以草酸为赋形剂的无环鸟苷共非晶化

S. Rohani, A. Sarkar
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引用次数: 1

摘要

本文提出了一种以草酸为赋形剂的无环鸟苷和草酸共无定形合成的新方法。描述了指定为acv -草酸的其制备方法及其在制药应用中的用途。采用粉末x射线衍射、差示扫描量热法和热重分析对共无定形acv -草酸进行了表征。对共无定形ACV-草酸的相对湿度稳定性进行了评价,并与母体ACV进行了比较。在35℃时,共无定形acv -草酸的水溶性比母体阿昔洛韦碱明显提高(约8倍)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-Amorphization of Acyclovir with Oxalic Acid as an Excipient
The present article provides a novel technique for the co-amorphous formation of acyclovir and oxalic acid as an excipient. Designated as ACV-oxalic acid, methods for the preparation thereof and its use in pharmaceutical applications are described. The co-amorphous ACV-oxalic acid was characterized by powder X-ray diffraction, differential scanning calorimetry and thermogravimetric analysis. Stability with respect to relative humidity (RH) for the co-amorphous ACV-oxalic acid was evaluated and compared with the parent ACV. The aqueous solubility of the co-amorphous ACV-oxalic acid was significantly improved (about 8 times more soluble) at 35°C compared to that of the parent Acyclovir base.
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