药物分析学报（英文）2016，Vol.6Issue(4)：268-275,8.
Validation of a liquid chromatographic method for the pharmaceutical quality control of products containing elacridar$
Validation of a liquid chromatographic method for the pharmaceutical quality control of products containing elacridar$
Emilia Sawicki 1Michel J. Hillebrand 1Hilde Rosing 1Jan H.M. Schellens 2Bastiaan Nuijen 1Jos H. Beijnen1
作者信息
- 1. Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
- 2. Division of Clinical Pharmacology, Department of Medical 0ncology, The Netherlands Cancer Institute /Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands
- 折叠
摘要
关键词
GF120918/Solid dispersion/Dissolution/Hydroxylation/HPLC-UVKey words
GF120918/Solid dispersion/Dissolution/Hydroxylation/HPLC-UV引用本文复制引用
Emilia Sawicki,Michel J. Hillebrand,Hilde Rosing,Jan H.M. Schellens,Bastiaan Nuijen,Jos H. Beijnen..Validation of a liquid chromatographic method for the pharmaceutical quality control of products containing elacridar$[J].药物分析学报（英文）,2016,6(4):268-275,8.
