用两种体外试验评价聚维酮碘的躯体毒性。

F K Kessler, D L Laskin, J F Borzelleca, R A Carchman
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引用次数: 0

摘要

采用L5178Y小鼠(TK+/-)淋巴瘤实验研究聚维酮碘(PVP-I)及其相关化合物的致突变性。已建立的诱变剂甲基磺酸乙酯(EMS)和二甲基亚硝胺(DMN)在本实验中具有高活性,而PVP- i、聚乙烯吡啶酮(PVP)、碘化钾(KI)和碘(I2)则无活性。此外,在存在大鼠肝微粒体激活部分(S-9)的情况下,PVP-I和I2作为诱变剂只有边际活性。利用Balb/c 3T3转化实验,我们评估了这些试剂和阳性诱变剂n -甲基-n -硝基-n -亚硝基胍(MNNG)的转化能力。除PVP-I (5 mg/ml)和MNNG(5微克/ml)外,所有浓度的化合物均无活性。然而,PVP-I的反应只是边际的。我们从这些研究中得出结论,PVP、PVP- i、KI和I2不具有任何生物学上显著的诱变或细胞转化能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of somatogenotoxicity of povidone-iodine using two in vitro assays.

The mutagenic potential of povidone-iodine (PVP-I) and some related compounds were studied using the L5178Y mouse (TK+/-) lymphoma assay. The established mutagens ethyl methanesulfonate (EMS) and dimethylnitrosamine (DMN) were highly active in this assay, whereas PVP-I, polyvinyl pyrolidone (PVP), potassium iodide (KI), and iodine (I2) were inactive. Furthermore, in the presence of a rat liver microsomal activating fraction (S-9), PVP-I and I2 had only marginal activity as mutagens. Using the Balb/c 3T3 transformation assay we assessed the transformational capacities of these same agents and the positive mutagen N-methyl-N-nitro-N-nitrosoguanidine (MNNG). All concentrations of the compounds tested were inactive in this assay except for PVP-I (5 mg/ml) and MNNG (5 micrograms/ml). However, the response with PVP-I was only marginal. We concluded from these studies that PVP, PVP-I, KI, and I2 did not possess any biologically significant mutagenic or cell transforming ability.

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