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Freeze-Dried Human Platelet-Rich Plasma Retains Activation and Growth Factor Expression after an Eight-Week Preservation Period

STUDY DESIGN: Controlled laboratory study. PURPOSE: This study aimed to evaluate the efficacy of platelet-rich plasma (PRP) stored at room temperature (RT), frozen, or after freeze-drying. OVERVIEW OF LITERATURE: PRP enriches tissue repair and regeneration, and is a novel treatment option for muscul...

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Detalles Bibliográficos
Autores principales: Shiga, Yasuhiro, Kubota, Go, Orita, Sumihisa, Inage, Kazuhide, Kamoda, Hiroto, Yamashita, Masaomi, Iseki, Toru, Ito, Michihiro, Yamauchi, Kazuyo, Eguchi, Yawara, Sainoh, Takeshi, Sato, Jun, Fujimoto, Kazuki, Abe, Koki, Kanamoto, Hirohito, Inoue, Masahiro, Kinoshita, Hideyuki, Furuya, Takeo, Koda, Masao, Aoki, Yasuchika, Toyone, Tomoaki, Takahashi, Kazuhisa, Ohtori, Seiji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Spine Surgery 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5481587/
https://www.ncbi.nlm.nih.gov/pubmed/28670400
http://dx.doi.org/10.4184/asj.2017.11.3.329
Descripción
Sumario:STUDY DESIGN: Controlled laboratory study. PURPOSE: This study aimed to evaluate the efficacy of platelet-rich plasma (PRP) stored at room temperature (RT), frozen, or after freeze-drying. OVERVIEW OF LITERATURE: PRP enriches tissue repair and regeneration, and is a novel treatment option for musculoskeletal pathologies. However, whether biological activity is preserved during PRP storage remains uncertain. METHODS: PRP was prepared from blood of 12 healthy human volunteers (200 mL/person) and stored using three methods: PRP was stored at RT with shaking, PRP was frozen and stored at −80℃, or PRP was freeze-dried and stored at RT. Platelet counts and growth factor content were examined immediately after preparation, as well as 2, 4, and 8 weeks after storage. Platelet activation rate was quantified by flow cytometry. RESULTS: Platelet counts were impossible to determine in many RT samples after 2 weeks, but they remained at constant levels in frozen and freeze-dried samples, even after 8 weeks of storage. Flow cytometry showed approximately 80% activation of the platelets regardless of storage conditions. Almost no growth factors were detected in the RT samples after 8 weeks, while low but significant expression was detected in the frozen and freeze-dried PRP. Over time, the mean relative concentrations of various growth factors decreased significantly or disappeared in the RT group. In the frozen group, levels were maintained for 4 weeks, but decreased significantly by 8 weeks (p <0.05). The freeze-dried group maintained baseline levels of growth factors for the entire 8-week duration. CONCLUSIONS: Freeze-drying enables PRP storage while maintaining bioactivity and efficacy for extended periods.