Phosphocholine-decorated superparamagnetic iron oxide nanoparticles: defining the structure and probing in vivo applications

被引:28
|
作者
Luchini, Alessandra [1 ,2 ]
Irace, Carlo [3 ]
Santamaria, Rita [3 ]
Montesarchio, Daniela [1 ]
Heenan, Richard K. [4 ]
Szekely, Noemi [5 ]
Flori, Alessandra [6 ]
Menichetti, Luca [6 ,7 ]
Paduano, Luigi [1 ,2 ]
机构
[1] Univ Naples Federico II, Dipartimento Sci Chim, Complesso Univ Monte S Angelo,via Cintia, I-80126 Naples, Italy
[2] CSGI Consorzio Interuniv Sviluppo Sistemi Grande, Pisa, Italy
[3] Univ Naples Federico II, Dipartimento Farm, Via D Montesano 49, I-80131 Naples, Italy
[4] Rutherford Appleton Lab, ISIS Facil, Sci & Technol Facil Council, Harwell Oxford, Didcot OX11 0QX, Oxon, England
[5] Garching Forschungszentrum, Julich Ctr Neutron Sci, Lichtenbergstr 1, D-85747 Garching, Germany
[6] Fdn CNR Reg Toscana G Monaterio, Via Moruzzi 1, I-56124 Pisa, Italy
[7] CNR, Inst Clin Physiol, Via Moruzzi 1, I-56124 Pisa, Italy
关键词
CONTRAST AGENTS; DOXORUBICIN;
D O I
10.1039/c5nr08486e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Superparamagnetic Iron Oxide Nanoparticles (SPIONs) are performing contrast agents for Magnetic Resonance Imaging (MRI). A functionalization strategy for SPIONs based on hydrophobic interactions is a versatile approach easily extendable to several kinds of inorganic nanoparticles and suitable for obtaining stable and biocompatible systems. Here we report on the original preparation of functionalized SPIONs with an 8 nm radius exploiting the hydrophobic interaction between a phosphocholine and an inner amphiphilic. With respect to other similarly functionalized SPIONs, characterized by the typical nanoparticle clustering that leads to large aggregates, our phosphocholine-decorated SPIONs are demonstrated to be monodisperse. We report the in vitro and in vivo study that proves the effective applicability of phosphocholine-decorated SPIONs as MRI contrast agents. The versatility of this functionalization approach is highlighted by introducing on the SPION surface a ruthenium-based potential antitumoral drug, named ToThyCholRu. Even if in this case we observed the formation of SPION clusters, ascribable to the presence of the amphiphilic ruthenium complex, interesting and promising antiproliferative activity points at the ToThyCholRu-decorated SPIONs as potential theranostic agents.
引用
收藏
页码:10078 / 10086
页数:9
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