Characteristics and photo-responsive release property of liposome containing 7-acetoxy coumarin

Journal of Nanoscience and Nanotechnology

Volumn 11, Issue 11, 2011, Pages 10262-10270

  Seo, Hee Jin ^a   Kim, Jin Chul ^a  

^a Kangwon National University   (South Korea)

Author keywords

7 Acetoxy Coumarin; Egg Phosphatidylcholine; Liposomes; Photo Responsive Release

Indexed keywords

7-ACETOXY COUMARIN; CARBOXYFLUORESCEIN; DISTILLED WATER; EGG PHOSPHATIDYLCHOLINE; H NMR SPECTRA; LIPOSOMAL MEMBRANES; LIPOSOMAL SUSPENSION; MIXTURE FILMS; PHOSPHATIDYLCHOLINE; PHOTO-RESPONSIVE RELEASE; PHOTODIMERIZATION; RELEASE PROPERTY; SODIUM ACETATE; UNSATURATED CHAINS;

DIMERIZATION; DIMERS; LIPOSOMES; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PHOSPHOLIPIDS;

IRRADIATION;

ACETIC ACID; COUMARIN DERIVATIVE; LIPOSOME; PHOSPHATIDYLCHOLINE;

ARTICLE; CHEMISTRY; DIMERIZATION; DRUG STABILITY; INFRARED SPECTROSCOPY; NUCLEAR MAGNETIC RESONANCE; PHOTOCHEMISTRY; RADIATION EXPOSURE; TRANSMISSION ELECTRON MICROSCOPY; ULTRAVIOLET RADIATION;

COUMARINS; DIMERIZATION; DRUG STABILITY; LIPOSOMES; MICROSCOPY, ELECTRON, TRANSMISSION; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PHOSPHATIDYLCHOLINES; PHOTOCHEMICAL PROCESSES; SODIUM ACETATE; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; ULTRAVIOLET RAYS;

EID: 84857188757     PISSN: 15334880     EISSN: None     Source Type: Journal    
DOI: 10.1166/jnn.2011.4996     Document Type: Article

References (28)

1. S. Wright and L. Huang, Adv. Drug Deliv. Rev. 3, 343 (1989).
2. V. A. Slepushkin, S. Simoes, P. Dazin, M. S. Newman, L. S. Guo, M. C. Pedroso de Lima, and N. Duzgunes, J. Biol. Chem. 272, 2382 (1997).
3. S. M. Jo, Y. Xia, H. Y. Lee, Y. C. Kim, and J. C. Kim, Korean J. Chem. Eng. 25, 1221 (2008).
4. J. A. Zasadzinski, B. Wong, N. Forbes, G. Braun and G. Wu, Curr. Opin. Colloid. Interface Sci. 16, 203 (2011).
5. P. Chandaroy, A. Sen, and S. W. Hui, J. Control. Release 76, 27 (2001).
6. J. C. Kim and J. D. Kim, Colloid. Surface B 24, 45 (2002).
7. K. Kono, H. Hayashi, and T. Takagishi, J. Control. Release 30, 69 (1994).
8. A. Yavlovich, A. Singh, S. Tarasov, J. Capala, R. Blumenthal, and A. Puri, J. Therm. Anal. Calorim. 98, 97 (2009).
9. C. G. Morgan, E. W. Thomas, S. S. Sandhu, Y. P. Yianni, and A. C. Mitchell, Biochim. Biophys. Acta 903, 504 (1987).
10. R. H. Bisby, C. Mead, and C. G. Morgan, Photochem. Photobiol. 72, 57 (2000).
11. C. G. Morgan, S. S. Sandhu, Y. P. Yianni, and N. J. F. Dodd, Biochim. Biophys. Acta 903, 495 (1987).
12. B. Chandra, R. Subramaniam, S. Mallik, and D. K. Srivastava, Org. Biomol. Chem. 4, 1730 (2006).
13. J. S. Katz and J. A. Burdick, Macromol. Biosci. 10, 339 (2010).
14. Y. Chem and K. H. Chen, J. Polym. Sci. Pol. Chem. 35, 613 (1997).
15. N. K. Mal, M. Fujiwara, Y. Tanaka, T. Taguchi, and M. Matsukata, Chem. Mater. 15, 3385 (2003).
16. H. C. Kim, S. Kreiling, A. Greiner, and N. Hampp, Chem. Phys. Lett. 372, 899 (2003).
17. J. Jiang, B. Qi, M. Lepage, and Y. Zhao, Macromolecules 40, 790 (2007).
18. J. He and Y. Zhao, Dyes. Pigments 89, 278 (2011).
19. Y. J. Hong, G. P. Choi, and J. C. Kim, Int. J. Biol. Macromol. 47, 635 (2010).
20. Y. J. Hong and J. C. Kim, J. Nanosci. Nanotechnol. 10, 8380 (2010).
21. Q. Jin, G. Liu, and J. Ji, Eur. Polym. J. 46, 2120 (2010).
22. S. M. Jo and J. C. Kim, Colloid. Polym. Sci. 287, 379 (2009).
23. S. G. Antimisiaris, P. Kallinteri, and D. G. Fatouros, Pharmaceutical Manufacturing Handbook: Production and Processes, edited by S. C. Gad, John Wiley & Sons, Inc., New Jersey (2008), p. 456.
24. B. Caruso, D. M. Maestri and M. M. Perillo, Colloid. Surface B 75, 57 (2010).
25. Y. Jiang, S. K. Noh, and S. I. Koo, J. Nutr. 131, 2358 (2001).
26. J. Malsam, F. Seiler, Y. Schollmeier, P. Rusu, J. M. Krause, and T. H. Sollner, Proc. Natl. Acad. Sci. U.S.A 106, 2001 (2009).
27. L. H. Lindner, M. E. Eichhorn, H. Eibl, N. Teichert, M. Schmitt- Sody, R. D. Issels, and M. Dellian, Clin. Cancer Res. 10, 2168 (2004).
28. N. A. Kuznetsova and O. L. Kaliya, Russ. Chem. Rev. 61, 1243 (1992).