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Nicotine & Tobacco Research Advance Access originally published online on November 23, 2009
Nicotine & Tobacco Research 2009 11(12):1458-1466; doi:10.1093/ntr/ntp161
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Published by Oxford University Press on behalf of the Society for Research on Nicotine and Tobacco 2009.

Interlaboratory comparability of serum cotinine measurements at smoker and nonsmoker concentration levels: A round-robin study

John T. Bernert, Peyton Jacob, III, David B. Holiday, Neal L. Benowitz, Connie S. Sosnoff, Mira V. Doig, Colin Feyerabend, Kenneth M. Aldous, Mehran Sharifi, Mark D. Kellogg and Loralie J. Langman

John T. Bernert, Ph.D., Division of Laboratory Science, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA
Peyton Jacob, III, Ph.D., Department of Medicine, University of California at San Francisco
David B. Holiday, Ph.D., RTI International, Atlanta Regional Office, Atlanta, GA
Neal L. Benowitz, M.D., Department of Medicine, University of California at San Francisco
Connie S. Sosnoff, M.S., Division of Laboratory Science, National Center for Environmental Health, Centers for Disease Control and Prevention, Atlanta, GA
Mira V. Doig, Ph.D., ABS Laboratories Ltd, Welwyn Garden City, Herts, UK
Colin Feyerabend, Ph.D., ABS Laboratories Ltd, Welwyn Garden City, Herts, UK
Kenneth M. Aldous, Ph.D., Biggs Laboratory, Wadsworth Center, New York State Department of Health, Empire State Plaza, Albany
Mehran Sharifi, Ph.D., LabStat International ULC, Kitchener, Ontario, Canada
Mark D. Kellogg, Ph.D., Department of Laboratory Medicine, Children’s Hospital Boston, Boston, MA
Loralie J. Langman, Ph.D., Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN

Corresponding Author: John T. Bernert, Centers for Disease Control and Prevention, 4770 Buford Highway, N.E., Mailstop F-47, Atlanta, GA 30341, USA. Telephone: 770-488-7911; Fax: 770-488-0181; E-mail: jtb2{at}cdc.gov


   Abstract

Introduction: Cotinine, the primary proximate metabolite of nicotine, is commonly measured as an index of exposure to tobacco in both active users of tobacco and nonsmokers with possible exposure to secondhand smoke (SHS). A number of laboratories have implemented analyses for measuring serum cotinine in recent years, but there have been few interlaboratory comparisons of the results. Among nonsmokers exposed to SHS, the concentration of cotinine in blood can be quite low, and extensive variability in these measurements has been reported in the past.

Methods: In this study, a group of seven laboratories, all experienced in serum cotinine analysis, measured eight coded serum pools with concentrations ranging from background levels of about 0.05 ng/ml to relatively high concentrations in the active smokers range. All laboratories used either gas–liquid chromatography with nitrogen–phosphorus detection or liquid chromatography with mass spectrometric detection.

Results: All seven laboratories reliably measured the cotinine concentrations in samples that were within the range of their methods. In each case, the results for the pools were correctly ranked in order, and no significant interlaboratory bias was observed at the 5% level of significance for results from any of the pools.

Discussion: We conclude that present methods of chromatographic analysis of serum cotinine, as used by these experienced laboratories, are capable of providing accurate and precise results in both the smoker and the nonsmoker concentration range.

Received: May 6, 2009; Accepted: September 22, 2009
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