strength, Young’s modulus and strain at yield) after hydrolysis, although the polymers were more brittle than before irradiation. There was also no observable change in the thermal stability of the polymers as they were degraded. Given its superior resistance to hydrolytic degradation, crosslinked PLLA-ir and PLGA-ir could potentially be ideal choices for biomedical applications like fixation or load bearing devices, over an implantation period of 3 to 6 months. |
author2 |
Loo Say Chye Joachim |
author_facet |
Loo Say Chye Joachim Han, Sheng Chou. |
format |
Final Year Project |
author |
Han, Sheng Chou. |
author_sort |
Han, Sheng Chou. |
title |
Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers |
title_short |
Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers |
title_full |
Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers |
title_fullStr |
Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers |
title_full_unstemmed |
Hydrolytic degradation of cross-linked irradiated PLLA and PLGA polymers |
title_sort |
hydrolytic degradation of cross-linked irradiated plla and plga polymers |
publishDate |
2009 |
url |
http://hdl.handle.net/10356/15309 |
_version_ |
1759855889827758080 |