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Updated: Jul 16, 2026

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Effects of Allogeneic Platelet-Rich Plasma (PRP) on the Healing Process of Sectioned Achilles Tendons of Rats: A Methodological Description
Published on: March 19, 2018
Wound-healing properties of trehalose-stabilized freeze-dried outdated platelets
Ruth Sum1, Sarah Hager, Giorgio Pietramaggiori
1From Adlyfe Inc., and Cellphire Inc., Rockville, Maryland 22101, USA.
Transfusion
|March 27, 2007
Summary
Stabilized freeze-dried outdated platelets (FDPOs) effectively accelerate wound healing. These preparations promote cell proliferation and tube formation, showing comparable results to fresh platelets in mice models.
Area of Science:
- Biomedical Science
- Regenerative Medicine
- Wound Healing Research
Background:
- Platelet (PLT)-derived products are recognized for wound healing, with ongoing research into their therapeutic potential.
- Stabilized freeze-dried platelets from outdated sources (FDPOs) are explored for their wound healing capabilities.
- Comparison is made between FDPOs, stabilized freeze-dried platelets from dated sources (FDPIs), and room-temperature fresh platelets (RT-PLTs).
Purpose of the Study:
- To compare the in vitro and in vivo wound healing properties of FDPOs, FDPIs, and RT-PLTs.
- To assess the concentration of key growth factors, PDGF-betabeta and TGF-beta1, in these preparations.
- To evaluate the impact on endothelial cell proliferation and tube formation, crucial for wound repair.
Main Methods:
- In vitro assessment of endothelial cell proliferation and tube formation induced by FDPIs, FDPOs, and RT-PLTs.
- In vivo study using full-thickness wounds in db/db mice treated with FDPIs and FDPOs.
- Measurement of wound closure rate and histological evaluation of cellular makeup, including reepithelialization, granulation, and angiogenesis.
Main Results:
- FDPOs maintain concentrations of PDGF-betabeta and TGF-beta1 comparable to FDPIs and RT-PLTs.
- FDPOs effectively promote endothelial cell proliferation and tube formation in vitro.
- Multiple FDPO applications significantly accelerated wound closure and enhanced reepithelialization in mice.
Conclusions:
- FDPOs demonstrate comparable wound healing enhancement to FDPIs and RT-PLTs in db/db mice.
- Wound closure was achieved 6 days earlier in FDPO-treated groups compared to controls.
- Histological analysis revealed reduced granulation tissue and increased cellular angiogenesis in FDPO-treated wounds.
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