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Volumn 837, Issue 1-2, 2006, Pages 49-58

Development and validation of a quantitative assay for the measurement of two HIV-fusion inhibitors, enfuvirtide and tifuvirtide, and one metabolite of enfuvirtide (M-20) in human plasma by liquid chromatography-tandem mass spectrometry

Author keywords

Enfuvirtide; HIV fusion inhibitor; LC MS MS; Peptide; Tifuvirtide

Indexed keywords

CONCENTRATION (PROCESS); COPOLYMERIZATION; ENZYME INHIBITION; FUSION REACTIONS; IMMUNOLOGY; METABOLITES; POLYPEPTIDES; VIRUSES;

EID: 33744502918     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2006.03.059     Document Type: Article
Times cited : (49)

References (35)
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    • http://www.emea.eu.int/humandocs/PDFs/EPAR/fuzeon/169503en6.pdf, Scientific discussion for the approval of Fuzeon, European Medicines Agency (EMEA), 2005.
  • 17
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    • http://www.rocheuk.com/ProductDB/Documents/rx/spc/fuzeon_SPC.pdf, Summary of product characteristics; Fuzeon, Roche registration Ltd, UK 2005.
  • 31
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    • http://www.fda.gov/cder/guidance/4252fnl.htm, Guidance for Industry, Bioanalytical Method Validation, U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CEDR), Center for Veterinary Medicine (CVM), BP, May 2001.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.