Access to different nanostructures via self-assembly of thiourea-containing pegylated amphiphiles

Macromolecular Rapid Communications

Volumn 34, Issue 8, 2013, Pages 652-658

  Venkataraman, Shrinivas ^a   Chowdhury, Zarir Ashraf ^b,d   Lee, Ashlynn L ^a   Tong, Yen Wah ^b   Akiba, Isamu ^c   Yang, Yi Yan ^a  

^a INSTITUTE OF BIOENGINEERING AND NANOTECHNOLOGY   (Singapore)

^b NATIONAL UNIVERSITY OF SINGAPORE   (Singapore)

^c UNIVERSITY OF KITAKYUSHU   (Japan)

^d LONZA AG   (Switzerland)

Author keywords

amphiphilic block copolymer; morphology; nanostructures; self assembly; small angle X ray scattering

Indexed keywords

AMPHIPHILIC BLOCK COPOLYMERS; CHEMICAL COMPOSITIONS; HYDROPHOBIC AND HYDROPHILIC; HYDROPHOBIC COMPONENTS; HYDROPHOBIC GROUPS; ORGANIC SOLVENT-FREE; SMALL ANGLE X-RAY SCATTERING; STRUCTURAL CHARACTERIZATION;

BLOCK COPOLYMERS; HEAT TREATMENT; HYDROPHOBICITY; MICELLES; MOLECULAR RECOGNITION; MORPHOLOGY; NANOSTRUCTURES; ORGANIC SOLVENTS; SELF ASSEMBLY; THIOUREAS; TISSUE ENGINEERING;

AMPHIPHILES;

ANTINEOPLASTIC ANTIBIOTIC; DOXORUBICIN; DRUG CARRIER; MACROGOL DERIVATIVE; NANOMATERIAL; THIOUREA;

ARTICLE; CELL STRAIN HEPG2; CELL SURVIVAL; CHEMICAL PHENOMENA; CHEMISTRY; DRUG EFFECT; HUMAN; MICELLE; SMALL ANGLE SCATTERING; TEMPERATURE; TISSUE ENGINEERING; X RAY DIFFRACTION;

ANTIBIOTICS, ANTINEOPLASTIC; CELL SURVIVAL; DOXORUBICIN; DRUG CARRIERS; HEP G2 CELLS; HUMANS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; MICELLES; NANOSTRUCTURES; POLYETHYLENE GLYCOLS; SCATTERING, SMALL ANGLE; TEMPERATURE; THIOUREA; TISSUE ENGINEERING; X-RAY DIFFRACTION;

EID: 84876270127     PISSN: 10221336     EISSN: 15213927     Source Type: Journal    
DOI: 10.1002/marc.201200751     Document Type: Article

References (42)

1. J.-H. Ryu, D.-J. Hong, M. Lee, Chem. Commun. 2008, 1043.
2. C. Wang, Z. Wang, X. Zhang, Acc. Chem. Res. 2012, 45, 608.
3. S. J. Holder, N. A. J. M. Sommerdijk, Polym. Chem. 2011, 2, 1018.
4. R. C. Hayward, D. J. Pochan, Macromolecules 2010, 43, 3577.
5. T. Aida, E. W. Meijer, S. I. Stupp, Science 2012, 335, 813.
6. S. Venkataraman, J. L. Hedrick, Z. Y. Ong, C. Yang, P. L. R. Ee, P. T. Hammond, Y. Y. Yang, Adv. Drug Delivery Rev. 2011, 63, 1228.
7. V. P. Torchilin, Adv. Drug Delivery Rev. 2012, 64, 302.
8. H. Otsuka, Y. Nagasaki, K. Kataoka, Adv. Drug Delivery Rev. 2012, 64, 246.
9. R. Custelcean, Chem. Commun. 2008, 295.
10. P. Cordier, F. Tournilhac, C. Soulie-Zialovic, L. Leibler, Nature 2008, 451, 977.
11. N. E. Botterhuis, S. Karthikeyan, D. Veldman, S. C. J. Meskers, R. P. Sijbesma, Chem. Commun. 2008, 3915.
12. L. A. Estroff, A. D. Hamilton, Angew. Chem. Int. Ed. 2000, 39, 3447.
13. L. A. Estroff, A. D. Hamilton, Chem. Rev. 2004, 104, 1201.
14. N. Chbotareva, P. H. H. Bomans, P. M. Frederik, N. A. J. M. Sommerdijk, R. P. Sijbesma, Chem. Commun. 2005, 4967.
15. S. H. Kim, F. Nederberg, R. Jakobs, J. P. K. Tan, K. Fukushima, A. Nelson, E. W. Meijer, Y. Y. Yang, J. L. Hedrick, Angew. Chem. Int. Ed. 2009, 48, 4508.
16. A. S. Hoffman, J. Controlled Release 2008, 132, 153.
17. M. E. Davis, Z. G. Chen, D. M. Shin, Nat. Rev. Drug Discov. 2008, 7, 771.
18. J. A. Champion, S. Mitragotri, Proc. Natl. Acad. Sci. USA 2006, 103, 4930.
19. J. A. Champion, S. Mitragotri, Pharm. Res. 2009, 26, 244.
20. D. A. Canelas, K. P. Herlihy, J. M. DeSimone, Wiley Interdiscip. Rev. Nanomed. Nanobiotechnol. 2009, 1, 391.
21. S. E. A. Gratton, P. Ropp, P. D. Pohlhaus, J. Luft, V. J. Madden, M. E. Napier, J. M. DeSimone, Proc. Natl. Acad. Sci. USA 2008, 105, 11613.
22. Y. Geng, P. Dalhaimer, S. Cai, R. Tsai, M. Tewari, T. Minko, D. E. Discher, Nat. Nanotechnol. 2007, 2, 249.
23. K. Zhang, H. Fang, Z. Chen, J.-S. A. Taylor, K. L. Wooley, Bioconjug. Chem. 2008, 19, 1880.
24. K. Grodowska, A. Parczewski, Acta Poloniae Pharmaceutica Drug Res. 2010, 67, 3.
25. C. E. Mora-Huertas, H. Fessi, A. Elaissari, Int. J. Pharm. 2010, 385, 113.
26. C. Fong, D. Wells, I. Krodkiewska, P. G. Hartley, C. J. Drummond, Chem. Mater. 2006, 18, 594.
27. Y. Hu, M. Rogunova, V. Topolkaraev, A. Hiltner, E. Baer, Polymer 2003, 44, 5701.
28. W.-C. Lai, W.-B. Liau, T.-T. Lin, Polymer 2004, 45, 3073.
29. J. H. Jung, Y. Do, Y.-A. Lee, T. Shimizu, Chem. Eur. J. 2005, 11, 5538.
30. J. H. Jung, G. John, M. Masuda, K. Yoshida, S. Shinkai, T. Shimizu, Langmuir 2001, 17, 7229.
31. J. H. Jung, G. John, K. Yoshida, T. Shimizu, J. Am. Chem. Soc. 2002, 124, 10674.
32. S. J. Lee, E. Kim, M. L. Seo, Y. Do, Y.-A. Lee, S. S. Lee, J. H. Jung, M. Kogiso, T. Shimizu, Tetrahedron 2008, 64, 1301.
33. S. Mahabir, W. Wan, J. Katsaras, M.-P. Nieh, J. Phys. Chem. B. 2010, 114, 5729.
34. M.-P. Nieh, P. Dolinar, N. Kučerka, S. R. Kline, L. M. Debeer-Schmitt, K. C. Littrell, J. Katsaras, Langmuir 2011, 27, 14308.
35. M.-P. Nieh, V. A. Raghunathan, S. R. Kline, T. A. Harroun, C.-Y. Huang, J. Pencer, J. Katsaras, Langmuir 2005, 21, 6656.
36. Z. Li, Z. Chen, H. Cui, K. Hales, K. Qi, K. L. Wooley, D. J. Pochan, Langmuir 2005, 21, 7533.
37. Z. Li, Z. Chen, H. Cui, K. Hales, K. L. Wooley, D. J. Pochan, Langmuir 2007, 23, 4689.
38. W. F. Edmonds, Z. Li, M. A. Hillmyer, T. P. Lodge, Macromolecules 2006, 39, 4526.
39. T. P. Lodge, M. A. Hillmyer, Z. Zhou, Y. Talmon, Macromolecules 2004, 37, 6680.
40. R. R. Taribagil, M. A. Hillmyer, T. P. Lodge, Macromolecules 2009, 42, 1796.
41. J. Qian, M. Zhang, I. Manners, M. A. Winnik, Trends Biotechnol. 2009, 28, 84.
42. N. Petzetakis, A. P. Dove, R. K. O'Reilly, Chem. Sci. 2011, 2, 955.