首页> 外文会议>Symposia on Biomaterials for Drug Delivery and Tissue Engineering Nov 27-29, 2000, Boston, Massachusetts, U.S.A. >Microstructural Characterization of Polyanhydride Blends for Controlled Drug Delivery
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Microstructural Characterization of Polyanhydride Blends for Controlled Drug Delivery

机译:用于控制药物输送的聚酸酐混合物的微观结构表征

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This research examines the microstructure of polyanhydride blends for use in drug delivery devices. Atomic force microscopy (AFM) and small-angle X-ray scattering (SAXS) studies were performed on the homopolymers and blends of the polyanhydrides poly( 1,6-carboxyphenoxy hexane) (CPH) and poly(sebacic anhydride) (SA). AFM of the CPH/SA blends 20:80, 50:50, and 80:20 showed distinct patterns indicating spinodal decomposition and phase separation on the micron-scale. Because it has been shown that incorporated drugs will thermodynamically partition into phase-separated domains depending on their hydrophobicity, polyanhydride blends will be able to encapsulate larger bioactive compounds including nucleotides, proteins, and vaccines. Preliminary SAXS studies of the CPH/SA blend systems provide information on the crystalline morphology of the polymer. A peak shift to a lower q from poly(SA) to the blends indicates that the poly(CPH) is incorporated into and causes swelling of the interlamellar amorphous regions of poly(SA).
机译:这项研究检查了用于药物输送装置的聚酸酐共混物的微观结构。对聚酸酐聚(1,6-羧基苯氧基己烷)(CPH)和聚(癸二酸酐)(SA)的均聚物和共混物进行了原子力显微镜(AFM)和小角X射线散射(SAXS)研究。 CPH / SA共混物20:80、50:50和80:20的AFM显示出明显的模式,表明旋节线分解和微米级的相分离。由于已显示掺入的药物将根据其疏水性在热力学上划分为相分离的域,因此聚酸酐共混物将能够封装更大的生物活性化合物,包括核苷酸,蛋白质和疫苗。对CPH / SA共混体系的初步SAXS研究提供了有关聚合物晶体形态的信息。从聚(SA)到共混物向较低q峰移动表明聚(CPH)被并入聚(SA)的层间非晶区域并引起膨胀。

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