"Carryback": effect of viscous liquid controls on the preceding sample analyzed with the SMA II continuous-flow analyzer

We systematically studied the "carryback" effect of ethylene glycol-based controls on the preceding sample on an SMA II continuous-flow analyzer. Including Beckman Level 1 unassayed liquid control material as a sample lowered the 12 analyte values of the preceding sample by an average of 2...

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Published inClinical chemistry (Baltimore, Md.) Vol. 31; no. 11; pp. 1896 - 1899
Main Authors Winter, SD, Kerr, C, McAvoy, M, Gallomore, MD, Smith, C, Lepoff, RB
Format Journal Article
LanguageEnglish
Published Washington, DC Am Assoc Clin Chem 01.11.1985
American Association for Clinical Chemistry
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Summary:We systematically studied the "carryback" effect of ethylene glycol-based controls on the preceding sample on an SMA II continuous-flow analyzer. Including Beckman Level 1 unassayed liquid control material as a sample lowered the 12 analyte values of the preceding sample by an average of 2.7%, Level 2 (the most viscous) by an average of 4.4%, and Level 3 by 3.2%. Water-reconstituted lyophilized control material caused no carryback effect, but lyophilized control reconstituted with 330 mL/L ethylene glycol decreased the preceding sample's results by 4.1% (average carryback). We believe that carryback is caused by the drag placed on the sample line by a viscous sample, which decreases the volume of the preceding sample that is delivered to the reagent or pre-dilution mixing coils. Our findings were confirmed on another SMA II. Limited study of a SMAC analyzer gave inconclusive results, but further evaluation of continuous-flow systems for carryback is warranted. Carryback substantially increases total analytical variability.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0009-9147
1530-8561
DOI:10.1093/clinchem/31.11.1896