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Volumn , Issue 3, 2010, Pages 65-74

New liquid chromatography coupled with mass spectrometry method for ciprofloxacin monitoring in human plasma

Author keywords

Ciprofloxacin; Human plasma; LC MS; Pharmacokinetics; Therapeutic drug monitoring

Indexed keywords


EID: 79251633768     PISSN: 12247154     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (3)

References (9)
  • 1
    • 0003984765 scopus 로고    scopus 로고
    • Medical Economics Company, Inc at Montvale, NJ, USA, sec. 5
    • Physician's Desk Reference, Medical Economics Company, Inc at Montvale, NJ, USA, 2001, sec. 5, 848.
    • (2001) Physician's Desk Reference , pp. 848
  • 7
    • 79251604841 scopus 로고    scopus 로고
    • The European Agency for the Evaluation of Medicinal Products, Note for Guidance on the Investigation of Bioavailability and Bioequivalence, CPMP/EWP/QWP/1401/98, July 2001, London, UK,
    • The European Agency for the Evaluation of Medicinal Products, Note for Guidance on the Investigation of Bioavailability and Bioequivalence, CPMP/EWP/QWP/1401/98, July 2001, London, UK, http://www.emea.europa.eu/pdfs/human/qwp/140198enfin.pdf
  • 8
    • 79251616446 scopus 로고    scopus 로고
    • U. S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry. Bioavailability and Bioequivalence studies for orally administered drug products - general considerations, March 2003, Rockville, USA
    • U. S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research. Guidance for Industry. Bioavailability and Bioequivalence studies for orally administered drug products - general considerations, March 2003, Rockville, USA, http://www.fda.gov/cder/guidance/5356fnl.pdf
  • 9
    • 79251615937 scopus 로고    scopus 로고
    • U.S. Department of Health and Human Services, Food and Drug Administration, Guidance for Industry - Bioanalytical Method Validation, May
    • U.S. Department of Health and Human Services, Food and Drug Administration, Guidance for Industry - Bioanalytical Method Validation, May 2001, http://www.fda.gov/cder/guidance/4252fnl.pdf
    • (2001)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.