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用于估算低溶解度药物旋转圆盘固有溶出速率的粉末溶出法。

Powder dissolution method for estimating rotating disk intrinsic dissolution rates of low solubility drugs.

作者信息

Tsinman Konstantin, Avdeef Alex, Tsinman Oksana, Voloboy Dmytro

机构信息

pION INC, Woburn, MA 01801, USA.

出版信息

Pharm Res. 2009 Sep;26(9):2093-100. doi: 10.1007/s11095-009-9921-3. Epub 2009 Jun 19.

Abstract

PURPOSE

The objective was to investigate the applicability and limitations of a novel approach for measuring intrinsic dissolution rates (IDR) of very small quantities of compounds introduced as powders to buffered solutions and comparing these results to disk IDR obtained using the traditional Wood's apparatus.

METHODS

The powder dissolution profiles of 13 model drugs were determined at 37 degrees C in USP buffers at pH 1.2, 4.5, and 6.8, stirred at 100 RPM. As little as 0.06 mg of drug were added to 1 mL buffer media. Drug concentration was measured by an in situ fiber optic UV method. The results were converted to rotating disk IDR values by a novel mathematical procedure.

RESULTS

The comparison of the powder-based IDR values to those obtained by traditional Wood's apparatus indicated r(2) = 0.97 (n = 26).

CONCLUSION

The results demonstrate that using potentially 10,000-fold less drug material does not sacrifice the quality of the measurement, and lends support to an earlier study that the disk IDR measurement may possibly serve as a surrogate for the BCS solubility classification.

摘要

目的

本研究旨在探讨一种新方法的适用性和局限性,该方法用于测量以粉末形式加入缓冲溶液中的极少量化合物的固有溶解速率(IDR),并将这些结果与使用传统伍德装置获得的圆盘IDR进行比较。

方法

在37℃下,于pH值为1.2、4.5和6.8的USP缓冲液中,以100转/分钟的速度搅拌,测定13种模型药物的粉末溶解曲线。向1 mL缓冲介质中加入低至0.06 mg的药物。通过原位光纤紫外法测量药物浓度。通过一种新的数学程序将结果转换为旋转圆盘IDR值。

结果

基于粉末的IDR值与通过传统伍德装置获得的值的比较表明,r(2)=0.97(n = 26)。

结论

结果表明,使用可能少10000倍的药物材料不会牺牲测量质量,并支持早期的一项研究,即圆盘IDR测量可能作为BCS溶解度分类的替代方法。

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