Hydroxypropyl- β-cyclodextrin inclusion complexes for transdermal delivery: Preparation, inclusion properties, stability, and release behavior

Journal of Industrial and Engineering Chemistry

Volumn 12, Issue 1, 2006, Pages 50-59

  Cho, Seung Hei ^a   Kim, So Yeon ^a   Lee, Sang In ^b   Lee, Young Moo ^a  

^a Hanyang University   (South Korea)

^b Macrocare Tech Ltd   (South Korea)

Author keywords

cyclodextrin; Hydroxypropyl cyclodextrin; Inclusion complex; Vitamin; Water solubility

Indexed keywords

EID: 31944445779     PISSN: 1226086X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. J. L. Atwood, J. E. D. Davis, D. D. MacNicol, F. Vogtle, J.-M. Lehn, J. Szejtli, and Osa, Comprehensive supramolecular chemistry, Volume 3. Elsevier Science, New York (1996).
2. E. M. Martin Del Valle, Process Biochemistry, 39, 1033 (2004).
3. M. Singh Sharma and U. C. Banerjee, Biotechnology Advances, 20, 341 (2002).
4. G. Gattuso, S. A. Nepogodiev, and J. F. Stoddart, Chem. Rev., 98, 1919 (1998).
5. H. Matsuda and H. Arima, Adv. Drug Delivery Rev., 36, 81 (1999).
6. R. A. Rajewski and V. J. Stella, J. Pharm. Sci., 85, 1142 (1996).
7. L. Szente and J. Szejtli, Adv. Drug Delivery Rev., 36, 17 (1999).
8. B. Lindberg and J. Lindberg, Carbohydr. Res., 222, 113 (1991).
9. S. Jambhekar, R. Casella, and T. Maher, Int. J. Pharmaceutics, 270, 149 (2004).
10. J. Manosroi, M. G. Apriyani, K. Foe, and A. Manosroi, Int. J. Pharmaceutics, 293, 235 (2005).
11. G. Wenz and T. Hofler, Carbohydr. Res., 322, 153 (1999).
12. S. Shuang and M. M. F. Choi, J. Chromatogr. A, 919, 321 (2001).
13. S. Sabah and G. K. E. Scriba, J. Chromatogr. A, 833, 261 (1999).
14. M. P. Lupo, Clinics in Dermatology, 19, 467 (2001).
15. N. Failloux, I. Bonnet, E. Perrier, and M.-H. Baron, J. Roman Spectrosc., 35, 140 (2004).
16. J. S. Lee, Y. S. Nam, B. Y. Kang, S. H. Han, and I. S. Chang, J. Appl. Polym. Sci., 92, 517 (2004).
17. S. Scalia, A. Renda, G. Ruberto, F. Bonina, and E. Menegatti, J. Pharm. Biomed. Anal., 13, 273 (1995).
18. R. M. McClain, E. Wolz, A. Davidovich, F. Pfannkuch, and J. Bausch, Food Chem. Toxicol., 43, 1461 (2005).
19. Z. Yu, Y. Tang, D. Hu, and J. Li, Biochem. Biophys. Res. Commun., 333, 827 (2005).
20. J. Pitha, C. Rao, B. Lindberg, and P. Seffers, Distribution of substituents in 2-hydroxypropyl ethers of cyclomaltoheptaose, Carbohydr. Res., 200, 429 (1990).
21. J. Reuben, C. T. Rao, and J. Pitha, Carbohydr. Res., 258, 281 (1994).
22. L. Van Santvliet, K. Caljon, L. Pieters, and A. Ludwig, Int. J. Pharmaceutics, 171, 147 (1998).
23. C. Amnuaikit, I. Ikeuchi, K. Ogawara, K. Higaki, and T. Kimura, Int. J. Pharmaceutics, 289, 167 (2005).
24. I. C. Yue, J. Poff, M. E. Cortes, R. D. Sinisterra, C. B. Faris, P. Hildgen, R. Langer, and V. P. Shastri, Biomaterials, 25, 3743 (2004).
25. T. Cerchiara, B. Luppi, F. Bigucci, and V. Zecchi, Int. J. Pharmaceutics, 258, 209 (2003).