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通过核靶向多功能上转换纳米探针进行核内同时成像和药物递释。

Simultaneous nuclear imaging and intranuclear drug delivery by nuclear-targeted multifunctional upconversion nanoprobes.

机构信息

State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China.

出版信息

Biomaterials. 2012 Oct;33(29):7282-90. doi: 10.1016/j.biomaterials.2012.06.035. Epub 2012 Jul 12.

Abstract

Nuclear-targeted therapy by delivering anticancer drug directly into cancer cell nuclei can elicit synergistic therapeutic effects and kill these cancer cells with much enhanced efficiencies. Besides nuclear targeting, another difficulty in nuclear-targeted therapy is how to achieve real-time monitoring of the therapy process simultaneously. In this article we report on the development of multifunctional upconversion nanoparticles (UCNPs) which were able to target cancer cell nuclei, and thus deliver the anticancer drug directly to the nuclear region and simultaneously image cell nucleus by magnetic resonance (MR)/upconversion fluorescent for real-time guidance of their therapeutic action simultaneously. The Er/Yb-doped NaYF(4) core and NaGdF(4) shell endow the core/shell structured UCNPs with enhanced upconversion fluorescent imaging and more sensitive T(1)-MR imaging performances, and the surface conjugation of TAT peptide served as a key role in the nuclear targeting and nuclear transport process. This multifunctional UCNPs-based nano-theranostic was used to improve the efficacy of DOX in Hela humor tumor models, by direct DOX delivery to the nucleus under the synchronous monitoring of the nano-theranostics. Further development of this technology may provide more exciting opportunities in treating cancer disease by nuclear-targeted therapy.

摘要

通过将抗癌药物直接递送到癌细胞核内进行核靶向治疗,可以产生协同的治疗效果,并以更高的效率杀死这些癌细胞。除了核靶向外,核靶向治疗的另一个难点是如何实现治疗过程的实时监测。在本文中,我们报告了多功能上转换纳米粒子(UCNPs)的开发,这些纳米粒子能够靶向癌细胞核,从而将抗癌药物直接递送到核区域,并通过磁共振(MR)/上转换荧光同时对细胞核进行成像,实时指导其治疗作用。掺铒/掺镱的 NaYF(4) 核和 NaGdF(4) 壳赋予了核壳结构的 UCNPs 增强的上转换荧光成像和更敏感的 T(1)-MR 成像性能,而 TAT 肽的表面缀合在核靶向和核转运过程中起着关键作用。这种基于多功能 UCNPs 的纳米治疗被用于提高 DOX 在 Hela 肿瘤模型中的疗效,通过在纳米治疗的同步监测下将 DOX 直接递送到细胞核内。这项技术的进一步发展可能为通过核靶向治疗治疗癌症疾病提供更多令人兴奋的机会。

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