Dual-responsive crosslinked pluronic micelles as a carrier to deliver anticancer drug taxol

Macromolecular Research

Volumn 21, Issue 1, 2013, Pages 92-99

  Abdullah Al Nahain, ^a   Nam, Jeong A ^a   Mok, Hyejung ^b   Lee, Yong Kyu ^a   Park, Sung Young ^a  

^a Chungju National University   (South Korea)

^b Konkuk University   (South Korea)

Author keywords

Crosslinking; Pluronic; Redox potential; Stimuli sensitive polymers; Target delivery.

Indexed keywords

A549 CELLS; ANTICANCER DRUG; BIODEGRADABLE MICELLES; CELLULAR UPTAKE; CONFOCAL LASER SCANNING MICROSCOPY; CROSS-LINKED POLYMERS; CROSSLINKED; CYTOTOXIC; DRUG DELIVERY SYSTEM; EMISSION INTENSITY; HYDROPHOBIC DRUG; LOADING EFFICIENCY; MICELLES STABILITY; PH-RESPONSIVE; PHYSIOLOGICAL CONDITION; PLURONIC MICELLES; PLURONICS; REDOX POTENTIALS; SHORT PERIODS; STIMULI-SENSITIVE POLYMERS; TARGET DELIVERY; TRANSMISSION ELECTRON MICROSCOPY IMAGES;

CONFOCAL MICROSCOPY; CROSSLINKING; CYTOTOXICITY; DRUG DELIVERY; DYNAMIC LIGHT SCATTERING; LOADING; MOLECULAR BIOLOGY; POLYMERS; REDOX REACTIONS; TRANSMISSION ELECTRON MICROSCOPY;

MICELLES;

EID: 84873409441     PISSN: 15985032     EISSN: 20927673     Source Type: Journal    
DOI: 10.1007/s13233-013-1011-z     Document Type: Article

References (41)

1. M. Liu, J. Fu, J. Li, L. Wang, Q. Tan, X. Ran, Z. Peng, and H. Zeng, Int. J. Pharm., 391, 292 (2010).
2. Y. Shen, E. Jin, B. Zhang, C. J. Murphy, M. Sui, J. Zhao, J. Wang, J. Tang, M. Fan, E. V. Kirk, and W. J. Murdoch, J. Am. Chem. Soc., 132, 4259 (2010).
3. A. Klaikherd, C. Nagamani, and S. Thayumanavan, J. Am. Chem. Soc., 131, 4830 (2009).
4. H. R. Ihre, O. L. P. D. Jesús, F. C. Szoka, and J. M. J. Fréchet, Bioconjug. Chem., 13, 443 (2002).
5. G. S. Kwon and K. Kataoka, Adv. Drug Deliv. Rev., 16, 295 (1995).
6. L. Mingjun, K. Kenji, and M. J. F. Jean, J. Control. Release, 65, 121 (2000).
7. A. Napoli, M. J. Boerakker, N. Tirelli, R. J. M. Nolte, N. A. J. M. Sommerdijk, and J. A. Hubbell, Langmuir, 20, 3487 (2004).
8. A. Marin, H. Sun, G. A. Husseini, W. G. Pitt, D. A. Christensen, and N. Y. Rapoport, J. Control. Release, 84, 39 (2002).
9. D. Schmaljohann, Adv. Drug Deliv. Rev., 58, 1655 (2006).
10. F. Meng, Z. Zhong, and J. Feijen, Biomacromolecules, 10, 197 (2009).
11. J. Du, X. Du, C. Mao, and J. Wang, J. Am. Chem. Soc., 133, 17560 (2011).
12. C. J. F. Rijcken, O. Soga, W. E. Hennink, and C. F. van Nostrum, J. Control. Release, 120, 131 (2007).
13. D. Velluto, D. Demurtas, and J. A. Hubbell, Mol. Pharm., 5, 632 (2008).
14. H. Sun, B. Guo, R. Cheng, F. Meng, H. Liu, and Z. Zhon, Biomaterials, 30, 6358 (2009).
15. Y. Kakizawa and K. Kataoka, Adv. Drug Deliv. Rev., 54, 203 (2002).
16. Y. S. Ahn, H. J. Baik, B. R. Lee, E. S. Lee, K. T. Oh, D. H. Lee, and Y. S. Youn, Macromol. Res., 18, 747 (2010).
17. J. H. Kim, Y. T. Oh, K. S. Lee, J. M. Yun, B. T. Park, and K. T. Oh, Macromol. Res., 19, 453 (2011).
18. Y. Bae, N. Nishiyama, and K. Kataoka, Bioconjug. Chem., 18, 1131 (2007).
19. Y. Lee, S. Y. Park, H. Mok, and T. G. Park, Bioconjug. Chem., 19, 525 (2008).
20. C. Ding, J. Gu, X. Qu, and Z. Yang, Bioconjug. Chem., 20, 1163 (2009).
21. H. Østergaard, C. Tachibana, and J. R. Winther, J. Cell Biol., 166, 337 (2004).
22. J. Ryu, R. Roy, J. Ventura, and S. Thayumanavan, Langmuir, 26, 7086 (2010).
23. M. Schultz, S. Dutta, and K. D. Tew, Adv. Drug Deliv. Rev., 26, 91 (1997).
24. Y. Lee, H. Koo, G. Jin, H. Mo, M. Y. Cho, J. Park, J. S. Choi, and J. S. Park, Biomacromolecules, 6, 24 (2005).
25. K. H. Bae, S. H. Choi, S. Y. Park, Y. Lee, and T. G. Park, Langmuir, 22, 6380 (2006).
26. S. Alexander, T. Cosgrove, S. W. Prescott, and T. C. Castle, Langmuir, 27, 8054 (2011).
27. W. Zhang, K. Gilstrap, L. Wu, R. B. K. C, M. A. Moss, Q. Wang, X. Lu, and X. He, ACS Nano, 4, 6747 (2010).
28. K. Lee, K. H. Bae, Y. Lee, S. H. Lee, C. Ahn, and T. G. Park, Macromol. Biosci., 10, 239 (2010).
29. S. Ruthstein, A. Potapov, A. M. Raitsimring, and D. Goldfarb, J. Phys. Chem. B, 109, 22843 (2005).
30. J. A Nam, A. A. Nahain, S. Hong, K. D. Lee, H. Lee, and S. Y. Park, Macromol. Biosci., 11, 1594 (2011).
31. L. Li, and B. Tan, J. Colloid Interface Sci., 317, 326 (2008).
32. E. Ruel-Gariépy and J. Leroux, Eur. J. Pharm. Biopharm., 58, 409 (2004).
33. C. Y. Gong, S. Shi, P. W. Dong, B. Yang, X. R. Qi, G. Guo, Y. C. Gu, X. Zhao, Y. Q. Wei, and Z. Y. Qian, J. Pharm. Sci., 98, 4684 (2009).
34. K. E. Schmalenberg, L. Frauchiger, L. Nikkhouy-Albers, and K. E. Uhrich, Biomacromolecules, 2, 851 (2001).
35. F. Alexis, E. Pridgen, L. K. Molnar, and O. C. Farokhzad, Mol. Pharm., 5, 505 (2008).
36. O. Onaca, R. Enea, D. W. Hughes, and W. Meier, Macromol. Biosci., 9, 129 (2009).
37. A. P. Goodwin, J. L. Mynar, Y. Ma, G. R. Fleming, and J. M. J. Fréchet, J. Am. Chem. Soc., 127, 9952 (2005).
38. A. A. Nahain, H. Lee, Y. S. Lee, K. D. Lee, and S. Y. Park, Macromol. Biosci., 11, 1264 (2011).
39. J. Liu, Y. Pang, W. Huang, Z. Zhu, X. Zhu, Y. Zhou, and D. Yan, Biomacromolecules, 12, 2407 (2011).
40. Y. Li, A. Nese, N. V. Lebedeva, T. Davis, K. Matyjaszewski, and S. S. Sheiko, J. Am. Chem. Soc., 133, 17479 (2011).
41. C. Ding, L. Zhao, F. Liu, J. Cheng, J. Gu, S. Dan, C. Liu, X. Qu, and Z. Yang, Biomacromolecules, 11, 1043 (2010).