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功能化单壁碳纳米管作为用于肿瘤靶向药物递送的合理设计载体。

Functionalized single-walled carbon nanotubes as rationally designed vehicles for tumor-targeted drug delivery.

作者信息

Chen Jingyi, Chen Shuyi, Zhao Xianrui, Kuznetsova Larisa V, Wong Stanislaus S, Ojima Iwao

机构信息

Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, New York 11973, USA.

出版信息

J Am Chem Soc. 2008 Dec 10;130(49):16778-85. doi: 10.1021/ja805570f.

Abstract

A novel single-walled carbon nanotube (SWNT)-based tumor-targeted drug delivery system (DDS) has been developed, which consists of a functionalized SWNT linked to tumor-targeting modules as well as prodrug modules. There are three key features of this nanoscale DDS: (a) use of functionalized SWNTs as a biocompatible platform for the delivery of therapeutic drugs or diagnostics, (b) conjugation of prodrug modules of an anticancer agent (taxoid with a cleavable linker) that is activated to its cytotoxic form inside the tumor cells upon internalization and in situ drug release, and (c) attachment of tumor-recognition modules (biotin and a spacer) to the nanotube surface. To prove the efficacy of this DDS, three fluorescent and fluorogenic molecular probes were designed, synthesized, characterized, and subjected to the analysis of the receptor-mediated endocytosis and drug release inside the cancer cells (L1210FR leukemia cell line) by means of confocal fluorescence microscopy. The specificity and cytotoxicity of the conjugate have also been assessed and compared with L1210 and human noncancerous cell lines. Then, it has unambiguously been proven that this tumor-targeting DDS works exactly as designed and shows high potency toward specific cancer cell lines, thereby forming a solid foundation for further development.

摘要

一种新型的基于单壁碳纳米管(SWNT)的肿瘤靶向药物递送系统(DDS)已被开发出来,它由连接到肿瘤靶向模块以及前药模块的功能化单壁碳纳米管组成。这种纳米级药物递送系统有三个关键特性:(a)使用功能化单壁碳纳米管作为用于递送治疗药物或诊断剂的生物相容性平台;(b)偶联抗癌剂(带有可裂解连接子的紫杉烷)的前药模块,该前药模块在被内化并原位释放药物后在肿瘤细胞内被激活为其细胞毒性形式;(c)在纳米管表面连接肿瘤识别模块(生物素和一个间隔物)。为了证明这种药物递送系统的功效,设计、合成、表征了三种荧光和荧光生成分子探针,并通过共聚焦荧光显微镜对癌细胞(L1210FR白血病细胞系)内的受体介导的内吞作用和药物释放进行了分析。还评估了缀合物的特异性和细胞毒性,并与L1210和人非癌细胞系进行了比较。然后,已明确证明这种肿瘤靶向药物递送系统的工作方式与设计完全一致,并且对特定癌细胞系显示出高效能,从而为进一步开发奠定了坚实基础。

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