期刊文献+

温度和pH敏感高分子含钆核磁共振成像造影剂的合成及性能 被引量:4

Synthesis and Proporties of Temperature and p H-sensitive and Gadolinium Contained Polymeric Magnetic Resonance Imaging Contrast Agent
下载PDF
导出
摘要 以N-异丙基丙烯酰胺为温度敏感单体,以甲基丙烯酸为p H敏感单体,与三丙烯酸菲洛啉钆进行无皂乳液聚合,一步合成了具有温度和pH敏感的高分子含钆核磁共振成像(MRI)造影剂(TPRPP).动态光散射测试结果表明,TPRPP的粒径随温度或p H值的变化而发生较大的改变.体外MRI测试结果表明,TPRPP的横向弛豫时间(T_1)的加权弛豫率约为11.3 L/(mmol·s),为临床造影剂Magnevist~的2.6倍.体内MRI结果表明,TPRPP在肝和脾中具有明显的正增强效果.研究结果表明,TPRPP是一种优异的多功能MRI造影剂,具有极大的临床研究价值. Paramagnetic,temperature and p H-sensitive polymeric particles were prepared with N-isopropylacrylamide,methacrylic acid,styrene,and polymerizable Gd(AA)_3phen·H_2O using emulsifier-free emulsion polymerization technique. Dynamic light scattering result shows that the diameter of the polymeric particles changes by about 60 nm as a result of variations in either the temperature or p H,indicating that the particles are p H and temperature-sensitive. The T1-weighted relaxivity values at 3 T are about 11. 3 L /( mmol · s)which is 2. 6 times higher than clinical Magnevist~. In vivo MR imaging reveals that the TPRPPs can be effectively imaged in the liver and spleen,suggesting that they are excellent magnetic resonance imaging agents.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2016年第1期155-160,共6页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:51273058 81171386 81372369)资助~~
关键词 温度和p H敏感高分子 核磁共振成像 无皂乳液聚合 钆造影剂 Temperature and p H-sensitive polymer Magnetic resonance imaging(MRI) Emulsifier-free emulsion polymerization Gadolinium contrast agent
  • 相关文献

参考文献24

  • 1LiY. , BeijaM. , Laurent S., ElstL. V., MullerR. N., DuongH. T. T., LoweA. B., DavisT. P., BoyerC., Macrotm~lecules, 2012, 45(10), 4196----4204.
  • 2Liu Y. J., FengL. X., LiuT. X., ZhangL., YaoY., Yu D. X., WangL. L., ZhangN. , Nanoscale, 2014, 6(6), 3231--3242.
  • 3Cheng Z. , Thorek D. L. , Tsourkas A. , Angew. Chem. Int. Ed. Engl. , 2010, 49(2) , 346--350 Liu Y. G. , Zhang N. , Biomaterials, 2012, 33(21 ) , 5363--5375.
  • 4Wu X. , Wang Z. , Zhu D. , Zong S. , Yang L. , Zhong Y. , Cui Y. , ACS Appl. Mater. lnteoCaces, 2013, 5(21), 10895--10903.
  • 5Davies G. L., Kramberger I., Davis J. J., Chem. Commun. (Camb), 2013, 49(84), 9704--9721.
  • 6Nwe K. , Huang C. H. , Tsourkas A. , J. Med. Chem. , 2013, 56(20), 7862--7869.
  • 7Kim K. S. , Park W. , Hu J. , Bae Y. H. , Na K. , Biomaterials, 2014, 35(1), 337--343.
  • 8Kono K. , Nakashima S. , Kokuryo D. , Aoki I. , Shimomoto H. , Aoshima S. , Maruyama K. , Yuba E. , Kojima C. , Harada A. Ishizaka Y. , Biomaterials, 2011, 32 ( 5 ), 1387--1395.
  • 9Liu Q. M. , Zhu H. Z. , Qi~ J. Y. , Dong H. Q. , Du J. Z. , Biomacrornoleeules, 2014, 15(5), 1586--1592.
  • 10Liu Q. M. , Chen S. ,Chen J. , Du J. Z. , Macromolecules, 2015, 48(3) , 739--749.

同被引文献15

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部