Fabre T, Schappacher M, Bareille R, Dupuy B, Soum A, Bertrand-Barat J, Baquey C
Inserm U 443, Université Victor Segalen, Bordeaux, France.
Biomaterials. 2001 Nov;22(22):2951-8. doi: 10.1016/s0142-9612(01)00012-6.
Future surgical strategies to restore neurological function in peripheral nerve loss may involve replacement of nerve tissue with cultured Schwann cells using biodegradable guiding implants. Random copolymers of trimethylene carbonate and epsilon caprolactone (P(epsilonCL-TMC), 50: 50) have been synthesized by ring opening polymerization using rare earth alkoxides as initiator. Their potential use as nerve guide repairs has been assessed through indirect and direct in vitro biocompatibility tests and in vivo soft tissue response to EDI subclass macrophages. In vitro, we exposed monolayers of human skin fibroblasts and an established continuous cell line (Hela) to liquid extracts (either pure or diluted in the culture medium) of epsilonCL-TMC copolymer including positive (phenol) and negative controls. Then, colorimetric assays (Neutral red and MTT) were performed. The extracts of epsilonCL-TMC induced no significant cytotoxic effect. We also exposed in vitro Schwann cells to pieces of P(epsilonCL-TMC) and P(LA-GA) copolymers. We evaluated cell attachment at 1 and 3 h by measuring the activity of the lysosomal enzyme (N-acetyl-beta-hexosaminidase) and cell proliferation at 1, 3, 6 and 9 days by measuring the cell metabolic activity (MTT assay). Values for attachment slightly decreased between 1 and 3 h but were significantly higher than on agars (negative control). Cells plated on epsilonCL-TMC showed a rate of proliferation comparable with that of normalized controls and higher than on PGA-PLA at day 9. Finally, we evaluated in vivo the soft tissue response after implantation of cylindrical tubes of P(epsilonCL-TMC) and P(LA-GA) copolymers with an immunohistochemistry staining procedure for the newly recruited ED1 macrophages. An image analysis system automatically measured the optical density of labelled positive ED1 cells at 9, 21 and 60 days after implantation. epsilonCL-TMC copolymer showed a mild soft tissue reaction with no adverse chronic inflammatory reaction. These data allowed us to consider this conduit as a potential effective substitute in nerve repair. El sevier Science Ltd. All rights reserved.
未来用于恢复周围神经损伤后神经功能的手术策略可能包括使用可生物降解的引导植入物,将培养的施万细胞替代神经组织。碳酸三亚甲基酯和ε-己内酯的无规共聚物(P(εCL-TMC),50:50)已通过以稀土醇盐为引发剂的开环聚合反应合成。已通过间接和直接的体外生物相容性测试以及体内对EDI亚类巨噬细胞的软组织反应,评估了它们作为神经引导修复材料的潜在用途。在体外,我们将人皮肤成纤维细胞单层和已建立的连续细胞系(Hela)暴露于εCL-TMC共聚物的液体提取物(纯提取物或在培养基中稀释的提取物)中,包括阳性(苯酚)和阴性对照。然后,进行比色测定(中性红和MTT)。εCL-TMC的提取物未诱导出明显的细胞毒性作用。我们还将体外施万细胞暴露于P(εCL-TMC)和P(LA-GA)共聚物片上。我们通过测量溶酶体酶(N-乙酰-β-己糖胺酶)的活性在1小时和3小时评估细胞附着情况,并通过测量细胞代谢活性(MTT测定)在1天、3天、6天和9天评估细胞增殖情况。附着值在1小时到3小时之间略有下降,但明显高于琼脂上的值(阴性对照)。接种在εCL-TMC上的细胞在第9天显示出与正常对照相当的增殖速率,且高于PGA-PLA上的细胞。最后,我们通过免疫组织化学染色程序对新募集的ED1巨噬细胞进行体内评估,将P(εCL-TMC)和P(LA-GA)共聚物的圆柱形管植入后,用图像分析系统在植入后9天、21天和60天自动测量标记阳性的ED1细胞的光密度。εCL-TMC共聚物显示出轻微的软组织反应,没有不良的慢性炎症反应。这些数据使我们能够将这种导管视为神经修复中的一种潜在有效替代物。爱思唯尔科学有限公司。保留所有权利。