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Volumn 879, Issue 2, 2011, Pages 219-224

Quantitation of ursolic acid in human plasma by ultra performance liquid chromatography tandem mass spectrometry and its pharmacokinetic study

Author keywords

Clinical pharmacokinetics; UPLC MS MS; Ursolic acid

Indexed keywords

ACQUITY; AMMONIUM FORMATE; ANTI-INFLAMMATORIES; ANTICANCER ACTIVITIES; ANTIULCER; CLINICAL PHARMACOKINETICS; ETHYL ACETATES; EXTRACTION RECOVERY; HIGH SELECTIVITY; HUMAN PLASMAS; INTERNAL STANDARDS; ION SUPPRESSION; LIQUID CHROMATOGRAPHY/TANDEM MASS SPECTROMETRY; LIQUID-LIQUID EXTRACTION; LOWER LIMIT OF QUANTITATIONS; MATRIX; MOBILE PHASE; MULTIPLE REACTION MONITORING; PHARMACOKINETIC STUDIES; PLASMA SAMPLES; STORAGE PERIODS; TRITERPENES; ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY; UPLC/MS/MS; URSOLIC ACID; VALIDATED METHODS;

EID: 78651252487     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2010.11.037     Document Type: Article
Times cited : (54)

References (10)
  • 9
    • 78651253386 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Veterinary Medicine (CVM) Guidance for Industry - Bioanalytical Method Validation
    • U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM) Guidance for Industry - Bioanalytical Method Validation, 1-5-2001. http://www.fda.gov/cder/guidance/4252fnl.pdf.
    • (2001) , vol.5 , Issue.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.