›› 2019, Vol. 39 ›› Issue (10): 889-894.

• 基础研究 • 上一篇    下一篇

3种不同压膜方法对浓缩生长因子膜细胞因子释放以及降解的影响

文超举1,刘春影2,裴婷婷3,秦洁4,周延民2   

  1. 1. 贵州医科大学附属口腔医院口腔种植科
    2. 吉林大学口腔医院种植科
    3. 吉林大学口腔医院
    4. 吉林大学口腔医学院口腔种植科
  • 收稿日期:2019-04-11 修回日期:2019-05-02 出版日期:2019-10-28 发布日期:2019-10-28
  • 通讯作者: 周延民 E-mail:wen33090102@126.com
  • 基金资助:
    慢性牙周炎致老年认知功能障碍机制的研究;浓缩血小板纤维蛋白在上颌窦底提升术中的机理与临床应用研究;微创上颌窦底提升术缩短治疗周期的临床应用研究

A comparative study of CGF membranes made by three different compression methods on the effect of the releasing of growth factors in vitro and degradability in vivo

  • Received:2019-04-11 Revised:2019-05-02 Online:2019-10-28 Published:2019-10-28
  • Contact: yanmin -zhou E-mail:wen33090102@126.com

摘要: 目的 探讨不同压膜方法制备的浓缩生长因子(CGF)纤维膜细胞因子释放以及降解速度的差异,为其应用提供理论依据。方法 用3种方法(纱布法、压膜器法、注射器法)将CGF纤维凝胶压制成膜,扫描电镜和透射电镜分别观察不同纤维膜表面形态和膜内纤维密度。体外ELISA法检测3组纤维膜不同时间点细胞因子(TGF-β1、VEGF、PDGF-AB)的释放值。将3组CGF纤维膜植入大耳白兔背部皮下,于第1、2、3、4、5周分别取出样本固定,行HE染色和Mallory三色染色,测量组织切片内剩余纤维膜的厚度。结果 虽然3组CGF膜表面形貌及膜内纤维密度差别较大,但在同一时间点,3种不同的方法对体外CGF膜内TGF-β1、VEGF、PDGF-AB的释放量以及体内降解率的影响并没有统计学的差异(P<0.05),CGF膜在体外能持续缓慢释放细胞因子至第33天,在体内于第5周降解完全。结论 不同压膜方法对CGF膜细胞因子释放及降解无显著性影响;在临床应用时,纱布和压膜器都是将CGF凝胶压制成膜以适应种植位点的良好选择。

关键词: 浓缩生长因子, 因子释放, 降解

Abstract: Objective  To evaluate the differences in the cytokine release in vitro and the degradation rate in vivo of concentrated growth factor (CGF) membranes for standardized protocol of CGF membrane preparation with three designed compression methods: dry gauze, a compressor and a special syringe. Methods Microsurface textures and fibrin densities of the compressed CGF membranes were examined via scanning electron microscopy and transmission electron microscopy. Cytokine release (TGF-β1, VEGF, PDGF-AB) and the degradation rate were analyzed with one-way ANOVA and Kruskal-Wallis H test by conducting enzyme-linked immunosorbent assay, haematoxylin-eosin and Mallory phosphotungstic acid-haematoxylin staining. Results No significant difference in the release of main cytokines and the degradation rate was noted amongst the three compression methods, although the surface topographies and fibrin densities of the three-group membranes were quite different. The main cytokines in vitro exhibited steady controlled release until the 33rd day, and the release amount did not decrease evidently at different time points. In vivo, all the fibrin membranes were degraded completely within 5 weeks. Conclusions No significant difference was found in cytokine release and degradability amongst the CGF membranes with different compression methods. The results provided theoretical basis for standardized protocol of CGF membrane preparation.

Key words: concentrated growth factors, cytokine release, degradation

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