References
- Ball, V. 2017. Composite materials and films based on melanins, polydopamine, and other catecholamine-based materials. Biomimetics 2 (4):12. doi:10.3390/biomimetics2030012.
- Barclay, T. G., H. M. Hegab, S. R. Clarke, and M. Ginic-Markovic. 2017. Versatile surface modification using polydopamine and related polycatecholamines: Chemistry, structure, and applications. Advanced Materials Interfaces 4 (19):1601192. doi:10.1002/admi.201601192.
- Circu, M., and C. Filip. 2018. Closer to the polydopamine structure: New insights from a combined 13C/1H/2H solid-state NMR study on deuterated samples. Polymer Chemistry 9 (24):3379–87. doi:10.1039/C8PY00633D.
- Dhanak, D., S. D. Knight, and G. L. Warren. pub. date: 1. Apr. 2004. Urotensin-LL Receptor Antagonists. Patent US 2004/0063757 A1.
- Dreyer, D. R., D. J. Miller, B. D. Freeman, D. R. Paul, and C. W. Bielawski. 2013. Perspectives on poly(dopamine). Chemical Science 4 (10):3796–802. doi:10.1039/c3sc51501j.
- Kaupp, G., M. R. Naimi-Jamal, and J. Schmeyers. 2003. Solvent-free Knoevenagel condensations and Michael additions in the solid state and in the melt with quantitative yield. Tetrahedron 59 (21):3753–60. doi:10.1016/S0040-4020(03)00554-4.
- Kharas, G. B., B. L. Hill, V. M. Gaizutis, I. T. Garcia, L. Gutierrez, M. E. Huddle, M. S. Jalili, N. W. Nlandu, K. H. Nymerg, J. S. Yonan, et al. 2013. Novel copolymers of styrene. 3. Oxy Ring-disubstituted 2-cyano-3-phenyl-2-propenamides. Journal of Macromolecular Science, Part A 50 (6):575–80. doi:10.1080/10601325.2013.784166.
- Kurhanewicz, J. D. B., J. H. Vigneron, J. A. Ardenkjaer-Larsen, K. Bankson, C. H. Brindle, F. A. Cunningham, K. R. Gallagher, A. Keshari, C. Kjaer, D. A. Laustsen, et al. 2019. Hyperpolarized 13C MRI: Path to clinical translation in oncology. Neoplasia (New York, NY) 21 (1):1–16. doi:10.1016/j.neo.2018.09.006.
- Lee, H., S. M. Dellatore, W. M. Miller, and P. B. Messersmith. 2007. Mussel-inspired surface chemistry for multifunctional coatings. Science (New York, NY) 318 (5849):426–30. doi:10.1126/science.1147241.
- Li, Q., Z. Dong, M. Chen, and L. Feng. 2021. Phenolic molecules constructed nanomedicine for inovative cancer treatment. Coordination Chemistry Reviews 439:213912. doi:10.1016/j.ccr.2021.213912.
- Liebscher, J. 2019. Chemistry of polydopamine – Scope, variation and limitation. European Journal of Organic Chemistry 31–32:4976–94.
- Liu, X., Z. Xie, W. Shi, Z. He, Y. Liu, H. Su, Y. Sun, and D. Ge. 2019. Polynorepinephrine nanoparticles: A novel photothermal nanoagent for chemo-photothermal cancer therapy. ACS Applied Materials & Interfaces 11 (22):19763–73. doi:10.1021/acsami.9b03458.
- Lyu, Q., N. Hsueh, and C. L. L. Chai. 2019. Unravelling the polydopamine mystery: Is the end in sight? Polymer Chemistry 10 (42):5771–7. doi:10.1039/C9PY01372E.
- Mabuchi, M., J. Shimada, K. Okamoto, Y. Kawakami, S. Fujita, and K. Matsushige. 2001. Time-resolved fluorescence spectroscopy of dopamine in the single cells. Advances in Fluorescence Sensing Technology V. Proceedings 4252:140–8.
- Mee, S. P. H., V. Lee, J. E. Baldwin, and A. Cowley. 2004. Total synthesis of 5,50,6,60-tetrahydroxy-3,30-biindolyl, the proposed structure of a potent antioxidant found in beetroot (Beta vulgaris). Tetrahedron 60 (16):3695–712. doi:10.1016/j.tet.2004.02.043.
- Ouwerkerk, N., J. van Boom, J. Lugtenburg, and J. Raap. 2002. Synthesis of [1′,2′,5′,2-13C4]-2′-Deoxy-D-adenosine by a Chemoenzymatic Strategy to Enable Labelling of Any of the 215 Carbon-13 and Nitrogen-15 Isotopomers. European Journal of Organic Chemistry 14:2356–62.
- Samala, G., P. B. Devi, R. Nallangi, J. P. Sridevi, S. Saxena, P. Yogeeswar, and D. Sriram. 2014. Development of novel tetrahydrothieno[2,3-c]pyridine-3-carboxamide based Mycobacterium tuberculosispantothenate synthetase inhibitors: Molecular hybridization from known antimycobacterialleads. Bioorganic & Medicinal Chemistry 22 (6):1938–47. doi:10.1016/j.bmc.2014.01.030.
- Ueki, R. K., H. Yamaguchi, S. Nonaka, and A. Sando. 2012. 1H NMR probe for in situ monitoring of dopamine metabolism and its application to inhibitor screening. Journal of the American Chemical Society 134 (30):12398–401. − doi:10.1021/ja305051u.
- Wang, H., Y. Sun, and B. Tang. 2002. Study on fluorescence property of dopamine and determination of dopamine by fluorimetry. Talanta 57 (5):899–907. doi:10.1016/S0039-9140(02)00123-6.
- Wunderlich, C. H., R. Spitzer, T. Santner, K. Fauster, M. Tollinger, and C. Kreutz. 2012. Synthesis of (6-(13)C)pyrimidine nucleotides as spin-labels for RNA dynamics. Journal of the American Chemical Society 134 (17):7558–69. doi:10.1021/ja302148g.
- Xiao, M., M. D. Shawkey, and A. Dhinojwala. 2020. Bioinspired melanin-based optically active materials. Advanced Optical Materials 8 (19):2000932. doi:10.1002/adom.202000932.
- Xie, W. E., Y. Pakdel, Y. Liang, Y. J. Kim, D. Liu, L. Sun, and X. Wang. 2019. Natural eumelanin and its derivatives as multifunctional materials for bioinspired applications: A review. Biomacromolecules 20 (12):4312–31. − doi:10.1021/acs.biomac.9b01413.
- Yamada, H., T. Kameda, Y. Kimura, H. Imai, H. Matsuda, S. Sando, A. Toshimitsu, Y. Aoyama, and T. Kondo. 2016. (13)C/(15)N-Enriched l-Dopa as a triple-resonance NMR probe to monitor neurotransmitter dopamine in the brain and liver extracts of mice. ChemistryOpen 5 (2):125–8. doi:10.1002/open.201500196.
- Zhang, X., S. Wang, L. Xu, L. Feng, Y. Ji, L. Tao, S. Li, and Y. Wei. 2012. Biocompatible polydopamine fluorescent organic nanoparticles: Facile preparation and cell imaging. Nanoscale 4 (18):5581–4. doi:10.1039/c2nr31281f.