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Volumn 76, Issue 5, 2008, Pages 1015-1021

Development and validation of reversed phase liquid chromatographic method utilizing ultraviolet detection for quantification of irinotecan (CPT-11) and its active metabolite, SN-38, in rat plasma and bile samples: Application to pharmacokinetic studies

Author keywords

Bile; Irinotecan (CPT 11); Pharmacokinetics; Plasma; SN 38; Ultraviolet detection

Indexed keywords

ACETONITRILE; BIOCHEMISTRY; BODY FLUIDS; CHROMATOGRAPHIC ANALYSIS; DICHLOROMETHANE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; LIQUIDS; METABOLITES; PHARMACOKINETICS; PLASMAS; RATS;

EID: 50349101344     PISSN: 00399140     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.talanta.2008.04.058     Document Type: Article
Times cited : (48)

References (22)
  • 18
    • 84925625685 scopus 로고    scopus 로고
    • Topic Q2B: Validation of analytical procedures: Methodology
    • Topic Q2B: Validation of analytical procedures: Methodology. International Conference on Harmonisation (ICH) (1996)
    • (1996) International Conference on Harmonisation (ICH)
  • 21
    • 50349100907 scopus 로고    scopus 로고
    • http://www.fda.gov/cder/guidance/4252fnl.pdf


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.