journal article·2013-10-22

Magnetic Nanobeads as Potential Contrast Agents for Magnetic Resonance Imaging

Michele H. Pablico-Lansigan, William J. Hickling, Emily A. Japp, Olga C. Rodriguez, Anup Ghosh, Chris Albanese, Maki Nishida, Edward Van Keuren, Stanley Fricke, Norman Dollahon, Sarah L. Stoll

ACS Nano· Volume 7· Issue 10
Publisher page

Abstract

Metal-oxo clusters have been used as building blocks to form hybrid nanomaterials and evaluated as potential MRI contrast agents. We have synthesized a biocompatible copolymer based on a water stable, nontoxic, mixed-metal-oxo cluster, Mn8Fe4O12(L)16(H2O)4, where L is acetate or vinyl benzoic acid, and styrene. The cluster alone was screened by NMR for relaxivity and was found to be a promising T2 contrast agent, with r1 = 2.3 mM(-1) s(-1) and r2 = 29.5 mM(-1) s(-1). Initial cell studies on two human prostate cancer cell lines, DU-145 and LNCap, reveal that the cluster has low cytotoxicity and may be potentially used in vivo. The metal-oxo cluster Mn8Fe4(VBA)16 (VBA = vinyl benzoic acid) can be copolymerized with styrene under miniemulsion conditions. Miniemulsion allows for the formation of nanometer-sized paramagnetic beads (~80 nm diameter), which were also evaluated as a contrast agent for MRI. These highly monodispersed, hybrid nanoparticles have enhanced properties, with the option for surface functionalization, making them a promising tool for biomedicine. Interestingly, both relaxivity measurements and MRI studies show that embedding the Mn8Fe4 core within a polymer matrix decreases r2 effects with little effect on r1, resulting in a positive T1 contrast enhancement.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Magnetism in coordination complexes · Nanoparticle-Based Drug Delivery

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

Affiliations

Department of Chemistry, Georgetown University, 37th and O Streets NW, Washington, D.C. 20057, United States

Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, D.C. 20057, United States

Department of Physics, Georgetown University, Washington, D.C. 20057, United States

Children’s National Medical Center, George Washington University, Washington, D.C. 20010, United States

Department of Biology, Villanova University, Villanova, Pennsylvania 19085, United States

References (70)

Show source-provided references
1. Strijkers G. · Anti-Cancer Agents Med. Chem. · 2007 · 7 · 29110.2174/187152007780618135 ↗
2. Caravan P. · Chem. Rev. · 1999 · 99 · 229310.1021/cr980440x ↗
3. Pankhurst Q. A. · J. Phys. D: Appl. Phys. · 2003 · 36 · R16710.1088/0022-3727/36/13/201 ↗
4. Laurent S. · Chem. Rev. · 2008 · 108 · 206410.1021/cr068445e ↗
5. Chavhan G. B. · Radiographics · 2009 · 29 · 143310.1148/rg.295095034 ↗
6. Kowalewski J. · Prog. NMR Spectrosc. · 1984 · 17 · 14110.1016/0079-6565(85)80007-8 ↗
7. Lowe M. P. · Aust. J. Chem. · 2002 · 55 · 55110.1071/CH02172 ↗
8. Wolff S. · Magn. Reson. Med. · 1989 · 10 · 13510.1002/mrm.1910100113 ↗
9. Saritas E. U. · J. Magn. Reson. · 2013 · 229 · 11610.1016/j.jmr.2012.11.029 ↗
10. Manjunath V. · Clin. Nephrol. · 2011 · 75 · 27910.5414/CNP75279 ↗
11. Weinreb J. C. · J. Magn. Reson. Imaging · 2009 · 30 · 123610.1002/jmri.21979 ↗
12. Sadowski E. A. · Radiology · 2007 · 243 · 14810.1148/radiol.2431062144 ↗
13. Kuo P. H. · Radiology · 2007 · 242 · 64710.1148/radiol.2423061640 ↗
14. Serkan K. · Appl. Geochem. · 2011 · 26 · 187710.1016/j.apgeochem.2011.06.011 ↗
15. Kümmerer K. · Environ. Sci. Technol. · 2000 · 34 · 57310.1021/es990633h ↗
16. Liu Y. · Med. Res. Rev. · 2010 · 33 · 310.1002/med.20233 ↗
17. Liu Y. · Biomaterials · 2011 · 32 · 516710.1016/j.biomaterials.2011.03.077 ↗
18. Liong M. · ACS Nano · 2008 · 2 · 88910.1021/nn800072t ↗
19. Holzapfel V. · J. Phys.: Condens. Matter · 2006 · 18 · S2581
20. Hong G. · Biomed. Microdevices · 2008 · 10 · 69310.1007/s10544-008-9180-9 ↗
21. Shapiro E. M. · Magn. Reson. Med. · 2005 · 53 · 32910.1002/mrm.20342 ↗
22. Shapiro E. M. · Proc. Natl. Acad. Sci. U. S. A. · 2004 · 101 · 1090110.1073/pnas.0403918101 ↗
23. Rodriguez O. · Cell Cycle · 2006 · 5 · 11310.4161/cc.5.1.2295 ↗
24. Tassa C. · Acc. Chem. Res. · 2011 · 44 · 84210.1021/ar200084x ↗
25. Koretsky A. P. · NMR Biomed. · 2004 · 17 · 52710.1002/nbm.940 ↗
26. Pan D. · Tetrahedron · 2011 · 67 · 843110.1016/j.tet.2011.07.076 ↗
27. Pan D. · WIREs Nanomed. Nanobiotechnol. · 2010 · 3 · 16210.1002/wnan.116 ↗
28. Kueny-Stotz M. · Eur. J. Inorg. Chem. · 2012 · 198710.1002/ejic.201101163 ↗
29. Drahoš B. · Eur. J. Inorg. Chem. · 2012 · 197510.1002/ejic.201101336 ↗
30. Lauterbur P. · Nature · 2004 · 1
31. Bryant L. H. · Inorg. Chem. · 1999 · 38 · 100210.1021/ic981197n ↗
32. Krause, W.Contrast Agents I, Magnetic Resonance Imaging;Springer-Verlag:New York, 2002; p165.
33. Federle M. · J. Magn. Reson. Imaging · 2000 · 12 · 68910.1002/1522-2586(200011)12:5<689::AID-JMRI5>3.0.CO;2-Z ↗
34. Troughton J. S. · Inorg. Chem. · 2004 · 43 · 631310.1021/ic049559g ↗
35. Hernandez G. · Bioconjugate Chem. · 2001 · 1
36. Niesman M. · Invest. Radiol. · 1990 · 25 · 54510.1097/00004424-199005000-00012 ↗
37. Taylor K. M. L. · J. Am. Chem. Soc. · 2008 · 130 · 1435810.1021/ja803777x ↗
38. Li Z. · J. Inorg. Biochem. · 2007 · 101 · 103610.1016/j.jinorgbio.2007.04.003 ↗
39. Na H. B. · Angew. Chem., Int. Ed. Engl. · 2007 · 46 · 539710.1002/anie.200604775 ↗
40. Bennewitz M. F. · ACS Nano · 2011 · 5 · 343810.1021/nn1019779 ↗
41. Cersosimo M. G. · Neurotoxicology · 2006 · 27 · 34010.1016/j.neuro.2005.10.006 ↗
42. Cage B. · Polyhedron · 2007 · 26 · 241310.1016/j.poly.2006.12.009 ↗
43. Isaacman S. · Polyhedron · 2005 · 24 · 269110.1016/j.poly.2005.03.138 ↗
44. Steckel J. S. · Nano Lett. · 2004 · 4 · 39910.1021/nl0343553 ↗
45. Mertzman J. E. · Chem. Commun. · 2009 · 78810.1039/b815424d ↗
46. Wang Y. · Chem. Commun. · 2011 · 47 · 354110.1039/c0cc03758c ↗
47. Schake A. · Inorg. Chem. · 1994 · 33 · 602010.1021/ic00104a009 ↗
48. Pablico M. H. · Langmuir · 2011 · 27 · 1257510.1021/la2029774 ↗
49. Derfus A. M. · Nano Lett. · 2004 · 4 · 1110.1021/nl0347334 ↗
50. Li H. · Macromol. Rapid Commun. · 2008 · 29 · 43110.1002/marc.200700702 ↗
51. Landfester K. · J. Polym. Sci., Part A: Polym. Chem. · 2010 · 48 · 49310.1002/pola.23786 ↗
52. Palacio F. · J. Mater. Chem. · 2004 · 14 · 187310.1039/B400590B ↗
53. Willemin S. · New J. Chem. · 2004 · 28 · 91910.1039/B402080D ↗
54. Elizondo G. · Radiology · 1991 · 178 · 7310.1148/radiology.178.1.1898538 ↗
55. Rodríguez E. · NMR Biomed. · 2005 · 18 · 30010.1002/nbm.959 ↗
56. Gupta A. K. · Biomaterials · 2005 · 26 · 399510.1016/j.biomaterials.2004.10.012 ↗
57. Tromsdorf U. I. · Nano Lett. · 2007 · 7 · 242210.1021/nl071099b ↗
58. Jun Y.-W. · Acc. Chem. Res. · 2008 · 41 · 17910.1021/ar700121f ↗
59. Jun Y.-W. · Angew. Chem., Int. Ed. · 2008 · 47 · 512210.1002/anie.200701674 ↗
60. Jun Y.-W. · J. Am. Chem. Soc. · 2005 · 127 · 573210.1021/ja0422155 ↗
61. Lee J. E.-H. · Nat. Med. · 2006 · 13 · 95
62. Duan H. · J. Phys. Chem. C · 2008 · 112 · 812710.1021/jp8029083 ↗
63. Vestal C. R. · J. Am. Chem. Soc. · 2003 · 125 · 982810.1021/ja035474n ↗
64. Di Marco M. · J. Am. Chem. Soc. · 2006 · 128 · 1005410.1021/ja061674y ↗
65. Kucheryavy P. · Langmuir · 2013 · 29 · 71010.1021/la3037007 ↗
66. Daou T. J. · Chem. Mater. · 2008 · 20 · 586910.1021/cm801405n ↗
67. Hu F. · Nanoscale · 2010 · 2 · 188410.1039/c0nr00173b ↗
68. LaConte L. E. W. · J. Magn. Reson. Imaging · 2007 · 26 · 163410.1002/jmri.21194 ↗
69. Marie E. · Colloids Surf., A · 2007 · 308 · 2510.1016/j.colsurfa.2007.05.025 ↗
70. Ladaviere C. · Colloid Polym. Sci. · 2007 · 285 · 62110.1007/s00396-006-1579-3 ↗