首页> 外文期刊>Designed Monomers and Polymers: An International Journal on Monomer and Macromolecular Synthesis >Development of pH-sensitive polycaprolactone-based microspheres for in vitro release studies of Triprolidine Hydrochloride
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Development of pH-sensitive polycaprolactone-based microspheres for in vitro release studies of Triprolidine Hydrochloride

机译:基于pH敏感的聚己内酯基微球的开发,用于盐酸曲普立定的体外释放研究

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A series of different blend ratios of polycaprolactone (PCL) and cellulose acetate phthalate microspheres were prepared by double emulsion solvent evaporation method. Triprolidine hydrochloride (TPH) is propylamine antihistamine drug, which was successfully loaded in to these microspheres via in situ method. The maximum loading of TPH was found to be about 66%. The resulting microspheres were characterized by differential scanning calorimetry (DSC), X-ray diffraction (X-RD), particle size analysis, and scanning electron microscopic (SEM) studies. The DSC study indicates the blend compatibility of polymers. X-RD studies showed that the TPH drug particles are molecularly dispersed in the microspheres. Particle size and SEM studies indicated the formation of spherical microspheres with distinct size. The in vitro release studies revealed that the release of TPH depends upon the pH condition, blend composition, and drug content. The time taken for the release of TPH from microspheres was more than 10 h. Klend microspheres;; compatibility;; antihistamine drug;; in vitro release
机译:采用双乳液溶剂蒸发法制备了一系列不同比例的聚己内酯(PCL)和醋酸纤维素邻苯二甲酸酯微球。盐酸曲普利啶(TPH)是丙胺抗组胺药,已通过原位方法成功地装载到这些微球中。发现TPH的最大负载为约66%。通过差示扫描量热法(DSC),X射线衍射(X-RD),粒度分析和扫描电子显微镜(SEM)研究对所得微球进行表征。 DSC研究表明聚合物的共混物相容性。 X-RD研究表明TPH药物颗粒分子分散在微球中。粒度和SEM研究表明,球形微球的形成具有不同的大小。体外释放研究表明,TPH的释放取决于pH条件,混合物成分和药物含量。从微球中释放TPH的时间超过10小时。 K 混合微球;;兼容性;;抗组胺药;体外释放

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