Tsuchiya T, Nakaoka R, Degawa H, Nakamura A
Division of Medical Devices, National Institute of Health Sciences, Tokyo, Japan.
J Biomed Mater Res. 1996 Jul;31(3):299-303. doi: 10.1002/(SICI)1097-4636(199607)31:3<299::AID-JBM2>3.0.CO;2-H.
The tumor-initiating activities of the methanol extracts of polyetherurethanes (PEUs) were first detected in the presence of 12-0-tetradecanyl-phorbol-13-acetate (TPA) using Balb 3T3 transformation assay. A model hard segment of PEUs, 4,4'-di(ethoxycarboamide) diphenylmethane (MDU), showed initiating activity, while chemical moieties other than the hard segment were shown to be negative in the test. The transformation assay was carried out using glass dishes half coated with two different PEUs, PU4 and PU8. In the presence of TPA, the transforming activities correlated with the tumorigenic potential in the rat implantation study on the coated surface of PEUs, but not on the uncoated glass area. From these results it was concluded that initiation was caused by the hard-segment moiety such as MDU structure derived not only from the leachable extracts but also from the biodegradable substances by the direct interaction of cells with the coated materials.
首次使用Balb 3T3转化试验,在12-O-十四烷酰佛波醇-13-乙酸酯(TPA)存在的情况下,检测了聚醚聚氨酯(PEU)甲醇提取物的肿瘤起始活性。PEU的一种模型硬段,4,4'-二(乙氧基碳酰胺)二苯甲烷(MDU),显示出起始活性,而硬段以外的化学部分在试验中显示为阴性。转化试验使用半涂有两种不同PEU(PU4和PU8)的玻璃培养皿进行。在TPA存在的情况下,在PEU包被表面的大鼠植入研究中,转化活性与致瘤潜力相关,但在未包被的玻璃区域则不相关。从这些结果可以得出结论,起始是由硬段部分引起的,例如MDU结构,其不仅来源于可浸出提取物,还来源于细胞与包被材料直接相互作用产生的可生物降解物质。