Synthesis and physicochemical characterization of reduction-sensitive block copolymer for intracellular delivery of doxorubicin

Macromolecular Research

Volumn 21, Issue 1, 2013, Pages 100-107

  Thambi, Thavasyappan ^a   Saravanakumar, Gurusamy ^a   Chu, Jun Uk ^b   Heo, Roun ^a   Ko, Hyewon ^a   Deepagan, Veerasikku Gopal ^a   Kim, Jong Ho ^c   Park, Jae Hyung ^a  

^a Sungkyunkwan University   (South Korea)

^b Korea Institute of Science and Technology   (South Korea)

^c Kyung Hee University   (South Korea)

Author keywords

Amphiphilic block copolymer; Doxorubicin.; Glutathione; Reduction sensitive micelle

Indexed keywords

AMPHIPHILIC BLOCK COPOLYMERS; AMPHIPHILIC DIBLOCK COPOLYMERS; AMPHIPHILICS; ANTICANCER DRUG; AQUEOUS CONDITION; DISULFIDE BONDS; DOXORUBICIN; GLUTATHIONES; HIGH LOADINGS; HYDROPHOBIC CORE; IN-VITRO; INTRACELLULAR DELIVERY; L-GLUTAMATE; MACROINITIATORS; PHYSICO-CHEMICAL CHARACTERIZATION; PHYSIOLOGIC CONDITIONS; SPHERICAL MICELLES; SYNTHETIC METHODS; TRIPEPTIDE;

BIOMATERIALS; BLOCK COPOLYMERS; COVALENT BONDS; CYTOLOGY; HYDROPHOBICITY; MICELLES; PEPTIDES; POLYETHYLENE OXIDES;

POLYETHYLENE GLYCOLS;

EID: 84873406861     PISSN: 15985032     EISSN: 20927673     Source Type: Journal    
DOI: 10.1007/s13233-013-1014-9     Document Type: Article

References (37)

1. K. Kataoka, A. Harada, and Y. Nagasaki, Adv. Drug Deliv. Rev., 47, 113 (2001).
2. A. Rösler, G. W. M. Vandermeulen, and H.-A. Klok, Adv. Drug Deliv. Rev., 53, 95 (2001).
3. Y. Matsumura and H. Maeda, Cancer Res., 46, 6387 (1986).
4. H. Maeda, J. Wu, T. Sawa, Y. Matsumura, and K. Hori, J. Control. Release, 65, 271 (2000).
5. Y. Nakada, R. Tudomi, K. Sakurai, and Y. Takahashi, Int. J. Pharm., 175, 109 (1998).
6. R. Gref, Y. Minamitake, M. T. Peracchia, V. Trubetskoy, V. Torchilin, and R. Langer, Science, 263, 1600 (1994).
7. X. Shuai, H. Ai, N. Nasongkla, S. Kim, and J. Gao, J. Control. Release, 98, 415 (2004).
8. Y. Machida, H. Onishi, A. Kurita, H. Hata, and A. Morikawa, J. Control. Release, 66, 159 (2000).
9. Y. Dong and S.-S. Feng, Biomaterials, 25, 2843 (2004).
10. M. A. C. Stuart, W. T. S. Huch, J. Genzer, M. Muller, C. Ober, M. Stamm, G. B. Sukhorukov, I. Szleifer, V. V. Tsukruk, M. Urban, F. Winnik, S. Zauscher, I. Luzinov, and S. Minko, Nat. Mater., 9, 101 (2010).
11. F. Meng, W. E. Hennink, and Z. Zhong, Biomaterials, 30, 2180 (2009).
12. R. Natalya, Prog. Polym. Sci., 32, 962 (2007).
13. F. Meng, Z. Zhong, and J. Feijen, Biomacromolecules, 10, 197 (2009).
14. Y. Shamay, L. Adar, G. Ashkenasy, and A. David, Biomaterials, 32, 1377 (2011).
15. H. Zhang, H. Xia, J. Wang, and Y. Li, J. Control. Release, 139, 31 (2009).
16. T. Thambi, V. G. Deepagan, C. K. Yoo, and J. H. Park, Polymer, 52, 4753 (2011).
17. K. H. Min, J. H. Kim, S. M. Bae, H. Shin, M. S. Kim, S. Park, H. Lee, R. W. Park, I. S. Kim, K. Kim, I. C. Kwon, S. Y. Jeong, and D. S. Lee, J. Control. Release, 144, 259 (2010).
18. J. Lu, N. Li, Q. Xu, J. Ge, J. Lu, and X. Xia, Polymer, 51, 1709 (2010).
19. S. Q. Liu, Y. W. Tong, and Y.-Y. Yang, Biomaterials, 26, 5064 (2005).
20. S. Cerritelli, D. Velluto, and J. A. Hubbell, Biomacromolecules, 8, 1966 (2007).
21. A. N. Koo, H. J. Lee, S. E, Kim, J. H. Chang, C. Park, C. Kim, J. H. Park, and S. C. Lee, Chem. Commun., 6570 (2008).
22. T.-B. Ren, Y. Feng, Z.-H. Zhang, L. Li, and Y.-Y. Li, Soft Matter, 7, 2329 (2011).
23. H. Sun, B. Guo, R. Cheng, F. Meng, H. Liu, and Z. Zhong, Biomaterials, 30, 6358 (2009).
24. T. Thambi, H. Y. Yoon, K. Kim, I. C. Kwon, C. K. Yoo, and J. H. Park, Bioconjug. Chem., 22, 1924 (2011).
25. D. P. Jones, J. L. Carlson, P. S. Samiec, P. Sternberg, V. C. Mody, R. L. Reed, and L. A. Brown, Clin. Chim. Acta, 275, 175 (1998).
26. Y. Sun, X. Yan, T. Yuan, J. Liang, Y. Fan, Z. Gu, and X. Zhang, Biomaterials, 31, 7124 (2010).
27. S. Stolnik, L. Illum, and S. S. Davis, Adv. Drug Deliv. Rev., 16, 195 (1995).
28. B. Romberg, W. Hennink, and G. Storm, Pharm. Res., 25, 55 (2008).
29. Y. Lee, S. Y. Park, C. Kim, and T. G. Park, J. Control. Release, 135, 89 (2009).
30. W. H. Daly and D. Poché, Tetrahedron Lett., 29, 5859 (1988).
31. M. Wilhelm, C. L. Zhao, Y. Wang, R. Xu, M. A. Winnik, J. L. Mura, G. Riess, and M. D. Croucher, Macromolecules, 24, 1033 (1991).
32. L.-Y. Tang, Y.-C. Wang, Y. Li, Z.-H. Du, and J. Wang, Bioconjug. Chem., 20, 1095 (2009).
33. H. S. Yoo, E. A. Lee, and T. G. Park, J. Control. Release, 82, 17 (2002).
34. K. Y. Choi, H. Chung, K. H. Min, H. Y. Yoon, K. Kim, J. H. Park, I. C. Kwon, and S. Y. Jeong, Biomaterials, 31, 106 (2010).
35. C. Kim, S. C. Lee, S. W. Kang, I. C. Kwon, Y.-H. Kim, and S. Y. Jeong, Langmuir, 16, 4792 (2000).
36. S. Kwon, J. H. Park, H. Chung, I. C. Kwong, S. Y. Jeong, and I.-S. Kim, Langmuir, 19, 10188 (2003).
37. Y. Li, R. Tong, H. Xia, H. Zhang, and J. Xuan, Chem. Commun., 46, 7739 (2010).