Mesoporous silica nanoparticles as a delivery system of gadolinium for effective human stem cell tracking

被引:169
作者
Hsiao, Jong-Kai [3 ,4 ,6 ]
Tsai, Chih-Pin [2 ]
Chung, Tsai-Hua [1 ]
Hung, Yann [2 ]
Yao, Ming [4 ,5 ]
Liu, Hon-Man [3 ,4 ]
Mou, Chung-Yuan [2 ]
Yang, Chung-Shi [1 ]
Chen, Yao-Chang [4 ,5 ]
Huang, Dong-Ming [1 ]
机构
[1] Natl Hlth Res Inst, Ctr Nanomed Res, Zhunan 350, Miaoli County, Taiwan
[2] Natl Taiwan Univ, Dept Chem, Taipei 10764, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Med Imaging, Taipei, Taiwan
[4] Natl Taiwan Univ, Coll Med, Taipei 10764, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
[6] Natl Taiwan Univ, Inst Biomed Engn, Taipei 10764, Taiwan
关键词
biocompatibility; gadolinium; magnetic resonance imaging; silica; stem cells;
D O I
10.1002/smll.200701316
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The progress of using gadolinium (Gd)-based nanoparticles in cellular tracking lags behind that of superparamagnetic iron oxide (SPIO) nanoparticles in magnetic resonance imaging (MRI). Here, dual functional Gd-fluorescein isothiocyanate mesoporous silica nanoparticles (Gd-Dye@MSN) that possess green fluorescence and paramagnetism are developed in order to evaluate their potential as effective T1-enhancing trackers for human mesenchymal stem cells (hMSCs). hMSCs are labeled efficiently with Gd-Dye@MSN via endocytosis. Labeled hMSCs are unaffected in their viability, proliferation, and differentiation capacities into adipocytes, osteocytes, and chondrocytes, which can still be readily MRI detected. Imaging, with a clinical 1.5-T MRI system and a low incubation dosage of Gd, low detection cell numbers, and short incubation times is demonstrated on both loaded cells and hMSC-injected mouse brains. This study shows that the advantages of biocompatibility, durability, high internalizing efficiency, and pore architecture make MSNs an ideal vector of T1-agent for stem-cell tracking with MRI.
引用
收藏
页码:1445 / 1452
页数:8
相关论文
共 32 条
[21]   Stem cells - hype and hope [J].
McKay, R .
NATURE, 2000, 406 (6794) :361-364
[22]   Bone marrow cells regenerate infarcted myocardium [J].
Orlic, D ;
Kajstura, J ;
Chimenti, S ;
Jakoniuk, I ;
Anderson, SM ;
Li, BS ;
Pickel, J ;
McKay, R ;
Nadal-Ginard, B ;
Bodine, DM ;
Leri, A ;
Anversa, P .
NATURE, 2001, 410 (6829) :701-705
[23]   Multilineage potential of adult human mesenchymal stem cells [J].
Pittenger, MF ;
Mackay, AM ;
Beck, SC ;
Jaiswal, RK ;
Douglas, R ;
Mosca, JD ;
Moorman, MA ;
Simonetti, DW ;
Craig, S ;
Marshak, DR .
SCIENCE, 1999, 284 (5411) :143-147
[24]  
Platas-Iglesias C, 2002, CHEM-EUR J, V8, P5121, DOI 10.1002/1521-3765(20021115)8:22<5121::AID-CHEM5121>3.0.CO
[25]  
2-W
[26]   Synthesis and Characterization of a Gd-DOTA-D-Permeation Peptide for Magnetic Resonance Relaxation Enhancement of Intracellular Targets [J].
Prantner, Andrew M. ;
Sharma, Vijay ;
Garbow, Joel R. ;
Piwnica-Worms, David .
Molecular Imaging, 2003, 2 (04) :333-341
[27]   Effect of surface functionalization of MCM-41-type mesoporous silica nanoparticleson the endocytosis by human cancer cells [J].
Slowing, Igor ;
Trewyn, Brian G. ;
Lin, Victor S. -Y. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (46) :14792-14793
[28]   Mesoporous silica nanospheres as highly efficient MRI contrast agents [J].
Taylor, Kathryn M. L. ;
Kim, Jason S. ;
Rieter, William J. ;
An, Hongyu ;
Lin, Weili ;
Lin, Wenbin .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (07) :2154-+
[29]   Human mesenchymal stem cells differentiate to a cardiomyocyte phenotype in the adult murine heart [J].
Toma, C ;
Pittenger, MF ;
Cahill, KS ;
Byrne, BJ ;
Kessler, PD .
CIRCULATION, 2002, 105 (01) :93-98
[30]   High-contrast paramagnetic fluorescent mesoporous silica nanorods as a multifunctional cell-imaging probe [J].
Tsai, Chih-Pin ;
Hung, Yann ;
Chou, Yi-Hsin ;
Huang, Dong-Ming ;
Hsiao, Jong-Kai ;
Chang, Chen ;
Chen, Yao-Chang ;
Mou, Chung-Yuan .
SMALL, 2008, 4 (02) :186-191