Yamaguchi Sadahiro, Aizawa Hachidai, Sato Atsushi, Tsujino Tetsuhiro, Isobe Kazushige, Kitamura Yutaka, Watanabe Taisuke, Okudera Hajime, Mourão Carlos Fernando, Kawase Tomoyuki
Tokyo Plastic Dental Society, Tokyo, Japan.
Department of Oral Surgery, Dentistry School, Fluminense Federal University, Rio de Janeiro, Brazil.
Front Bioeng Biotechnol. 2020 Jun 16;8:600. doi: 10.3389/fbioe.2020.00600. eCollection 2020.
Platelet-rich fibrin (PRF) matrices were originally prepared using plain glass tubes without the aid of coagulation factors because coagulation factor XII is activated by glass surfaces. Recently, the use of silica-coated plastic tubes as a substitute of glass tubes has been recommended for PRF preparation. This recommendation is owing not only to the shortage of glass tubes for medical use in the market, but also the higher coagulation activity of silica-coated plastic tubes and equal quality of PRF. However, these matrices are not the same. To evaluate the differences, we compared glass- and silica-coated plastic tubes in terms of platelet distribution and quantity in concentrated growth factors (CGF). CGF matrices were immediately prepared from freshly collected blood samples, fixed after red thrombus removal, and divided into two equal pieces sagittally. One piece was used for CD41 detection and the other was applied as an isotype control. Platelet distribution in CGF matrices was examined, without embedding or sectioning, by a novel method using invisible near-infrared imaging. The dehydrated membranous CGF matrix was more transparent. Thus, the fluorescence signal was clearly detectable with less scattering. Platelets were distributed mainly in the distal side of the glass-prepared CGF matrix, but homogeneously in the silica-prepared CGF matrix. Platelet count was positively correlated with fluorescence intensity. Although not yet fully developed, this imaging technique enabled us to recognize the differences in platelet distribution and quantity in CGF matrices by excluding bias caused by the technical limitations of scanning electron microscopy and conventional immunohistochemical methods.
富含血小板纤维蛋白(PRF)基质最初是使用普通玻璃管制备的,无需凝血因子的帮助,因为凝血因子XII可被玻璃表面激活。最近,有人推荐使用二氧化硅涂层塑料管替代玻璃管来制备PRF。提出这一建议不仅是因为市场上医用玻璃管短缺,还因为二氧化硅涂层塑料管具有更高的凝血活性以及PRF质量相当。然而,这些基质并不相同。为了评估差异,我们比较了玻璃管和二氧化硅涂层塑料管在浓缩生长因子(CGF)中的血小板分布和数量。CGF基质由新鲜采集的血液样本立即制备,去除红色血栓后固定,并沿矢状面分成两个相等的部分。一部分用于检测CD41,另一部分用作同型对照。通过一种使用不可见近红外成像的新方法,在不进行包埋或切片的情况下检查CGF基质中的血小板分布。脱水的膜状CGF基质更透明。因此,荧光信号散射较少,清晰可检测。血小板主要分布在玻璃制备的CGF基质的远端,但在二氧化硅制备的CGF基质中分布均匀。血小板计数与荧光强度呈正相关。尽管这项成像技术尚未完全成熟,但它使我们能够通过排除扫描电子显微镜和传统免疫组织化学方法的技术局限性所导致的偏差,识别CGF基质中血小板分布和数量的差异。