Fluorescence-tagged amphiphilic brush copolymer encapsulated Gd2O3 core-shell nanostructures for enhanced T1 contrast effect and fluorescent imaging

被引:1
作者
Wang, Fenghe [1 ]
Peng, Erwin [1 ]
Liu, Feng [2 ]
Li, Pingjing [2 ]
Li, Sam Fong Yau [2 ,3 ]
Xue, Jun Min [1 ]
机构
[1] Natl Univ Singapore, Fac Engn, Dept Mat Sci & Engn, 7 Engn Dr 1, Singapore 117574, Singapore
[2] NERI, Dept Chem, 3 Sci Dr 3, Singapore 117573, Singapore
[3] Natl Univ Singapore, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore
关键词
magnetic resonance imaging; contrast agent; gadolinium oxide; fluorescent imaging; HIGH-RESOLUTION MRI; IN-VIVO; OXIDE NANOPARTICLES; MOLECULAR PROBES; GENE DELIVERY; QUANTUM DOTS; RESONANCE; AGENTS; ACID; TUMORS;
D O I
10.1088/0957-4484/27/42/425101
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To obtain suitable T-1 contrast agents for magnetic resonance imaging (MRI) application, aqueous Gd2O3 nanoparticles (NPs) with high longitudinal relativity (r(1)) are demanded. High quality Gd2O3 NPs are usually synthesized through a non-hydrolytic route which requires post-synthetic modification to render the NPs water soluble. The current challenge is to obtain aqueous Gd2O3 NPs with high colloidal stability and enhanced r(1) relaxivity. To overcome this challenge, fluorescence-tagged amphiphilic brush copolymer (AFCP) encapsulated Gd2O3 NPs were proposed as suitable T-1 contrast agents. Such a coating layer provided (i) superior aqueous stability, (ii) biocompatibility, as well as (iii) multi-modality (conjugation with fluorescence dye). The polymeric coating layer thickness was simply adjusted by varying the phase-transfer parameters. By reducing the coating thickness, i.e. the distance between the paramagnetic centre and surrounding water protons, the r(1) relaxivity could be enhanced. In contrast, a thicker polymeric layer coating prevents Gd3+ ions leakage, thus improving its biocompatibility. Therefore, it is important to strike a balance between the biocompatibility and the r(1) relaxivity behaviour. Lastly, by conjugating fluorescence moiety, an additional imaging modality was enabled, as demonstrated from the cell-labelling experiment.
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页数:12
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