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Volumn 1216, Issue 20, 2009, Pages 4423-4433

Fast analysis of doping agents in urine by ultra-high-pressure liquid chromatography-quadrupole time-of-flight mass spectrometry. I. Screening analysis

Author keywords

Doping agents; Fast analysis; Matrix effect; Quadrupole time of flight; Screening; Ultra high pressure liquid chromatography

Indexed keywords

DOPING AGENTS; FAST ANALYSIS; MATRIX EFFECT; QUADRUPOLE TIME-OF-FLIGHT; ULTRA-HIGH-PRESSURE LIQUID CHROMATOGRAPHY;

EID: 64649083661     PISSN: 00219673     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chroma.2009.03.033     Document Type: Article
Times cited : (115)

References (33)
  • 2
    • 64649105434 scopus 로고    scopus 로고
    • World Anti-doping Agency (WADA), the World Anti-Doping Code, Minimal Required Performance Limits, Technical Document TD2004MRPL, Montreal, 2004, www.wada-ama.org (accessed December 2008).
    • World Anti-doping Agency (WADA), the World Anti-Doping Code, Minimal Required Performance Limits, Technical Document TD2004MRPL, Montreal, 2004, www.wada-ama.org (accessed December 2008).
  • 20
    • 64649101654 scopus 로고    scopus 로고
    • World Anti-Doping Agency (WADA), International Standard for Laboratories V5.0, Montreal, 2008, www.wada-ama.org (accessed December 2008).
    • World Anti-Doping Agency (WADA), International Standard for Laboratories V5.0, Montreal, 2008, www.wada-ama.org (accessed December 2008).
  • 21
    • 64649106436 scopus 로고    scopus 로고
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, ICH Harmonised Tripartite Guideline, Validation of Analytical Procedures: Text and Methodology, Q2 R1, Geneva, 2005
    • International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, ICH Harmonised Tripartite Guideline, Validation of Analytical Procedures: Text and Methodology, Q2 (R1), Geneva, 2005.
  • 22
    • 0003484310 scopus 로고    scopus 로고
    • Food and Drug Administration, US Department of Health and Human Services, FDA, Centre for Drug Evaluation and Research, Rockville, MD
    • Food and Drug Administration, Guidance for Industry: Bioanalytical Method Validation, US Department of Health and Human Services, FDA, Centre for Drug Evaluation and Research, Rockville, MD, 2001.
    • (2001) Guidance for Industry: Bioanalytical Method Validation


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.