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Preparation and Characterization of Spherical Amorphous Solid Dispersion with Amphotericin B

机译:两性霉素B球形非晶态固体分散体的制备与表征

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摘要

In the present study, new polymer microspheres of amphotericin B (AmB) were prepared by a spray drying technique using cyclodextrin polymers (Poly-CD) to improve the solubility and dissolution of AmB, to prevent in vivo toxic AmB aggregations. Formulations were characterized through scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry (DSC), thermal analysis, Raman spectroscopy, particle size, drug purity test and in vitro release studies. The analysis indicated that the chemical structure of AmB remained unchanged in the amorphous solid dispersion, but the structure was changed from crystalline to amorphous. AmB was completely release from such optimized formulations in dissolution media in 40 min. This work may contribute to a new generation of spherical amorphous solid dispersion using a cyclodextrin polymer, which has implications for the possibility of drug development for oral utilization or as powder aerosols for pulmonary administration.
机译:在本研究中,使用环糊精聚合物(Poly-CD)通过喷雾干燥技术制备了两性霉素B(AmB)的新聚合物微球,以提高AmB的溶解度和溶解度,以防止体内毒性AmB聚集。通过扫描电子显微镜(SEM),傅立叶变换红外光谱(FT-IR),差示扫描量热法(DSC),热分析,拉曼光谱,粒径,药物纯度测试和体外释放研究来对制剂进行表征。分析表明,AmB的化学结构在无定形固体分散体中保持不变,但是结构从结晶变为无定形。在40分钟内,AmB在溶解介质中完全从此类优化配方中释放出来。这项工作可能有助于使用环糊精聚合物的新一代球形无定形固体分散体,这对药物开发用于口服或作为肺部给药的粉末气雾剂具有重要意义。

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