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用抗体功能化的放射性标记碳纳米管进行肿瘤靶向

Tumor targeting with antibody-functionalized, radiolabeled carbon nanotubes.

作者信息

McDevitt Michael R, Chattopadhyay Debjit, Kappel Barry J, Jaggi Jaspreet Singh, Schiffman Scott R, Antczak Christophe, Njardarson Jon T, Brentjens Renier, Scheinberg David A

机构信息

Molecular Pharmacology and Chemistry Department, Departments of Medicine and Radiology, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

J Nucl Med. 2007 Jul;48(7):1180-9. doi: 10.2967/jnumed.106.039131.

Abstract

UNLABELLED

Single-walled carbon nanotubes (CNT) are mechanically robust graphene cylinders with a high aspect ratio that are comprised of sp(2)-bonded carbon atoms and possessing highly regular structures with defined periodicity. CNT exhibit unique mechanochemical properties that can be exploited for the development of novel drug delivery platforms. We hypothesized that novel prototype nanostructures consisting of biologics, radionuclides, fluorochromes, and CNT could be synthesized and designed to target tumor cells.

METHODS

Tumor-targeting CNT constructs were synthesized from sidewall-functionalized, water-soluble CNT platforms by covalently attaching multiple copies of tumor-specific monoclonal antibodies, radiometal-ion chelates, and fluorescent probes. The constructs were characterized spectroscopically, chromatographically, and electrophoretically. The specific reactivity of these constructs was evaluated in vitro by flow cytometry and cell-based immunoreactivity assays and in vivo using biodistribution in a murine xenograft model of lymphoma.

RESULTS

A soluble, reactive CNT platform was used as the starting point to build multifunctional constructs with appended antibody, metal-ion chelate, and fluorescent chromophore moieties to effect specific targeting, to carry and deliver a radiometal-ion, and to report location, respectively. These nanoconstructs were found to be specifically reactive with the human cancer cells they were designed to target in vivo in a model of disseminated human lymphoma and in vitro by flow cytometry and cell-based immunoreactivity assays versus appropriate controls.

CONCLUSION

The key achievement in these studies was the selective targeting of tumor in vitro and in vivo by the use of specific antibodies appended to a soluble, nanoscale CNT construct. The ability to specifically target tumor with prototype-radiolabeled or fluorescent-labeled, antibody-appended CNT constructs was encouraging and suggested further investigation of CNT as a novel delivery platform.

摘要

未标注

单壁碳纳米管(CNT)是具有高纵横比的机械坚固的石墨烯圆柱体,由sp(2)键合的碳原子组成,具有高度规则的结构和确定的周期性。碳纳米管具有独特的机械化学性质,可用于开发新型药物递送平台。我们假设可以合成并设计由生物制剂、放射性核素、荧光染料和碳纳米管组成的新型原型纳米结构,以靶向肿瘤细胞。

方法

通过共价连接多个肿瘤特异性单克隆抗体、放射性金属离子螯合物和荧光探针,从侧壁功能化的水溶性碳纳米管平台合成肿瘤靶向碳纳米管构建体。通过光谱、色谱和电泳对构建体进行表征。通过流式细胞术和基于细胞的免疫反应性测定在体外评估这些构建体的特异性反应性,并在体内使用淋巴瘤小鼠异种移植模型中的生物分布进行评估。

结果

使用可溶性、反应性碳纳米管平台作为起点,构建具有附加抗体、金属离子螯合物和荧光发色团部分的多功能构建体,分别实现特异性靶向、携带和递送放射性金属离子以及报告位置。在弥散性人类淋巴瘤模型中,通过流式细胞术和基于细胞的免疫反应性测定与适当对照相比,发现这些纳米构建体在体内与它们设计靶向的人类癌细胞具有特异性反应。

结论

这些研究的关键成就是通过使用附着在可溶性纳米级碳纳米管构建体上的特异性抗体在体外和体内对肿瘤进行选择性靶向。用原型放射性标记或荧光标记的、附着抗体的碳纳米管构建体特异性靶向肿瘤的能力令人鼓舞,并建议进一步研究碳纳米管作为一种新型递送平台。

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