메뉴 건너뛰기




Volumn 868, Issue 1-2, 2008, Pages 110-115

Development and validation of a sensitive liquid chromatography/mass spectrometry method for quantitation of flavopiridol in plasma enables accurate estimation of pharmacokinetic parameters with a clinically active dosing schedule

Author keywords

Flavopiridol; Genistein; LCMS; Pharmacokinetics; Plasma; Quantitation

Indexed keywords

BIOASSAY; LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; PARAMETER ESTIMATION; PHARMACOKINETICS; PLASMAS;

EID: 44449083839     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2008.04.023     Document Type: Article
Times cited : (13)

References (29)
  • 26
    • 85069423527 scopus 로고    scopus 로고
    • US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Guidance for Industry, Bioanalytical Method Validation, 2001.
    • US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Guidance for Industry, Bioanalytical Method Validation, 2001.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.