a Drug Applied Research Center, Tabriz University of Medical Sciences , Tabriz , Iran.
b Pharmacology and Toxicology Department , School of Pharmacy, Tabriz University of Medical Sciences , Tabriz , Iran.
Artif Cells Nanomed Biotechnol. 2018 Mar;46(2):411-420. doi: 10.1080/21691401.2017.1315427. Epub 2017 Apr 20.
The objective of present study was in vitro and in vivo evaluation of hepatoprotective and antioxidant activity of Quercetin nanoparticles (Q NPs) against toxicity induced by aflatoxin B1. The Q NPs were prepared using precipitation method. Hepatocytes were prepared by the method of collagenase enzyme perfusion via portal vein. The NPs were characterized in terms of size and morphology using dynamic light scattering (DLS) and transmission electron microscopy (TEM), respectively. The level of parameters, such as cell death, ROS formation, lipid peroxidation, mitochondrial membrane potential and cellular glutathione (GSH) content, in the aflatoxin B1-treated and non-treated hepatocytes were determined and the mentioned markers were assessed in the presence of Q NPs. The prepared NPs showed particle size of 52.70 nm with polydispersity index (PDI) of 0.18. In contrast to free Q, the administration of Q NPs more efficiently decreased the rate of ROS formation, lipid peroxidation and improved cell viability, mitochondrial membrane potential and glutathione level and showed a significant hepatoprotective efiect by reducing levels of aspartate aminotransferase, alanine aminotransferase and alkaline phosphatase. It is suggested that the Q NPs is a promising candidate for drug delivery, which enhances the hepatoprotective effect of Q against the cytotoxic effects of aflatoxin B1.
本研究的目的是体外和体内评价槲皮素纳米粒(Q NPs)对黄曲霉毒素 B1 诱导的毒性的肝保护和抗氧化活性。Q NPs 采用沉淀法制备。肝细胞通过门静脉胶原酶灌注法制备。分别采用动态光散射(DLS)和透射电子显微镜(TEM)对 NPs 的粒径和形态进行了表征。测定了黄曲霉毒素 B1 处理和未处理的肝细胞中细胞死亡、ROS 形成、脂质过氧化、线粒体膜电位和细胞内谷胱甘肽(GSH)含量等参数的水平,并在 Q NPs 存在的情况下评估了上述标记物。所制备的 NPs 的粒径为 52.70nm,多分散指数(PDI)为 0.18。与游离 Q 相比,Q NPs 的给药更有效地降低了 ROS 形成、脂质过氧化的速率,并提高了细胞活力、线粒体膜电位和谷胱甘肽水平,并通过降低天冬氨酸氨基转移酶、丙氨酸氨基转移酶和碱性磷酸酶的水平显示出显著的肝保护作用。结果表明,Q NPs 是一种有前途的药物递送候选物,可增强 Q 对黄曲霉毒素 B1 的细胞毒性的肝保护作用。