Dendrimers for drug delivery
Source abstract
Abstract
Due to their nanometric size, dendrimers have been considered as potentially suitable as new vehicles for drug delivery since their infancy. The association of a dendrimer and a drug may occur in different ways, either through covalent or non-covalent interactions. A non-covalent interaction can be the simple encapsulation inside dendrimers that enhances the solubility of lipophilic drugs in water, or electrostatic interactions between the surface and charged drugs (or DNA, RNA, or siRNA). The covalent association may occur through stable bonds, in particular for dendrimers that are considered as active per se, or through cleavable bonds that should be cleaved only when reaching the target (often cancerous cells). In addition, the full structure of the dendrimer can be disassembled under the influence of a trigger such as pH variations. This review will present these strategies and their consequences for drug delivery.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Dendrimers and Hyperbranched Polymers · RNA Interference and Gene Delivery · Synthesis and Characterization of Heterocyclic Compounds
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CNRS
LCC (Laboratoire de Chimie de Coordination)
F-31077 Toulouse Cedex 4, France
Université de Toulouse
UPS
References (100+)
Show source-provided references
1. Dendrimers. Towards Catalytic, Material and Biomedical Uses, ed. A. M. Caminade, C. O. Turrin, R. Laurent, A. Ouali and B. Delavaux-Nicot, John Wiley & Sons, Chichester (UK), 2011, p. 528
2. Tomalia · Polym. J. · 1985 · 17 · 11710.1295/polymj.17.117 ↗
3. Dendrimers in Biomedical Applications, ed. B. Klajnert, L. Peng and V. Cena, RSCPublishing, Cambridge, UK, 2013, p. 204
4. Lee · Nat. Biotechnol. · 2005 · 23 · 151710.1038/nbt1171 ↗
5. Menjoge · Drug Discovery Today · 2010 · 15 · 17110.1016/j.drudis.2010.01.009 ↗
6. Mintzer · Chem. Soc. Rev. · 2011 · 40 · 17310.1039/B901839P ↗
7. Rolland · New J. Chem. · 2009 · 33 · 180910.1039/b901054h ↗
8. Khandare · Chem. Soc. Rev. · 2012 · 41 · 282410.1039/C1CS15242D ↗
9. Oliveira · Prog. Polym. Sci. · 2010 · 35 · 116310.1016/j.progpolymsci.2010.04.006 ↗
10. Ottaviani · J. Am. Chem. Soc. · 1995 · 117 · 438710.1021/ja00120a022 ↗
11. Shiao · New J. Chem. · 2012 · 36 · 32410.1039/C2NJ20873C ↗
12. Dendrimer-based Drug Delivery Systems. From Theory to Practice, ed. Y. Cheng, John Wiley & Sons, Hoboken, NJ, USA, 2012, p. 514
13. D'Emanuele · Adv. Drug Delivery Rev. · 2005 · 57 · 214710.1016/j.addr.2005.09.012 ↗
14. Jain · Expert Opin. Drug Delivery · 2007 · 4 · 49510.1517/17425247.4.5.495 ↗
15. Tomalia · Biochem. Soc. Trans. · 2007 · 35 · 6110.1042/BST0350061 ↗
16. Paleos · Mol. Pharm. · 2007 · 4 · 16910.1021/mp060076n ↗
17. Medina · Chem. Rev. · 2009 · 109 · 314110.1021/cr900174j ↗
18. Mignani · Adv. Drug Delivery Rev. · 2013 · 64 · 131610.1016/j.addr.2013.01.001 ↗
19. Mammen · Angew. Chem., Int. Ed. · 1998 · 37 · 275410.1002/(SICI)1521-3773(19981102)37:20<2754::AID-ANIE2754>3.0.CO;2-3 ↗
20. Svenson · Nanomedicine · 2008 · 3 · 67910.2217/17435889.3.5.679 ↗
21. Maeda · Bioconjugate Chem. · 1992 · 3 · 35110.1021/bc00017a001 ↗
22. Maeda · J. Controlled Release · 2000 · 65 · 27110.1016/S0168-3659(99)00248-5 ↗
23. Taurin · J. Controlled Release · 2012 · 164 · 26510.1016/j.jconrel.2012.07.013 ↗
24. Prabhakar · Cancer Res. · 2013 · 73 · 241210.1158/0008-5472.CAN-12-4561 ↗
25. Schwartz · N. Engl. J. Med. · 2004 · 350 · 107910.1056/NEJMp048021 ↗
26. C.-O. Turrin and A.-M.Caminade, in Dendrimers: Towards Catalytic, Material and Biomedical Uses, ed. A.-M. Caminade, C.-O. Turrin, R. Laurent, A. Ouali and B. Delavaux-Nicot, John Wiley & Sons Ltd., Chichester, UK, 2011, pp. 437–461
27. C.-O. Turrin and A.-M.Caminade, in Dendrimers: towards Catalytic, Material and Biomedical Uses, ed. A.-M. Caminade, C.-O. Turrin, R. Laurent, A. Ouali and B. Delavaux-Nicot, John Wiley & Sons Ltd., Chichester, UK, 2011, pp. 463–484
28. Hawker · J. Chem. Soc., Chem. Commun. · 1990 · 101010.1039/C39900001010 ↗
29. Roy · J. Chem. Soc., Chem. Commun. · 1993 · 186910.1039/c39930001869 ↗
30. http://www.starpharma.com/vivagel
31. Tyssen · PLoS One · 2010 · 5 · e1230910.1371/journal.pone.0012309 ↗
32. Bestman-Smith · Antimicrob. Agents Chemother. · 2001 · 45 · 222910.1128/AAC.45.8.2229-2237.2001 ↗
33. Jansen · Eur. J. Inorg. Chem. · 1999 · 142910.1002/(SICI)1099-0682(199909)1999:9<1429::AID-EJIC1429>3.0.CO;2-8 ↗
34. C.-O. Turrin and A.-M.Caminade, in Dendrimers: Towards Catalytic, Material and Biomedical Uses, ed. A.-M. Caminade, C.-O. Turrin, R. Laurent, A. Ouali and B. Delavaux-Nicot, John Wiley & Sons Ltd., Chichester, UK, 2011, pp. 485–509
35. Hayder · Sci. World J. · 2011 · 11 · 136710.1100/tsw.2011.129 ↗
36. Supattapone · J. Virol. · 2001 · 75 · 345310.1128/JVI.75.7.3453-3461.2001 ↗
37. Solassol · J. Gen. Virol. · 2004 · 85 · 179110.1099/vir.0.19726-0 ↗
38. Griffe · Angew. Chem., Int. Ed. · 2007 · 46 · 252310.1002/anie.200604651 ↗
39. Portevin · J. Transl. Med. · 2009 · 7 · 8210.1186/1479-5876-7-82 ↗
40. Poupot · FASEB J. · 2006 · 20 · 233910.1096/fj.06-5742com ↗
41. Fruchon · J. Leukocyte Biol. · 2009 · 85 · 55310.1189/jlb.0608371 ↗
42. Hayder · Sci. Transl. Med. · 2011 · 3 · 1110.1126/scitranslmed.3002212 ↗
43. Blattes · Proc. Natl. Acad. Sci. U. S. A. · 2013 · 110 · 879510.1073/pnas.1221708110 ↗
44. Zhu · J. Mater. Chem. B · 2013 · 1 · 419910.1039/c3tb20724b ↗
45. Barth · Bioconjugate Chem. · 1994 · 5 · 5810.1021/bc00025a008 ↗
46. Yang · J. Neuro-Oncol. · 2009 · 95 · 35510.1007/s11060-009-9945-x ↗
47. Thomas · Mol. Pharm. · 2012 · 9 · 266910.1021/mp3002232 ↗
48. Goller · Tetrahedron Lett. · 2001 · 42 · 358710.1016/S0040-4039(01)00509-3 ↗
49. Zhu · Pharm. Res. · 2010 · 27 · 16110.1007/s11095-009-9992-1 ↗
50. Gingras · Angew. Chem., Int. Ed. · 2007 · 46 · 101010.1002/anie.200601962 ↗
51. Quintana · Pharm. Res. · 2002 · 19 · 131010.1023/A:1020398624602 ↗
52. Leamon · Drug Discovery Today · 2001 · 6 · 4410.1016/S1359-6446(00)01594-4 ↗
53. Majoros · Biomacromolecules · 2006 · 7 · 57210.1021/bm0506142 ↗
54. Mullen · ACS Nano · 2010 · 4 · 65710.1021/nn900999c ↗
55. Zong · Biomacromolecules · 2012 · 13 · 98210.1021/bm201639c ↗
56. Lim · Org. Lett. · 2008 · 10 · 20110.1021/ol7024907 ↗
57. Caminade · New J. Chem. · 2012 · 36 · 21710.1039/C1NJ20458K ↗
58. Lee · Proc. Natl. Acad. Sci. U. S. A. · 2006 · 103 · 1664910.1073/pnas.0607705103 ↗
59. Tannock · Cancer Res. · 1989 · 49 · 4373
60. Griffiths · Br. J. Cancer · 1991 · 64 · 42510.1038/bjc.1991.326 ↗
61. Medina · Biomaterials · 2013 · 34 · 465510.1016/j.biomaterials.2013.02.070 ↗
62. McGrath · Mol. Pharm. · 2005 · 2 · 25310.1021/mp050047x ↗
63. Calderon · Biochimie · 2010 · 92 · 124210.1016/j.biochi.2010.02.017 ↗
64. de Groot · Angew. Chem., Int. Ed. · 2003 · 42 · 449010.1002/anie.200351942 ↗
65. Amir · Angew. Chem., Int. Ed. · 2003 · 42 · 449410.1002/anie.200351962 ↗
66. Tang · Tetrahedron Lett. · 2006 · 47 · 767110.1016/j.tetlet.2006.08.110 ↗
67. Cheng · Eur. J. Med. Chem. · 2008 · 43 · 229110.1016/j.ejmech.2007.12.021 ↗
68. Kaminskas · Mol. Pharm. · 2012 · 9 · 35510.1021/mp2005966 ↗
69. El Kazzouli · New J. Chem. · 2012 · 36 · 22710.1039/C1NJ20459A ↗
70. Newkome · Angew. Chem., Int. Ed. · 1991 · 30 · 117810.1002/anie.199111781 ↗
71. Naylor · J. Am. Chem. Soc. · 1989 · 111 · 233910.1021/ja00188a079 ↗
72. Jansen · Science · 1994 · 266 · 122610.1126/science.266.5188.1226 ↗
73. Jansen · J. Am. Chem. Soc. · 1995 · 117 · 441710.1021/ja00120a032 ↗
74. Li · J. Polym. Sci. Part a-Polym. Chem. · 2010 · 48 · 55110.1002/pola.23757 ↗
75. Tekade · Chem. Rev. · 2009 · 109 · 4910.1021/cr068212n ↗
76. Ma · Eur. J. Med. Chem. · 2007 · 42 · 9310.1016/j.ejmech.2006.07.015 ↗
77. Yiyun · Eur. J. Med. Chem. · 2005 · 40 · 118810.1016/j.ejmech.2005.06.010 ↗
78. Wang · J. Am. Chem. Soc. · 2013 · 135 · 980510.1021/ja402903h ↗
79. Morgan · Cancer Res. · 2006 · 66 · 1191310.1158/0008-5472.CAN-06-2066 ↗
80. Neerman · Mol. Pharm. · 2004 · 1 · 39010.1021/mp049957p ↗
81. Kulhari · Mol. Pharm. · 2013 · 10 · 252810.1021/mp300650y ↗
82. Hu · Chem. Rev. · 2012 · 112 · 385610.1021/cr200333h ↗
83. Zhao · J. Am. Chem. Soc. · 2010 · 132 · 1318210.1021/ja106128u ↗
84. Hu · J. Phys. Chem. B · 2010 · 114 · 714810.1021/jp1007889 ↗
85. Kolhe · Int. J. Pharm. · 2003 · 259 · 14310.1016/S0378-5173(03)00225-4 ↗
86. Zhao · J. Phys. Chem. B · 2009 · 113 · 1417210.1021/jp907437e ↗
87. Blanzat · ChemBioChem · 2005 · 6 · 220710.1002/cbic.200500203 ↗
88. Perez-Anes · Org. Biomol. Chem. · 2009 · 7 · 349110.1039/b908352a ↗
89. Spataro · Eur. J. Med. Chem. · 2010 · 45 · 32610.1016/j.ejmech.2009.10.017 ↗
90. Al-Jamal · Adv. Drug Delivery Rev. · 2005 · 57 · 223810.1016/j.addr.2005.09.015 ↗
91. Azagarsamy · J. Am. Chem. Soc. · 2009 · 131 · 1418410.1021/ja906162u ↗
92. Caminade · Chem. –Eur. J. · 2008 · 14 · 742210.1002/chem.200800584 ↗
93. Mehrabadi · Curr. Opin. Solid State Mater. Sci. · 2012 · 16 · 31010.1016/j.cossms.2013.01.003 ↗
94. Ramaswamy · Int. J. Pharm. · 2003 · 254 · 1710.1016/S0378-5173(02)00670-1 ↗
95. Rettig · Expert Opin. Biol. Ther. · 2007 · 7 · 79910.1517/14712598.7.6.799 ↗
96. Mintzer · Chem. Rev. · 2009 · 109 · 25910.1021/cr800409e ↗
97. Dufes · Adv. Drug Delivery Rev. · 2005 · 57 · 217710.1016/j.addr.2005.09.017 ↗
98. Guillot-Nieckowski · New J. Chem. · 2007 · 31 · 111110.1039/B614877H ↗
99. Shcharbin · Biochemistry · 2009 · 74 · 1070
100. Marvaniya · J. Chem. Pharm. Res. · 2010 · 2 · 97