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在人体受试者中局部给予酮洛芬制剂后,从角质层中消除酮洛芬。

Elimination of ketoprofen from the stratum corneum after topical administration with ketoprofen formulations in human subjects.

机构信息

Medical Corporation Shinanokai Shinanozaka Clinic, 20 Samon-cho, Shinjuku-ku, Tokyo 160-0017, Japan.

Department of Dermatology, Keio University School of Medicine, 25 Shinano-machi, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

Int J Pharm. 2014 Apr 25;465(1-2):197-201. doi: 10.1016/j.ijpharm.2014.02.015. Epub 2014 Feb 12.

Abstract

PURPOSE

To assess the drug concentrations and elimination rate of ketoprofen in the stratum corneum following topical administration of two different formulations in human subjects for reference in the risk management of photocontact dermatitis caused by topical ketoprofen.

METHODS

Ketoprofen tape and gel were used as test formulations. The stratum corneum at the application sites was removed by tape-stripping at scheduled times after removal of the formulations. The ketoprofen concentration in the stratum corneum was determined by liquid chromatography with tandem mass spectrometry.

RESULTS

The ketoprofen concentration in the stratum corneum decreased and the elimination half-life in the stratum corneum was comparable between tape and gel after removal of the test formulations. The ketoprofen concentration in the stratum corneum decreased more rapidly after the subjects took a shower. Ketoprofen was not detected in the stratum corneum adjacent to the tape application sites.

CONCLUSIONS

Ketoprofen in the stratum corneum appears to reach the lower limit of quantitation (0.005 μg) 12-16 days after removal of tape or gel. This period is similar to that recommended for avoiding ultraviolet light after removal of topical ketoprofen formulations in the Summary of Product Characteristics for topical ketoprofen in the European Union.

摘要

目的

评估两种不同制剂外用后角质层中酮洛芬的药物浓度和消除率,为外用酮洛芬引起光接触性皮炎的风险管理提供参考。

方法

酮洛芬贴剂和凝胶用作试验制剂。在去除制剂后,按预定时间通过胶带剥离去除应用部位的角质层。采用液相色谱-串联质谱法测定角质层中酮洛芬的浓度。

结果

去除试验制剂后,角质层中酮洛芬的浓度下降,角质层中的消除半衰期在贴剂和凝胶之间具有可比性。受试者洗澡后,角质层中的酮洛芬下降更快。在胶带应用部位相邻的角质层中未检测到酮洛芬。

结论

去除胶带或凝胶后 12-16 天,角质层中的酮洛芬似乎达到定量下限(0.005μg)。这一时间与欧盟外用酮洛芬制剂产品特性摘要中建议的在去除外用酮洛芬制剂后避免紫外线的时间相似。

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