journal article·2012-08-28Open access

Gadolinium-Encapsulating Iron Oxide Nanoprobe as Activatable NMR/MRI Contrast Agent

Santimukul Santra, Samuel D. Jativa, Charalambos Kaittanis, Guillaume Normand, Jan Grimm, J. Manuel Perez

ACS Nano· Volume 6· Issue 8

Abstract

Herein we report a novel gadolinium-encapsulating iron oxide nanoparticle-based activatable NMR/MRI nanoprobe. In our design, Gd-DTPA is encapsulated within the poly(acrylic acid) (PAA) polymer coating of a superparamagnetic iron oxide nanoparticle (IO-PAA), yielding a composite magnetic nanoprobe (IO-PAA-Gd-DTPA) with quenched longitudinal spin-lattice magnetic relaxation (T(1)). Upon release of the Gd-DTPA complex from the nanoprobe's polymeric coating in acidic media, an increase in the T(1) relaxation rate (1/T(1)) of the composite magnetic nanoprobe was observed, indicating a dequenching of the nanoprobe with a corresponding increase in the T(1)-weighted MRI signal. When a folate-conjugated nanoprobe was incubated in HeLa cells, a cancer cell line overexpressing folate receptors, an increase in the 1/T(1) signal was observed. This result suggests that, upon receptor-mediated internalization, the composite magnetic nanoprobe degraded within the cell's lysosome acidic (pH 5.0) environment, resulting in an intracellular release of Gd-DTPA complex with subsequent T(1) activation. In addition, when an anticancer drug (Taxol) was coencapsulated with the Gd-DTPA within the folate receptor targeting composite magnetic nanoprobe, the T(1) activation of the probe coincided with the rate of drug release and corresponding cytotoxic effect in cell culture studies. Taken together, these results suggest that our activatable T(1) nanoagent could be of great importance for the detection of acidic tumors and assessment of drug targeting and release by MRI.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoparticle-Based Drug Delivery · Lanthanide and Transition Metal Complexes · Advanced MRI Techniques and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Nanoscience Technology Center and Chemistry Department, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, Florida 32826, United States

Department of Radiology, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, New York 10065, United States

References (68)

Show source-provided references
1. Winter P. M. · Curr. Cardiol. Rep. · 2006 · 8 · 6510.1007/s11886-006-0013-2 ↗
2. Hu X. · Annu. Rev. Biomed. Eng. · 2004 · 6 · 15710.1146/annurev.bioeng.6.040803.140017 ↗
3. Aime S. · J. Magn. Reson. Imaging · 2002 · 16 · 39410.1002/jmri.10180 ↗
4. Louie A. · Chem. Rev. · 2010 · 110 · 314610.1021/cr9003538 ↗
5. Mulder W. J. · Bioconjugate Chem. · 2004 · 15 · 79910.1021/bc049949r ↗
6. Mazooz G. · Cancer Res. · 2005 · 65 · 136910.1158/0008-5472.CAN-04-2269 ↗
7. Josephson L. · Bioconjugate Chem. · 1999 · 10 · 18610.1021/bc980125h ↗
8. Caravan P. · Chem. Rev. · 1999 · 99 · 229310.1021/cr980440x ↗
9. Song Y. · Bioconjugate Chem. · 2010 · 21 · 226710.1021/bc1002828 ↗
10. Frullano L. · J. Biol. Inorg. Chem. · 2007 · 12 · 93910.1007/s00775-007-0265-3 ↗
11. Tu C. Q. · Chem. Commun. · 2007 · 1331
12. Uzgiris E. E. · Biomacromolecules · 2004 · 5 · 5410.1021/bm034197+ ↗
13. Endres P. J. · Bioconjugate Chem. · 2008 · 19 · 204910.1021/bc8002919 ↗
14. Laurent S. · Chem. Rev. · 2008 · 108 · 206410.1021/cr068445e ↗
15. Hu F. · Chem. Commun. · 2010 · 46 · 7310.1039/B916562B ↗
16. Cho S. J. · Nanotechnology · 2006 · 17 · 64010.1088/0957-4484/17/3/004 ↗
17. Huber M. M. · Bioconjugate Chem. · 1998 · 9 · 24210.1021/bc970153k ↗
18. Hooker J. M. · Nano Lett. · 2007 · 7 · 220710.1021/nl070512c ↗
19. Crich S. G. · Magn. Reson. Med. · 2004 · 51 · 93810.1002/mrm.20072 ↗
20. Brekke C. · NMR Biomed. · 2007 · 20 · 7710.1002/nbm.1077 ↗
21. Anderson E. A. · Nano Lett. · 2006 · 6 · 116010.1021/nl060378g ↗
22. Santra S. · Small · 2009 · 5 · 186210.1002/smll.200900389 ↗
23. Chen T. · ACS Nano · 2011 · 5 · 786610.1021/nn202073m ↗
24. Kim H. M. · ACS Nano · 2011 · 5 · 823010.1021/nn202912b ↗
25. Paquet C. · ACS Nano · 2011 · 5 · 310410.1021/nn2002272 ↗
26. Poselt E. · ACS Nano · 2012 · 6 · 161910.1021/nn204591r ↗
27. Tromsdorf U. I. · Nano Lett. · 2007 · 7 · 242210.1021/nl071099b ↗
28. Tu C. · Biomaterials · 2011 · 32 · 720910.1016/j.biomaterials.2011.06.026 ↗
29. Bae K. H. · Bioconjugate Chem. · 2010 · 21 · 50510.1021/bc900424u ↗
30. Bull S. R. · Nano Lett. · 2005 · 5 · 110.1021/nl0484898 ↗
31. Bull S. R. · Bioconjugate Chem. · 2005 · 16 · 134310.1021/bc050153h ↗
32. Datta A. · J. Am. Chem. Soc. · 2008 · 130 · 254610.1021/ja0765363 ↗
33. Drake P. · J. Mater. Chem. · 2007 · 17 · 491410.1039/b711962c ↗
34. Pan D. · J. Am. Chem. Soc. · 2008 · 130 · 918610.1021/ja801482d ↗
35. Song Y. · J. Am. Chem. Soc. · 2008 · 130 · 666210.1021/ja0777990 ↗
36. Song Y. · Angew. Chem., Int. Ed. · 2009 · 48 · 914310.1002/anie.200904666 ↗
37. Cheng Z. · Angew. Chem., Int. Ed. · 2010 · 49 · 34610.1002/anie.200905133 ↗
38. Cheng Z. L. · Adv. Funct. Mater. · 2009 · 19 · 375310.1002/adfm.200901253 ↗
39. Allen M. J. · Chem. Biol. · 2004 · 11 · 30110.1016/j.chembiol.2004.03.003 ↗
40. Manus L. M. · Nano Lett. · 2010 · 10 · 48410.1021/nl903264h ↗
41. Mastarone D. J. · J. Am. Chem. Soc. · 2011 · 133 · 532910.1021/ja1099616 ↗
42. Major J. L. · Acc. Chem. Res. · 2009 · 42 · 89310.1021/ar800245h ↗
43. Kalman F. K. · Inorg. Chem. · 2007 · 46 · 526010.1021/ic0702926 ↗
44. Duimstra J. A. · J. Am. Chem. Soc. · 2005 · 127 · 1284710.1021/ja042162r ↗
45. Caravan P. · J. Am. Chem. Soc. · 2002 · 124 · 315210.1021/ja017168k ↗
46. Caravan P. · Chem. Soc. Rev. · 2006 · 35 · 51210.1039/b510982p ↗
47. Aime S. · Acc. Chem. Res. · 2009 · 42 · 82210.1021/ar800192p ↗
48. Tu C. · Annu. Biomed. Eng. · 2011 · 39 · 133510.1007/s10439-011-0270-0 ↗
49. Major J. L. · Proc. Natl. Acad. Sci. U.S.A. · 2007 · 104 · 1388110.1073/pnas.0706247104 ↗
50. Zhang X. A. · Proc. Natl. Acad. Sci. U.S.A. · 2007 · 104 · 1078010.1073/pnas.0702393104 ↗
51. Louie A. Y. · Nat. Biotechnol. · 2000 · 18 · 32110.1038/73780 ↗
52. Urbanczyk-Pearson L. M. · Nat. Protoc. · 2008 · 3 · 34110.1038/nprot.2007.529 ↗
53. Frullano L. · Inorg. Chem. · 2006 · 45 · 848910.1021/ic0612045 ↗
54. Lee J. · Chem. Biol. · 2007 · 14 · 82410.1016/j.chembiol.2007.06.006 ↗
55. Yang H. · Biomaterials · 2011 · 32 · 458410.1016/j.biomaterials.2011.03.018 ↗
56. Perez J. M. · Nat. Biotechnol. · 2002 · 20 · 81610.1038/nbt720 ↗
57. Kaittanis C. · PloS One · 2012 · 7 · e3532610.1371/journal.pone.0035326 ↗
58. Kaittanis C. · J. Am. Chem. Soc. · 2009 · 131 · 1278010.1021/ja9041077 ↗
59. Kaittanis C. · J. Am. Chem. Soc. · 2011 · 133 · 366810.1021/ja1109584 ↗
60. Haun J. B. · Sci. Trans. Med. · 2011 · 3 · 71ra16
61. Asati A. · Angew. Chem., Int. Ed. · 2009 · 48 · 230810.1002/anie.200805279 ↗
62. Asati A. · ACS Nano · 2010 · 4 · 532110.1021/nn100816s ↗
63. Santra S. · Langmuir · 2010 · 26 · 536410.1021/la9037843 ↗
64. Lattuada L. · Tetrahedron Lett. · 2003 · 44 · 389310.1016/S0040-4039(03)00829-3 ↗
65. Weinmann H. J. · Am. J. Roentgenol. · 1984 · 142 · 61910.2214/ajr.142.3.619 ↗
66. McCarthy J. R. · Nano Lett. · 2005 · 5 · 255210.1021/nl0519229 ↗
67. Sun E. Y. · Mol. Imaging · 2006 · 5 · 122
68. Perez J. M. · Small · 2008 · 4 · 55210.1002/smll.200700824 ↗