메뉴 건너뛰기




Volumn 33, Issue 19-20, 2012, Pages 2978-2986

Easy sample treatment for the determination of enrofloxacin and ciprofloxacin residues in raw bovine milk by capillary electrophoresis

Author keywords

CE; Fluoroquinolones; Milk; Routine analysis; Sample treatment

Indexed keywords

ANTIBIOTICS; MAMMALS;

EID: 84867682038     PISSN: 01730835     EISSN: 15222683     Source Type: Journal    
DOI: 10.1002/elps.201200316     Document Type: Article
Times cited : (33)

References (34)
  • 5
    • 77952193613 scopus 로고    scopus 로고
    • Commission of the European communities, Commission regulation No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin
    • Commission of the European communities, Commission regulation No. 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, Off. J. Eur. Commun. 2010, L15, 1-72.
    • (2010) Off. J. Eur. Commun. , vol.15 L , pp. 1-72
  • 6
    • 85153544802 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration (FDA). Code of Federal Regulation, Title 21 (Food and Drugs). Revised April 1.
    • U.S. Food and Drug Administration (FDA). Code of Federal Regulation, 2006. Title 21 (Food and Drugs), Vol. 6, Part 556. Revised April 1.
    • (2006) , vol.6 , Issue.PART 556
  • 32
    • 85153549133 scopus 로고    scopus 로고
    • ICH Harmonised Tripartite Guideline: Validation of Analytical Procedures: Text and Methodology, Q2(R1), Geneva, Switzerland,
    • ICH Harmonised Tripartite Guideline: Validation of Analytical Procedures: Text and Methodology, Q2(R1), Geneva, Switzerland 2005, http://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q2_R1/Step4/Q2_R1_Guideline.pdf
    • (2005)
  • 33
    • 85153548565 scopus 로고    scopus 로고
    • Guidance for Industry: Bioanalytical Method Validation, US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Biologics Evaluation and Research (CBER), 2001, Rockville, USA
    • Guidance for Industry: Bioanalytical Method Validation, US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Biologics Evaluation and Research (CBER), 2001, Rockville, USA, http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM070107.pdf
  • 34
    • 0013285756 scopus 로고    scopus 로고
    • Commission of the European Communities, Commission Decision 2002/657/EC of 12 August implementing Council Directive 96/23/EC concerning the performance of analytical methods and the interpretation of the results
    • Commission of the European Communities, Commission Decision 2002/657/EC of 12 August implementing Council Directive 96/23/EC concerning the performance of analytical methods and the interpretation of the results, Off. J. Eur. Comun. 2002, L221, 8-36.
    • (2002) Off. J. Eur. Comun. , vol.221 L , pp. 8-36


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.