Journal of Adhesion and Interface (접착 및 계면)

The Society of Adhesion and Interface, Korea (한국접착및계면학회)
권호 표지
DOI QR코드

DOI QR Code

Beyond Mussel-inspired Polydopamice Coatings: Derivatives of Catecholamines

카테콜아민의 화학치환: 홍합 모방 코팅 물질인 도파민을 넘어서

  • Received : 2018.08.29
  • Accepted : 2018.09.15
  • Published : 2018.09.30
Download PDF
⟨ Previous Next ⟩

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.

홍합족사 단백질을 모방한 카테콜아민 화합물을 통한 물질 무관 코팅방법이 2007년 본 연구진에 의해 발표 된 이래로, 이를 이용하고 발전시키고자 세계 유수의 연구진들이 다양한 방향으로 연구를 진행하고 있다. 이에 본 연구진은 본 지를 통해, 카테콜아민계 물질의 작용기 치환 방법을 통해 카테콜아민의 범용성을 확장시킨 사례들을 알아보고, 이를 통한 카테콜아민계 물질의 발전 가능성에 대해 기술해 보고자 한다.

Keywords

References

  1. J. H. Waite, Integr. Comp. Biol., 42, 1172, (2002). https://doi.org/10.1093/icb/42.6.1172
  2. H. G. Silverman, and F. F. Roberto, Mar. Biotechnol., 9, 661, (2007). https://doi.org/10.1007/s10126-007-9053-x
  3. H. Lee, N. F. Scherer, and P. B. Messersmith, Proc. Natl. Acad. Sci. U. S. A., 103, 12999, (2006). https://doi.org/10.1073/pnas.0605552103
  4. H. Lee, S. M. Dellatore, M. W. Miller and P. B. Messersmith, Science, 318, 426, (2007). https://doi.org/10.1126/science.1147241
  5. M. E. Rice, B. Moghaddam, Anal. Chem., 59, 1534-1538, (1987). https://doi.org/10.1021/ac00138a011
  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). https://doi.org/10.1021/acs.biomac.5b01126
  8. J. Cui, J. Iturri, J. Paez, Z. Shafiq, C. Serrano, M. d'Ischia, A. del Campo, Macromol. Chem. Phys., 215, 2403-2413, (2014). https://doi.org/10.1002/macp.201400366
  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). https://doi.org/10.1039/C5TC00672D
  10. R. Shevate, M. Kumar, M. Karunakaran, M. N. Hedhili, K. -V. Peinemann, J. Membr. Sci., 529, 185-194, (2017). https://doi.org/10.1016/j.memsci.2017.01.058
  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). https://doi.org/10.1021/jm8002284
  13. C. Zingle, D. Tritsch, C. G.-Billiard, M. Rohmer, Bioorg. Med. Chem., 22, 3713-3719, (2014). https://doi.org/10.1016/j.bmc.2014.05.004
  14. J. -K. Kim, H. A. Lee, H. Lee, H. J. Chung, Chem. Mater., 30, 1467-1471, (2018). https://doi.org/10.1021/acs.chemmater.7b05136