Near-infrared-emitting semiconductor quantum dots for tumor imaging and targeting.

Andrey L Rogach, Manfred Ogris
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Abstract

Visualizing tumors with the help of near-infrared-emitting probes allows not only in vivo imaging, but also online analysis during surgical resection. Near-infrared-emitting semiconductor quantum dots (QDs) are highly fluorescent nanocrystals that can be modified to meet the needs of tumor-selective probes by variations in size, composition and internal structure (core-only, type I and type II core-shell QDs). The passive accumulation of probes in tumors, as a result of leaky vasculature, can be achieved with systemically injected QDs designed to circulate in the bloodstream and avoid clearance via the kidneys or the reticuloendothelial system. With the help of chemical strategies, QDs are decorated with surface ligands, including antibodies or peptides that bind antigens on tumor cells or tumor endothelium, which further improves the specificity of accumulation within tumors. Encapsulation of QDs into macromolecular structures allows the in vivo tracking of gene and drug carriers in real time. Considerable research has been undertaken to avoid acute and chronic toxicities of QDs by reducing the dose or replacing toxic elements with more biocompatible materials. This review discusses the benefits and potential disadvantages of QDs, and highlights recent advances in the application of these probes for tumor imaging and targeting.

用于肿瘤成像和靶向的近红外发射半导体量子点。
在近红外探针的帮助下,肿瘤的可视化不仅可以进行体内成像,还可以在手术切除期间进行在线分析。近红外发射半导体量子点(QDs)是一种高荧光纳米晶体,可以通过改变大小、组成和内部结构(仅核、I型和II型核壳量子点)来满足肿瘤选择性探针的需要。由于血管渗漏,探针在肿瘤中的被动积累可以通过全身注射QDs来实现,这些QDs可以在血液中循环,避免通过肾脏或网状内皮系统被清除。在化学策略的帮助下,量子点被表面配体修饰,包括结合肿瘤细胞或肿瘤内皮上抗原的抗体或肽,进一步提高了在肿瘤内积累的特异性。将量子点封装到大分子结构中,可以实时跟踪基因和药物载体的体内情况。为了避免量子点的急性和慢性毒性,已经进行了大量的研究,通过减少剂量或用更具有生物相容性的材料取代有毒元素。本文讨论了量子点的优点和潜在的缺点,并重点介绍了这些探针在肿瘤成像和靶向中的应用的最新进展。
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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来源期刊
Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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