Development and validation of hydrophilic interaction liquid chromatography-tandem mass spectrometric method for the analysis of paroxetine in human plasma

Biomedical Chromatography

Volumn 18, Issue 1, 2004, Pages 28-36

  Naidong, Weng ^a   Eerkes, Angela ^a  

^a 206 Carnegie Center   (United States)

Author keywords

HILIC MS MS; Human plasma; Paroxetine

Indexed keywords

DRUG INTERACTIONS; HIGH PRESSURE LIQUID CHROMATOGRAPHY; HYDROPHILICITY; PATIENT MONITORING; PLASMA (HUMAN); QUALITY CONTROL; SILICA; SOLVENT EXTRACTION;

HILIC-MS/MS; HUMAN PLASMAS; HYDROPHILIC INTERACTION LIQUID CHROMATOGRAPHIES; INTERNAL STANDARDS; LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY; LIQUID CHROMATOGRAPHY/TANDEM MASS SPECTROMETRY; PAROXETINE; SIMPLE++; SPECTROMETRIC METHODS; TANDEM MASS SPECTROMETRIC;

MASS SPECTROMETRY;

FENTANYL; PAROXETINE; SILICON DIOXIDE; TERT BUTYL METHYL ETHER;

ACCURACY; ANALYTICAL ERROR; ARTICLE; CONCENTRATION (PARAMETERS); CONTROLLED STUDY; DRUG INFORMATION; DRUG ISOLATION; DRUG MONITORING; DRUG STRUCTURE; EVAPORATION; HYDROPHILICITY; LIQUID CHROMATOGRAPHY; LIQUID LIQUID EXTRACTION; PUBLISHING; QUALITY CONTROL; QUANTITATIVE ANALYSIS; SENSITIVITY ANALYSIS; STANDARD; TANDEM MASS SPECTROMETRY; VALIDATION PROCESS;

EID: 1142299604     PISSN: 02693879     EISSN: None     Source Type: Journal    
DOI: 10.1002/bmc.288     Document Type: Article

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