Yu Yajuan, Shen Jian, Fang Guizhen, Wang Lingcong, Lei Shu, Cai Danli, Shi Ying, Jin Shuifang, Lu Qiaoli, Wang Sisi, Sun Yunlei, Yao Jinmei, Hu Peiya, Wu Xiaofei, He Xujun
ICU Specialty Nurse, Department of Intensive Care Units, Zhejiang Provincial Hospital of Traditional Chinese Medicine, Xiasha Campus; The First Affiliated Hospital and First Clinical College of Zhejiang Chinese Medical University, Hangzhou, 310018, Zhejiang, China.
Technologist-in-charge, Department of Blood Transfusion, Zhejiang Provincial People's Hospital; People's Hospital of Hangzhou Medical College, Hangzhou, 310014, Zhejiang, China.
J Wound Care. 2019 Apr 1;28(Sup4):S23-S30. doi: 10.12968/jowc.2019.28.Sup4.S23.
To verify the feasibility of treating pressure ulcers (PUs) with autologous platelet-rich fibrin-based (PRF) bioactive membrane, both in vitro and in vivo.
An animal model using adult male Sprague-Dawley rats was used. Pressure was periodically exerted on the skin to induce localised ischaemia by using an external magnet and transplanted metal disc. After a PU developed, the rats were divided into two groups: a treatment group and a control group. Rats in the treatment group were then treated with PRF bioactive membrane every three days.
A total of 20 rats were used in this study. At days three and seven, the PU area in the PRF bioactive membrane-treated group was significantly smaller than that in the control group, and after 14 days of treatment, the PUs in the PRF bioactive membrane treatment group had healed. Haemotoxylin and eosin staining, immunohistochemistry and Western blot results indicated that PRF bioactive membrane induced wound healing by increasing the thickness of the regenerated epidermis and by upregulating vascular endothelial growth factor expression. Further, we found that different concentrations of rat autologous PRF soluble factors extraction components could significantly promote rat aortic endothelial cell proliferation, wound healing and migration ability in vitro.
Overall, results indicate that PRF bioactive membrane promotes PU healing in rats. Thus, it may represent a natural and effective wound-healing tool for use in the treatment of clinical skin PUs in humans in the future.
在体外和体内验证使用基于富血小板纤维蛋白(PRF)的自体生物活性膜治疗压疮(PU)的可行性。
使用成年雄性Sprague-Dawley大鼠建立动物模型。通过使用外部磁铁和移植的金属盘定期对皮肤施加压力以诱导局部缺血。在形成压疮后,将大鼠分为两组:治疗组和对照组。然后每三天用PRF生物活性膜治疗治疗组的大鼠。
本研究共使用了20只大鼠。在第3天和第7天,PRF生物活性膜治疗组的压疮面积明显小于对照组,并且在治疗14天后,PRF生物活性膜治疗组的压疮已经愈合。苏木精和伊红染色、免疫组织化学和蛋白质印迹结果表明,PRF生物活性膜通过增加再生表皮的厚度和上调血管内皮生长因子的表达来诱导伤口愈合。此外,我们发现不同浓度的大鼠自体PRF可溶性因子提取成分在体外可显著促进大鼠主动脉内皮细胞增殖、伤口愈合和迁移能力。
总体而言,结果表明PRF生物活性膜可促进大鼠压疮愈合。因此,它可能代表一种天然且有效的伤口愈合工具,未来可用于治疗人类临床皮肤压疮。