journal article·2015Open access

Smart branched polymer drug conjugates as nano-sized drug delivery systems

A. Duro-Castano, J. Movellan, M. J. Vicent

Biomaterials Science· Volume 3· Issue 10

Abstract

Polymer-drug conjugates represent excellent nanopharmaceutical candidates, as they offer multiple advantages related to their intrinsic characteristics. Many of the said characteristics are provided by the covalent bonding between the drug and the polymer. However, their clinical development has been slow and only one polymer-drug conjugate has reached the market, thus there remains an urgent need for the development of new and smart polymeric systems. Desirable characteristics of these new systems include higher molecular weight and degree of homogeneity, predictable conformations in solution, multivalency, and increased drug loading capacity, amongst others. With these aims in mind, branched polymers are ideal candidates due to their unique rheological, mechanical, and biomedical properties derived from their structure, inaccessible for linear polymers. Within this review, the synthetic strategies developed and the main efforts towards branched polymer implementation as carriers for polymer-drug conjugates will be addressed.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Dendrimers and Hyperbranched Polymers · Nanoparticle-Based Drug Delivery · Advanced Polymer Synthesis and Characterization

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

Affiliations

Centro de Investigación Príncipe Felipe

Polymer Therapeutics Lab.

E-46012 Valencia

Spain

Funding

European Research Council

References (100+)

Show source-provided references
1. Gaspar · Mol. Pharm. · 2011 · 8 · 210110.1021/mp200394t ↗
2. http://www.etp-nanomedicine.eu/public/press-documents/publications/etpn-publications/etpn-white-paper-H2020
3. Nitta · Int. J. Mol. Sci. · 2013 · 14 · 162910.3390/ijms14011629 ↗
4. Duncan · J. Controlled Release · 2014 · 190 · 37110.1016/j.jconrel.2014.05.001 ↗
5. Duncan · Nat. Rev. Drug Discovery · 2003 · 2 · 34710.1038/nrd1088 ↗
6. Scott · CNS Drugs · 2013 · 27 · 97110.1007/s40263-013-0117-3 ↗
7. Powell · Biofouling · 2013 · 29 · 41310.1080/08927014.2013.777954 ↗
8. Powell · Am. J. Respir. Cell Mol. Biol. · 2013 · 50 · 48310.1165/rcmb.2013-0287OC ↗
9. Kopeček · Adv. Drug Delivery Rev. · 2013 · 65 · 4910.1016/j.addr.2012.10.014 ↗
10. Canal · Curr. Opin. Biotechnol. · 2011 · 22 · 89410.1016/j.copbio.2011.06.003 ↗
11. Pasut · Polymers · 2014 · 6 · 16010.3390/polym6010160 ↗
12. Pelegri-O'Day · J. Am. Chem. Soc. · 2014 · 136 · 1432310.1021/ja504390x ↗
13. Gonzalez-Toro · Eur. Polym. J. · 2013 · 49 · 290610.1016/j.eurpolymj.2013.05.002 ↗
14. Yang · Biomaterials · 2013 · 34 · 843010.1016/j.biomaterials.2013.07.037 ↗
15. Li · Biomaterials · 2014 · 35 · 952910.1016/j.biomaterials.2014.07.059 ↗
16. Matsumura · Cancer Sci. · 2009 · 100 · 57210.1111/j.1349-7006.2009.01103.x ↗
17. Merkel · J. Controlled Release · 2014 · 190 · 41510.1016/j.jconrel.2014.06.009 ↗
18. Osada · Polym. J. · 2014 · 46 · 46910.1038/pj.2014.49 ↗
19. Tschiche · Nanomedicine · 2014 · 9 · 66710.2217/nnm.14.32 ↗
20. Mehrabadi · Curr. Opin. Solid State Mater. Sci · 2012 · 16 · 31010.1016/j.cossms.2013.01.003 ↗
21. Kesharwani · Biomaterials · 2012 · 33 · 713810.1016/j.biomaterials.2012.06.068 ↗
22. Matsumura · Cancer Res. · 1986 · 46 · 6387
23. Maeda · Int. Immunopharmacol. · 2003 · 3 · 31910.1016/S1567-5769(02)00271-0 ↗
24. Maeda · Adv. Drug Delivery Rev. · 2013 · 65 · 7110.1016/j.addr.2012.10.002 ↗
25. Maeda · Cancer Sci. · 2013 · 104 · 77910.1111/cas.12152 ↗
26. Prabhakar · Cancer Res. · 2013 · 73 · 241210.1158/0008-5472.CAN-12-4561 ↗
27. Duncan · Trends Biotechnol. · 2006 · 24 · 3910.1016/j.tibtech.2005.11.006 ↗
28. R. Webster , V.Elliott, B. K.Park, D.Walker, M.Hankin and P.Taupin, PEG and PEG conjugates toxicity: towards an understanding of the toxicity of PEG and its relevance to PEGylated biologicals, PEGylated Protein Drugs: Basic Science and Clinical Applications, ed. F. M. Veronese, Birkhäuser, Basel, 2009, p. 12710.1007/978-3-7643-8679-5_8 ↗
29. Barz · Polym. Chem. · 2011 · 2 · 190010.1039/c0py00406e ↗
30. Duro-Castano · Polymers · 2014 · 6 · 51510.3390/polym6020515 ↗
31. Hardwicke · Mol. Pharm. · 2010 · 7 · 69910.1021/mp9002656 ↗
32. http://www.xeneticbio.com/publications.aspx
33. Yurkovetskiy · Curr. Bioact. Compd. · 2011 · 7 · 1510.2174/157340711795163839 ↗
34. Perner · Trials · 2011 · 12 · 2410.1186/1745-6215-12-24 ↗
35. Dhal · Adv. Drug Delivery Rev. · 2009 · 61 · 112110.1016/j.addr.2009.05.004 ↗
36. Duncan · Adv. Drug Delivery Rev. · 2013 · 65 · 6010.1016/j.addr.2012.08.012 ↗
37. Santamaria · PLoS One · 2009 · 4 · 663410.1371/journal.pone.0006634 ↗
38. Tomalia · J. Polym. Sci., Part A: Polym. Chem. · 2002 · 40 · 271910.1002/pola.10301 ↗
39. Voit · Chem. Rev. · 2009 · 109 · 592410.1021/cr900068q ↗
40. Zhou · Angew. Chem., Int. Ed. · 2004 · 43 · 489610.1002/anie.200460325 ↗
41. Zhou · J. Phys. Chem. B · 2007 · 111 · 126210.1021/jp0673563 ↗
42. Fasting · Angew. Chem., Int. Ed. · 2012 · 51 · 1047210.1002/anie.201201114 ↗
43. Zhou · Chem. Commun. · 2009 · 117210.1039/b814560c ↗
44. Zhou · Adv. Mater. · 2010 · 22 · 456710.1002/adma.201000369 ↗
45. Deshpande · J. Controlled Release · 2004 · 97 · 14310.1016/j.jconrel.2004.02.019 ↗
46. Sant · J. Biomed. Mater. Res., Part A · 2008 · 87 · 88510.1002/jbm.a.31800 ↗
47. Shi · ACS Nano · 2013 · 7 · 1061210.1021/nn403069n ↗
48. Garofalo · Biomacromolecules · 2013 · 15 · 40310.1021/bm401812r ↗
49. Seib · J. Controlled Release · 2007 · 117 · 29110.1016/j.jconrel.2006.10.020 ↗
50. Mintzer · Chem. Soc. Rev. · 2011 · 40 · 17310.1039/B901839P ↗
51. Svenson · Adv. Drug Delivery Rev. · 2005 · 57 · 210610.1016/j.addr.2005.09.018 ↗
52. Wolinsky · Adv. Drug Delivery Rev. · 2008 · 60 · 103710.1016/j.addr.2008.02.012 ↗
53. Menjoge · Drug Discovery Today · 2010 · 15 · 17110.1016/j.drudis.2010.01.009 ↗
54. Lee · Nat. Biotechnol. · 2005 · 23 · 151710.1038/nbt1171 ↗
55. Konkolewicz · Macromolecules · 2001 · 44 · 706710.1021/ma200656h ↗
56. N. Hadjichristidis , M.Pitsikalis, H.Iatrou, P.Driva, G.Sakellariou and M.Chatzichristidi, 6.03 - Polymers with Star-Related Structures: Synthesis, Properties, and Applications, in Polymer Science: A Comprehensive Reference, ed. K. M. Möller, Elsevier, Amsterdam, 2012, pp. 29–111
57. Inoue · Macromol. Biosci. · 2003 · 3 · 2610.1002/mabi.200390002 ↗
58. Inoue · J. Am. Chem. Soc. · 1994 · 116 · 1078310.1021/ja00102a053 ↗
59. N. Hadjichristidis , M.Pitsikalis and H.Iatrou, Polymers with Star-Related Structures, Macromolecular Engineering, Wiley-VCH Verlag GmbH & Co. KGaA, 2007, pp. 909–972
60. Zhu · Macromol. Chem. Phys. · 2006 · 207 · 84410.1002/macp.200600008 ↗
61. Wang · Bioconjugate Chem. · 2005 · 16 · 39710.1021/bc049784m ↗
62. Wang · Bioconjugate Chem. · 2008 · 19 · 142310.1021/bc7004285 ↗
63. Liu · Nat. Mater. · 2011 · 10 · 39810.1038/nmat2999 ↗
64. Hadjichristidis · Polymer · 1985 · 26 · 108710.1016/0032-3861(85)90233-2 ↗
65. M. Pitsikalis , S.Pispas, J. W.Mays and N.Hadjichristidis, Nonlinear block copolymer architectures, Blockcopolymers-Polyelectrolytes-Biodegradation, Springer, 1998, pp. 1–137
66. Schultz · J. Chem. Inf. Comput. Sci. · 1998 · 38 · 8510.1021/ci9700900 ↗
67. Knoll · Macromol. Symp. · 1998 · 132 · 23110.1002/masy.19981320122 ↗
68. D. C. Forman , F.Wieberger, A.Gröschel, A. H. E.Müller, H.-W.Schmidt and C. K.Ober, Comparison of star and linear ArF resists, 2010, pp. 76390–76398
69. He · Langmuir · 2009 · 25 · 489210.1021/la804056p ↗
70. Strandman · Macromolecules · 2008 · 41 · 885510.1021/ma801475p ↗
71. Strandman · Polymer · 2007 · 48 · 700810.1016/j.polymer.2007.10.002 ↗
72. Strandman · Polymer · 2006 · 47 · 652410.1016/j.polymer.2006.07.057 ↗
73. Wei · Biomaterials · 2007 · 28 · 9910.1016/j.biomaterials.2006.08.030 ↗
74. Nabid · Polymer · 2011 · 52 · 279910.1016/j.polymer.2011.04.054 ↗
75. Xue · J. Mater. Chem. · 2012 · 22 · 740310.1039/c2jm15918j ↗
76. Djordjevic · AAPS PharmSci. · 2003 · 5 · 110.1208/ps050426 ↗
77. A. Duro-Castano , R. M.England, M.Oteo, E.Romero, M. A.Morcillo and M. J.Vicent, Mol. Pharm., 2015
78. Chen · Polym. Chem. · 2014 · 5 · 17510.1039/C3PY00942D ↗
79. Chen · Macromol. Rapid Commun. · 2013 · 34 · 150710.1002/marc.201300487 ↗
80. Schaefgen · J. Am. Chem. Soc. · 1948 · 70 · 270910.1021/ja01188a026 ↗
81. Morton · J. Polym. Sci. · 1962 · 57 · 47110.1002/pol.1962.1205716537 ↗
82. J. D. Ferry , Viscoelastic properties of polymers, John Wiley & Sons, 1980
83. Burchard · Adv. Polym. Sci. · 1983 · 48 · 110.1007/3-540-12030-0_1 ↗
84. H. Yamakawa , Modern theory of polymer solutions, Electronic edn, Harper & Row, Kyoto, 1971
85. Wang · Biomacromolecules · 2000 · 1 · 31310.1021/bm0000236 ↗
86. Jelínková · Pharm. Res. · 2003 · 20 · 155810.1023/A:1026170830782 ↗
87. Etrych · Eur. J. Pharm. Sci. · 2011 · 42 · 52710.1016/j.ejps.2011.03.001 ↗
88. Etrych · J. Controlled Release · 2011 · 154 · 24110.1016/j.jconrel.2011.06.015 ↗
89. Etrych · J. Controlled Release · 2007 · 122 · 3110.1016/j.jconrel.2007.06.007 ↗
90. Cao · Biomacromolecules · 2010 · 11 · 368010.1021/bm101154r ↗
91. Kowalczuk · Int. J. Pharm. · 2011 · 404 · 22010.1016/j.ijpharm.2010.11.004 ↗
92. Li · Adv. Healthcare Mater. · 2015 · 4 · 14810.1002/adhm.201400164 ↗
93. Navath · J. Controlled Release · 2010 · 142 · 44710.1016/j.jconrel.2009.10.035 ↗
94. Sedlák · Bioorg. Med. Chem. Lett. · 2008 · 18 · 295210.1016/j.bmcl.2008.03.065 ↗
95. Bílková · Int. J. Pharm. · 2010 · 386 · 110.1016/j.ijpharm.2009.10.034 ↗
96. Yang · J. Biomater. Sci., Polym. Ed. · 2003 · 14 · 104310.1163/156856203769231556 ↗
97. Flory · J. Am. Chem. Soc. · 1952 · 74 · 271810.1021/ja01131a008 ↗
98. Kim · Abstr. Pap. Am. Chem. Soc. · 1988 · 196 · 104
99. Kim · J. Am. Chem. Soc. · 1990 · 112 · 459210.1021/ja00167a094 ↗
100. Kim · Macromolecules · 1992 · 25 · 556110.1021/ma00047a001 ↗