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Volumn 852, Issue 1-2, 2007, Pages 174-179

An optimized analytical method of fluconazole in human plasma by high-performance liquid chromatography with ultraviolet detection and its application to a bioequivalence study

Author keywords

Bioequivalence; Fluconazole; High performance liquid chromatography (HPLC); Human plasma; Validation

Indexed keywords

CONCENTRATION (PROCESS); DICHLOROMETHANE; LIQUID CHROMATOGRAPHY; PLASMA (HUMAN); ULTRAVIOLET DETECTORS;

EID: 34249717358     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2007.01.012     Document Type: Article
Times cited : (43)

References (20)
  • 17
    • 34249653552 scopus 로고    scopus 로고
    • FDA 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, http://www.fda.gov/cder/guidance/index.htm.
  • 19
    • 34249654577 scopus 로고    scopus 로고
    • KFDA Guidance for Industry, Statistical Approaches to Establishing Bioequivalence, Bioequivalence Division, Pharmacology Department, National Institute of Toxicology Department, 2003, http://ezdrug.kfda.go.kr/kfda2.
  • 20
    • 34249658991 scopus 로고    scopus 로고
    • FDA Guidance for Industry, Statistical Approaches to Establishing Bioequivalence, US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), 2001, http://www.fda.gov/cder/guidance/index.htm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.