In-vitro production and pre-validation of lyophilized canine platelet-rich plasma for therapeutic use

富血小板血浆 体外 免疫原性 化学 血小板 冷冻干燥 体内 分子生物学 免疫学 色谱法 免疫系统 生物 生物化学 生物技术
作者
Natália Pereira Paiva Freitas,Maria Márcia Souto Maior,Beatriz A.P. Silva,Marcus Rafael Lobo Bezerra,José Ferreira Nunes,Saul Gaudêncio Neto,Kaio César Simiano Tavares,Leonardo Tondello Martins
出处
期刊:Pesquisa Veterinaria Brasileira [Colégio Brasileiro de Patologia Animal (CBPA)]
卷期号:41 被引量:3
标识
DOI:10.1590/1678-5150-pvb-6999
摘要

ABSTRACT: Platelet-rich plasma (PRP) has been considered a promising therapeutic alternative, since platelets are rich in growth factors that are used in the Regenerative Medicine field. However, fresh PRP cannot be stored for long periods. This study aimed to develop a protocol for obtaining lyophilized canine PRP capable of maintaining viability after its reconstitution. For that purpose, canine PRP extraction and lyophilization protocols were initially tested. Subsequently, assays were carried out to quantify the growth factors VEGF and TGF-β, before and after the lyophilization process, gelation test and the three-dimensional gel structure analysis of the reconstituted lyophilized PRP by electron microscopy, as well as in vitro cell proliferation test in lyophilized PRP gel. Additionally, the immunogenicity test was performed, using allogeneic samples of lyophilized PRP. The results showed that the lyophilized PRP had adequate therapeutic concentrations of growth factors VEGF and TGF-β (9.1pg/mL and 6161.6pg/mL, respectively). The reconstituted PRP gel after lyophilization showed an in vitro durability of 10 days. Its electron microscopy structure was similar to that of fresh PRP. In the cell proliferation test, an intense division process was verified in mesenchymal stem cells (MSCs) through the three-dimensional mesh structure of the lyophilized PRP gel. The immunogenicity test showed no evidence of an immune reaction. The findings were promising, suggesting the possibility of having a lyophilized canine PRP that can be marketed. New in vivo and in vitro studies must be carried out for therapeutic confirmation.
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