論文

査読有り 国際誌
2020年2月25日

A Comparative Study of The Effects of Anticoagulants on Pure Platelet-Rich Plasma Quality and Potency.

Biomedicines
  • Hachidai Aizawa
  • ,
  • Hideo Kawabata
  • ,
  • Atsushi Sato
  • ,
  • Hideo Masuki
  • ,
  • Taisuke Watanabe
  • ,
  • Tetsuhiro Tsujino
  • ,
  • Kazushige Isobe
  • ,
  • Masayuki Nakamura
  • ,
  • Koh Nakata
  • ,
  • Tomoyuki Kawase

8
3
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.3390/biomedicines8030042

It is generally accepted that citrate or the A-form of acid-citrate-dextrose (ACD-A) are suitable for preparing platelet-rich plasma (PRP) for regenerative therapy. However, this is based on evidence from blood transfusions and not from regenerative medicine. Thus, we examined the effects of anticoagulants, such as ACD-A, ethylenediaminetetraacetic acid (EDTA), and heparin, on the regenerative quality of PRP to address this gap. The blood samples were collected in the presence of anticoagulants and were processed to prepare pure-PRP. Platelet size, activation status, and intra-platelet free Ca2+ concentration were determined while using a hematology analyzer and flow cytometer. Platelet-derived growth factor-BB (PDGF-BB) was quantified while using an ELISA. In pure-PRP samples, EDTA caused platelet swelling and activation, but yielded the highest number of platelets. Heparin aggregated platelets and disturbed the overall counting of blood cells. However, no significant differences in PDGF-BB levels were observed among the anticoagulants tested. Moreover, when considering the easy preparation of platelet suspensions, without the need for high-level pipetting skills, these findings suggest the comparable potency of EDTA-derived pure-PRP in tissue regeneration and support the use of EDTA in the preparation of pure-PRP. Further in vivo studies are required in animal models to exclude the possible negative effects of including EDTA in pure-PRP preparations.

リンク情報
DOI
https://doi.org/10.3390/biomedicines8030042
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/32106422
PubMed Central
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7148468
ID情報
  • DOI : 10.3390/biomedicines8030042
  • PubMed ID : 32106422
  • PubMed Central 記事ID : PMC7148468

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