Collaborative Research Group, Tokyo Plastic Dental Society, Tokyo, Japan.
Implant Dentistry, Nihon University School of Dentistry, Dental Hospital, Tokyo, Japan.
Platelets. 2022 Jan 2;33(1):110-115. doi: 10.1080/09537104.2020.1856359. Epub 2020 Dec 7.
Platelet-rich fibrin (PRF) has been widely applied in regenerative therapy owing to its simple preparation protocol. To date, the original protocol for preparing leukocyte-rich (L)-PRF has been modified to produce derivatives such as advanced (A)-PRF, concentrated growth factors (CGF), and horizontal (H)-PRF. However, these derivatives have not been rigorously compared to explore possible differences. We previously developed and validated a nondestructive near-infrared (NIR) imaging method to quantitatively examine the platelet distribution in PRF matrices. To further evaluate the characteristics of platelets in PRF, we herein examined the distribution of activated platelets. Four types of PRF matrices were prepared under different centrifugal conditions from blood samples obtained from the same healthy donors. After fixation and compression, the matrices were stained immunohistochemically without sectioning and visualized using an NIR imager. Qualitative morphological analysis revealed that whole platelets were distributed widely and homogeneously in H-PRF and A-PRF, but localized along the distal tube surface in L-PRF and CGF. Activated platelets were distributed as were whole platelets in A-PRF, L-PRF, and CGF, but localized mainly in the "buffy coat" region in H-PRF. Quantitative analysis revealed that there was no significant difference in the ratio of activated to whole platelets between PRF derivatives. These findings suggest that platelet activation is similarly induced in fibrin matrices regardless of centrifugal speed or rotor angulation. However, only the H-PRF group was distinguishable from the other PRF derivatives in terms of activated platelet distribution.
富血小板纤维蛋白 (PRF) 因其制备方案简单而被广泛应用于再生治疗。迄今为止,原始的白细胞丰富 (L)-PRF 制备方案已被修改,以产生衍生产品,如先进 (A)-PRF、浓缩生长因子 (CGF) 和水平 (H)-PRF。然而,这些衍生产品尚未经过严格比较,以探讨可能的差异。我们之前开发并验证了一种非破坏性的近红外 (NIR) 成像方法来定量检查 PRF 基质中的血小板分布。为了进一步评估 PRF 中血小板的特性,我们在此检查了激活血小板的分布。从相同的健康供体获得的血液样本在不同的离心条件下制备了四种类型的 PRF 基质。固定和压缩后,不进行切片即可对基质进行免疫组织化学染色,并使用 NIR 成像仪进行可视化。定性形态分析表明,在 H-PRF 和 A-PRF 中,完整血小板广泛且均匀地分布,而在 L-PRF 和 CGF 中,血小板局部化地沿远端管表面分布。激活的血小板与 A-PRF、L-PRF 和 CGF 中的完整血小板一样分布,但在 H-PRF 中主要定位于“白血球层”区域。定量分析表明,PRF 衍生物之间激活血小板与完整血小板的比率没有显著差异。这些发现表明,无论离心速度或转子角度如何,血小板在纤维蛋白基质中的激活方式相似。然而,只有 H-PRF 组在激活血小板分布方面与其他 PRF 衍生物有区别。