Schartel B, Volland C, Li Y X, Wendorff J W, Kissel T
Department of Physical Chemistry, Philipps-University Marburg, Germany.
J Microencapsul. 1997 Jul-Aug;14(4):475-88. doi: 10.3109/02652049709033832.
The mechanical and dielectric properties of three kinds of poly(lactic acid-coglycolic acid) (PLG) with different molecular weights and polydispersities fractioned by ultrafiltration were investigated by dynamic mechanical thermal analysis (DMTA) and dielectric measurement. All samples showed typical behaviour of amorphous polymer under different fields. Two relaxation processes were found, a secondary relaxation in glassy state at low temperature and a glass transition relaxation. The molecular weights and polydispersities of PLGs influenced significantly both relaxation, especially the relaxation strength and location. The strength of secondary relaxation was reduced and the glass transition shifted to a higher temperature when the molecular weight of PLG increased and the polydispersity decreased. The shift of glass transition temperature (Tg) might decrease the motion of the macromolecules and resulted in a higher moduli of rubbery PLG at the temperature of the drug system (37 degrees C) and lowered the diffusivity of the drug in polymeric matrix and then the initial burst and fast diffusional release of captopril from commercial PLG were improved.
通过动态热机械分析(DMTA)和介电测量,研究了三种通过超滤分级的具有不同分子量和多分散性的聚乳酸-乙醇酸共聚物(PLG)的机械性能和介电性能。所有样品在不同条件下均表现出典型的非晶态聚合物行为。发现了两个弛豫过程,一个是低温玻璃态下的次级弛豫,另一个是玻璃化转变弛豫。PLG的分子量和多分散性对这两种弛豫都有显著影响,尤其是弛豫强度和位置。当PLG分子量增加且多分散性降低时,次级弛豫强度降低,玻璃化转变向更高温度移动。玻璃化转变温度(Tg)的移动可能会降低大分子的运动,导致药物体系温度(37℃)下橡胶态PLG具有更高的模量,并降低药物在聚合物基质中的扩散率,进而改善卡托普利从市售PLG中的初始突释和快速扩散释放。