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siRNA-aptamer chimeras on nanoparticles: preserving targeting functionality for effective gene silencing.纳米颗粒上的 siRNA-aptamer 嵌合体:保留靶向功能以实现有效的基因沉默。
ACS Nano. 2011 Oct 25;5(10):8131-9. doi: 10.1021/nn202772p. Epub 2011 Sep 21.
2
Cytotoxicity and oxidative stress induced by different metallic nanoparticles on human kidney cells.不同金属纳米颗粒对人肾细胞的细胞毒性和氧化应激作用。
Part Fibre Toxicol. 2011 Mar 3;8:10. doi: 10.1186/1743-8977-8-10.
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Biocompatible quantum dots for biological applications.用于生物应用的生物相容性量子点。
Chem Biol. 2011 Jan 28;18(1):10-24. doi: 10.1016/j.chembiol.2010.11.013.
4
The effect of acyclovir on the tubular secretion of creatinine in vitro.阿昔洛韦对体外肌酐管状分泌的影响。
J Transl Med. 2010 Dec 30;8:139. doi: 10.1186/1479-5876-8-139.
5
Comparative tissue distributions of cadmium chloride and cadmium-based quantum dot 705 in mice: Safety implications and applications.氯化镉和基于镉的量子点 705 在小鼠体内的组织分布比较:安全性影响及应用。
Nanotoxicology. 2011 Mar;5(1):91-7. doi: 10.3109/17435390.2010.502260. Epub 2010 Dec 14.
6
Cd/Se/Te-based quantum dot 705 modulated redox homeostasis with hepatotoxicity in mice.基于 Cd/Se/Te 的量子点 705 调节了小鼠的氧化还原平衡并具有肝毒性。
Nanotoxicology. 2011 Dec;5(4):650-63. doi: 10.3109/17435390.2010.539712. Epub 2010 Dec 10.
7
Quantum dot cytotoxicity in vitro: an investigation into the cytotoxic effects of a series of different surface chemistries and their core/shell materials.量子点体外细胞毒性:不同表面化学特性及其核/壳材料的细胞毒性作用研究。
Nanotoxicology. 2011 Dec;5(4):664-74. doi: 10.3109/17435390.2010.534196. Epub 2010 Nov 24.
8
Silica-polymer dual layer-encapsulated quantum dots with remarkable stability.具有显著稳定性的硅-聚合物双层包裹量子点。
ACS Nano. 2010 Oct 26;4(10):6080-6. doi: 10.1021/nn1017044.
9
An investigation into the potential for different surface-coated quantum dots to cause oxidative stress and affect macrophage cell signalling in vitro.研究不同表面涂层量子点在体外引起氧化应激和影响巨噬细胞信号转导的潜力。
Nanotoxicology. 2010 Jun;4(2):139-49. doi: 10.3109/17435390903276925.
10
Role of heme oxygenase in preserving vascular bioactive NO.血红素加氧酶在维持血管生物活性一氧化氮中的作用。
Nitric Oxide. 2010 Dec 15;23(4):251-7. doi: 10.1016/j.niox.2010.08.002. Epub 2010 Aug 14.

血红素加氧酶表达作为暴露于两亲聚合物包覆的 CdSe/ZnS 量子点的生物标志物。

Heme oxygenase expression as a biomarker of exposure to amphiphilic polymer-coated CdSe/ZnS quantum dots.

机构信息

Department of Environmental and Occupational Health Sciences, University of Washington , Seattle, WA 98195, USA.

出版信息

Nanotoxicology. 2013 Mar;7(2):181-91. doi: 10.3109/17435390.2011.648224. Epub 2012 Jan 20.

DOI:10.3109/17435390.2011.648224
PMID:22264017
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4084970/
Abstract

Because of their unique optical properties, quantum dots (QDs) have become a preferred system for ultrasensitive detection and imaging. However, since QDs commonly contain Cd and other heavy metals, concerns have been raised regarding their toxicity. QDs are thus commonly synthesised with a ZnS cap structure and/or coated with polymeric stabilisers. We recently synthesised amphiphilic polymer-coated tri-n-octylphosphine oxide - poly(maleic anhydride-alt-1-tetradecene (TOPO-PMAT) QDs, which are highly stable in aqueous environments. The effects of these QDs on viability and stress response in five cell lines of mouse and human origins are reported here. Human and mouse macrophages and human kidney cells readily internalised these QDs, resulting in modest toxicity. TOPO-PMAT QD exposure was highly correlated with the induction of the stress response protein heme oxygenase-1 (HMOX1). Other stress biomarkers (glutamate cysteine ligase modifier subunit, NAD(P)H, necrosis) were only moderately affected. HMOX1 may thus be a useful biomarker of TOPO-QDOT QD exposure across cell types and species.

摘要

由于其独特的光学特性,量子点 (QD) 已成为超灵敏检测和成像的首选系统。然而,由于 QD 通常含有 Cd 和其他重金属,因此人们对其毒性表示担忧。因此,QD 通常采用 ZnS 帽结构合成和/或用聚合物稳定剂进行涂层。我们最近合成了两亲聚合物涂层的三辛基氧化膦-聚(马来酸酐-alt-1-十四烯)(TOPO-PMAT)QD,在水相环境中具有高度稳定性。本文报道了这些 QD 对来自小鼠和人类的五种细胞系的活力和应激反应的影响。人和小鼠巨噬细胞和人肾细胞很容易内化这些 QD,导致适度的毒性。TOPO-PMAT QD 的暴露与应激反应蛋白血红素加氧酶-1 (HMOX1) 的诱导高度相关。其他应激生物标志物(谷胱甘肽半胱氨酸连接酶修饰亚基、NAD(P)H、坏死)仅受到中度影响。因此,HMOX1 可能是跨细胞类型和物种的 TOPO-QDOT QD 暴露的有用生物标志物。