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

Stability of plasma enzymes during storage.

Author(s): Juul P

Publication: Clin Chem, 1967, Vol. 13, Page 416-22

PubMed ID: 6024052 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of storage on enzyme stability in whole blood, plasma and serum from healthy individuals.

Conclusion of Paper

Generally, the stability of enzymes in whole blood, plasma, and serum was analyte specific and differed based on storage conditions. Lactate dehydrogenase (LDH) was unstable in serum stored without the clot at -20 degrees C, but other analytes measured remained stable under these conditions. Amylase was stable in citrated plasma stored at 38 degrees C, but other analytes measured were unstable under these conditions.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of storage and anticoagulant on enzyme stability in whole blood, plasma and serum, stored with or without the clot, from healthy individuals. Only 1-2 specimens were examined under each condition.

    Summary of Findings:

    Acetylcholinesterase (AChE) was stable in citrated or heparinated whole blood at 4 degrees C for at least 7 days. Pseudocholinesterase (ChE) was relatively stable in whole blood under all storage conditions, in serum with the clot at -20, 4, or 22 degrees C, or in citrated plasma at 4 degrees C, but ChE levels declined in citrated plasma stored at 38 degrees C. Both glutamic-oxaloacetic transaminase (GOT) and glutamic-pyruvic transaminase (GPT) were stable in citrated plasma and whole blood stored at 4 degrees C and in serum without the clot stored at -20, 4 and 22 degrees C, but GOT and GPT levels declined in citrated plasma stored at 38 degrees C and increased in heparinated whole blood stored at 4 degrees C for more than a week and in serum stored on the clot at 22 degrees C. LDH was stable in heparinated plasma at 4 degrees C but decreased in citrated plasma stored at 4 degrees C and increased in citrated or heparinated whole blood stored at 4 degrees C or serum stored on the clot at 22 degrees C. Acid phosphatase (Acid Ph) was stable at -20 degrees C but increased when in contact with erythrocytes and decreased when stored at temperatures above -20 degrees C. Alkaline phosphatase (Alk Ph) decreased with storage of whole blood and plasma but was stable in serum at all temperatures examined. Amylase was stable under all temperatures and conditions.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Protein Enzyme assay
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Storage duration 0 days
    1 days
    7 days
    8 days
    30 days
    60 days
    120 days
    Storage Storage temperature -20 degrees C
    4 degrees C
    22 degrees C
    38 degrees C
    Storage Storage conditions On the clot
    Without clot
    Biospecimen Aliquots and Components Blood and blood products Plasma
    Serum
    Whole blood
    Biospecimen Acquisition Anticoagulant Citrate
    Heparin
    None

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