Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-23T10:44:13.612Z Has data issue: false hasContentIssue false

Preparation of Asymmetric Thermosensitive Double-layer Gel

Published online by Cambridge University Press:  01 February 2011

Takashi Iizawa
Affiliation:
[email protected], Hiroshima University, Chemical Engineering, Higashi-hiroshima, Japan
Akihiro Terao
Affiliation:
[email protected], Hiroshima University, Chemical Engineering, Higashi-Hiroshima, Japan
Get access

Abstract

Heterogeneous amidation of poly(acrylic acid) gel-1,8-diazabicyclo-[5,4,0]-7-undecene salt (DAA) in N-methyl-2-pyrrolidone containing an excess of alkylamine and triphenylphosphite occurred from the surface to give the corresponding DAA-poly(N-alkylacrylamide) (PNAA) core-shell type gel, consisting of an unreacted DAA core and a quantitatively amidated shell layer. Further amidation of the DAA-PNAA core-shell type gel with a second alkylamine afforded a novel core-shell type gel consisting of two PNAA layers: PNAA(2) and PNAA(1). The resulting cylindrical PNAA(2)-PNAA(1) core-shell type gels were resistant to marked deformation caused by swelling/de-swelling because of their axial symmetry. This paper proposes a new approach to the preparation of asymmetric thermosensitive PNAA(2)-PNAA(1) double-layer gels by several procedures using the synthetic method of the core-shell type gels containing of poly(N-isopropylacrylamide) and poly(N-n-propylacrylamide) layers. Among the obtained asymmetric double-layer gels the model I type gel (cylindrical grooved PNNPA-PNIPA core-shell type gel) was markedly bent in water at temperatures between the lower critical solution temperatures of both layers.

Type
Research Article
Copyright
Copyright © Materials Research Society 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Ito, S., Kobunshi Ronbunshu, 46, 437 (1989).Google Scholar
2. Osada, Y., Okuzaki, H., Hori, H., Nature, 355, 242 (1992)Google Scholar
3. (a) Freitas, R. F. S. and Cussler, E. L., Chem. Eng. Sci., 42, 97 (1987).Google Scholar
(b) Cai, W., and Gupta, R. B., Ind. Eng. Chem. Res., 40, 3406 (2001).Google Scholar
4. Seida, Y. and Nakano, Y., J. Chem. Eng. Jpn., 29, 767 (1996).Google Scholar
5. Dong, L. C. and Hoffman, A. S., J. Controlled Release, 15, 141 (1990).Google Scholar
6. Park, T. G. and Hoffman, A. S., J. Biomed. Res., 24, 21 (1990).Google Scholar
7. Iizawa, T., Terao, A., Ohuchida, M., Matsuura, Y. and Onohara, Y., Polymer J., 39, 63 (2007).Google Scholar
8. (a) Iizawa, T., Matsuno, N., Takeuchi, M., and Matsuda, F., Polymer J., 31, 1277 (1999).Google Scholar
(b) Iizawa, T., Matsuno, N., Takeuchi, M., and Matsuda, F., Polymer J., 34, 63 (2002).Google Scholar
(c) Iizawa, T., Matsuura, Y., Hashida, K., and Onohara, Y., Polymer J., 35, 815 (2003).Google Scholar
(d) Iizawa, T., Matsuura, Y., and Onohara, Y., Polymer, 46, 8098 (2005)Google Scholar
9. Yagi, S. and Kunii, T., Kogyo Kagaku Zashi, 56, 131 (1953)..Google Scholar