journal article·2018

Cyclotriphosphazene core-based dendrimers for biomedical applications: an update on recent advances

Le Wang, Yun-Xia Yang, Xiangyang Shi, Serge Mignani, Anne-Marie Caminade, Jean-Pierre Majoral

Publisher page

Abstract

This review is focused on the recent use of cyclotriphosphazene-based dendrimers in biomedicine. Since its synthesis for the first time in 1834, cyclotriphosphazene has been an important compound of phosphorus chemistry as a scaffold, and a large number of cyclotriphosphazene derivatives have been synthesized and applied in various fields such as biology, catalysis, fluorescence, nanomaterials, etc. Today, one of the most important uses concerns its biomedical applications. In this review, the recent developments (since 2012) of cyclotriphosphazene for major pharmaceutical applications are highlighted and analyzed.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Dendrimers and Hyperbranched Polymers · Lanthanide and Transition Metal Complexes · Luminescence and Fluorescent Materials

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

Affiliations

College of Chemistry and Chemical Engineering

Shanghai University of Engineering Science

Shanghai

China

College of Chemistry

Chemical Engineering and Biotechnology

Donghua University

CQM – Centro de Química da Madeira

MMRG

Universidade da Madeira

Campus da Penteada

9020-105 Funchal

Laboratoire de Chimie de Coordination (LCC)

CNRS

205, route de Narbonne

F-31077 Toulouse

France

Funding

Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China

References (64)

Show source-provided references
1. Allcock · Chem. Rev. · 1972 · 72 · 31510.1021/cr60278a002 ↗
2. Chandrasekhar · Appl. Organomet. Chem. · 1993 · 7 · 110.1002/aoc.590070102 ↗
3. Steiner · Coord. Chem. Rev. · 2002 · 227 · 19310.1016/S0010-8545(02)00012-7 ↗
4. Chandrasekhar · Coord. Chem. Rev. · 2007 · 251 · 104510.1016/j.ccr.2006.07.005 ↗
5. Xu · Polym. Adv. Technol. · 2017 · 28 · 138210.1002/pat.4015 ↗
6. Liang · Polym. Degrad. Stab. · 2017 · 135 · 14010.1016/j.polymdegradstab.2016.11.023 ↗
7. Chen · J. Appl. Polym. Sci. · 2016 · 134 · 4466010.1002/app.44660 ↗
8. Dagger · J. Power Sources · 2017 · 342 · 26610.1016/j.jpowsour.2016.12.007 ↗
9. Wen · Ind. Eng. Chem. Res. · 2016 · 55 · 801810.1021/acs.iecr.6b01527 ↗
10. Jiménez · Chem. – Eur. J. · 2012 · 18 · 1680110.1002/chem.201202748 ↗
11. He · Macromolecules · 2012 · 45 · 793110.1021/ma3016745 ↗
12. Kobr · J. Org. Chem. · 2013 · 78 · 176810.1021/jo3009897 ↗
13. Çetindere · Dyes Pigm. · 2017 · 139 · 51710.1016/j.dyepig.2016.12.035 ↗
14. Çoşut · Dyes Pigm. · 2013 · 98 · 44210.1016/j.dyepig.2013.03.028 ↗
15. Kagit · Inorg. Chem. · 2014 · 53 · 214410.1021/ic402783x ↗
16. Biswal · New J. Chem. · 2017 · 41 · 411610.1039/C7NJ00136C ↗
17. Naik · Mater. Chem. Phys. · 2016 · 180 · 3810.1016/j.matchemphys.2016.05.020 ↗
18. Caminade · Coord. Chem. Rev. · 2016 · 308 · 47810.1016/j.ccr.2015.06.007 ↗
19. Caminade · Dalton Trans. · 2016 · 45 · 181010.1039/C5DT03047A ↗
20. Franc · J. Org. Chem. · 2007 · 72 · 870710.1021/jo701462f ↗
21. Rao · Inorg. Chem. · 2010 · 49 · 1060610.1021/ic1016092 ↗
22. Mignani · Chem. Rev. · 2014 · 114 · 132710.1021/cr400362r ↗
23. Mukundam · J. Mater. Chem. C · 2016 · 4 · 352310.1039/C6TC00909C ↗
24. Allcock · Polym. Chem. · 2012 · 3 · 57810.1039/C1PY00468A ↗
25. Tinkle · Ann. N. Y. Acad. Sci. · 2014 · 1313 · 3510.1111/nyas.12403 ↗
26. Mignani · Prog. Polym. Sci. · 2013 · 38 · 99310.1016/j.progpolymsci.2013.03.003 ↗
27. El Brahmi · Nanoscale · 2015 · 7 · 391510.1039/C4NR05983B ↗
28. Solassol · J. Gen. Virol. · 2004 · 85 · 179110.1099/vir.0.19726-0 ↗
29. Lazniewska · Mol. Pharmaceutics · 2013 · 10 · 348410.1021/mp4003255 ↗
30. Loup · Chem. – Eur. J. · 1999 · 5 · 364410.1002/(SICI)1521-3765(19991203)5:12<3644::AID-CHEM3644>3.0.CO;2-I ↗
31. Hayder · Sci. Transl. Med. · 2011 · 3 · 81ra3510.1126/scitranslmed.3002212 ↗
32. Caminade · Chem. Commun. · 2017 · 53 · 983010.1039/C7CC04949H ↗
33. N. Howlader , A. M.Noone , M.Krapcho , D.Miller , K.Bishop , C. L.Kosary , M.Yu , J.Ruhl , Z.Tatalovich , A.Mariotto , D. R.Lewis , H. S.Chen , E. J.Feuer and K. A.Cronin , SEER Cancer Statistics Review, National Cancer Institute. Bethesda, MD, 1975–2014
34. Hare · Adv. Drug Delivery Rev. · 2017 · 108 · 2510.1016/j.addr.2016.04.025 ↗
35. Davies · Science · 1994 · 264 · 37510.1126/science.8153624 ↗
36. Görgülü · J. Mol. Struct. · 2015 · 1087 · 110.1016/j.molstruc.2015.01.033 ↗
37. El Brahmi · Mol. Pharmaceutics. · 2013 · 10 · 145910.1021/mp4000184 ↗
38. Wasiak · Mol. Pharmaceutics · 2012 · 9 · 45810.1021/mp2005627 ↗
39. Patel · J. Antimicrob. Chemother. · 2009 · 64 · 26710.1093/jac/dkp203 ↗
40. Davies · Microbiol. Mol. Biol. Rev. · 2010 · 74 · 41710.1128/MMBR.00016-10 ↗
41. Li · Bioorg. Med. Chem. · 2011 · 19 · 441310.1016/j.bmc.2011.06.049 ↗
42. Ahamad · Middle East J. Cancer · 2012 · 15 · 476
43. Koran · Res. Chem. Intermed. · 2013 · 39 · 110910.1007/s11164-012-0670-2 ↗
44. Asmafiliz · New J. Chem. · 2016 · 40 · 960910.1039/C6NJ02052F ↗
45. Allkock · Biomaterials · 1992 · 13 · 85710.1016/0142-9612(92)90179-R ↗
46. Mignani · Prog. Polym. Sci. · 2017 · 64 · 2310.1016/j.progpolymsci.2016.09.006 ↗
47. Kuo · J. Controlled Release · 2007 · 120 · 5110.1016/j.jconrel.2007.03.019 ↗
48. World Health Orgnization (WHO), Global Tuberculosis Report. WHO/HTM/TB/2014.08, WHO, Geneva, Switzerland, 2014
49. Costa-Gouveia · Drug Discovery Today · 2017 · 22 · 60010.1016/j.drudis.2017.01.011 ↗
50. Blattes · Proc. Natl. Acad. Sci. U. S. A. · 2013 · 110 · 879510.1073/pnas.1221708110 ↗
51. Caminade · Nat. Commun. · 2015 · 6 · 772210.1038/ncomms8722 ↗
52. de Jong · New J. Chem. · 2015 · 39 · 719410.1039/C5NJ00620A ↗
53. Wang · Phosphorus, Sulfur Silicon Relat. Elem. · 2013 · 188 · 5410.1080/10426507.2012.741159 ↗
54. Le · Eur. J. Inorg. Chem. · 2011 · 674
55. Zhu · Chemistry · 2014 · 20 · 1450710.1002/chem.201403883 ↗
56. Servin · Inorg. Chim. Acta · 2018 · 470 · 10610.1016/j.ica.2017.04.044 ↗
57. Yuan · Theranostics · 2016 · 6 · 93010.7150/thno.14855 ↗
58. Morozowich · Macromolecules · 2011 · 44 · 135510.1021/ma1027406 ↗
59. Toti · J. Controlled Release · 2007 · 119 · 3410.1016/j.jconrel.2007.01.003 ↗
60. Sun · ACS Appl. Mater. Interfaces · 2015 · 7 · 499010.1021/acsami.5b00175 ↗
61. Wei · J. Mater. Chem. A · 2015 · 3 · 460410.1039/C4TA06828A ↗
62. Chang · Mater. Lett. · 2014 · 125 · 12810.1016/j.matlet.2014.03.137 ↗
63. Hu · Langmuir · 2013 · 29 · 915610.1021/la402119s ↗
64. Meng · Polym. Chem. · 2015 · 6 · 315510.1039/C5PY00196J ↗