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

The use of potassium dichromate and ethyl alcohol as blood preservatives for analysis of organochlorine contaminants.

Author(s): Schecter A, Pavuk M, Päpke O, Malisch R

Publication: Chemosphere, 2004, Vol. 57, Page 1-7

PubMed ID: 15288193 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of preservation with potassium dichromate, 20% ethanol, or 40% ethanol and room temperature shipping and storage rather than frozen shipping and storage on levels of 4 polychlorinated biphenyls (PCBs), 6 dioxins and 9 dibenzofurans in blood specimens.

Conclusion of Paper

Preservation of blood specimens in 20% or 40% ethanol led to higher fat and lipid content than observed in potassium dichromate-preserved or frozen specimens, and in specimens preserved in 20% ethanol, fat and lipid content increased with storage. The increased lipid content led to decreased normalized levels of contaminants in ethanol-preserved specimens compared to potassium dichromate-preserved or frozen specimens. Preservation or storage in potassium dichromate had no effects on the measurement of contaminant levels, regardless of normalization method.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of preservation with potassium dichromate, 20% ethanol, or 40% ethanol and room temperature shipping and storage rather than frozen shipping and storage on levels of 4 PCBs, 6 dioxins and 9 dibenzofurans in blood. Leftover blood from 249 patients was pooled, aliquoted, and either frozen or preserved with potassium dichromate, 20% ethanol, or 40% ethanol. Frozen specimens were shipped on dry ice and stored frozen (temperature not specified), but potassium dichromate and ethyl alcohol-preserved specimens were shipped and stored at ambient temperatures.

    Summary of Findings:

    The fat content was 0.35% in frozen blood specimens, 0.34% in potassium dichromate specimens, 0.48% in 20% ethanol-preserved specimens and 0.52% in 40% ethanol-preserved specimens. The lipid content was also higher in specimens preserved with 40% ethanol than in frozen or potassium dichromate specimens, and it remained relatively stable during storage; however, the lipid content of specimens preserved in 20% ethanol increased with storage such that on day 25, lipid content was comparable to that in 40% ethanol-preserved specimens. When the levels of contaminants were normalized to lipid content, contaminant levels in ethanol-preserved specimens were lower than in frozen specimens and were changed during storage in 20% ethanol. However, when contaminant levels are normalized for wet weight and not lipid weight, preservation method had no effect on contaminant levels. Regardless of method used for normalization, contaminant levels were not affected by preservation or storage in potassium dichromate when compared to frozen specimens.

    Biospecimens
    Preservative Types
    • Frozen
    • Other Preservative
    • Ethanol
    Diagnoses:
    • Not specified
    Platform:
    AnalyteTechnology Platform
    Small molecule GC-MS
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Storage duration 6 days
    25 days
    34 days
    Storage Between site transportation method Mailed
    Storage Specimen transport duration/condition At room temperature
    On dry ice
    Biospecimen Preservation Type of fixation/preservation Ethanol
    Frozen
    Potassium dichromate
    Biospecimen Preservation Concentration of fixative 20% Ethanol
    40% Ethanol

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