Systematic study of enhanced cytotoxicity effects of gold-based nanoparticles in targeted cancer radiotherapy

K. Song, P. Xu, Yongde Meng, Jie Chen, Xiaoyan Yang, W. Roa, B. Kong, J. Xing
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引用次数: 3

Abstract

Worldwide, cancers are the leading causes of human mortality. To successfully treat advanced-stage cancers, it is important to increase cytotoxicity of targeted tumor cells while reducing side effects on normal cells during radiotherapy. Nanotechnology provides a promising solution to achieve this targeted treatment[1–3]. An ideal strategy is to develop effective nanoscale radio-sensitizers targeting specifically at tumor cells. In this paper, we focus on gold-based nanoparticles as radio-sensitizers. Naked gold nanoparticles (GNPs) can accumulate at tumor tissues based on passively targeting mechanism and thus it can be used as a radio-sensitizer to kill cancers. However, GNPs conjugated with tumor-specific ligands are more promising for tumor diagnosis and treatment at the molecular scale. We have designed glucose-capped GNPs (or Glu-GNPs) to achieve specific targeting. Our preliminary results show a remarkable increase in cell-uptake of Glu-GNPs and also a significant increase of radiation cytotoxicity after applying irradiations.
金基纳米颗粒在肿瘤靶向放疗中增强细胞毒性作用的系统研究
在世界范围内,癌症是人类死亡的主要原因。为了成功治疗晚期癌症,重要的是在放疗过程中增加靶向肿瘤细胞的细胞毒性,同时减少对正常细胞的副作用。纳米技术为实现这种靶向治疗提供了一个很有前景的解决方案[1-3]。一个理想的策略是开发有效的纳米级放射性增敏剂,专门针对肿瘤细胞。本文主要研究了金基纳米粒子作为辐射增敏剂。裸金纳米颗粒(GNPs)可以通过被动靶向机制在肿瘤组织中积累,因此可以作为一种放射性增敏剂来杀伤肿瘤。然而,与肿瘤特异性配体结合的GNPs在分子尺度上更有希望用于肿瘤的诊断和治疗。我们设计了葡萄糖限制GNPs(或Glu-GNPs)来实现特定的靶向。我们的初步结果显示,在施加辐照后,细胞对Glu-GNPs的摄取显着增加,并且辐射细胞毒性也显着增加。
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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