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Volumn 879, Issue 11-12, 2011, Pages 695-706

Development and validation of a liquid chromatography/tandem mass spectrometry procedure for the quantification of sunitinib (SU11248) and its active metabolite, N-desethyl sunitinib (SU12662), in human plasma: Application to an explorative study

Author keywords

LC MS MS analysis; N desethyl sunitinib; Sunitinib; Tandem mass spectrometry; Tyrosine kinase inhibitors

Indexed keywords

LC-MS/MS; N-DESETHYL SUNITINIB; SUNITINIB; TANDEM MASS SPECTROMETRY; TYROSINE KINASE INHIBITORS;

EID: 79952902010     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2011.02.006     Document Type: Article
Times cited : (38)

References (29)
  • 18
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    • in: Proceedings of the AAPS Conference, November
    • D. Song, W. Wong, P. Giannousis, in: Proceedings of the AAPS Conference, November 2002.
    • (2002)
    • Song, D.1    Wong, W.2    Giannousis, P.3
  • 20
    • 79952899113 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services, Food and Drug Administration, Guidance for industry: bioanalytical method validation
    • U.S. Department of Health and Human Services, Food and Drug Administration, Guidance for industry: bioanalytical method validation, 2001.
    • (2001)
  • 21
    • 79952897596 scopus 로고    scopus 로고
    • European Medicines Agency, Committee for Medicinal Products for Human Use, Guideline on validation of bioanalytical methods
    • European Medicines Agency, Committee for Medicinal Products for Human Use, Guideline on validation of bioanalytical methods, 2009.
    • (2009)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.