Multi hydroxylated [Gd@C82(OH)22]n nanoparticles:: Antineoplastic activity of high efficiency and low toxicity

被引:273
作者
Chen, CY
Xing, GM
Wang, JX
Zhao, YL [1 ]
Li, B
Tang, J
Jia, G
Wang, TC
Sun, J
Xing, L
Yuan, H
Gao, YX
Meng, H
Chen, Z
Zhao, F
Chai, ZF
Fang, XH
机构
[1] Chinese Acad Sci, Inst High Energy Phys, Lab Bioenvironm Hlth Sci Nanoscale Mat, Beijing 100049, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Key Lab Nucl Analyt Techniques, Beijing 100049, Peoples R China
[3] Peking Univ, Hosp 3, Dept Clin Lab, Sch Publ Hlth, Beijing 100083, Peoples R China
[4] Chinese Acad Sci, Inst Chem, Key Lab Mol Nanostruct & Nanotechnol, Beijing 100080, Peoples R China
[5] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
关键词
D O I
10.1021/nl051624b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
[Gd@C-82(OH)(22)](n) particles (22 nm in a saline solution) of a dose level as low as 10(-7) mol/kg exhibit a very high antineoplastic efficiency (similar to 60%) in mice. A dose increment of 1 x 10(-7) mol/kg increases the tumor inhibition rate 26%. [Gd@C-82(OH)(22)](n) particles have a strong capacity to improve immunity and interfere with tumor invasion in normal muscle cells, nearly without toxicity in vivo and in vitro. Unlike conventional antineoplastic chemicals, the high antitumor efficiency of nanoparticles is not due to toxic effects to cells because they do not kill the tumor cells directly and only about 0.05% of the used dose is found in the tumor tissues. Results suggest that fullerene derivatives with proper surface modifications and sizes may help realize the dream of tumor chemotherapeutics of high-efficacy and low-toxicity.
引用
收藏
页码:2050 / 2057
页数:8
相关论文
共 30 条
[11]   Delivery of molecular medicine to solid tumors [J].
Jain, RK .
SCIENCE, 1996, 271 (5252) :1079-1080
[12]   SOLID C-60 - A NEW FORM OF CARBON [J].
KRATSCHMER, W ;
LAMB, LD ;
FOSTIROPOULOS, K ;
HUFFMAN, DR .
NATURE, 1990, 347 (6291) :354-358
[13]   C-60 - BUCKMINSTERFULLERENE [J].
KROTO, HW ;
HEATH, JR ;
OBRIEN, SC ;
CURL, RF ;
SMALLEY, RE .
NATURE, 1985, 318 (6042) :162-163
[14]   Design and synthesis of novel [60]fullerene derivatives as potential HIV aspartic protease inhibitors [J].
Marcorin, GL ;
Da Ros, T ;
Castellano, S ;
Stefancich, G ;
Bonin, I ;
Miertus, S ;
Prato, M .
ORGANIC LETTERS, 2000, 2 (25) :3955-3958
[15]   Paramagnetic water-soluble metallofullerenes having the highest relaxivity for MRI contrast agents [J].
Mikawa, M ;
Kato, H ;
Okumura, M ;
Narazaki, M ;
Kanazawa, Y ;
Miwa, N ;
Shinohara, H .
BIOCONJUGATE CHEMISTRY, 2001, 12 (04) :510-514
[16]   Evaluation of water-soluble metallofullerenes as MRI contrast agents [J].
Okumura, M ;
Mikawa, M ;
Yokawa, T ;
Kanazawa, Y ;
Kato, H ;
Shinohara, H .
ACADEMIC RADIOLOGY, 2002, 9 :S495-S497
[17]  
ROS DT, 1999, CHEM COMMUN, P663
[18]   The differential cytotoxicity of water-soluble fullerenes [J].
Sayes, CM ;
Fortner, JD ;
Guo, W ;
Lyon, D ;
Boyd, AM ;
Ausman, KD ;
Tao, YJ ;
Sitharaman, B ;
Wilson, LJ ;
Hughes, JB ;
West, JL ;
Colvin, VL .
NANO LETTERS, 2004, 4 (10) :1881-1887
[19]   SYNTHESIS AND VIRUCIDAL ACTIVITY OF A WATER-SOLUBLE, CONFIGURATIONALLY STABLE, DERIVATIZED C60 FULLERENE [J].
SCHINAZI, RF ;
SIJBESMA, R ;
SRDANOV, G ;
HILL, CL ;
WUDL, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (08) :1707-1710
[20]  
Simonin JP, 2001, J PHYS CHEM B, V105, P5262, DOI [10.1021/jp004077l, 10.1021/jp0040771]