Histological Preparation Technique of Blood Derivative Injectable Platelet-Rich Fibrin (I-Prf) for Microscopic Analyzes

H. Varela, R. F. Araújo, R. C. Vasconcelos, V. B. Garcia, L. B. Souza, A. Araújo
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引用次数: 8

Abstract

Objective: The objective of the present study was to describe the histological preparation technique of blood derivative injectable platelet-rich fibrin (i-PRF) for microscopic analyzes.Materials and methods: Blood samples were collected from 15 volunteers to prepare i-PRF samples. The difference between i-PRF and oral mucosa tissue experimental protocol for histological preparation was elaborated in Step 1 - fixation, with 01 hour for i-PRF fixation and 24 hours for oral mucosa tissue. The other histological preparation protocol steps used for the processing and staining of the specimens were similar to that used for oral mucosa tissue. Tissue and i-PRF samples were analyzed by immunofluorescence, immunohistochemistry and microscopic histology.Results: In comparing i-PRF and oral mucosal tissue, it was observed that both had similarities in morphology and coloration of the visualized structures. The technique demonstrates immunostaining regulation of TGF-β from i- PRF. VEGF was fully detectable using the immunofluorescence technique applied to i-PRF. The method showed a fundamental advantage in reducing the fixation time, since the established fixation time in oral mucosa tissue is at least 24 hours. For the i-PRF, it was observed that the fixation was 01 hour, so the reduced fixation time shows an advantage in reducing the total working time without compromising the quality of the analyzed samples.Conclusions: The method showed a distinct advantage in reducing the fixation time of i-PRF. These initial analyses revealed that the slow polymerization during i-PRF preparation generates a blood derivative with a special fibrin network rich in platelets and leukocytes, and the presence of immunostaining for TGF-β and immunofluorescence of VEGF.
血液衍生物可注射富血小板纤维蛋白(I-Prf)显微分析的组织学制备技术
目的:介绍可注射富血小板纤维蛋白(i-PRF)的组织学制备技术。材料与方法:采集15名志愿者血样,制备i-PRF样本。在步骤1 -固定中阐述了i-PRF与口腔黏膜组织组织学准备实验方案的区别,i-PRF固定时间为01小时,口腔黏膜组织固定时间为24小时。用于标本处理和染色的其他组织学准备步骤与用于口腔黏膜组织的步骤相似。采用免疫荧光、免疫组织化学和显微组织学对组织和i-PRF样本进行分析。结果:将i-PRF与口腔黏膜组织进行比较,发现两者在可视化结构的形态和颜色上具有相似性。该技术证实了i- PRF对TGF-β的免疫染色调节。应用i-PRF的免疫荧光技术可完全检测到VEGF。该方法在减少固定时间方面具有根本优势,因为在口腔黏膜组织中建立的固定时间至少为24小时。对于i-PRF,观察到固定时间为01小时,因此减少固定时间在减少总工作时间而不影响分析样品质量方面具有优势。结论:该方法在缩短i-PRF固定时间方面具有明显优势。这些初步分析表明,i-PRF制备过程中的缓慢聚合产生了具有富含血小板和白细胞的特殊纤维蛋白网络的血液衍生物,并且存在TGF-β的免疫染色和VEGF的免疫荧光。
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