|
Volumn 44, Issue 4, 2007, Pages 924-930
|
Development and full validation of a sensitive quantitative assay for the determination of clemastine in human plasma by liquid chromatography-tandem mass spectrometry
|
Author keywords
Clemastine; Determination; Human plasma; LC MS MS; Quantitative assay
|
Indexed keywords
ACETIC ACID ETHYL ESTER;
CLEMASTINE;
DIPHENHYDRAMINE;
PARACETAMOL;
PSEUDOEPHEDRINE;
ACCURACY;
ANALYTIC METHOD;
AREA UNDER THE CURVE;
ARTICLE;
CONTROLLED STUDY;
DRUG BLOOD LEVEL;
DRUG DETERMINATION;
HUMAN;
HUMAN EXPERIMENT;
LIQUID CHROMATOGRAPHY;
MALE;
NORMAL HUMAN;
PRIORITY JOURNAL;
QUALITY CONTROL;
QUANTITATIVE ANALYSIS;
STANDARD;
TANDEM MASS SPECTROMETRY;
VALIDATION PROCESS;
ACETAMINOPHEN;
ADULT;
CALIBRATION;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CLEMASTINE;
DRUG COMBINATIONS;
DRUG STABILITY;
EPHEDRINE;
FREEZING;
HISTAMINE H1 ANTAGONISTS;
HUMANS;
MALE;
QUALITY CONTROL;
REFERENCE STANDARDS;
REPRODUCIBILITY OF RESULTS;
SOLUTIONS;
SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;
TANDEM MASS SPECTROMETRY;
TEMPERATURE;
|
EID: 34447643215
PISSN: 07317085
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jpba.2007.03.019 Document Type: Article |
Times cited : (14)
|
References (13)
|