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http://dx.doi.org/10.17702/jai.2018.19.3.123

Beyond Mussel-inspired Polydopamice Coatings: Derivatives of Catecholamines  

Lee, Haesung A. (Department of chemistry, KAIST)
LEE, Haeshin (Department of chemistry, KAIST)
Publication Information
Journal of Adhesion and Interface / v.19, no.3, 2018 , pp. 123-128 More about this Journal
Abstract
As a mussel-inspired surface independent modification chemistry using catecholamine family molecule was suggested on 2007, there are tremendous efforts being done by researchers from around the world to adjust and develop diverse applications using catecholamine family. Accordingly, we will discuss about the novel method to extend catecholamine applications, which is through the functional group substitution of catecholamine molecules.
Keywords
Polydopamine; catechol derivatives; dopamine derivatives; mussel; surface;
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1 J. H. Waite, Integr. Comp. Biol., 42, 1172, (2002).   DOI
2 H. G. Silverman, and F. F. Roberto, Mar. Biotechnol., 9, 661, (2007).   DOI
3 H. Lee, N. F. Scherer, and P. B. Messersmith, Proc. Natl. Acad. Sci. U. S. A., 103, 12999, (2006).   DOI
4 H. Lee, S. M. Dellatore, M. W. Miller and P. B. Messersmith, Science, 318, 426, (2007).   DOI
5 M. E. Rice, B. Moghaddam, Anal. Chem., 59, 1534-1538, (1987).   DOI
6 L. G. -Fernandez, J. Cui, C. Serrano, Z. Shafiq, R. A. Gropeanu, V. S. Miguel, J. I. Ramos, M. Wang, G. K. Auernhammer, S. Ritz, A. A. Golriz, R. Berger, M. Wagner, A. del Campo, Adv. Mater., 225, 529-533, (2013).
7 J. I. Paez, O. Ustahuseyin, C. Serrano, X. -A. Ton, Z. Shafiq, G. K. Auernhammer, M. d'Ischia, A. del Campo, Biomacromolecules, 16, 3811-3818, (2015).   DOI
8 J. Cui, J. Iturri, J. Paez, Z. Shafiq, C. Serrano, M. d'Ischia, A. del Campo, Macromol. Chem. Phys., 215, 2403-2413, (2014).   DOI
9 N. F. D. Vecchia, R. Marega, M. Ambrico, M. Iacomino, R. Micillo, A. Napolitano, D. Bonifazibe, M. d'Ischia, J. Mater. Chem. C, 3, 6525-6531, (2015).   DOI
10 R. Shevate, M. Kumar, M. Karunakaran, M. N. Hedhili, K. -V. Peinemann, J. Membr. Sci., 529, 185-194, (2017).   DOI
11 G. Kumar, T. Banerjee, N. Kapoor, N. Surolia, A. Surolia, IUBMB Life, 3, 204-213, (2010).
12 X. Ge, B. Wakim, D. S. Sem, J. Med. Chem., 51, 4571-4580, (2008).   DOI
13 C. Zingle, D. Tritsch, C. G.-Billiard, M. Rohmer, Bioorg. Med. Chem., 22, 3713-3719, (2014).   DOI
14 J. -K. Kim, H. A. Lee, H. Lee, H. J. Chung, Chem. Mater., 30, 1467-1471, (2018).   DOI