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The role of surface chemistry in determining invivo biodistribution and toxicity of CdSe/ZnS core-shell quantum dots

机译:表面化学在确定CdSe / ZnS核-壳量子点的体内生物分布和毒性中的作用

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摘要

To examine the effect of surface chemistry and surface charge on invivo biodistribution and toxicity of CdSe/ZnS core-shell quantum dots (QDs), QDs with positive, negative, or PEG coating are used in this study for invivo evaluation in a mouse model. The results suggest that QDs coated with cationic polydiallyldimethylammonium chloride (PDDA) preferentially deposit in the lung other than in the liver, while the negative and PEGylated QDs render abundant accumulation in the liver. At higher doses positive QDs with PDDA coating show severe acute toxicity due to pulmonary embolism. Independent of their surface coatings, all QDs cause injuries in specific tissues like liver, spleen, lung, and kidney, after acute and long-term exposure, and the degree of injuries is dominated by their surface properties. For the positively charged QDs, the acute phase toxicity is primarily contributed by the coating material PDDA, while coating on QDs may amplify both invitro and invivo toxicity of PDDA. PEGylated QDs display the slightest chronic injuries in the long-term toxicity examination in comparison to positive or negative ones.
机译:为了检查表面化学和表面电荷对CdSe / ZnS核-壳量子点(QD)的体内生物分布和毒性的影响,在本研究中使用具有正,负或PEG涂层的QD在小鼠模型中进行体内评估。结果表明,涂​​覆有阳离子聚二烯丙基二甲基氯化铵(PDDA)的QD优先沉积在肺中,而不是沉积在肝脏中,而阴性和PEG化的QD则在肝脏中积累丰富。较高剂量的带有PDDA涂层的阳性QD由于肺栓塞表现出严重的急性毒性。所有QD都不受其表面涂层的影响,在急性和长期暴露后会在特定组织(例如肝脏,脾脏,肺和肾脏)中造成伤害,并且伤害的程度由其表面特性决定。对于带正电荷的QD,急性期毒性主要由涂料PDDA引起,而QD上的涂层可能会放大PDDA的体外和体内毒性。在长期毒性检查中,与阳性或阴性相比,聚乙二醇化的量子点显示出最小的慢性伤害。

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