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Hyaluronic Acid-Gadolinium Complex Nanospheres as Lymphatic System-Specific Contrast Agent for Magnetic Resonance Imaging 被引量:2

Hyaluronic Acid-Gadolinium Complex Nanospheres as Lymphatic System-Specific Contrast Agent for Magnetic Resonance Imaging
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摘要 A novel MRI contrast agent, hyaluronic acid gadolinium complex (HA-Gd-DTPA) nanospheres, is prepared by the synthesis of hyaluronic acid gadolinium complexes and their assembly. The physicochemical properties are characterized, and the lymphatic targeting in vitro and in vivo are also evaluated. The results show that the HA-Gd-DTPA nanospheres with suitable and stable physicochemical properties could be used for in vivo lymphatic targeting studies. Furthermore, the HA-Gd-DTPA nanospheres have obviously higher relaxation efficiency and MRI contrast between blood vessel and lymph vessel in rabbit than that of Magnevist. Thus, the novel MRI contrast agent can be taken up selectively by lymphatic system and used as a potential MRI contrast agents in lymphatic system. A novel MRI contrast agent, hyaluronic acid gadolinium complex (HA-Gd-DTPA) nanospheres, is prepared by the synthesis of hyaluronic acid gadolinium complexes and their assembly. The physicochemical properties are characterized, and the lymphatic targeting in vitro and in vivo are also evaluated. The results show that the HA-Gd-DTPA nanospheres with suitable and stable physicochemical properties could be used for in vivo lymphatic targeting studies. Furthermore, the HA-Gd-DTPA nanospheres have obviously higher relaxation efficiency and MRI contrast between blood vessel and lymph vessel in rabbit than that of Magnevist. Thus, the novel MRI contrast agent can be taken up selectively by lymphatic system and used as a potential MRI contrast agents in lymphatic system.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2015年第10期1153-1158,共6页 中国化学(英文版)
关键词 magnetic resonance imaging hyaluronic acid lymphatic system magnetic resonance imaging, hyaluronic acid, lymphatic system
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  • 1Zhang, J. C.; Qiao, Z. Y.; Yang, P. P.; Pan, J.; Wang, L.; Wang, H. Chin. J.. Chem. 2015, 33, 35.
  • 2Yang, E P.; Wang, L.; Wang, H. Chin. J. Chem. 2015, 33, 59.
  • 3Yan, G. E; Robinson, L.; Hogg, E Radiography 2007, 13, e5.
  • 4Moon, M. J.; Thomas, R. G.; Heo, S. U.; Park, M. S.; Bae, W. K.;Heo, S. H.; Yim, N. Y.; Jeong, Y. Y. Mol. Imaging Biol. 2015, DOI: 10.1007/s11307-014-0819-z.
  • 5Guo, R.; Yao, Y.; Cheng, G. C.; Wang, S. H.; Li, Y.; Shen, M. W.; Zhang, Y. H.; Baker Jr., J. R.; Wang, J. H.; Shi, X. Y. RSC Adv. 2012, 2, 99.
  • 6Tao, Y. H.; Han, J. F.; Dou, H. Y..1. Mater. Chem. 2012, 22, 11808.
  • 7Yang, D.; Yang, F.; Hu, J. H.; Long, J.; Wang, C. C.; Fu, D. L.; Ni, Q. X. Chem. Commun. 2009, 4447.
  • 8Kobayashi, H.; Kawamoto, S.; Bemardo, M.; Brechbiel, M. W.; Knopp, M. V.; Choyke, P. L. ,L Control. Release 2006, 111,343.
  • 9Lambregts, D. M.; Beets, G. L.; Maas, M.; Kesse|s, A. G.; Bakers, F. C.; Cappendijk, V. C.; Engelen, S. M.; Lahaye, M. J.; de Bru'ine, A. P.; Lammering, G.; Leiner, T.; Verwoerd, J. L.; Wildberger, J. E.; Beets-Tan, R. G. Ann. Surg. 2011, 253,539.
  • 10Triantafyllou, M.; Studer, U. E.; Birkh~iuser, F. D.; Fleischmann, A.; Bains, L. J.; Petra|ia, G.; Christe, A.; Froehlich, J. M.; Thoeny, H. C. Eur J. Cancer 2013, 49, 616.

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