Abdulmajeed Aous A, Kokkari Anne K, Käpylä Jarmo, Massera Jonathan, Hupa Leena, Vallittu Pekka K, Närhi Timo O
J Mater Sci Mater Med. 2014 Jan;25(1):151-62. doi: 10.1007/s10856-013-5040-0.
This in vitro study was designed to evaluate both blood and human gingival fibroblast responses to bisphenol A-glycidyl methacrylate-triethyleneglycol dimethacrylate (BisGMA-TEGDMA)/bioactive glass (BAG) composite, aimed to be used as composite implant abutment surface modifier. Three different types of substrates were investigated: (a) plain polymer (BisGMA 50 wt%-TEGDMA 50 wt%), (b) BAG-composite (50 wt% polymer + 50 wt% fraction of BAG-particles, <50 μm), and (c) plain BAG plates (100 wt% BAG). The blood response, including the blood-clotting ability and platelet adhesion morphology were evaluated. Human gingival fibroblasts were plated and cultured on the experimental substrates for up to 10 days, then the cell proliferation rate was assessed using AlamarBlue assay™. The BAG-composite and plain BAG substrates had a shorter clotting time than plain polymer substrates. Platelet activation and aggregation were most extensive, qualitatively, on BAG-composite. Analysis of the normalized cell proliferation rate on the different surfaces showed some variations throughout the experiment, however, by day 10 the BAG-composite substrate showed the highest (P < 0.001) cell proliferation rate. In conclusion, the presence of exposed BAG-particles enhances fibroblast and blood responses on composite surfaces in vitro.
本体外研究旨在评估血液和人牙龈成纤维细胞对双酚A-甲基丙烯酸缩水甘油酯-三乙二醇二甲基丙烯酸酯(BisGMA-TEGDMA)/生物活性玻璃(BAG)复合材料的反应,该复合材料旨在用作复合种植体基台表面改性剂。研究了三种不同类型的基质:(a)纯聚合物(BisGMA 50 wt%-TEGDMA 50 wt%),(b)BAG复合材料(50 wt%聚合物+50 wt% BAG颗粒,<50μm),以及(c)纯BAG板(100 wt% BAG)。评估了血液反应,包括血液凝固能力和血小板粘附形态。将人牙龈成纤维细胞接种在实验基质上并培养长达10天,然后使用AlamarBlue检测法评估细胞增殖率。BAG复合材料和纯BAG基质的凝血时间比纯聚合物基质短。定性地说,BAG复合材料上的血小板活化和聚集最为广泛。对不同表面上归一化细胞增殖率的分析表明,在整个实验过程中存在一些差异,然而,到第10天时,BAG复合材料基质显示出最高(P < 0.001)的细胞增殖率。总之,暴露的BAG颗粒的存在增强了体外复合表面上的成纤维细胞和血液反应。