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Related Concept Videos

Structure and Function of Platelets01:18

Structure and Function of Platelets

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The cell fragments known as platelets are disc-shaped, with an average diameter of about 3 μm and a thickness of roughly 1 μm. They play a crucial role in the body's vascular clotting system, which also involves plasma proteins, blood cells, and blood vessel tissues.
Platelets are continually replenished, circulating in the bloodstream for 9-12 days before being removed by phagocytes, primarily in the spleen. A microliter of circulating blood contains between 150,000 and 450,000...
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The platelet phase, the second stage of hemostasis, commences around 15-20 seconds after an injury. It follows and overlaps with the vascular phase, during which blood vessels constrict to minimize blood loss.
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Procoagulant Platelet Characterization by Measuring Phosphatidylserine Exposure and Microvesicle Release from Human Purified Platelets
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Procoagulant Platelet Characterization by Measuring Phosphatidylserine Exposure and Microvesicle Release from Human Purified Platelets

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Frozen platelets.

Kathleen Kelly1, Larry J Dumont1

  • 1Blood Systems Research Institute, 717 Yosemite Street, Denver, CO, 80230, United States.

Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis
|January 8, 2019
PubMed
Summary
This summary is machine-generated.

Cryopreservation of platelets using dimethyl sulfoxide (DMSO) offers a viable alternative to room temperature storage. Frozen platelets demonstrate safety and potential benefits in hemostasis, supporting their use in various applications.

Keywords:
Cryopreserved plateletsFrozen platelets

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Area of Science:

  • Hematology
  • Biopreservation
  • Transfusion Medicine

Background:

  • Platelet storage limitations necessitate alternative preservation methods.
  • Cryopreservation has emerged as a promising alternative for extending platelet viability.
  • Current methods involve freezing with dimethyl sulfoxide (DMSO) and mechanical freezers.

Purpose of the Study:

  • To evaluate the efficacy and safety of cryopreserved platelets.
  • To assess the in vitro and in vivo characteristics of frozen platelets.
  • To determine the potential of frozen platelets as an alternative to room temperature platelets.

Main Methods:

  • Platelets were frozen in 6% dimethyl sulfoxide (DMSO).
  • Storage was conducted in mechanical freezers at -80°C for up to 2 years.
  • In vitro assays included morphology, flow cytometry, and thrombin capacity.
  • In vivo studies and limited clinical trials were conducted.

Main Results:

  • Frozen platelets exhibited a primed, hypercoagulable in vitro phenotype post-thaw.
  • In vivo studies indicated a role in hemostasis maintenance.
  • Limited clinical trials suggested safety and potential benefits.

Conclusions:

  • Cryopreserved platelets are a safe and potentially beneficial alternative.
  • Frozen platelet development addresses limitations of room temperature storage.
  • Further research is needed to correlate in vitro assays with clinical outcomes.