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Volumn 856, Issue 1-2, 2007, Pages 141-147
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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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Author keywords
17 OHPC; Liquid chromatography mass spectrometry; MPA; Pregnancy
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Indexed keywords
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
MASS SPECTROMETRY;
PHASE SEPARATION;
PLASMA (HUMAN);
EXTRACTION CARTRIDGE;
MEDROXYPROGESTERONE ACETATE (MPA);
DRUG PRODUCTS;
ACETONITRILE;
FORMIC ACID;
HYDROXYPROGESTERONE CAPROATE;
MEDROXYPROGESTERONE ACETATE;
WATER;
ACCURACY;
ARTICLE;
BLOOD ANALYSIS;
BLOOD SAMPLING;
CONCENTRATION (PARAMETERS);
CONTROLLED STUDY;
DRUG BLOOD LEVEL;
DRUG DETERMINATION;
ELECTROSPRAY MASS SPECTROMETRY;
EXTRACTION;
FEMALE;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
HUMAN EXPERIMENT;
MASS SPECTROMETRY;
PREGNANCY;
PRIORITY JOURNAL;
PROCESS DEVELOPMENT;
SOLID PHASE EXTRACTION;
SPECTROMETER;
SPECTROPHOTOMETER;
STANDARD;
VALIDATION PROCESS;
17-ALPHA-HYDROXYPROGESTERONE;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
FEMALE;
GAS CHROMATOGRAPHY-MASS SPECTROMETRY;
HUMANS;
PREGNANCY;
REFERENCE STANDARDS;
REPRODUCIBILITY OF RESULTS;
SENSITIVITY AND SPECIFICITY;
SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;
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EID: 34548132381
PISSN: 15700232
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jchromb.2007.05.028 Document Type: Article |
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Times cited : (6)
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References (11)
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