NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Effect of anticoagulants and cell separation media as preanalytical determinants on zymographic analysis of plasma matrix metalloproteinases.

Author(s): Mannello F, Luchetti F, Canonico B, Papa S

Publication: Clin Chem, 2003, Vol. 49, Page 1956-7

PubMed ID: 14578336 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to assess the potential influence anticoagulants and cell separation media have on matrix metalloproteinase (MMP) levels in plasma and leukocyte specimens.

Conclusion of Paper

The type and concentration of anticoagulant used altered quantifiable MMP levels in plasma specimens in an analyte-specific manner.

Studies

  1. Study Purpose

    The purpose of this study was to assess the potential influence anticoagulants and cell separation media have on matrix metalloproteinase (MMP) levels in plasma and leukocyte specimens.

    Summary of Findings:

    Circulating MMP expression was influenced both by the type and concentration of anticoagulant used. MMP expression was lower in K2EDTA compared to lithium heparin plasma specimens, and K2EDTA resulted in a dose-dependent decrease and increase in MMP-9 and MMP-2 levels, respectively. Analysis of plasma obtained from a single volunteer served to reduce variability and highlighted increased levels of proMMP-2 and proMMP-9 in buffered/acidic citrate plasma or K2EDTA and sodium fluoride/potassium oxalate plasma specimens, respectively.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Protein Zymography
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Biospecimen Acquisition Anticoagulant Buffered acidic citrate
    Citrate-phosphate-dextrose
    Lithium heparin
    Potassium EDTA
    Sodium fluoride/potassium oxalate
    None
    Acid-citrate-dextrose

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