碲化镉量子点的抗凝血性能

Ciarán M. Maguire, Michelle Lavin, Mairead Doyle, Mary Byrne, Adriele Prina-Mello, James S. O'Donnell, Yuri Volkov
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引用次数: 8

摘要

量子点(QDs)的尺寸依赖光学特性经常被用于医学成像和标签应用。同样,在这里,它们也引发了深刻的大小依赖的抗凝血特性。与3.6 nm的碲化镉量子点相比,3.2 nm的碲化镉量子点(QDs)在固有凝血途径周围具有显著的抗凝作用。在量子点的浓度范围内进行了几项临床相关的诊断试验,结果表明,3.2 nm量子点在整个内在途径上引起了它们的反应,但单个内在凝血因子的活性不受影响。该机制似乎也受到钙离子浓度的强烈影响,而不是镉离子从量子点中浸出。静态和基于剪切的初级止血试验也进行了,显示出深刻的抗凝作用,这是独立于血小板和磷脂。本文的数据表明,量子点的物理化学性质可能在血流止血和凝血级联的调节中发挥作用,其机制尚未完全了解。这项研究对在体内使用类似量子点作为诊断或治疗工具,以及对使用此类材料的人员的职业健康和安全具有启示意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The anticoagulant properties of cadmium telluride quantum dots

The size-dependent optical properties of quantum dots (QDs) are frequently exploited for use in medical imaging and labelling applications. Similarly, presented here, they also elicit profound size-dependent anticoagulant properties. Cadmium telluride quantum dot (QDs) (3.2 nm) were shown to have a dramatic anticoagulant effect centred on around the intrinsic coagulation pathway, compared to their 3.6 nm counterparts. Several clinically relevant diagnostic tests were carried out over a concentration range of the QDs and demonstrated that the 3.2 nm QDs elicited their response on the intrinsic pathway as a whole, yet the activity of the individual intrinsic coagulation factors was not affected. The mechanism appears also to be strongly influenced by the concentration of calcium ions and not cadmium ions leached from the QDs. Static and shear-based primary haemostasis assays were also carried out, demonstrating a profound anticoagulant effect which was independent of platelets and phospholipids. The data presented here suggest that the physical–chemical properties of the QDs may have a role in the modulation of haemostasis and the coagulation cascade, in a yet not fully understood mechanism. This study has implications for the use of similar QDs as diagnostic or therapeutic tools in vivo, and for the occupational health and safety of those working with such materials.

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