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Initial attachment of osteoblasts to various guided bone regeneration membranes: an in vitro study

机译:成骨细胞对各种引导骨再生膜的初始附着:体外研究

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摘要

Guided bone regeneration (GBR) has proved to be a suitable and somehow predictable technique for promoting bone regeneration. Avariety of synthetic and naturally derived GBR barriers have been used in clinics to facilitate bone regeneration. These barriers may differ in composition and structure and these may affect the outcomes of GBR. Therefore, the present study was undertaken to evaluate the in vitro ability of osteoblasts (MC3T3-E1) to attach to various GBR membranes. Materials and methods:  Six GBR/GTR (guided tissue regeneration) membranes [BioMend ® (BM), Resolut ® (RL), Guidor ® (GD), EpiGuide ® (EG), Gore-Tex ® (GT) and Millipore filter ® (MP)] were tested. For controls, cells were directly plated on culture dishes (CD). Each test membrane was secured to the bottom of a culture dish with a double-sided adhesive tape. All samples were triplicate. At 1.5 and 24 h after plating of 2 ml (5 × 10 4 cells/ml) of MC3T3-E1 (passage 7) cells, the specimens were rinsed with phosphate-buffered saline to wash out any unattached cells and then fixed with a 10% buffered formalin solution for 1 d. After washing with distilled water, the cells were stained with hematoxylin. The number of attached cells was counted under a light microscope equipped with an ocular-micrometer in a unit area of 0.25 mm 2 (five areas on each membrane). In addition, cell morphology attached to the membranes was evaluated under scanning electron microscope. Results:  Data were presented as mean ± standard error and analyzed for statistical difference using a generalized Wilcoxon's test. Cell attachment at 1.5 h was as follows: MP (27.5 ± 2.1) > RL (17.0 ± 1.4) ≈ BM (14.5 ± 1.4) ≈ EG (11.4 ± 1.0) > GD (5.2 ± 0.8) ≈ GT (3.1 ± 0.6); and at 24 h was: MP (67.6 ± 3.6) > RL (35.8 ± 1.8) > BM (15.4 ± 0.9) ≈ EG (13.3 ± 1.3) > GD (5.9 ± 0.7) ≈ GT (5.6 ± 1.3). At 24 h, the scanning electron microscope finding revealed that cells attached on MP, RL, BM and EG were flatter in shape, like cells on CD, than cells on GD and GT, where cells were rather round. Conclusions:  Results from this study suggested that MP, BM, RL and EG enhanced the early osteoblast attachment. However, the true benefit of this observation in clinic remains to be determined.
机译:被证明是引导骨再生(GBR)是一种适用于促进骨再生的可预测技术。诊所中使用了合成和天然衍生的GBR屏障的变性,以促进骨再生。这些屏障可能在组成和结构中不同,并且这些屏障可能会影响GBR的结果。因此,对本研究进行了评价成骨细胞(MC3T3-E1)的体外能力,以连接到各种GBR膜。材料和方法:六GBR / GTR(引导组织再生)膜[BioMend®(BM),Resolut®(RL),Guidor®(GD),EpiGuide®(EG),Gore-Tex的®(GT)和Millipore过滤® (MP)]进行了测试。对于对照,细胞直接涂在培养皿(CD)上。将每个测试膜用双面胶带固定在培养皿的底部。所有样品都是三份。在1.5和24小时后镀2毫升(5×10 4个细胞/ mL)的MC3T3-E1(通过7)细胞,用磷酸盐缓冲盐水冲洗样品,以清洗任何未附加的细胞,然后用10固定1 D%缓冲福尔马林溶液。用蒸馏水洗涤后,用苏木精染色细胞。在配备有0.25mm 2的单位区域(每个膜上的五个区域)的光学显微镜下计算附着细胞的数量。此外,在扫描电子显微镜下评价附着于膜的细胞形态。结果:数据呈现为平均值±标准误差,并使用广泛的Wilcoxon测试分析统计差异。在1.5小时的细胞附着进行如下:MP(27.5±2.1)> RL(17.0±1.4)≈BM(14.5±1.4)≈EG(11.4±1.0)> GD(5.2±0.8)≈GT(3.1±0.6) ;在24小时,MP(67.6±3.6)> RL(35.8±1.8)> BM(15.4±0.9)≈(13.3±1.3)> Gd(5.9±0.7)≈GT(5.6±1.3)。在24小时时,扫描电子显微镜发现揭示了在MP,RL,BM上附着的细胞,例如CD上的细胞,比GD和GT上的细胞相当,其中细胞相当圆形。结论:本研究的结果表明,MP,BM,R1和例如增强了早期成骨细胞附着。然而,临床中该观察的真正益处仍有待确定。

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