New Strategy for Controlled Release of Drugs. Potential Pinpoint Targeting with Multiresponsive Tetraaniline Diblock Polymer Vesicles: Site-Directed Burst Release with Voltage
Source abstract
Abstract
A series of amphiphlic diblock polymers, tetraaniline block with different length of poly(N-isopropylacrylamide) (TA-b-PNIPAM), have been successfully synthesized. In a suitable solution, the as-synthesized diblock polymers can form stable large compound vesicles (LCVs) with multiple bimolecular-layer structure through self-assembly. These factors, such as the block length, different organic solvent, solvent ratio, pH value, temperature, and voltage, which affect the morphology and properties of the assembled aggregates, are systematically investigated. When the degree of polymerization of PNIPAM block is close to 10, the as-synthesized diblock polymer may form stable LCVs with the uniform size as well as few defects in the mixed solvent of dimethylformamide/water (v/v = 3:7). The assembled LCVs possess the properties of triple-responsive capacity on temperature, pH, and voltage. Variation in any of these factors can cause some changes in the morphology of LCVs. The drug release properties for doxorubicin (DOX) loaded by LCVs affected by temperature, voltage, and different pH values have been investigated. It is interesting that the structure of LCVs can be destructed completely by applying a voltage at 0.6 V. With such an advantage, the drugs loaded by the LCVs could burst release into designated place by using appropriate circuit design or instrument, thus achieving maximum efficacy of the loaded drugs or other bioactive molecules without any unnecessary chemical substances added. This approach allows us to concentrate more on material design aspects only, without regard to the complex targeting issue which is the biggest obstacle of such materials in practical applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence and Fluorescent Materials · Conducting polymers and applications · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
PCFM Lab, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 51025, China
Department of Chemistry, Tsinghua University, Beijing 100084, China
References (70)
Show source-provided references
1. Stuart M. A. C. · Nat. Mater. · 2010 · 9 · 10110.1038/nmat2614 ↗
2. Sun T. · Acc. Chem. Res. · 2005 · 38 · 64410.1021/ar040224c ↗
3. Senaratne W. · Biomacromolecules · 2005 · 6 · 242710.1021/bm050180a ↗
4. Liu Z. · Adv. Mater. · 2000 · 12 · 28810.1002/(SICI)1521-4095(200002)12:4<288::AID-ADMA288>3.0.CO;2-1 ↗
5. Kelley E. G. · Chem. Soc. Rev. · 2013 · 42 · 705710.1039/c3cs35512h ↗
6. Besnard L. · Adv. Mater. · 2013 · 25 · 284410.1002/adma.201204496 ↗
7. Jäkle F. · Chem. Rev. · 2010 · 110 · 398510.1021/cr100026f ↗
8. Hoffman A. S. · Adv. Drug Delivery Rev. · 2013 · 65 · 1010.1016/j.addr.2012.11.004 ↗
9. Nash M. A. · ACS Nano · 2012 · 6 · 677610.1021/nn3015008 ↗
10. Tokarev I. · Soft Matter · 2012 · 8 · 598010.1039/c2sm25069a ↗
11. Yoshida R. · Biophysics · 2012 · 8 · 16310.2142/biophysics.8.163 ↗
12. Gracia R. · Polym. Chem. · 2013 · 4 · 220610.1039/c3py21118e ↗
13. Li G. · ACS Nano · 2013 · 7 · 247010.1021/nn305814q ↗
14. Kelly J. C. · Adv. Mater. · 2012 · 24 · 88610.1002/adma.201103340 ↗
15. Zapotoczny S. · Methods Mol. Biol. · 2012 · 811 · 5110.1007/978-1-61779-388-2_4 ↗
16. Jochum F. D. · Chem. Soc. Rev. · 2013 · 42 · 746810.1039/C2CS35191A ↗
17. Zhang J. · ACS Macro Lett. · 2013 · 2 · 6710.1021/mz300613q ↗
18. Habibi Y. · Chem. Rev. · 2010 · 110 · 347910.1021/cr900339w ↗
19. Yan X. · Adv. Mater. · 2012 · 24 · 36210.1002/adma.201103220 ↗
20. Liu Y. · J. Am. Chem. Soc. · 2013 · 135 · 476510.1021/ja3122608 ↗
21. Kashem M. M. A. · ACS Macro Lett. · 2012 · 1 · 39610.1021/mz200141q ↗
22. Kazakov S. · Macromolecules · 2002 · 35 · 191110.1021/ma011644+ ↗
23. Nardin C. · Eur. Phys. J. E: Soft Matter Biol. Phys. · 2001 · 4 · 40310.1007/s101890170095 ↗
24. Wang C. · Langmuir · 2010 · 26 · 71610.1021/la902427r ↗
25. Hatch A. C. · Lab Chip · 2011 · 11 · 250910.1039/c0lc00553c ↗
26. Kim K. T. · Nanoscale · 2010 · 2 · 84410.1039/b9nr00409b ↗
27. Shi Z. · Macromol. Rapid Commun. · 2008 · 29 · 41210.1002/marc.200700673 ↗
28. Thompson C. J. · Colloid Polym. Sci. · 2008 · 286 · 151110.1007/s00396-008-1925-8 ↗
29. Rösler A. · Adv. Drug Delivery Rev. · 2012 · 64 · 27010.1016/j.addr.2012.09.026 ↗
30. Dimitrov I. · Prog. Polym. Sci. · 2007 · 32 · 127510.1016/j.progpolymsci.2007.07.001 ↗
31. Luo Y. · J. Polym. Sci., Part A: Polym. Chem. · 2012 · 50 · 205310.1002/pola.25980 ↗
32. Königer A. · Soft Matter · 2013 · 9 · 141810.1039/C2SM27417E ↗
33. Nakayama M. · Macromol. Biosci. · 2012 · 12 · 75110.1002/mabi.201200018 ↗
34. Moughton A. O. · Chem. Commun. · 2010 · 46 · 109110.1039/B922289H ↗
35. Wan X. · Langmuir · 2011 · 27 · 408210.1021/la104911r ↗
36. Liu X. · Biomacromolecules · 2012 · 13 · 130710.1021/bm2018382 ↗
37. Roy D. · ACS Macro Lett. · 2013 · 2 · 13210.1021/mz300620v ↗
38. Deka S. R. · Nanoscale · 2011 · 3 · 61910.1039/C0NR00570C ↗
39. He X. · React. Funct. Polym. · 2011 · 71 · 54410.1016/j.reactfunctpolym.2011.02.001 ↗
40. Tang Y. · J. Colloid Interface Sci. · 2013 · 397 · 2410.1016/j.jcis.2013.01.018 ↗
41. Qiao J. · J. Mater. Chem. · 2012 · 22 · 1154310.1039/c2jm31093g ↗
42. Zhu Z. · Macromolecules · 2005 · 38 · 980310.1021/ma051808c ↗
43. Borchert U. · Langmuir · 2006 · 22 · 584310.1021/la060227t ↗
44. Wu X. L. · Bioconjugate Chem. · 2010 · 21 · 20810.1021/bc9005283 ↗
45. Du Y. · Biomaterials · 2012 · 33 · 729110.1016/j.biomaterials.2012.06.034 ↗
46. Kim H. · J. Am. Chem. Soc. · 2011 · 133 · 520610.1021/ja200297j ↗
47. Hoag H. · Nature · 2003 · 423 · 79610.1038/423796a ↗
48. Stieglitz T. · Sens. Actuators, A · 2001 · 90 · 20310.1016/S0924-4247(01)00520-9 ↗
49. Stieglitz T. · Med. Device Tech. · 1999 · 10 · 28
50. Kim H. · J. Mater. Chem. · 2010 · 20 · 118610.1039/B914912K ↗
51. Zhang W. J. · Synth. Met. · 1997 · 84 · 11910.1016/S0379-6779(97)80674-1 ↗
52. Wei Y. · J. Chem. Educ. · 2001 · 78 · 55110.1021/ed078p551 ↗
53. Kujawa P. · Macromolecules · 2006 · 39 · 34110.1021/ma051876z ↗
54. Gupta N. · Int. J. Mater. Chem. · 2012 · 2 · 7910.5923/j.ijmc.20120202.07 ↗
55. Bates F. S. · Annu. Rev. Phys. Chem. · 1990 · 41 · 52510.1146/annurev.pc.41.100190.002521 ↗
56. Yu K. · Macromolecules · 1998 · 31 · 350910.1021/ma971419l ↗
57. Yu Y. · Macromolecules · 1998 · 31 · 114410.1021/ma971254g ↗
58. Zang L. · Acc. Chem. Res. · 2008 · 41 · 159610.1021/ar800030w ↗
59. Podlogar F. · Int. J. Pharm. · 2004 · 276 · 11510.1016/j.ijpharm.2004.02.018 ↗
60. Yu Y. · Langmuir · 2001 · 17 · 670510.1021/la010640v ↗
61. Burke S. E. · Polymer · 2001 · 42 · 911110.1016/S0032-3861(01)00385-8 ↗
62. Shao Z. · J. Mater. Chem. · 2012 · 22 · 1623010.1039/c2jm32278a ↗
63. Ford W. E. · ACS Nano · 2013 · 7 · 194310.1021/nn3050769 ↗
64. Basavaiah K. · E-J. Chem. · 2012 · 9 · 117510.1155/2012/679462 ↗
65. Zhang G. · Adv. Polym. Sci. · 2006 · 195 · 10110.1007/12_050 ↗
66. Zhang W. · Macromolecules · 2005 · 38 · 90910.1021/ma048227s ↗
67. Li J. · J. Polym. Sci., Part A: Polym. Chem. · 2007 · 45 · 515610.1002/pola.22260 ↗
68. Chen L. · Mater. Lett. · 2005 · 59 · 244610.1016/j.matlet.2005.03.018 ↗
69. Wei Z. · Macromol. Rapid Commun. · 2008 · 29 · 28010.1002/marc.200700741 ↗
70. Udeh C. U. · J. Mater. Chem. · 2011 · 21 · 1813710.1039/c1jm12557e ↗