Targeted tumor dual mode CT/MR imaging using multifunctional polyethylenimine-entrapped gold nanoparticles loaded with gadolinium

被引:37
作者
Zhou, Benqing [1 ,2 ]
Xiong, Zuogang [1 ]
Wang, Peng [2 ]
Peng, Chen [1 ]
Shen, Mingwu [2 ]
Mignani, Serge [3 ,4 ]
Majoral, Jean-Pierre [5 ,6 ]
Shi, Xiangyang [1 ,2 ,4 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Sch Med, Dept Radiol, Shanghai, Peoples R China
[2] Donghua Univ, Coll Chem Chem Engn & Biotechnol, State Key Lab Modifcat Chem Fibers & Polymer Mat, Shanghai, Peoples R China
[3] Univ Paris 05, PRES Sorbonne Paris Cite, Lab Chim & Biochim Pharmacol & Toxicol, Paris, France
[4] Univ Madeira, MMRG, CQM, Funchal, Portugal
[5] CNRS, Lab Chim Coordinat, Toulouse, France
[6] Univ Toulouse, INPT, UPS, Toulouse, France
基金
中国国家自然科学基金;
关键词
Polyethylenimine; gold nanoparticles; CT imaging; MR imaging; tumor targeting; IRON-OXIDE NANOPARTICLES; HYALURONIC-ACID; FOLIC-ACID; CORE/SHELL NANOSTARS; PHOTOTHERMAL THERAPY; FACILE SYNTHESIS; CONTRAST AGENTS; RGD PEPTIDE; PEI; EFFICIENCY;
D O I
10.1080/10717544.2017.1422299
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We report the construction and characterization of polyethylenimine (PEI)-entrapped gold nanoparticles (AuNPs) chelated with gadolinium (Gd) ions for targeted dual mode tumor CT/MR imaging in vivo. In this work, polyethylene glycol (PEG) monomethyl ether-modified PEI was sequentially modified with Gd chelator and folic acid (FA)-linked PEG (FA-PEG) was used as a template to synthesize AuNPs, followed by Gd(III) chelation and acetylation of the remaining PEI surface amines. The formed FA-targeted PEI-entrapped AuNPs loaded with Gd (FA-Gd-Au PENPs) were well characterized in terms of structure, composition, morphology, and size distribution. We show that the FA-Gd-Au PENPs with an Au core size of 3.0 nm are water dispersible, colloidally stable, and noncytotoxic in a given concentration range. Thanks to the coexistence of Au and Gd elements within one nanoparticulate system, the FA-Gd-Au PENPs display a better X-ray attenuation property than clinical iodinated contrast agent (e.g. Omnipaque) and reasonable r(1) relaxivity (1.1 mM(-1)s(-1)). These properties allow the FA-targeted particles to be used as an efficient nanoprobe for dual mode CT/MR imaging of tumors with excellent FA-mediated targeting specificity. With the demonstrated organ biocompatibility, the designed FA-Gd-Au PENPs may hold a great promise to be used as a nanoprobe for CT/MR dual mode imaging of different FA receptor-overexpressing tumors.
引用
收藏
页码:178 / 186
页数:9
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