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Frontiers of Chemistry in China

ISSN 1673-3495

ISSN 1673-3614(Online)

CN 11-5726/O6

Front. Chem. China    2010, Vol. 5 Issue (2) : 166-170    https://doi.org/10.1007/s11458-010-0108-6
Research articles
A conjugated polymer - Gd (III) complex as pH sensitive contrast agent in magnetic resonance imaging
Qingling XU1,Libing LIU1,Minghui YU1,Qiong YANG1,Shu WANG1,Litao ZHU2,
1.Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China; 2.State Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing 100875, China;
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Abstract A novel pH-responsive contrast agent (PFP-aa/Gd) for magnetic resonance imaging (MRI) was prepared by binding Gd(III) to a water-soluble conjugated polyfluorene with pendant carboxylate and amine moieties. The PFP-aa is a good chelator for Gd3+ and the PFP-aa/Gd complex has good stability. As the pH changes from 10.0 to 4.0, both the carboxylate and amine are protonated, thus PFP-aa exhibits positive charges and forms tight aggregation, which reduces molecular tumbling and accelerates the exchange of bound water leading to the increase of relaxivity R1. More importantly, the R1 increases by about eight fold as the pH changes from 8.0 to 6.0, which makes PFP-aa/Gd suitable as a potential marker of the pH below physiological level. In comparison to other contrast agents, the unique sensitivity of the water relaxivity of PFP-aa/Gd indicates that this complex could be used in MRI experiments to monitor physiological pH change.
Keywords magnetic resonance imaging      pH-sensitive      conjugated polymer      Gd(III) chelate      
Issue Date: 05 June 2010
 Cite this article:   
Qingling XU,Minghui YU,Libing LIU, et al. A conjugated polymer - Gd (III) complex as pH sensitive contrast agent in magnetic resonance imaging[J]. Front. Chem. China, 2010, 5(2): 166-170.
 URL:  
https://academic.hep.com.cn/fcc/EN/10.1007/s11458-010-0108-6
https://academic.hep.com.cn/fcc/EN/Y2010/V5/I2/166
Meade, T. J.; Taylor, A. K.; Bull, S. R., Curr. Opin. Neurobiol. 2003, 13, 597–602

doi: 10.1016/j.conb.2003.09.009
Kircher, M. F.; Mahmood, U.; King, R. S.; Weissleder, R.; Josephson, L., Cancer Res. 2003, 63, 8122–8125
Caravan, P.; Ellison, J. J.; McMurry, T. J.; Lauffer, R. B., Chem. Rev. 1999, 99, 2293–2352

doi: 10.1021/cr980440x
Aime, S.; Botta, M.; Fasano, M.; Terreno, E., Chem. Soc. Rev. 1998, 27, 19–29

doi: 10.1039/a827019z
Werner, E. J.; Avedano, S.; Botta, M.; Hay, B. P.; Moore, E. G.; Aime, S.; Raymond, K. N., J. Am. Chem. Soc. 2007, 129, 1870–1871

doi: 10.1021/ja068026z
Gerweck, L. E.; Seetharaman, K., Cancer Res. 1996, 56, 1194–1198
Jayasundar, R.; Honess, D.; Hall, L. D.; Bleehen, N. M., Magn. Reson. Med. 2000, 43, 1–8

doi: 10.1002/(SICI)1522-2594(200001)43:1<1::AID-MRM1>3.0.CO;2-2
Lokling, K. E.; Skurtveit, R.; Bjornerud, A.; Fossheim, S. L., Magn. Reson. Med. 2004, 51, 688–696

doi: 10.1002/mrm.20009
Aime, S.; Fedeli, F.; Sanino, A.; Terreno, E., J. Am. Chem. Soc. 2006, 128, 11326–11327

doi: 10.1021/ja062387x
Løklinga, K. E.; Fossheimb, S. L.; Skurtveitb, R.; Bjørnerudb, A.; Klavenessa, J., Magn. Reson. Imaging 2001, 19, 731–738

doi: 10.1016/S0730-725X(01)00380-0
Tóth, E.; Bolskar, R. D.; Borel, A.; González, G.; Helm, L.; Merbach, A. E.; Sitharaman, B.; Wilson, L. J., J. Am. Chem. Soc. 2005, 127, 799–805

doi: 10.1021/ja044688h
Rudovský, J.; Botta, M.; Hermann, P.; Hardcastle, K. I.; Lukeš, I.; Aime, S., Bioconjugate Chem. 2006, 17, 975–987

doi: 10.1021/bc060149l
Mikawa, M.; Miwa, N.; Bräutigam, M.; Akaike, T.; Maruyama1, A., J. Biomed. Mater. Res. 2000, 49, 390–395

doi: 10.1002/(SICI)1097-4636(20000305)49:3<390::AID-JBM12>3.3.CO;2-H
Xu, Q.; Zhu, L.; Yu, M.; Feng, F.; An, L.; Xing, C.; Wang, S., Polymer 2009, doi:

doi: 10.1016/j.polymer.2009.04.003
André, J. P.; Tóth, É.; Fischer, H.; Seelig, A.; Mäcke, H. R.; Merbach, A. E., Chem. Eur. J. 1999, 5, 2977–2983

doi: 10.1002/(SICI)1521-3765(19991001)5:10<2977::AID-CHEM2977>3.0.CO;2-T
Wang, S.; Bazan, G. C., Chem. Commun. 2004, 21, 2508–2509

doi: 10.1039/b410002f
Xu, Q.; An, L.; Yu, M.; Wang, S., Macromol. Rapid Commun. 2008, 29, 390–395

doi: 10.1002/marc.200700745
Lakowicz, J. R., Principles of Fluorescence Spectroscopy; Kluwer Academic/Plenum: New York, 1999
Zhang, S.; Wu, K.; Sherry, A. D., Angew. Chem. Int. Ed. 1999, 38, 3192–3194

doi: 10.1002/(SICI)1521-3773(19991102)38:21<3192::AID-ANIE3192>3.0.CO;2-#
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