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Volumn 879, Issue 23, 2011, Pages 2265-2273

Development and validation of a selective and sensitive LC-MS/MS method for determination of cycloserine in human plasma: Application to bioequivalence study

Author keywords

Bioequivalence; Cycloserine; Human plasma; LC MS MS; Solid phase extraction

Indexed keywords

BIOEQUIVALENCE; CYCLOSERINE; HUMAN PLASMAS; LC-MS/MS; SOLID PHASE EXTRACTION;

EID: 79960557826     PISSN: 15700232     EISSN: 1873376X     Source Type: Journal    
DOI: 10.1016/j.jchromb.2011.06.011     Document Type: Article
Times cited : (44)

References (21)
  • 2
    • 16844364421 scopus 로고    scopus 로고
    • Churchill Livingstone, New York, R.G. Finch, D. Greenwood, S.R. Norrby, R. Whitley (Eds.)
    • Greenwood D., Whitley R. Antibiotic and Chemotherapy 2002, 11. Churchill Livingstone, New York. 8th ed. R.G. Finch, D. Greenwood, S.R. Norrby, R. Whitley (Eds.).
    • (2002) Antibiotic and Chemotherapy , pp. 11
    • Greenwood, D.1    Whitley, R.2
  • 4
    • 0001794737 scopus 로고
    • Springer-Verlag, Berlin, Heidelberg, New York, D. Gottlieb, P.D. Shaw (Eds.)
    • Neuhhaus F.C. Antibiotics. I. Mechanism of Action 1967, 40. Springer-Verlag, Berlin, Heidelberg, New York. D. Gottlieb, P.D. Shaw (Eds.).
    • (1967) Antibiotics. I. Mechanism of Action , pp. 40
    • Neuhhaus, F.C.1
  • 18
    • 79960559987 scopus 로고    scopus 로고
    • Guidance for Industry, Bionanlytical Method Validation, US Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM), May.
    • Guidance for Industry, Bionanlytical Method Validation, US Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM), May 2001.
    • (2001)
  • 20
    • 79960564576 scopus 로고    scopus 로고
    • Guidance for Industry: ICH E6 Good Clinical Practice, U.S. Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER), Centre for Biologics Evaluation and Research (CBER), April
    • Guidance for Industry: ICH E6 Good Clinical Practice, U.S. Department of Health and Human Services, Food and Drug Administration, Centre for Drug Evaluation and Research (CDER), Centre for Biologics Evaluation and Research (CBER), April 1996.
    • (1996)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.