Centre for Nano Safety, School of Life Sciences, Edinburgh Napier University, Edinburgh, UK.
Nanotoxicology. 2011 Dec;5(4):664-74. doi: 10.3109/17435390.2010.534196. Epub 2010 Nov 24.
The aim of this study was to assess the effects of a series of different surface coated quantum dots (QDs) (organic, carboxylated [COOH] and amino [NH₂] polytethylene glycol [PEG]) on J774.A1 macrophage cell viability and to further determine which part of the QDs cause such toxicity. Cytotoxic examination (MTT assay and LDH release) showed organic QDs to induce significant cytotoxicity up to 48 h, even at a low particle concentration (20 nM), whilst both COOH and NH₂ (PEG) QDs caused reduced cell viability and cell membrane permeability after 24 and 48 h exposure at 80 nM. Subsequent analysis of the elements that constitute the QD core, core/shell and (organic QD) surface coating showed that the surface coating drives QD toxicity. Elemental analysis (ICP-AES) after 48 h, however, also observed a release of Cd from organic QDs. In conclusion, both the specific surface coating and core material can have a significant impact on QD toxicity.
本研究旨在评估一系列不同表面涂层量子点(QD)(有机、羧基[COOH]和氨基[NH₂]聚乙二醇[PEG])对 J774.A1 巨噬细胞活力的影响,并进一步确定 QD 引起毒性的原因。细胞毒性检测(MTT 检测和 LDH 释放)表明,有机 QD 在低粒子浓度(20 nM)下甚至在 48 小时内即可诱导显著的细胞毒性,而 COOH 和 NH₂(PEG)QD 在 80 nM 下暴露 24 和 48 小时后,导致细胞活力和细胞膜通透性降低。对构成 QD 核、核/壳和(有机 QD)表面涂层的元素进行后续分析表明,表面涂层导致 QD 毒性。然而,48 小时后的元素分析(ICP-AES)也观察到有机 QD 中 Cd 的释放。总之,特定的表面涂层和核心材料都可能对 QD 毒性产生重大影响。