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Volumn 879, Issue 30, 2011, Pages 3415-3422

Method development and validation of the simultaneous determination of a novel topoisomerase 1 inhibitor, the prodrug, and the active metabolite in human plasma using column-switching LC-MS/MS, and its application in a clinical trial

Author keywords

Column switching; Human plasma; LC MS MS; Pharmacokinetics; Topoisomerase 1 inhibitor

Indexed keywords

ACTIVE METABOLITES; ANALYTES; CITRIC ACID SOLUTION; CLINICAL SAMPLES; CLINICAL TRIAL; COLUMN SWITCHING; HUMAN PLASMAS; INTERNAL STANDARDS; LC-MS/MS; LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY; LOWER LIMIT OF QUANTITATIONS; METHOD DEVELOPMENT; MULTIPLE REACTION MONITORING; PLASMA PROTEIN; PRODRUGS; REANALYSIS; SENSITIVE METHOD; SIMULTANEOUS DETERMINATIONS; TOPOISOMERASES; VALIDATED METHODS;

EID: 80555131102     PISSN: 15700232     EISSN: 1873376X     Source Type: Journal    
DOI: 10.1016/j.jchromb.2011.09.015     Document Type: Article
Times cited : (9)

References (26)
  • 25
    • 80555146016 scopus 로고    scopus 로고
    • Guidance for Industry, Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM)
    • Guidance for Industry, Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM) (2001).
    • (2001)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.