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Volumn 879, Issue 19, 2011, Pages 1653-1658

Development and validation of a LC-ESI-MS/MS method for the determination of swertiamarin in rat plasma and its application in pharmacokinetics

Author keywords

LC ESI MS MS; Pharmacokinetics; Rat plasma; Swertiamarin

Indexed keywords

AGILENT; APPARENT VOLUME; ASSAY METHODS; BIOACTIVE SUBSTANCES; CHEMICAL STRUCTURE; FREEZE/THAW; INTERNAL DIAMETERS; INTERNAL STANDARDS; ION ELECTROSPRAY; IONISATION; LC-ESI-MS/MS; LIMIT OF DETECTION; LINEAR RANGE; LOWER LIMIT OF QUANTIFICATIONS; MOBILE PHASE; MULTIPLE-REACTION MONITORING MODES; ORAL ADMINISTRATION; PHARMACOKINETIC PARAMETERS; PHARMACOKINETIC PROPERTIES; PLASMA CONCENTRATION; RAT PLASMA; SAMPLE CLEAN-UP; SOLID-PHASE EXTRACTION; SWERTIAMARIN;

EID: 79955909249     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2011.04.003     Document Type: Article
Times cited : (17)

References (16)
  • 16
    • 84856070463 scopus 로고    scopus 로고
    • Guidance for Industry, Bioanalytical Method Validation, US Department of Health and Human Services Food and Drug Administration, Center for Drug Evaluation and Research (CDER), 2001 Center for Veterinary Medicine (CV), May
    • Guidance for Industry, Bioanalytical Method Validation, US Department of Health and Human Services Food and Drug Administration, Center for Drug Evaluation and Research (CDER), 2001 Center for Veterinary Medicine (CV), May 2001. http://www/fda.gov/cder/guidance/index.htm.
    • (2001)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.