目的现在较为广泛应用于临床的人工韧带[聚对苯二甲酸乙二醇脂(PET)]——因为所固有的疏水性,使其在临床应用受到一定局限,本实验拟寻找促进材料与骨的相容的新方法。方法运用临床常用的涂层技术,以生物玻璃(58S)作为涂层材料作用于PET纤维表面,将成骨细胞(MC3T3-E1)培养在以涂层PET纤维和未涂层PET纤维上,观察成骨细胞的细胞增殖能力和细胞活性。结果细胞计数的第1、3、5天,细胞数量在涂层组与空白组均呈现增长趋势,但是在5d涂层处理组明显高于未处理组[(6.25±0.27)×104比(8.92±0.17)×104,P〈0.05],而在噻唑蓝法(MTT)和碱性磷酸酶(ALP)活性测定中,涂层组在第1、3、5天均表现出明显的优势(P〈0.01)。结论经生物玻璃涂层处理的PET纤维组能显著提高成骨细胞的增殖及生物学活性。
Objective To search for a novel method to promote the compabibility of materials and bone. The anterior cruciate ligament (ACL) reconstruction using artificial ligament [ polyethylene tereph- thalates (PET)] , which has good biocompatibility and mechanical properties, is prevalent. However, the low tendon-to-bone healing rate due to the PET' s hydrophobicity limits the clinical application. Methods This study aimed to observe the effects of the coating bioactive glass (58S) synthetic anterior eruciate liga- ment (ACL) on osteoblastie proliferation and eytoaetivity in vitro. By using coating technique, bioaetive glass (58S) was coated on the polyethylene terephthalates (PET) fibers. The scanning electron micro- graphs showed that bioaetive glass (58S) were spindle-shaped and well-orientated on the PET fibers. Then, MC3T3-E1 osteoblasts were seeded onto the PET or the coating PET. Results The number of osteo- blasts was significantly increased in the coating PET (8.92 ± 0. 17 ) as compared with the PET (6. 25± 0. 27 ) by using automated cell counter at the 5th day (P 〈 0. 05 ). Alkaline phosphatase activity and meth- yl thiazol tetrazolium (MTF) test also showed that the coating fibrous scaffold induced significnat osteogen- esis and cell proliferation as compared to PET without coating. Conclusion The coating bioaetive glass (58S) provides an instructive microenvironment for osteoblast proliferation.