Multifold enhanced T2 relaxation of ZnFe2O4 nanoparticles by jamming them inside chitosan nanospheres

被引:28
作者
Lin, Ying [1 ,2 ]
Yao, Wei [1 ,2 ]
Cheng, Yuan [1 ,2 ]
Qian, Hanqing [1 ,2 ]
Wang, Xin [1 ,2 ]
Ding, Yin [3 ]
Wu, Wei [1 ,2 ]
Jiang, Xiqun [1 ,2 ]
机构
[1] Nanjing Univ, Coll Chem & Chem Engn, Lab Mesoscop Chem, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Coll Chem & Chem Engn, Dept Polymer Sci & Engn, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Coll Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210093, Jiangsu, Peoples R China
关键词
IRON-OXIDE NANOPARTICLES; MAGNETIC NANOPARTICLES; CELLULAR UPTAKE; DRUG-DELIVERY; MRI CONTRAST; IN-VIVO; NANOCRYSTALS; INTEGRINS; CARRIERS; THERAPY;
D O I
10.1039/c2jm15133b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
ZnFe2O4 nanoparticles were tightly packed and encapsulated in chitosan nanospheres by a nonsolvent-aided counterion complexation method. The obtained hybrid nanospheres exhibited not only the superparamagnetic properties provided by pure ZnFe2O4 nanoparticles but also a much higher r(2) relaxivity value than separate ZnFe2O4 nanoparticles, representing an approximately 3 to 16 fold increase. This was attributed to the high ZnFe2O4 payload and ZnFe2O4 nanoparticle clustering effect in the core of the nanospheres. The MR images generated in vivo demonstrated that the hybrid nanospheres showed an excellent contrast in T-2 weighted MRI and a high MRI sensitivity in the tumor sites for both passive and active targeting samples. In addition, the biodistribution analysis revealed that the obtained hybrid nanospheres could accumulate at tumor sites via passive and active targeting strategies.
引用
收藏
页码:5684 / 5693
页数:10
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