采用23全实验设计优化固体分散法制备女贞滴丸的配方参数。

Kai-Rong Wu, Wen-Ho Chuo, Yuh-Tyng Huang
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引用次数: 0

摘要

齐墩果酸(OA)是中药女贞子(FLL)的有效成分。它的临床使用受到限制,因为它不溶于水,目前的给药形式有限。因此,采用固体分散技术的热熔法制备了FFL滴丸。采用23因子设计考察滴丸制备材料(如PEG4000和PEG6000的不同比例、FLL提取物的添加量和Tween 80的百分比)对滴丸圆度、重量变化和崩解时间等参数的影响。利用23全因子设计寻找溶出度试验的最佳处方。结果表明:Tween 80的添加对滴丸圆度、重量变化和崩解时间有显著影响;FLL提取液载荷影响圆度和重量变化;PEG4000和PEG6000的不同配比只影响崩解时间。最优滴丸的溶出释放时间为30 min,释放率为70%,比市售的FLL中药快。此外,释放量高于市售制剂。本研究采用固体分散技术成功地制备了FLL滴丸。提高了FLL的水不溶性,提高了药物的溶出释放率,增加了FLL的应用价值,减少了传统给药剂型的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimization of Formulation Parameters in Preparation of <i>Fructus ligustri lucidi</i> Dropping Pills by Solid Dispersion Using 2<sup>3</sup> Full Experimental Design.

Optimization of Formulation Parameters in Preparation of <i>Fructus ligustri lucidi</i> Dropping Pills by Solid Dispersion Using 2<sup>3</sup> Full Experimental Design.

Optimization of Formulation Parameters in Preparation of <i>Fructus ligustri lucidi</i> Dropping Pills by Solid Dispersion Using 2<sup>3</sup> Full Experimental Design.

Optimization of Formulation Parameters in Preparation of Fructus ligustri lucidi Dropping Pills by Solid Dispersion Using 23 Full Experimental Design.

Oleanolic acid (OA) is an active ingredient of the traditional Chinese medicine (TCM) Fructus ligustri lucidi (FLL). Its clinical use is restricted because it is water-insoluble and has limited dosage forms of administration at present. Hence, the FFL dropping pills were prepared by the hot-melt method of solid dispersion technology. A 23 factorial design was used to examine the effects of the materials used to prepare the dropping pills (e.g., different ratios of PEG4000 and PEG6000, FLL extract loading, and percentage of Tween 80) on parameters such as dropping pill roundness, weight variation, and disintegration time. Moreover, 23 full factorial design was utilized to search for the optimal formulation for dissolution experiments. The results showed that the percentage of Tween 80 demonstrated significant effects on dropping pill roundness, weight variation, and disintegration time; FLL extract loading affected roundness and weight variation; and different ratios of PEG4000 and PEG6000 only affected disintegration time. The optimal formulation of the dropping pills released 70% of the drug after 30 min of dissolution release, which was faster than commercially available FLL Chinese medicines. Furthermore, the amount released was higher than that of commercially available formulations. In this study, a solid dispersion technique was used to successfully produce FLL dropping pills. In addition to improving the water insolubility of FLL and increasing the dissolution release percentage of the drug, we increased the application value of FLL and reduced the issues of traditional administration dosage forms.

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