中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
In vitro assessment of the dual-targeting behavior of a peptide-based magnetic resonance imaging contrast agent

文献类型:期刊论文

作者Dai, JW (戴建武); Deng, ZW (邓宗武); Zhang, HL (张海禄)
刊名INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
出版日期2014-01
卷号33期号:1页码:215-220
关键词Arg-Gly-Asp Asn-Gly-Arg dual targeting ast agent magnetic resonance imaging contr
通讯作者Yu, KC (Yu, Kaichao)
英文摘要In this study, a peptide-based dual-targeting magnetic resonance imaging (MRI) contrast agent (S8) was designed and synthesized. Arg-Gly-Asp (RGD) and Asn-Gly-Arg (NGR) were combined in the targeting vector so as to allow binding, on the surface of tumor cells, to integrin (v3) and aminopeptidase N (CD13), respectively. The longitudinal relaxivity (r(1)) value of S8 was 8.297 mM(-1)sec(-1) at a magnetic field of 11.7 T, which is approximately double the r(1) value (4.25 mM(-1)sec(-1)) of Magnevist, a commercially available contrast agent. MDA-MB-231 human breast cancer cells (which overexpress (v3)) and human prostate cancer cells PC-3 (which overexpress CD13) were used to investigate the tumor-targeting behavior of S8. The results from the present study indicate that the designed contrast agent, S8, targets both MDA-MB-231 and PC-3 cells.
收录类别SCI
语种英语
WOS记录号WOS:000330785400028
公开日期2014-12-19
源URL[http://ir.sinano.ac.cn/handle/332007/1690]  
专题苏州纳米技术与纳米仿生研究所_纳米仿生研究部_邓宗武团队
苏州纳米技术与纳米仿生研究所_纳米生物医学与安全研究部_戴建武团队
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GB/T 7714
Dai, JW ,Deng, ZW ,Zhang, HL . In vitro assessment of the dual-targeting behavior of a peptide-based magnetic resonance imaging contrast agent[J]. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,2014,33(1):215-220.
APA Dai, JW ,Deng, ZW ,&Zhang, HL .(2014).In vitro assessment of the dual-targeting behavior of a peptide-based magnetic resonance imaging contrast agent.INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE,33(1),215-220.
MLA Dai, JW ,et al."In vitro assessment of the dual-targeting behavior of a peptide-based magnetic resonance imaging contrast agent".INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 33.1(2014):215-220.

入库方式: OAI收割

来源:苏州纳米技术与纳米仿生研究所

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