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Volumn 879, Issue 23, 2011, Pages 2265-2273
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Development and validation of a selective and sensitive LC-MS/MS method for determination of cycloserine in human plasma: Application to bioequivalence study
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Author keywords
Bioequivalence; Cycloserine; Human plasma; LC MS MS; Solid phase extraction
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Indexed keywords
BIOEQUIVALENCE;
CYCLOSERINE;
HUMAN PLASMAS;
LC-MS/MS;
SOLID PHASE EXTRACTION;
CARBOXYLIC ACIDS;
CHROMATOGRAPHY;
EXTRACTION;
HIGH PRESSURE LIQUID CHROMATOGRAPHY;
IONS;
MASS SPECTROMETRY;
PLASMAS;
PYRIDINE;
STANDARDIZATION;
PLASMA (HUMAN);
CYCLOSERINE;
NICOTINIC ACID;
ACCURACY;
ADULT;
ARTICLE;
BIOEQUIVALENCE;
DILUTION;
DRUG BIOAVAILABILITY;
DRUG DETERMINATION;
HUMAN;
LIMIT OF DETECTION;
LIMIT OF QUANTITATION;
LIQUID CHROMATOGRAPHY;
MALE;
NORMAL HUMAN;
PRIORITY JOURNAL;
SOLID PHASE EXTRACTION;
TANDEM MASS SPECTROMETRY;
CHROMATOGRAPHY, LIQUID;
CYCLOSERINE;
HUMANS;
MALE;
TANDEM MASS SPECTROMETRY;
THERAPEUTIC EQUIVALENCY;
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EID: 79960557826
PISSN: 15700232
EISSN: 1873376X
Source Type: Journal
DOI: 10.1016/j.jchromb.2011.06.011 Document Type: Article |
Times cited : (44)
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References (21)
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