Biofunctionalized, Phosphonate-Grafted, Ultrasmall Iron Oxide Nanoparticles for Combined Targeted Cancer Therapy and Multimodal Imaging

被引:147
|
作者
Das, Monasmita [1 ]
Mishra, Debasish [2 ]
Dhak, Prasanta [1 ]
Gupta, Satyajit [1 ]
Maiti, Tapas Kumar [2 ]
Basak, Amit [1 ]
Pramanik, Panchanan [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Kharagpur 721302, W Bengal, India
[2] Indian Inst Technol, Dept Biotechnol, Kharagpur 721302, W Bengal, India
关键词
cancer therapy; drug delivery; magnetic materials; magnetic resonance imaging; nanoparticles; FOLATE RECEPTOR; MAGNETIC-RESONANCE; IN-VITRO; DRUG-DELIVERY; VIVO; FABRICATION; MONOLAYERS; MOLECULES; PLATFORM; CELLS;
D O I
10.1002/smll.200901219
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel, inexpensive biofunctionalization approach is adopted to develop a multimodal and theranostic nanoagent, which combines cancer-targeted magnetic resonance/optical imaging and pH-sensitive drug release into one system. This multifunctional nanosystem, based on an ultrasmall superparamagnetic iron oxide (USPIO) nanocore, is modified with a hydrophilic, biocompatible, and biodegradable coating of N-phosphonomethyl iminodiacetic acid (PMIDA). Using appropriate spacers, functional molecules, such as rhodamine B isothiocyanate, folic acid, and methotrexate., are coupled to the amine-derivatized USPIO-PMIDA support with the aim of endowing simultaneous targeting, imaging, and intracellular drug-delivering capability. For the first time, phosphonic acid chemistry is successfully exploited to develop a stealth, multifunctional nanoprobe that can selectively target, detect, and kill cancer cells overexpressing the folate receptor, while allowing real-time monitoring of tumor response to drug treatment through dual-modal fluorescence and magnetic resonance imaging.
引用
收藏
页码:2883 / 2893
页数:11
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