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A biodegradable, injectable, gel system based on MPEG-b-(PCL-ran-PLLA) diblock copolymers with an adjustable therapeutic window.

Authors
Kang, YM; Lee, SH; Lee, JY; Son, JS; Kim, BS; Lee, B; Chun, HJ; Min, BH; Kim, JH; Kim, MS
Citation
Biomaterials, 31(9):2453-2469, 2010
Journal Title
Biomaterials
ISSN
0142-96121878-5905
Abstract
In situ-forming gel systems have drawn increasing attention for their potential use in a variety of biomedical applications. Here, we examined an in situ-forming gel system comprised of MPEG-b-PCL and MPEG-b-(PCL-ran-PLLA) diblock copolymers with different PLLA contents (0-10 mol%) in the PCL segment. The crystalline region of the PCL-ran-PLLA segment decreased with increasing PLLA content. The MPEG-b-(PCL-ran-PLLA) diblock copolymer solutions were liquid at room temperature and only MPEG-b-(PCL-ran-PLLA) diblock copolymer solutions with a PLLA content < or = 5 mol% in the PCL segment showed a sol-to-gel transition as the temperature was increased. The viscosity change associated with sol-to-gel phase transition depended on the PLLA content in the PCL segment. A MPEG-b-PCL diblock copolymer solution incubated in vitro showed increasing viscosity without degradation, whereas the viscosity of MPEG-b-(PCL-ran-PLLA) diblock copolymer solutions continuously and sharply decreased with increasing PLLA content in the PCL segment. As the amount of PLLA increased, the size of in vivo-formed MPEG-b-(PCL-ran-PLLA) gels after initial injection tended to gradually decrease because of hydrolytic degradation of the PLLA in the PCL-ran-PLLA segment. An immunohistochemical examination showed that in vivo MPEG-b-(PCL-ran-PLLA) diblock copolymer gels provoked only a modest inflammatory response. Collectively, our results show that the MPEG-b-(PCL-ran-PLLA) diblock copolymer gel described here could serve as a minimally invasive, therapeutic, in situ-forming gel system that offers an experimental window adjustable from a few weeks to a few months.
MeSH terms
AnimalsBiocompatible Materials/chemical synthesis*Chromatography, GelCrystallizationFluorescent Antibody TechniqueGelsImplants, ExperimentalInjectionsLactic Acid/chemical synthesis*Magnetic Resonance SpectroscopyPhase TransitionPolyesters/chemical synthesis*Polyethylene Glycols/chemical synthesis*Polymers/chemical synthesis*RatsSolutionsStaining and LabelingTemperatureViscosityWater/chemistry
DOI
10.1016/j.biomaterials.2009.11.115
PMID
20022371
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Orthopedic Surgery
AJOU Authors
민, 병현
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