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Volumn 879, Issue 19, 2011, Pages 1686-1696

An LC-MS/MS procedure for the quantification of naproxen in human plasma: Development, validation, comparison with other methods, and application to a pharmacokinetic study

Author keywords

Liquid chromatography; Naproxen; Pharmacokinetics; Tandem mass spectrometry; Validation

Indexed keywords

BIOANALYTICAL ASSAYS; CONCENTRATION RANGES; HUMAN PLASMAS; INTERNAL STANDARDS; KETOPROFEN; LC-MS/MS; LOWER LIMIT OF QUANTITATIONS; NAPROXEN; NAPROXENS; PHARMACOKINETIC STUDIES; PROTEIN PRECIPITATION; RUNTIMES; SAMPLE PREPARATION; SIMULTANEOUS ACHIEVEMENT; TANDEM MASS SPECTROMETRY; VALIDATION;

EID: 79955918510     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2011.04.012     Document Type: Article
Times cited : (44)

References (72)
  • 14
    • 79955907059 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)
  • 15
    • 79955907306 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services, Food and Drug Administration, Guidance for industry: bioavailability and bioequivalence studies for orally administered drug products - general considerations
    • U.S. Department of Health and Human Services, Food and Drug Administration, Guidance for industry: bioavailability and bioequivalence studies for orally administered drug products - general considerations, 2003.
    • (2003)
  • 16
    • 79955897636 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.