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Impact of citrate- and chitosan-capped gold nanoparticles on the liver of Swiss albino mice: Histological and cyto-genotoxic study

机译:柠檬酸和壳聚糖封端的金纳米粒子对瑞士白化小鼠肝脏的影响:组织学和细胞遗传毒性研究

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摘要

The present study aimed to disclose the histological alterations and cyto-genotoxic potential induced by citrate- and chitosan-capped AuNPs on liver of adult Swiss albino mice. Animals were randomly divided into 8 groups. The first two groups were intraperitoneally (i.p) injected with physiological saline once and left for 10 days and every other day for 21 days, respectively, and kept as negative control groups. While the third and fourth groups were injected i.p with a single dose of 2 mg/kg of citrate- and chitosan-capped AuNPs, respectively, and left for 10 days. The fifth and sixth groups were injected i.p every other day for 21 days with 200 mu g/kg of citrate- and chitosan-capped AuNPs, respectively. Animals of the seventh and eighth groups were injected i.p with 50 mg/kg cyclophosphamide once and left for 10 days and with 20 mg/kg cyclophosphamide every other day for 21 days, respectively. The livers of mice were dissected and processed for microscopic examination and for analyzing the expression of inflammation-related genes using RT-PCR. In addition, bone marrow samples were taken to investigate the mitotic index and the chromosomal aberrations. The present study showed various degrees of structural changes in the liver of animals received AuNPs. Such changes were more prominent in animals treated with a single dose of AuNPs, particularly with citrate-capped AuNPs as compared to chitosan-capped AuNPs. Furthermore, genotoxic analysis did not reveal any genotoxicity for AuNPs with both coats. Therefore, chitosan-capped AuNPs were less hepatotoxic than citratecapped ones. However, it has not been proven that AuNPs are genotoxic by both coats.
机译:本研究旨在公开通过柠檬酸盐和壳聚糖覆盖的AUNP诱导的成人瑞士白化小鼠肝脏的组织学改变和细胞遗传毒性。将动物随机分为8组。前两组腹膜内(I.P)腹膜内注射一次生理盐水一次,留下10天,每隔一天,分别为21天,并保持为阴性对照组。虽然第三组和第四组分别注射了单剂量的2mg / kg柠檬酸盐和壳聚糖封端的肛门粥,并且留下10天。每隔一天注射第五组和第六组,分别用200μg/ kg柠檬酸盐和壳聚糖覆盖的agapps注入21天。将七和第八组的动物注射含有50mg / kg环磷酰胺的I.p,每隔一天用50mg / kg环膦酰胺注射10天,每隔一天用20mg / kg环磷酰胺21天。解剖和加工小鼠的肝脏以用于微观检查,并使用RT-PCR分析炎症相关基因的表达。此外,还考虑骨髓样品来研究有丝分裂指数和染色体畸变。本研究表明,动物肝脏的各种结构变化接受了AUNP。在用一剂AUNPS处理的动物中,这种变化更突出,特别是与含壳聚糖封端的AUNP相比的柠檬酸盐型耳孔。此外,遗传毒性分析并未揭示用两种涂层的AUNPS的任何遗传毒性。因此,壳聚糖覆盖的剖腹产比酸毒性毒性较少。然而,尚未证明AUNPS是两层涂层的基因毒性。

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