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Morphology and Release Kinetics of Protein-Loaded Porous Poly(L-Lactic Acid) Spheres Prepared by Freeze-Drying Technique

机译:冷冻干燥技术制备的蛋白质负载多孔聚L-乳酸球的形貌和释放动力学

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摘要

Freeze-drying a biodegradable polymer, poly(L-lactic acid) (PLLA), from 1,4-dioxane solutions provided very porous spherical particles of ca. 3 mm in radius with specific surface area of 8–13 m2 g−1. The surface of the particle was found to be less porous compared with its interior. To apply the freeze-dried PLLA (FDPLLA) to drug delivery system, its morphology and drug releasing kinetics were investigated, bovine serum albumin (BSA) being used as a model drug compound. Immersion of FDPLLA into a BSA aqueous solution gave BSA-loaded FDPLLA, where mass fraction of the adsorbed BSA reached up to 79%. Time-dependent release profile of BSA in water suggested a two-step mechanism: (1) very rapid release of BSA deposited on and near the particle surface, which results in an initial burst, and (2) leaching of BSA from the interior of the particle by the diffusion process. It was suggested that the latter process is largely governed by the surface porosity. The porosity of both the interior and surface was found to decrease remarkably as the concentration of the original PLLA/1,4-dioxane solution increases, C 0. Thus, C 0 is a key parameter that controls the loading and releasing of BSA.
机译:从1,4-二恶烷溶液中冷冻干燥可生物降解的聚合物,聚(L-乳酸)(PLLA),可提供约0.1毫米的非常多孔的球形颗粒。半径3 mm,比表面积8-13 m 2 g -1 。发现颗粒的表面与其内部相比多孔性较小。为了将冻干的PLLA(FDPLLA)应用于药物递送系统,研究了其形态和药物释放动力学,牛血清白蛋白(BSA)被用作模型药物化合物。将FDPLLA浸入BSA水溶液中,得到了负载BSA的FDPLLA,其中吸附的BSA的质量分数高达79%。 BSA在水中的时间依赖性释放曲线表明有两步机制:(1)沉积在颗粒表面及其附近的BSA释放非常快,这导致初始破裂,(2)BSA从内部浸出。粒子通过扩散过程。有人提出,后者的过程主要受表面孔隙度的支配。随着原始PLLA / 1,4-二恶烷溶液浓度的增加C 0,发现内部和表面的孔隙率均显着降低。因此,C 0是控制BSA负载和释放的关键参数。

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