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首页> 外文期刊>International Journal of Pharmaceutics >The parameters influencing the morphology of poly(epsilon-caprolactone) microspheres and the resulting release of encapsulated drugs
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The parameters influencing the morphology of poly(epsilon-caprolactone) microspheres and the resulting release of encapsulated drugs

机译:影响聚ε-己内酯微球形态和包封药物释放结果的参数

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Polymer microparticles used for drug encapsulation and delivery have various surface morphologies depending on the type of formulation ingredients and parameters of the manufacture process. This works aims at investigating the critical parameters governing the morphology of microparticles and to underline the influence of their surface state on the drug release. The classical fabrication process by the "emulsion-solvent evaporation" is addressed using poly(epsilon-caprolactone) as the polymer and methylene chloride as the volatile organic solvent. The typical surfactants poly(vinyl alcohol) and polysorbate 80 have been considered. Scanning electron microscopy observations showed the various surface morphologies mainly depending on the stirring rate, the viscosity of the oil phase and by the presence of inappropriate surfactants. Because of arrested coalescence during solvent evaporation, the evaporation of the organic solvent causing particles hardening is the most important parameter that controls the morphology. Indeed, slow evaporation allows partial coalescence of the soft particles swollen by the organic solvent, whereas the particles morphology is frozen rapidly upon fast evaporation, thus preventing damaged surface states. Moreover, an effective stabilizing system for the primary emulsion is also a determining factor to control the final morphology. The morphology of the particles has a definite influence on the drug delivery of cholecalciferol. The surface morphology should be taken into consideration in the design of polymer microparticles because it allows a control over the drug release kinetics. (C) 2015 Elsevier B.V. All rights reserved.
机译:用于药物包封和递送的聚合物微粒具有多种表面形态,具体取决于制剂成分的类型和制造工艺的参数。这项工作旨在研究控制微粒形态的关键参数,并强调其表面状态对药物释放的影响。使用聚(ε-己内酯)作为聚合物,使用二氯甲烷作为挥发性有机溶剂,解决了“乳液-溶剂蒸发”的经典制造过程。已经考虑了典型的表面活性剂聚(乙烯醇)和聚山梨酯80。扫描电子显微镜观察表明,主要取决于搅拌速率,油相的粘度和不适当的表面活性剂的存在,各种表面形态。由于在溶剂蒸发过程中停止了聚结,导致颗粒硬化的有机溶剂蒸发是控制形态的最重要参数。实际上,缓慢的蒸发允许被有机溶剂溶胀的软颗粒的部分聚结,而在快速蒸发时,颗粒的形态迅速冻结,从而防止了受损的表面状态。此外,用于初级乳液的有效稳定体系也是控制最终形态的决定因素。颗粒的形态对胆钙化固醇的药物递送具有确定的影响。在聚合物微粒的设计中应考虑表面形态,因为它可以控制药物释放动力学。 (C)2015 Elsevier B.V.保留所有权利。

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