Sulfoalkyl ether cyclodextrin based controlled release solid pha

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

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514778, 514964, 514965, 536103, A61K 31735, C07H 1312, C08B 3716

Patent

active

060461772

ABSTRACT:
Sulfoalkyl ether cyclodextrin (SAE-CD) based controlled release pharmaceutical formulations are provided by the present invention. The present solid pharmaceutical formulations consist of a core comprising a physical mixture of one or more SAE-CD derivatives, an optional release rate modifier, a therapeutic agent, a major portion of which is not complexed to the SAE-CD, and an optional release rate modifying coating surrounding the core. The present formulations are advantageously easier to prepare than other SAE-CD based formulations in the art yet provide similar or improved effectiveness. The SAE-CD derivative is used to modify the bioavailability and/or rate of bioabsorption of therapeutic agents. Multi-layered, osmotic pump, coated, and uncoated tablet, minitablet, pellet, micropellet, particle, powder, and granule dosage forms are disclosed herein.

REFERENCES:
patent: 3426011 (1969-02-01), Parmerter et al.
patent: 4535152 (1985-08-01), Szejtli et al.
patent: 4727064 (1988-02-01), Pitha
patent: 4774329 (1988-09-01), Friedman
patent: 4869904 (1989-09-01), Uekama et al.
patent: 4946686 (1990-08-01), McClelland et al.
patent: 5134127 (1992-07-01), Stella et al.
patent: 5874418 (1999-02-01), Stella et al.
Kaneto Uekama, Kazutaka Matsubara, Kentaro Abe, Yasuhide Horiuchi, Fumitoshi Hirayama, and Nobuo Suzuki, "Design and In Vitro Evaluation of Slow-Release Dosage Form of Pirentanide: Utility of .beta.-Cyclodextrin: Cellulose Derivative Combination as a Modified-Release Drug Carrier," Journal of Pharmaceutical Sciences, vol. 79, No. 3, Mar. 1990, pp. 244-248.
O.I. Corrigan and C.T. Stanley, "Dissolution Properties of Phenobarbitone-.beta.-Cyclodextrin Systems," Pharm. Acta. Hel., vol. 56, No. 7 (1981), pp. 204-208.
A. Martini, C. Torricelli, L. Muggetti, R. DePonti, "Use of Dehydrated Beta-Cyclodextrin As Pharmaceutical Excipient," Proceed. Intern.-Symp. Control. Rel. Bioact. Mater., 20 (1993), Controlled Release Society, Inc., pp. 304-305.
A. Gursoy, M. Turkoglu, B. Senyucel, F. Kalkan, and I. Okar, "Evaluation of Tableted Microspheres of Dipyridamole," Drug Development and Industrial Pharmacy, 21(4) (1995), pp. 503-507.
H.O. Ammar, M. Ghorab, S. A. El-nahhas, S. M. Omar and M. M. Ghorab, "Improvement of some pharmaceutical properties of drugs by cyclodextrin complexation," Pharmazie, vol. 51 (1996), pp. 42-51.
Kristiina Jarvinen, Tomi Jarvinen, Diane O. Thompson and Valentino J. Stella, "The effect of a modified .beta.-cyclodextrin, SBE4-.beta.-CD, on the aqueous stability and ocular absorption of pilocarpine," Current Eye Research (1994).
V. J. Stella, H. K. Lee, D. O. Thompson, "The effect of SBE4-.beta.-CD on i.m. prednisolone pharmacokinetics and tissue damage in rabbits: Comparison to a co-solvent solution and a water-soluble prodrug," International Journal of Pharmaceutics, vol. 120 (1995), pp. 197-204.
V. J. Stella, H. K. Lee, D. O. Thompson, "The effect of SBE4-.beta.-CD on i.v. methylprednisolone pharmacokinetics in rats: Comparison to a co-solvent solution and two water-soluble prodrugs," International Journal of Pharmaceutics, vol. 120 (1995), pp. 189-195.
C. X. Song, V. Labhasetwar, R. J. Levy, "Controlled release of U-97983 from double-layer biodegradable matrices: effect of additives on release mechanism and kinetics," Journal of Controlled Release, vol. 45 (1997), pp. 177-192.
Valentino J. Stella and Roger A. Rajewski, "Cyclodextrins: Their Future in Drug Formulation and Delivery," Pharmaceutical Research, vol. 14, No. 5 (1997), pp. 556-567.
K. Uekama, F. Hirayama, and T. Irie, "New Functions of Peracylated .beta.-Cyclodextrins as Sustained-Release Drug Carriers," Proceedings of the Eighth International Symposium on Cyclodextrins (1996), pp. 413-418.
Tomi Jarvinen, Kristiina Jarvinen, Nancy Schwarting, and Valentino J. Stella, ".beta.-Cyclodextrin Derivatives, SBE4-.beta.-CD and HP-.beta.-CD, Increase the Oral Bioavailability of Cinnarizine in Beagle Dogs," Journal of Pharmaceutical Sciences, vol. 84, No. 3, Mar. 1995, pp. 295-299.
Kazuto Okimoto, Masatoshi Miyake, Norlo Ohnishi, Roger A. Rajewski, Valentino J. Stella, Tetsumi Irie, and Kaneto Uekama, Design and Evaluation of an Osmotic Pump tablet (OPT) for Prednisolone, a Poorly Water Soluble Drug, Using (SBE).sub.7m -.beta.-CD, Pharmaceutical Research, vol. 15, No. 1 (1998), pp. 1562-1568.
P. Mura, G. P. Bettinetti, A. Liguori, G. Bramanti, "Improvement of Clonazepam Release from a Carbopol Hydrogel," Pharm. Acta Helv, vol. 67, No. 9-10 (1992), pp. 282-288.
M. Chino, T. Kasama, Y. Noguchi, A. Ueda, and Y. Koyama, "Sustained-Release of Drugs from Cyclodextrin-Containing Hydrogels," Proceed. Intern. Symp. Control. Rel. Bioact. Mater., vol. 19 (1992), pp. 98-99.
Paolo Gionchedi, Lauretta Maggi, Aldo La Manna and Ubaldo Conte, "Modification of the Dissolution Behaviour of a Water-insoluble Drug, Naftazone, for Zero-order Release Matrix Preparation," J. Pharm. Pharmacol. vol. 46 (1994), pp. 476-480.
Kazuto Okimoto, Roger A. Rajewski, Kaneto Uekama, Janan A. Jona, and Valentino J. Stella, "The Interaction of Charged and Uncharged Drugs with Neutral (HP-.beta.-CD) and Anionically Charged (SBE7-.beta.-CD) .beta.-Cyclodextrins," Pharmaceutical Research, vol. 13, No. 2 (1996), pp. 256-264.
Fumitoshi Hirayama, "Inclusion Ability of Hydrophobic Cyclodextrin Derivatives and Their Application as Controlled-Release Drug Carrier," Yakugaku Kenkyu No Shinpo (1990), (6), 90-98.
J. J. Torres-Labanderia, J. Blanco-Mendez and J. L. Vila-Jato, "Biopharmaceutical stability of the glibornuride/.beta.-cyclodextrin inclusion complex after one year of storage," S.T.P. Pharma. Sciences 4(3), 1994, pp. 235-239.
F.J. Otero-Espinar, S. Anguiano-Igea, N. Garcia-Gonzalez, J.L. Vila-Jato and J. Blanco-Mendez, "Oral bioavailability of naproxen-.beta.-cyclodextrin inclusion compound," International Journal of Pharmaceutics, 75 (1991), pp. 37-44.
Hideaki Yajima, Jun Sumaoka, Sachiko Miyama, and Makoto Komiyama, "Lanthanide Ions for the First Non-Enzymatic Formation of Adenosine 3''5''Cyclic Monophosphate from Adenosine Triphosphate under Physiological Conditions,", Biochem, 115 (1994), pp. 1038-1039.
M. T. Esclusa-Diaz, M. Gayo-Otero, M. B. Perez-Marcos, J. L. Vila-Jato, J. J. Torres-Labandeira, "Preparation and evaluation of ketoconazole-.beta.-cyclodextrin multicomponent complexes," International Journal of Pharmaceutics, 142 (1991), pp. 183-187.
Noriyuki Muranushi, Mariko Yoshida, Haruki Kinoshita, Fumiaki Hirose, Takayo Fukuda, Masami Doteuchi and Hideo Yamada, "Studies on benexata-CD: Effect of inclusion compound formation on the antiulcer activity of benexate, the effective ingredient of benexate-CD," Folia pharmacol. Japon. 91 (1988), pp. 377-383.
D. Peri, C. M. Wyandt, R. W. Cleary, A. H. Hikal and A. B. Jones, "Inclusion Complexes of Tolnaftate with -.beta.-Cyclodextrin and Hydroxypropyl-.beta.-Cyclodextrin," Drug Development and Industrial Pharmacy, 20(8) (1994), pp. 1401-1410.

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