Particle formation methods and their products

Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Particulate form

Reexamination Certificate

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C424S400000, C424S439000

Reexamination Certificate

active

07115280

ABSTRACT:
Preparation of particles of an active substance having a layer of an additive at the particle surfaces, by dissolving both the active substance and the additive in a vehicle to form a target solution, and contacting the target solution with an anti-solvent fluid using a SEDS™ particle formation process, to cause the active substance and additive to coprecipitate. The additive is typically a protective additive, in particular a taste and/or odour masking agent. Also provided is a particulate coformulation made by the method, which has a finite gradient in the relative additive concentration, which concentration increases radially outwards from the active-rich core to the additive-rich surface of the particles.

REFERENCES:
patent: 4341759 (1982-07-01), Bogentoft et al.
patent: 4397907 (1983-08-01), Rosser et al.
patent: 4423099 (1983-12-01), Mueller et al.
patent: 4624848 (1986-11-01), Lee
patent: 4760093 (1988-07-01), Blank et al.
patent: 4835187 (1989-05-01), Reuter et al.
patent: 4952402 (1990-08-01), Sparks et al.
patent: 5043280 (1991-08-01), Fischer et al.
patent: 5424076 (1995-06-01), Gorissen et al.
patent: 5795594 (1998-08-01), York et al.
patent: 5916596 (1999-06-01), Desai et al.
patent: 6117455 (2000-09-01), Takada et al.
patent: 6322897 (2001-11-01), Borchert et al.
patent: 2002/0000681 (2002-01-01), Gupta et al.
patent: 2004/0119179 (2004-06-01), Perrut et al.
patent: 0709085 (1995-10-01), None
patent: 1022020 (1995-10-01), None
patent: 2 371 501 (2002-07-01), None
patent: 4187739 (1992-07-01), None
patent: 9082319 (1997-03-01), None
patent: 9611238 (1996-08-01), None
patent: WO 81/02975 (1981-10-01), None
patent: WO 97/31691 (1997-09-01), None
patent: WO 98/13136 (1998-04-01), None
patent: WO 98/13136 (1998-04-01), None
patent: WO 99/17748 (1998-09-01), None
patent: WO 99/17742 (1999-04-01), None
patent: WO 99/19085 (1999-04-01), None
patent: WO 99/59710 (1999-11-01), None
patent: WO 99/59710 (1999-11-01), None
patent: WO 01/15664 (2000-08-01), None
patent: WO 01/03821 (2001-01-01), None
patent: WO 01/45731 (2001-06-01), None
patent: WO 01/45731 (2001-06-01), None
patent: WO 02/32462 (2002-04-01), None
patent: WO 02/38127 (2002-05-01), None
S.A. Wilkins et al., “The Formulation of Indomethacin: Polymer co-Precipitates by the Solution Enhanced Dispersion by Supercritical Fluids (SEDS) Process,” J. of Pharmacy and Pharmol., GB, London vol. 51, (Suppl.) 1999, p. 291.
G.K. Vudathala et al., “Microencapsultation of Solid Dispersions: Release of Griseofulvin from Griseofulvin: Phospholipid Correcipitates in Microspheres,” Pharm. Research, US, New Your, NY, vol. 9, No.6, Jun. 1, 1992, p. 759-763.
J.D. Meyer et al., “Preparation and in Vitro Characterization of Gentamycin-Impregnated biodegradable Beads Suitable for Treatment of Osteomyelitis,” J. of Pharm. Sci. . , American Pharmacuetical Assoc., Washington, US, vol. 87, No. 9, p. 1149-1154.
Ghaderi et al., “A New Method for Preparing Biodegradable Microparticles and Entrapment of Hydrocortisone in DL-PLG Microparticles Using Supercritical Fluids,” European J. of Pharm. Sci., vol. 10, No. 1, Mar. 2000, p. 1-9.
B. Kovacs et al., “Hydroxyethylcellulose for Tablet Coating,” Drug Dev. Ind. Pharm., 1990, 16, p. 2302-2323.
“Hydroxy Propylcellulose,” Handbook of Pharm. Excepients, 2nd Edn., 1994, p. 223.
J. Stafford, “Hydroxypropyl Methyphthalate as Enteric Coationg for Tablets/Granules,” Drug Dev. Ind. Pharm., 1982, 8, p. 513-530.
K. Lehman, “Coating of Tablets and Small Particles with Acylic Resins by Fluid Bed Technology (Eudragit),” Int. J. Pharm. Tech. Prod. Mfr., 1981, 2(4), p. 31-43.
J. D. Meyer et al., “Preparation and in Vitro Characterization of Gentamycin-Impregnatedbiodegradable Beads Suitable for Treatment of Osteomyelitis,” J. of Pharm. Sci., American Pharmaceutical Assoc., Washington, US, vol. 87, No. 9, Sep. 1, 1998, p. 1149-1154.
G. K. Vudathala et al., “Microencapsulation of Solid Dispersions: Release of Griseofulvin from Griseofulvin: Phospholipid Correcipitates in Microspheres,” Pharm. Research, US, New York, Ny, vol. 9, No. 6, Jun. 1, 1992, p. 759-763.
P. He et al., “Chitosan Microspheres Prepared by Spray Drying,” International J. of Pharm. (Amsterdam), vol. 187, No. 1, p. 53-65.
Moneghini M. et al., “Processing of Carbamazephine-PEG 4000 Solid Dispersions with Supercritical Carbon Dioxide:,” International J. of Pharm. Netherlands Jul. 3, 2001. vol. 222, No. 1, p. 129-138.
S.A. Wilkins et al., “The Formation o findomethacin: Polymer Co-Precipitates by the Solution Enhanced Dispersion by Supercritical Fluids (SEDS) Process,” J. of Pharmacy and Pharmacol., GB, London vol. 51 (Suppl.) 1991, p. 291.

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