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Volumn 879, Issue 19, 2011, Pages 1677-1685

Development and validation of a quantitative assay for the determination of tamoxifen and its five main phase I metabolites in human serum using liquid chromatography coupled with tandem mass spectrometry

Author keywords

Endoxifen; Liquid chromatography; Mass spectrometry; Metabolites; Tamoxifen

Indexed keywords

BIOANALYTICAL ASSAYS; CLINICAL STUDY; DOSE OPTIMIZATION; ENDOXIFEN; FOUR-PHASE; HUMAN SERUM; LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY ASSAYS; LOWER LIMIT OF QUANTIFICATIONS; MULTIPLE REACTION MONITORING; PHASE I; POSITIVE ION MODE; PROTEIN PRECIPITATION; QUANTITATIVE ASSAY; QUANTITATIVE DETERMINATIONS; REVERSED PHASE LIQUID-CHROMATOGRAPHY; SAMPLE PRETREATMENT; SERUM CONCENTRATION; TAMOXIFEN; TANDEM MASS SPECTROMETRY; TWO PHASE; VALIDATION RESULTS;

EID: 79955879330     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2011.04.011     Document Type: Article
Times cited : (52)

References (20)
  • 18
    • 84856075857 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration - Centre for Drug Evaluation and Research - Guidance for Industry Bioanalytical Method Validation
    • U.S. Food and Drug Administration - Centre for Drug Evaluation and Research - Guidance for Industry Bioanalytical Method Validation, 2001, http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM070107.pdf.
    • (2001)
  • 19
    • 84856075858 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration - Centre for Drug Evaluation and Research - Chemistry Review(s)
    • U.S. Food and Drug Administration - Centre for Drug Evaluation and Research - Chemistry Review(s), 2008, http://www.accessdata.fda.gov/drugsatfda_docs/label/2006/017970s054lbl.pdf.
    • (2008)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.