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用于定量测定硝酸益康唑和雌二醇经皮吸收的近红外光谱法。

Near infrared spectrometry for the quantification of human dermal absorption of econazole nitrate and estradiol.

作者信息

Medendorp Joseph P, Paudel Kalpana S, Lodder Robert A, Stinchcomb Audra L

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, 725 Rose Street, Lexington, Kentucky 40536-0082, USA.

出版信息

Pharm Res. 2007 Jan;24(1):186-93. doi: 10.1007/s11095-006-9140-0. Epub 2006 Nov 14.

DOI:10.1007/s11095-006-9140-0
PMID:17103333
Abstract

PURPOSE

The purpose of this study was to demonstrate the use of near-infrared (NIR) spectrometry for the in vitro quantification of econazole nitrate (EN) and estradiol (EST) in human skin.

METHODS

NIR spectra were collected from EN and EST powders to verify the presence of NIR chromophores. One percent EN cream, a saturated solution of EN, or 0.25% EST solution was applied to human skin. NIR spectra were collected and one-point net analyte signal (NAS) multivariate calibration was used to predict the drug concentrations. NIR results were validated against known skin concentrations measured by high-pressure liquid chromatography (HPLC) analysis of solvent extracts.

RESULTS

NIR spectroscopy measured dermal absorption from saturated solutions of EN on human skin with an r2=0.990, standard error of estimation (SEE)=2.46%, and a standard error of performance (SEP)=3.55%, EN cream on skin with an r2=0.987, SEE=2.30%, and SEP=2.66%, and 0.25% solutions of EST on skin with an r2=0.987, SEE=3.30%, and SEP=5.66%. Despite low permeation amounts of both drugs through the stratum corneum into human tissue, the NIR signal-to-noise ratio was greater than three, even for the lowest concentrations.

CONCLUSION

NIR analyses paralleled the results obtained from HPLC, and thus could serve as a viable alternative for measuring the topical bioavailability/bioequivalence of different EN and EST formulations. Because these experiments were conducted in human tissue, this research suggests an all-optical in vivo method of measurement for dermal absorption could be developed.

摘要

目的

本研究旨在证明近红外(NIR)光谱法可用于体外定量测定人皮肤中硝酸益康唑(EN)和雌二醇(EST)的含量。

方法

收集EN和EST粉末的近红外光谱,以验证近红外发色团的存在。将1%的EN乳膏、EN饱和溶液或0.25%的EST溶液涂抹于人皮肤。收集近红外光谱,并使用单点净分析物信号(NAS)多元校准来预测药物浓度。近红外结果通过对溶剂提取物进行高压液相色谱(HPLC)分析测得的已知皮肤浓度进行验证。

结果

近红外光谱法测量EN饱和溶液在人皮肤上的真皮吸收,r2 = 0.990,估计标准误差(SEE)= 2.46%,性能标准误差(SEP)= 3.55%;测量EN乳膏在皮肤上的真皮吸收,r2 = 0.987,SEE = 2.30%,SEP = 2.66%;测量0.25%的EST溶液在皮肤上的真皮吸收,r2 = 0.987,SEE = 3.30%,SEP = 5.66%。尽管两种药物通过角质层进入人体组织的渗透量较低,但即使对于最低浓度,近红外信噪比仍大于3。

结论

近红外分析结果与HPLC获得的结果相似,因此可作为测量不同EN和EST制剂局部生物利用度/生物等效性的可行替代方法。由于这些实验是在人体组织中进行的,本研究表明可以开发一种全光学体内测量真皮吸收的方法。

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