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Small Molecule Specific Run Acceptance, Specific Assay Operation, and Chromatographic Run Quality Assessment: Recommendation for Best Practices and Harmonization from the Global Bioanalysis Consortium Harmonization Teams

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  • Theme: Best Practices for Bioanalytical Methods: Recommendations from the Global Bioanalysis Consortium
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Abstract

Consensus practices and regulatory guidance for liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS) assays of small molecules are more aligned globally than for any of the other bioanalytical techniques addressed by the Global Bioanalysis Consortium. The three Global Bioanalysis Consortium Harmonization Teams provide recommendations and best practices for areas not yet addressed fully by guidances and consensus for small molecule bioanalysis. Recommendations from all three teams are combined in this report for chromatographic run quality, validation, and sample analysis run acceptance.

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References

  1. European Medicines Agency. Guideline on bioanalytical method validation 2011. http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2011/08/WC500109686.pdf. Accessed 26 Jan 2014.

  2. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CVM), May 2001. http://www.fda.gov/downloads/Drugs/Guidances/ucm070107.pdf . Accessed 29 Jan 2014.

  3. Dyson N. Chromatographic integration methods. 2nd ed. London: RSC Chromatography Monographs; 1998. doi:10.1039/9781847550514. 978-0-85404-510-5.

    Google Scholar 

  4. Meyer VR. Error sources in the determination of chromatographic peak ratios. In: Advances in chromatography. New York: Marcel Dekker; 1995. p. 383.

    Google Scholar 

  5. Hill HM, Smeraglia J, Brodie RR, Smith GT. Where do you draw the line? Points to consider when implementing the FDA method validation guidance on quantifying chromatographic peaks. Chromatographia. 2002;55(Suppl):S79–81.

    Article  CAS  Google Scholar 

  6. Snyder LR, Kirkland JJ, Dolan JW. Introduction to modern liquid chromatography. 3rd ed. Hoboken: Wiley; 2010. doi:10.1002/9780470508183. 978-0-470-16754-0.

    Google Scholar 

  7. Garofolo F, Rocci ML, Dumont I, Martinez S, Lowes S, Woolf E, et al. 2011 White paper on recent issues in bioanalysis and regulatory findings from audits and inspections. Bioanalysis. 2011;3(18):2081–96.

    Article  CAS  PubMed  Google Scholar 

  8. Ministério da Saúde, Agência Nacional de Vigilância Sanitária, Brazil. RESOLUÇÃO - RDC No 27, DE 17 DE MAIO DE 2012. http://bvsms.saude.gov.br/bvs/saudelegis/anvisa/2012/rdc0027_17_05_2012.html . Accessed 29 Jan 2014.

  9. Bergeron M, Bergeron A, Furtado M, Garofolo F. Impact of plasma and whole-blood anticoagulant counter ion choice on drug stability and matrix effects during bioanalysis. Bioanalysis. 2009;1(3):537–48.

    Article  CAS  PubMed  Google Scholar 

  10. Sennbro CJ, Knutsson M, van Amsterdam P, Timmerman P. Anticoagulant counter ion impact on bioanalytical LC-MS/MS assays: results from discussions and experiments within the European Bioanalysis Forum. Bioanalysis. 2011;3(21):2393–99.

    Article  CAS  PubMed  Google Scholar 

  11. Sennbro CJ, Knutsson M, Timmerman P, van Amsterdam P. Anticoagulant counter ion impact on bioanalytical LC-MS/MS assay performance: additional validation required? Bioanalysis. 2011;3(21):2389–91.

    Article  CAS  PubMed  Google Scholar 

  12. World Health Organization. Handbook: good laboratory practice (GLP): quality practices for regulated non-clinical research and development. 2nd ed. Geneva: WHO Special Programme for Research and Training in Tropical Diseases; 2009. 978-92-4-154755-0.

    Google Scholar 

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Correspondence to Douglas M. Fast.

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Guest Editors: Binodh DeSilva and Philip Timmerman

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Woolf, E.J., McDougall, S., Fast, D.M. et al. Small Molecule Specific Run Acceptance, Specific Assay Operation, and Chromatographic Run Quality Assessment: Recommendation for Best Practices and Harmonization from the Global Bioanalysis Consortium Harmonization Teams. AAPS J 16, 885–893 (2014). https://doi.org/10.1208/s12248-014-9633-4

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  • DOI: https://doi.org/10.1208/s12248-014-9633-4

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