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Regulations in the field of residue and doping analysis should ensure the risk of false positive declaration is well-defined

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Abstract

The purpose of this contribution is twofold, namely, to discuss the fundamental weaknesses of some decision criteria in the field of residue and doping analysis and to draw attention to a statistics-based solution that was proposed and thoroughly validated a decade ago, but nevertheless continues to be overlooked by practitioners.

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References

  1. Van Eenoo P, Delbeke FT (2004) Chromatographia 59:S39–S44. doi:10.1365/s10337-004-0198-8

    Article  Google Scholar 

  2. van der Voet H, de Boer WJ, de Ruig WG, van Rhijn JA (1998) J Chemometr 12:279–294. doi:10.1002/(SICI)1099-128X(199807/08)12:4<279::AID-CEM514>3.0.CO;2-7

    Article  Google Scholar 

  3. European Council (2002) Council Directive 2002/657/EC of 12 August 2002 implementing Council Directive 96/23/EC concerning the performance of analytical methods and the interpretation of results. Off J Eu Communities L 221:8–36

    Google Scholar 

  4. Food and Drug Administration (2003) US Department of Health and Human Services, Center for Veterinary Medicine, Guidance for Industry. Mass spectrometry confirmation of the identity of animal drug residues, http://www.fda.gov/cvm/guidance/guide118.pdf

  5. Association of Official Racing Chemists (2002) AORC guidelines for the minimum criteria for identification by chromatography and mass spectrometry, MS Criteria Working group, Version 19 June 2002, Internal communication to AORC members

  6. International Olympic Committee (1998) Analytical criteria for reporting low concentrations of anabolic steroids. Internal communication to IOC accredited laboratories, Lausanne, Switzerland

    Google Scholar 

  7. World Anti-Doping Agency (2004) Identification criteria for qualitative assays incorporating chromatography and mass spectrometry, Version 1.2, http://www.wada-ama.org/rtecontent/document/criteria_1_2.pdf

  8. Hughes CG (2002) Confirmation and quantitation of ractopamine in equine urine, Equine Pharmacology Department, Gluck Equine Research Center, University of Kentucky

  9. Fraga CF (2003) J Chromatogr A 1019:31–42. doi:10.1016/S0021-9673(03)01329-3

    Article  CAS  Google Scholar 

  10. Mazzarino M, Orengia M, Botrè F (2007) Rapid Commun Mass Spectrom 21:4117–4124. doi:10.1002/rcm.3326

    Article  CAS  Google Scholar 

  11. de Zeeuw RA (2004) J Chromatogr B 811:3–12

    Google Scholar 

  12. de Boer WJ, van der Voet H, de Ruig WG, van Rhijn JA, Cooper KM, Kennedy DG, Patel RKP, Porter S, Reuvers T, Marcos V, Muñoz P, Bosch J, Rodríguez P, Grases JM (1999) Analyst (Lond) 124:109–114. doi:10.1039/a807051b

    Article  Google Scholar 

  13. Bethem R, Boison J, Gale J, Heller D, Lehotay S, Loo J, Musser S, Price P, Stein S (2003) J Am Soc Mass Spectrom 14:528–541. doi:10.1016/S1044-0305(03)00137-5

    Article  CAS  Google Scholar 

  14. De Bièvre P (1997) Accredit Qual Assur 2:269. doi:10.1007/s007690050147

    Article  Google Scholar 

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Acknowledgments

Thanks should be expressed to H. van der Voet for his critical assessment of the manuscript and to P. Kootstra for drawing my attention to the work of de Zeeuw.

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Correspondence to Nicolaas (Klaas) M. Faber.

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Faber, N.(.M. Regulations in the field of residue and doping analysis should ensure the risk of false positive declaration is well-defined. Accred Qual Assur 14, 111–115 (2009). https://doi.org/10.1007/s00769-008-0468-5

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