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Volumn 864, Issue 1-2, 2008, Pages 137-148

HPLC-ESI-MS/MS validated method for simultaneous quantification of zopiclone and its metabolites, N-desmethyl zopiclone and zopiclone-N-oxide in human plasma

Author keywords

LC MS MS; N desmethyl zopiclone; Solid phase extraction; Zopiclone; Zopiclone N oxide

Indexed keywords

N-DESMETHYL ZOPICLONE; SOLID PHASE EXTRACTION; ZOPICLONE; ZOPICLONE-N-OXIDE;

EID: 40849147026     PISSN: 15700232     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jchromb.2008.02.004     Document Type: Article
Times cited : (27)

References (43)
  • 41
    • 40849099340 scopus 로고    scopus 로고
    • Guidance for Industry: Bioanalytical Method validation, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM), May 2001.
    • Guidance for Industry: Bioanalytical Method validation, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), Centre for Veterinary Medicine (CVM), May 2001.
  • 42
    • 40849087158 scopus 로고    scopus 로고
    • FDA Guidance for Industry: Bioavailability Studies for Orally Administered Drug-Products-General Considerations, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), 2000.
    • FDA Guidance for Industry: Bioavailability Studies for Orally Administered Drug-Products-General Considerations, U.S. Department of Health and Human Services, Food and Drug Administration Centre for Drug Evaluation and Research (CDER), 2000.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.