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Cytotoxicity evaluation of reactive metabolites using rat liver homogenate microsome-encapsulated alginate gel microbeads

机译:使用大鼠肝匀浆微粒体包裹的藻酸盐凝胶微珠评估反应性代谢产物的细胞毒性

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摘要

We present an improved cytotoxicity test for reactive metabolites, in which the S9 microsomal fraction of rat liver homogenate is encapsulated in alginate gel microbeads to avoid cytotoxic effects of S9-self-generated toxicants, microsomal lipid peroxides. The S9-encapsulated gel microbeads were prepared by a coaxial two-fluid nozzle and surfaces of the microbeads were coated with poly-L-lysine (PLL). Although the initial metabolic rate of the S9-encapsulated gel microbeads was about 20% slower than that of bare S9, the microbeads prevented the leakage of microsomal lipid peroxides thanks to the dense alginate and PLL polymer networks. In fact, the half maximal effective concentration of the indirect mutagen cyclophosphamide on NIH3T3 cells in the presence of the S9-encapsulated gel microbeads was about 5 times higher than that in the presence of bare S9. Use of the S9-encapsulated gel microbeads enabled the more accurate evaluation of the cytotoxicity of the reactive metabolites without the S9-based cytotoxicity.
机译:我们提出了一种针对反应性代谢产物的改进的细胞毒性试验,其中大鼠肝匀浆的S9微粒体部分封装在藻酸盐凝胶微珠中,以避免S9自身产生的有毒物质微粒体脂质过氧化物的细胞毒性作用。通过同轴双流体喷嘴制备S9包封的凝胶微珠,并将微珠表面涂以聚-L-赖氨酸(PLL)。尽管S9包封的凝胶微珠的初始代谢速率比裸露的S9慢约20%,但由于密集的藻酸盐和PLL聚合物网络,微珠阻止了微粒体脂质过氧化物的泄漏。实际上,在存在S9包封的凝胶微珠的情况下,间接诱变环磷酰胺在NIH3T3细胞上的最大有效浓度的一半是在裸露的S9的情况下的一半。使用S9封装的凝胶微珠可以更准确地评估反应性代谢产物的细胞毒性,而无需基于S9的细胞毒性。

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