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使用氨基膦酸偶联剂对磁铁矿纳米颗粒进行生物功能化:用于癌症特异性靶向的新型超分散氧化铁叶酸纳米共轭物。

Bio-functionalization of magnetite nanoparticles using an aminophosphonic acid coupling agent: new, ultradispersed, iron-oxide folate nanoconjugates for cancer-specific targeting.

作者信息

Das Manasmita, Mishra Debasish, Maiti T K, Basak A, Pramanik P

机构信息

Department of Chemistry, Indian Institute of Technology, Kharagpur, India.

出版信息

Nanotechnology. 2008 Oct 15;19(41):415101. doi: 10.1088/0957-4484/19/41/415101. Epub 2008 Sep 3.

DOI:10.1088/0957-4484/19/41/415101
PMID:21832636
Abstract

The present study describes a systematic approach towards the design and development of novel, bio-functionalized, magneto-fluorescent nanoparticles for cancer-specific targeting. Biocompatible, hydrophilic, magneto-fluorescent nanoparticles with surface-pendant amine, carboxyl or aldehyde groups, to be later used for bio-conjugation, were designed using an aminophosphonic acid coupling agent. These magneto-fluorescent nanoparticles were further functionalized with folic acid, using diverse conjugation strategies. A series of new iron-oxide folate nanoconjugates with excellent aqueous dispersion stability and reasonably good hydrodynamic sizes under a wide range of physiological conditions were developed. These ultradispersed nanosystems were analyzed for their physicochemical properties and cancer-cell targeting ability, facilitated by surface modification with folic acid. The nanoparticle size, charge, surface chemistry, magnetic properties and colloidal stability were extensively studied using a variety of complementary techniques. Confocal microscopy, performed with folate receptor positive human cervical HeLa cancer cells, established that these non-cytotoxic iron-oxide folate nanoconjugates were effectively internalized by the target cells through receptor-mediated endocytosis. Cell-uptake behaviors of nanoparticles, studied using magnetically activated cell sorting (MACS), clearly demonstrated that cells over-expressing the human folate receptor internalized a higher level of these nanoparticle-folate conjugates than negative control cells.

摘要

本研究描述了一种用于设计和开发新型生物功能化磁荧光纳米颗粒以实现癌症特异性靶向的系统方法。使用氨基膦酸偶联剂设计了具有表面悬挂胺基、羧基或醛基的生物相容性、亲水性磁荧光纳米颗粒,这些基团随后用于生物共轭。利用多种共轭策略,用叶酸对这些磁荧光纳米颗粒进行了进一步功能化。开发了一系列新型的氧化铁叶酸纳米共轭物,它们在广泛的生理条件下具有优异的水分散稳定性和合理良好的流体动力学尺寸。通过用叶酸进行表面修饰,对这些超分散纳米系统的物理化学性质和癌细胞靶向能力进行了分析。使用各种互补技术对纳米颗粒的大小、电荷、表面化学、磁性和胶体稳定性进行了广泛研究。对叶酸受体阳性的人宫颈HeLa癌细胞进行共聚焦显微镜检查,结果表明这些无细胞毒性的氧化铁叶酸纳米共轭物通过受体介导的内吞作用被靶细胞有效内化。使用磁激活细胞分选(MACS)研究纳米颗粒的细胞摄取行为,结果清楚地表明,过度表达人叶酸受体的细胞比阴性对照细胞内化更高水平的这些纳米颗粒 - 叶酸共轭物。

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