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Formation of Supramolecular Assemblies by Modulating Self-Assembling Properties of Diacetylenic Phosphocholines

Published online by Cambridge University Press:  21 March 2011

Alok Singh
Affiliation:
Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, Washington, DC 20375 USA
Eva M. Wong
Affiliation:
Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, Washington, DC 20375 USA
Mark S. Spector
Affiliation:
Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, Washington, DC 20375 USA
Joel M. Schnur
Affiliation:
Center for Bio/Molecular Science & Engineering, Naval Research Laboratory, Washington, DC 20375 USA
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Abstract

Diacetylenic phospholipid dispersions in water produce tubules (500 nm diameter) and helices from their initial vesicular morphology as a function of temperature and concentration. A binary mixture consisting of diacetylenic phospholipid, 1,2 bis (tricosa-10, 12-diynoyl)-sn-glycero-3-phosphocholine and a short chain phospholipid, 1,2-dinonanoyl –sn-glycero-3-phosphocholine was studied to explore the morphological transformation of lipids into tubules to develop an approach to control and produce tubules of different diameters. Circular dichroic spectra not only indicated the chiral nature of these tubules, but also provided distinct spectral signatures differentiating micro- and nanotubules. The effects of temperature and lipid concentration on the formation and stability of tubules were also explored. An equimolar lipid mixture provided structures with uniform morphology, which were stable for several hours up to 36°C. The thermal stability of nanotubules makes them an attractive candidate for many practical applications including controlled release technology.

Type
Research Article
Copyright
Copyright © Materials Research Society 2002

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References

REFERENCES

1. Schnur, J. M., Science 262, 1669 (1993).Google Scholar
2. Singh, A. and Schnur, J. M., “Polymerized Phospholipids” in Handbook of Phospholipids, Cevc, G., ed. (Marcel Dekker, 1995), pp 233291.Google Scholar
3. Bong, D.T., Clark, T. D., Granja, J. R., and Ghediri, M. R., Angew. Chem. Int. Ed. 40, 988 (2001).Google Scholar
4. Ariga, K., Kikuchi, J., Naito, M., Koyama, E., and Yamada, N., Langmuir 16, 4929 (2000).Google Scholar
5. Fuhrhop, J.H. and Helfrich, W., Chem. Rev 93, 1565 (1993).Google Scholar
6. Yager, P., Schoen, P. E., Mol. Cryst. Liq. Cryst. 106, 371 (1984).Google Scholar
7. Georger, J. H, Singh, A., Price, R. R., Schnur, J. M., Yager, P., and Schoen, P. E., J. Am. Chem. Soc. 109, 61696175 (1987).Google Scholar
8. Markowitz, M. A., Singh, A., and Schnur, J. M., Chem. Phys. Lipids 62, 193 (1992).Google Scholar
9. Singh, A., Markowitz, M. A., and Tsao, L., Chem. Phys. Lipids 63, 191 (1992).Google Scholar
10. Rhodes, D. G. and Singh, A., Chem. Phys. Lipids 59, 215 (1991).Google Scholar
11. Markowitz, M. A., Chang, E. L., and Singh, A., Bichem. Biophys. Res. Commun. 203, 296 (1994).Google Scholar
12. Svenson, S. and Messersmith, P. B., Langmuir 15, 4464 (1999).Google Scholar
13. Spector, M. S., Singh, A., Messersmith, P. B., and Schnur, J. M., Nano Letters 7, 375 (2001).Google Scholar
14. Nakashima, N., Ando, R., Muramatsu, T., and Kunitake, T., Langmuir 10, 232 (1994).Google Scholar
15. Singh, A. and Gaber, B. P., Applied Bioactive Polymeric Materials, Gebelein, C. G., Carraher, C. E., and Forster, V. R. eds. (Plenum Press, 1988) p.239.Google Scholar
16. Rhodes, D. G. and Singh, A., Chem. Phys. Lipids 59, 215 (1991).Google Scholar
17. Schnur, J. M., Ratna, B. R., Selinger, J. V., Singh, A., Jyothi, G., and Easwaran, K. R. K., Science 264, 945 (1994).Google Scholar