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首页> 外文期刊>Human and Experimental Toxicology >In vitro cytotoxicity evaluation of plastic biomedical devices.
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In vitro cytotoxicity evaluation of plastic biomedical devices.

机译:塑料生物医学设备的体外细胞毒性评估。

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Cytotoxic potential of four plastic biomedical devices (intravenous transfusion sets, IV sets; dextrose normal saline bottles, DNS bottles; Ringer lactate bottles, RL bottles; and Ryle's tubes) including 17 different brands was evaluated by investigating growth inhibition, percent survival, mitotic index and colony-forming ability (cfa) in L929, an adherent type mouse fibroblast cell line. Experimental sets were exposed with leachates of biomedical products in serum-free minimum essential medium (MEM) for 1 h at 37 degrees C in a CO2 incubator. After 1 h, medium was replaced with serum rich MEM containing essential amino acids and reincubated up to 96 h. Cells in serum-free MEM only were processed under identical conditions and served as the control. The leachates from all types of biomedical devices evaluated exhibited reduction in the growth and survival of the cell line in the first 12 h postexposure followed by their gradual recovery up to 96 h. A significant reduction in cell growth was apparent in the six brands of IV sets from 24 h onwards up to 36 h (59% growth inhibition). Though the cfa was also reduced in all the brands tested, the magnitude of reduction was less compared to growth inhibition. The results indicate that leachates of IV sets were more toxic compared to other biomedical devices screened, and growth inhibition assay was found to be more sensitive and suitable for cytotoxicity evaluation of biomedical devices.
机译:通过研究生长抑制,存活率,有丝分裂指数,评估了包括17个不同品牌的四种塑料生物医学设备(静脉输液器,静脉输液器,葡萄糖生理盐水瓶,DNS瓶,林格乳酸瓶,RL瓶和莱尔管)的细胞毒性潜力。和粘附型小鼠成纤维细胞系L929中的集落形成能力(cfa)。实验组在37°C的CO2恒温箱中在无血清最低必需培养基(MEM)中与生物医学产品浸出液接触1 h。 1小时后,将培养基换成富含血清的含必需氨基酸的MEM,并重新温育96小时。仅在相同条件下处理无血清MEM中的细胞,并作为对照。在暴露后的最初12 h,来自所有评估类型的生物医学设备的浸出液均表现出细胞系生长和存活率下降,随后逐渐恢复至96 h。从24小时起至36小时(59%的生长抑制),六个品牌的静脉输液器中细胞生长明显减少。尽管在所有测试的品牌中CFA都降低了,但与生长抑制相比,降低的幅度较小。结果表明,与其他筛选的生物医学装置相比,静脉输液组的浸出液毒性更高,并且发现生长抑制测定法更灵敏并且适合于生物医学装置的细胞毒性评估。

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