Tunable, Metal-Loaded Polydopamine Nanoparticles Analyzed by Magnetometry

Chemistry of Materials

Volumn 29, Issue 19, 2017, Pages 8195-8201

  Wang, Zhao ^a,b   Xie, Yijun ^a   Li, Yiwen ^d   Huang, Yuran ^a   Parent, Lucas R ^a,b,c   Ditri, Treffly ^a   Zang, Nanzhi ^a,b   Rinehart, Jeffrey D ^a   Gianneschi, Nathan C ^a,b,c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

^c Northwestern University   (United States)

^d SICHUAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; COBALT COMPOUNDS; COPPER; ELECTRONIC STRUCTURE; IRON COMPOUNDS; MAGNETIC COUPLINGS; MAGNETOMETERS; MAGNETOMETRY; METAL NANOPARTICLES; NANOPARTICLES; NEUROPHYSIOLOGY; NICKEL; ZINC COMPOUNDS;

DOPING RANGE; ELECTRONIC INTERACTIONS; HIGH SPINS; LOW ANISOTROPY; MAGNETOMETRY MEASUREMENTS; PARTICLE MORPHOLOGIES; POLYDOPAMINE; PREDICTIVE ABILITIES;

MANGANESE;

EID: 85031026875     PISSN: 08974756     EISSN: 15205002     Source Type: Journal    
DOI: 10.1021/acs.chemmater.7b02262     Document Type: Article

References (40)

1. Simon, J. D.; Peles, D. N. The Red and the Black Acc. Chem. Res. 2010, 43, 1452-1460 10.1021/ar100079y
2. Meredith, P.; Sarna, T. The physical and chemical properties of eumelanin Pigm. Cell Res. 2006, 19, 572-594 10.1111/j.1600-0749.2006.00345.x
3. Simon, J. D. Spectroscopic and Dynamic Studies of the Epidermal Chromophores trans-Urocanic Acid and Eumelanin Acc. Chem. Res. 2000, 33, 307-313 10.1021/ar970250t
4. Paris, I.; Martinez-Alvarado, P.; Perez-Pastene, C.; Vieira, M. N. N.; Olea-Azar, C.; Raisman-Vozari, R.; Cardenas, S.; Graumann, R.; Caviedes, P.; Segura-Aguilar, J. Monoamine transporter inhibitors and norepinephrine reduce dopamine-dependent iron toxicity in cells derived from the substantia nigra J. Neurochem. 2005, 92, 1021-1032 10.1111/j.1471-4159.2004.02931.x
5. Xiao, M.; Li, Y.; Zhao, J.; Wang, Z.; Gao, M.; Gianneschi, N. C.; Dhinojwala, A.; Shawkey, M. D. Stimuli-Responsive Structurally Colored Films from Bioinspired Synthetic Melanin Nanoparticles Chem. Mater. 2016, 28, 5516-5521 10.1021/acs.chemmater.6b02127
6. Xiao, M.; Li, Y.; Allen, M. C.; Deheyn, D. D.; Yue, X.; Zhao, J.; Gianneschi, N. C.; Shawkey, M. D.; Dhinojwala, A. Bio-Inspired Structural Colors Produced via Self-Assembly of Synthetic Melanin Nanoparticles ACS Nano 2015, 9, 5454-5460 10.1021/acsnano.5b01298
7. 1-Weighted Magnetic Resonance Imaging Biomacromolecules 2013, 14, 3491-3497 10.1021/bm4008138
8. Lee, B. P.; Messersmith, P. B.; Israelachvili, J. N.; Waite, J. H. Mussel-Inspired Adhesives and Coatings Annu. Rev. Mater. Res. 2011, 41, 99-132 10.1146/annurev-matsci-062910-100429
9. Zhou, D.; Yang, L.; Yu, L.; Kong, J.; Yao, X.; Liu, W.; Xu, Z.; Lu, X. Fe/N/C hollow nanospheres by Fe(iii)-dopamine complexation-assisted one-pot doping as nonprecious-metal electrocatalysts for oxygen reduction Nanoscale 2015, 7, 1501-1509 10.1039/C4NR06366J
10. Ai, K.; Liu, Y.; Ruan, C.; Lu, L.; Lu, G. Sp2 C-Dominant N-Doped Carbon Sub-micrometer Spheres with a Tunable Size: A Versatile Platform for Highly Efficient Oxygen-Reduction Catalysts Adv. Mater. 2013, 25, 998-1003 10.1002/adma.201203923
11. Yao, X.; Zhao, C.; Kong, J.; Wu, H.; Zhou, D.; Lu, X. Dopamine-assisted one-pot synthesis of zinc ferrite-embedded porous carbon nanospheres for ultrafast and stable lithium ion batteries Chem. Commun. 2014, 50, 14597-14600 10.1039/C4CC07350A
12. Liu, Y.; Ai, K.; Lu, L. Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields Chem. Rev. 2014, 114, 5057-5115 10.1021/cr400407a
13. Miao, Z.-H.; Wang, H.; Yang, H.; Li, Z.-L.; Zhen, L.; Xu, C.-Y. Intrinsically Mn2+-Chelated Polydopamine Nanoparticles for Simultaneous Magnetic Resonance Imaging and Photothermal Ablation of Cancer Cells ACS Appl. Mater. Interfaces 2015, 7, 16946-16952 10.1021/acsami.5b06265
14. Li, Y.; Xie, Y.; Wang, Z.; Zang, N.; Carniato, F.; Huang, Y.; Andolina, C. M.; Parent, L. R.; Ditri, T. B.; Walter, E. D.; Botta, M.; Rinehart, J. D.; Gianneschi, N. C. Structure and Function of Iron-Loaded Synthetic Melanin ACS Nano 2016, 10, 10186-10194 10.1021/acsnano.6b05502
15. Ang, J. M.; Du, Y.; Tay, B. Y.; Zhao, C.; Kong, J.; Stubbs, L. P.; Lu, X. One-Pot Synthesis of Fe(III)-Polydopamine Complex Nanospheres: Morphological Evolution, Mechanism, and Application of the Carbonized Hybrid Nanospheres in Catalysis and Zn-Air Battery Langmuir 2016, 32, 9265-9275 10.1021/acs.langmuir.6b02331
16. Hong, L.; Simon, J. D. Current Understanding of the Binding Sites, Capacity, Affinity, and Biological Significance of Metals in Melanin J. Phys. Chem. B 2007, 111, 7938-7947 10.1021/jp071439h
17. Simpson, M. J.; Wilson, J. W.; Robles, F. E.; Dall, C. P.; Glass, K.; Simon, J. D.; Warren, W. S. Near-Infrared Excited State Dynamics of Melanins: The Effects of Iron Content, Photo-Damage, Chemical Oxidation, and Aggregate Size J. Phys. Chem. A 2014, 118, 993-1003 10.1021/jp4107475
18. Sever, M. J.; Wilker, J. J. Visible absorption spectra of metal-catecholate and metal-tironate complexes Dalton Trans. 2004, 1061-1072 10.1039/B315811J
19. Ejima, H.; Richardson, J. J.; Liang, K.; Best, J. P.; van Koeverden, M. P.; Such, G. K.; Cui, J.; Caruso, F. One-Step Assembly of Coordination Complexes for Versatile Film and Particle Engineering Science 2013, 341, 154-157 10.1126/science.1237265
20. Rahim, M. A.; Björnmalm, M.; Bertleff-Zieschang, N.; Besford, Q.; Mettu, S.; Suma, T.; Faria, M.; Caruso, F. Rust-Mediated Continuous Assembly of Metal-Phenolic Networks Adv. Mater. 2017, 29, 1606717 10.1002/adma.201606717
21. Rahim, M. A.; Björnmalm, M.; Suma, T.; Faria, M.; Ju, Y.; Kempe, K.; Müllner, M.; Ejima, H.; Stickland, A. D.; Caruso, F. Metal-Phenolic Supramolecular Gelation Angew. Chem., Int. Ed. 2016, 55, 13803-13807 10.1002/anie.201608413
22. Holten-Andersen, N.; Harrington, M. J.; Birkedal, H.; Lee, B. P.; Messersmith, P. B.; Lee, K. Y. C.; Waite, J. H. pH-induced metal-ligand cross-links inspired by mussel yield self-healing polymer networks with near-covalent elastic moduli Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 2651-2655 10.1073/pnas.1015862108
23. Srivastava, T. N.; Mohan, G. Complex Compounds of Ga(III) and In(III) with Catechol Z. Anorg. Allg. Chem. 1970, 379, 82-87 10.1002/zaac.19703790115
24. Freeman, G. E.; Raymond, K. N. Specific sequestering agents for the actinides. 12. Synthetic and structural chemistry of gadolinium and holmium catecholates Inorg. Chem. 1985, 24, 1410-1417 10.1021/ic00203a029
25. Charkoudian, L. K.; Franz, K. J. Fe(III)-Coordination Properties of Neuromelanin Components: 5,6-Dihydroxyindole and 5,6-Dihydroxyindole-2-carboxylic Acid Inorg. Chem. 2006, 45, 3657-3664 10.1021/ic060014r
26. Hider, R. C.; Kong, X. Chemistry and biology of siderophores Nat. Prod. Rep. 2010, 27, 637-657 10.1039/b906679a
27. Ho, C.-C.; Ding, S.-J. The pH-controlled nanoparticles size of polydopamine for anti-cancer drug delivery J. Mater. Sci.: Mater. Med. 2013, 24, 2381-2390 10.1007/s10856-013-4994-2
28. Hong, S.; Na, Y. S.; Choi, S.; Song, I. T.; Kim, W. Y.; Lee, H. Non-Covalent Self-Assembly and Covalent Polymerization Co-Contribute to Polydopamine Formation Adv. Funct. Mater. 2012, 22, 4711-4717 10.1002/adfm.201201156
29. Dreyer, D. R.; Miller, D. J.; Freeman, B. D.; Paul, D. R.; Bielawski, C. W. Elucidating the Structure of Poly(dopamine) Langmuir 2012, 28, 6428-6435 10.1021/la204831b
30. Ju, K.-Y.; Lee, Y.; Lee, S.; Park, S. B.; Lee, J.-K. Bioinspired Polymerization of Dopamine to Generate Melanin-Like Nanoparticles Having an Excellent Free-Radical-Scavenging Property Biomacromolecules 2011, 12, 625-632 10.1021/bm101281b
31. Ball, V.; Frari, D. D.; Toniazzo, V.; Ruch, D. Kinetics of polydopamine film deposition as a function of pH and dopamine concentration: Insights in the polydopamine deposition mechanism J. Colloid Interface Sci. 2012, 386, 366-372 10.1016/j.jcis.2012.07.030
32. Estelrich, J.; Sánchez-Martín, M. J.; Busquets, M. A. Nanoparticles in magnetic resonance imaging: from simple to dual contrast agents Int. J. Nanomed. 2015, 10, 1727 10.2147/IJN.S76501
33. Brückner, C.; Caulder, D. L.; Raymond, K. N. Preparation and Structural Characterization of Nickel(II) Catecholates Inorg. Chem. 1998, 37, 6759-6764 10.1021/ic980620p
34. 2O, a Catecholato-Bridged Dimer of Iron(III) Inorg. Chem. 1996, 35, 3568-3576 10.1021/ic950499b
35. Gorun, S. M.; Lippard, S. J. Magnetostructural correlations in magnetically coupled (.mu.-oxo)diiron(III) complexes Inorg. Chem. 1991, 30, 1625-1630 10.1021/ic00007a038
36. Taylor, S. W.; Chase, D. B.; Emptage, M. H.; Nelson, M. J.; Waite, J. H. Ferric Ion Complexes of a DOPA-Containing Adhesive Protein from Mytilus edulis Inorg. Chem. 1996, 35, 7572-7577 10.1021/ic960514s
37. Huang, J.; Xie, J.; Chen, K.; Bu, L.; Lee, S.; Cheng, Z.; Li, X.; Chen, X. HSA coated MnO nanoparticles with prominent MRI contrast for tumor imaging Chem. Commun. 2010, 46, 6684-6686 10.1039/c0cc01041c
38. Kim, T.; Momin, E.; Choi, J.; Yuan, K.; Zaidi, H.; Kim, J.; Park, M.; Lee, N.; McMahon, M. T.; Quinones-Hinojosa, A.; Bulte, J. W. M.; Hyeon, T.; Gilad, A. A. Mesoporous Silica-Coated Hollow Manganese Oxide Nanoparticles as Positive T1 Contrast Agents for Labeling and MRI Tracking of Adipose-Derived Mesenchymal Stem Cells J. Am. Chem. Soc. 2011, 133, 2955-2961 10.1021/ja1084095
39. Bjørnerud, A. The Physics of Magnetic Resonance Imaging; FYS-KJM 4740 Lecture Notes; University of Oslo: Oslo, Norway, 2008.
40. Kim, B. H.; Lee, N.; Kim, H.; An, K.; Park, Y. I.; Choi, Y.; Shin, K.; Lee, Y.; Kwon, S. G.; Na, H. B.; Park, J.-G.; Ahn, T.-Y.; Kim, Y.-W.; Moon, W. K.; Choi, S. H.; Hyeon, T. Large-Scale Synthesis of Uniform and Extremely Small-Sized Iron Oxide Nanoparticles for High-Resolution T1Magnetic Resonance Imaging Contrast Agents J. Am. Chem. Soc. 2011, 133, 12624-12631 10.1021/ja203340u