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Use of Polyvinyl Alcohol as a Solubility-Enhancing Polymer for Poorly Water Soluble Drug Delivery (Part 1)

机译:聚乙烯醇作为水溶性差的药物递送的增溶剂聚合物的用途(第1部分)

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摘要

Polyvinyl alcohol (PVAL) has not been investigated in a binary formulation as a concentration-enhancing polymer owing to its high melting point/high viscosity and poor organic solubility. Due to the unique attributes of the KinetiSol® dispersing (KSD) technology, PVAL has been enabled for this application and it is the aim of this paper to investigate various grades for improvement of the solubility and bioavailability of poorly water soluble active pharmaceutical ingredients. Solid amorphous dispersions were created with the model drug, itraconazole (ITZ), at a selected drug loading of 20%. Polymer grades were chosen with variation in molecular weight and degree of hydroxylation to determine the effects on performance. Differential scanning calorimetry, powder X-ray diffraction, polarized light microscopy, size exclusion chromatography, and dissolution testing were used to characterize the amorphous dispersions. An in vivo pharmacokinetic study in rats was also conducted to compare the selected formulation to current market formulations of ITZ. The 4-88 grade of PVAL was determined to be effective at enhancing solubility and bioavailability of itraconazole.
机译:聚乙烯醇(PVAL)由于其高熔点/高粘度和较差的有机溶解度,因此没有作为提高浓度的聚合物在二元配方中进行研究。由于KinetiSol®分散(KSD)技术的独特属性,PVAL已被启用用于此应用,并且本文的目的是研究各种等级的产品以改善水溶性差的活性药物成分的溶解度和生物利用度。用模型药物伊曲康唑(ITZ)在选定的20%药物载量下创建固体无定形分散体。选择具有分子量和羟基化程度变化的聚合物等级,以确定对性能的影响。差示扫描量热法,粉末X射线衍射,偏光显微镜,尺寸排阻色谱法和溶出度测试用于表征无定形分散体。还进行了大鼠体内药代动力学研究,以将所选制剂与ITZ的当前市场制剂进行比较。确定PVAL的4-88级可有效提高伊曲康唑的溶解度和生物利用度。

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