Development and validation of a high-performance liquid chromatography-mass spectrometric assay for the determination of 17α-hydroxyprogesterone caproate (17-OHPC) in human plasma
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概要
- 論文の詳細を見る
- 2007-09-01
著者
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Venkataramanan Raman
Department Of Pharmaceutical Sciences University Of Pittsburgh School Of Pharmacy
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ZHANG Shimin
Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy
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MADA Sripal
Department of Pharmaceutical Sciences, University of Pittsburgh School of Pharmacy
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MATTISON Don
Center for Research for Mothers and Children, Obstetric-Fetal Pharmacology Research Units (OPRU) Net
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CARITIS Steve
Department of Obstetrics and Gynecology, Magee Women's Hospital
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Mada Sripal
Department Of Pharmaceutical Sciences University Of Pittsburgh School Of Pharmacy
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Zhang Shimin
Department Of Pharmaceutical Sciences University Of Pittsburgh School Of Pharmacy
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Zhang Shimin
Department Of Pharmaceutical Sciences School Of Pharmacy School Of Medicine University Of Pittsburgh
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Mattison Don
Center For Research For Mothers And Children Obstetric-fetal Pharmacology Research Units (opru) Netw
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Caritis Steve
Department Of Obstetrics And Gynecology Magee Women's Hospital
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Venkataramanan Raman
Department Of Pharmaceutical Sciences School Of Pharmacy School Of Medicine University Of Pittsburgh
関連論文
- Development and validation of a high-performance liquid chromatography-mass spectrometric assay for the determination of 17α-hydroxyprogesterone caproate (17-OHPC) in human plasma
- Determination of 13-O-demethyl tacrolimus in human liver microsomal incubates using liquid chromatography-mass spectrometric assay (LC-MS)