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

Automated preparation of whole blood-derived platelets suspended in two different platelet additive solutions and stored for 7 days.

Author(s): Cid J, Magnano L, Molina P, Diaz-Ricart M, Martínez N, Maymó RM, Puig L, Lozano M, Escolar G, Galán AM

Publication: Transfusion, 2014, Vol. 54, Page 426-33

PubMed ID: 23721299 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of blood processor type, storage solution and storage duration on markers of platelet (Plt) quality in Plt concentrates (PC).

Conclusion of Paper

For at least one timepoint (1, 5, or 7 days), blood processor type had significant effects on Plt volume, mean platelet component (MPC), glucose, lactate, and expression of von Willebrand Factor (vWF). Storage of PC at room temperature had significant effects on MPC, glucose, and lactate. PC storage solution had effects on glucose, lacate, pH, and the expression of CD62p, CD63. Expression of glycoprotein (GP) Ib, IIbIIA and IV, Factor V/Va, annexin V, and fibrinogen, partial pressure oxygen (PO2) and partial pressure carbon dioxide (PCO2) were not significantly affected by processor type, storage duration, or storage solution.

Studies

  1. Study Purpose

    The purpose of this study was to determine the effects of blood processor type, storage solution and storage at room temperature on markers of Plt quality in PC. Leukoreduced PC were obtained from whole blood 1 day after collection. Buffy coats were obtained from whole blood using the Atreus 2C+ and were held for~4 h before processing of the buffy coats to PC in PASII using the OrbiSac and or PC were obtained directly from whole blood using the Atreus 3C and stored in PASII or PASIIIM. Each PC consisted of Plts from 4-5 healthy donors, and 8 PC pools were analyzed for each processor/storage solution.

    Summary of Findings:

    Compared to PC obtained using the Atreus 2C/OrbiSac, PC obtained with the Atreus 3C had lower volume (p<0.01) and a higher Plt count/L (p<0.01), regardless of storage duration and solution. However, Plt count/unit was not affected by type of blood processor, storage duration or storage solution. During room temperature storage, MPC decreased in all specimens (p<0.05 day 7 versus day 1, all), and while significant differences between processors were not apparent on day 1 or 7, on day 5, PC obtained with the Atreus 3C had higher MPC than those obtained with Atreus 2C/OrbiSac, regardless of storage solution (p<0.05, both). During room temperature storage of PC, glucose decreased, and lactate levels increased, and on day 5 and 7, glucose levels were lower and lactate levels were higher in PC obtained using the Atreus 3C and stored in Plt additive solution (PAS)-II than in PC obtained using the Atreus 2C/OrbiSac and stored in PAS-II or obtained by the Atreus 3C and stored in PAS-IIIM. The pH was higher in PC obtained using the Atreus 3C and stored in PAS-IIIM on day 1 than in PC obtained using the Atreus 3C and stored in PAS-II and on day 5 and 7 than in PC obtained using the Atreus 2C/OrbiSac and stored in PAS-II. Expression of Plt activation markers was not affected by storage duration, but was higher on day 5 and 7 in Plts obtained using the Atreus 3C and stored in PAS-IIIM than in Plts obtained using the Atreus 2C/OrbiSac and stored in PAS-II (p<0.05, both) or those obtained by the Atreus 3C and stored in PAS-II (p<0.05, both). Expression of GPIb, GPIIbIIA and GPIV, Factor V/Va, annexin V, and fibrinogen were not significantly affected by processor type, storage duration, or storage solution. vWF expression was lower on day 5 in Plts prepared with the Atreus 3C (either in PAS-II or IIIM) than in Plts prepared with the Atreus 2C in PAS-II. Processor type, storage solution and storage duration did not affect PO2 and PCO2 in PC.

    Biospecimens
    Preservative Types
    • None (Fresh)
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Small molecule Clinical chemistry/auto analyzer
    Carbohydrate Clinical chemistry/auto analyzer
    Cell count/volume Flow cytometry
    Cell count/volume Hematology/ auto analyzer
    Gas Clinical chemistry/auto analyzer
    Protein Flow cytometry
    Glycoprotein Flow cytometry
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Time at room temperature 1 day
    5 days
    7 days
    Storage Short-term storage solution PAS-II
    PAS-IIIM
    Biospecimen Aliquots and Components Blood processing method Atreus 2C/OrbiSac
    Atreus3C

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