Water-insoluble drug delivery system

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

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C264S004100, C264S004300, C264S004600

Reexamination Certificate

active

06838090

ABSTRACT:
The present invention provides a drug delivery system comprising a water-insoluble drug, a water-miscible organic solvent for the water-insoluble drug, a surfactant, and water, as well as a process for preparing the same. This invention further provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and such a drug delivery system. In addition, the present invention provides a method of delivering a drug to a host by administering to the host the drug delivery system of the present invention.

REFERENCES:
patent: 4565806 (1986-01-01), Setälä
patent: 4684630 (1987-08-01), Repta et al.
patent: 4737323 (1988-04-01), Martin et al.
patent: 4816247 (1989-03-01), Desai et al.
patent: 4826689 (1989-05-01), Violanto
patent: 4842856 (1989-06-01), Hoederath et al.
patent: 4997454 (1991-03-01), Violante et al.
patent: 5039527 (1991-08-01), Tabibi et al.
patent: 5077057 (1991-12-01), Szoka, Jr.
patent: 5091188 (1992-02-01), Haynes
patent: 5270053 (1993-12-01), Schneider et al.
patent: 5516770 (1996-05-01), Waranis et al.
patent: 5530006 (1996-06-01), Waranis et al.
patent: 5616330 (1997-04-01), Kaufman et al.
patent: 5616341 (1997-04-01), Mayer et al.
patent: 5616587 (1997-04-01), François et al.
patent: 5616588 (1997-04-01), Waranis et al.
patent: 5656296 (1997-08-01), Khan et al.
patent: 5672358 (1997-09-01), Tabibi et al.
patent: 5690954 (1997-11-01), Illum et al.
patent: 5714520 (1998-02-01), Jones et al.
patent: 5731356 (1998-03-01), Jones et al.
patent: 5736159 (1998-04-01), Chen et al.
patent: 893949 (1982-11-01), None
patent: 41 25 255 (1993-02-01), None
patent: 41 25 255 (1993-02-01), None
patent: 214501 (1987-03-01), None
patent: 215313 (1987-03-01), None
patent: 502766 (1992-09-01), None
patent: 0 648 494 (1995-04-01), None
patent: 0 720 853 (1996-07-01), None
patent: 770387 (1997-05-01), None
patent: 2 609 631 (1988-07-01), None
patent: WO 9853799 (1998-12-01), None
Eiseman et al., “#536 Pharmacokinetics of 17-allylamino(17demethoxy)geldanamycin in SCID mice bearing MDA-MB-453 xenografts and alterations in the expression of p185arb-B2in the xenografts following treatment”, AACR-NCI-EORTC International Conference, Nov. 16-19, 1999, Washington, DC.
Eiseman et al., “#2063 Plasma pharmacokinetics and tissue distribution of 17-allylaminogeldanamycin (NSC 330507), a prodrug for geldanamycin, in DC2F1mice and Fisher 344 rats”, Proceedings of the American Association for Cancer Research, vol. 38, Mar. 1998, p. 308.
Page et al., #2067 Comparison of geldanamycin (NSC-122750) and 17-allylaminogeldanamycin (NSC0330507D) toxicity in rats, Proceedings of the American Association for Cancer Research, vol. 38, Mar. 1998, p. 308.
Egorin et al., “#3567 Metabolism of 17-(allylamino)-17-demethoxygeldanamycin (17AAG) (NSC 330507) by murine and human hepatic preparations”, Proceedings of the American Association for Cancer Research, vol. 38, Mar. 1998, p. 524.
Burger et al., “#504 Antitumor activity of 17-allylaminogeldanamycin (NSC 330507) in melanoma xanografts in associated with decline in Hsp90 protein expression”, 10thNCJ-EDRTC Symposium on New Drugs in Cancer Therapy, Jun. 16-19, 1999, Amsterdam.
Laurie McCarthy, “Nanonization” Technology Provides Solutions for the Insoluble, http:/
ews.pharmaceuticalonlin.com/feature-articles/19980113-72.html.
“KODAK Established Independent Business to Develop Small Particle Technology”, http://www.kodak.com/aboutKodak/corpInfo/pressReleases/pr951106-2.shtml.
“Nanoparticles”, Process and Characteristics, Formulations and Biodistribution, and Case Studies, http://www/stsduotek.com
anoport.htm © 1997-98.
Davis, “Biomedical applications of nanotechnology-implications for drug targeting and gen therapy”, Trends Biotechnol, Jun. 1997, 15(6):217-214 (Abstract only).
Sharma et al., “Novel taxol formulations: preparation and characterization of taxol-containing liposome”, Pharm Res, Jun. 1994, 11(6):889-896 (Abstract only).
Hauss et al., Lipid-based delivery systems for improving the ioavailability and lymphatic transport of a poorly water-woluble LTB4 inhibitor, J Pharm Sci, Feb. 1998, 87(2):164-169 (Abstract only).
Merisko-Liversidge et al., “Formulation and antitumor activity evaluation of nonocrystalline suspensions of poorly soluble anticancer drugs”, Parm Res, Feb. 1996, 13(2):272-278 (Abstract only).
Anderson et al., “Strategies in he design of solution-stable, water-soluble prodrugs II: properties of micellar prodrugs of methylprednisolone”, J Pharm Sci, Apr. 1985, 74(4):375-381 (Abstract only).
Storm et al., “Colloidal systems for tumor targeting”, Hybridoma, Feb. 1997, 16(1):119-125 (Abstract only).
Jones, “The surface properties of phospholipid liposome systems and their characterization”, Adv colloid Interface Sci, Jan. 3, 1995, 54:93-128 (Abstract only).
Storm et al., Biopharmaceutical aspects of lipid formulations of amphotericin B., Eur J Clin Microbiol Infect Dis, Jan. 1997, 16(1):64-73 (Abstract only).
Benita et al., “Submicron emulsions as colloidal drug carriers for Intravenous administration: comprehensive physicochemical characterization”, J Pharm Sci, Nov. 1993, 82(11):1069-1079 (Abstract only).
Gabizon, “Tailoring liposomes for cancer drug delivery: from the bench to the clinic”, Ann Biol Clin (Paris), 1993, 51(9):811-813 (Abstract only).
Marty et al., Nanoparticles—a new colloidal drug delivery system., Pharm Acta Helv, 1978, 53(1):17-23 (Title only).
Thompson, “Cyclodextrins—enabling excipients: Their present and future use in pharmaceuticals”, Critical Reviews in Therapeutic Drug Carrier Systems (USA), 1997, 14/1 (1-104) (Abstract only).
Sculier et al., “Intravenous Infusion of high doses of liposomes containing NSC 251635, a water-insoluble cytostatic agent. A pilot study with pharmacokinetic data”, J. Clin. Oncol. (USA), 1986, 4/5 (789-797), (Abstract only).
Torchilin et al., “Long acting thrombolytic immobilized enzymes”, J. Control. Release (Netherlands), 1985, vol. 2 (321-330) (Abstract only).
Laduron et al., “Chemotherapeutic efficacy of Nocodazole(Reg. Trademark) encapsulated in liposomes on L1210 murine leukemia”, Res. Commun. Chem. Pathol. Pharmacol. (USA), 1983, 39/3 (419-436) (Abstract only).
Alyautdin et al., “Delivery of loperamide across the blood-brain-barrier with polysorbate 80-coated polybutylcyanoacrylate nanoparticles”, Pharmaceutical Research (New York) 14(3), 1997, 325-328 (Abstract only).
Leroux et al., “Pharmacokinetics of a novel HIV-1 protease inhibitor Incorporated into biodegradable or enteric nanoparticles following intravenous and oral administration to mice”, Journal of Pharmaceutical Sciences (J-Pharm-Sci) 84:1387-1391, Dec. 1995 (3 pages).
Page et al., “Comparison of geldanamycin (NSC0122750) and 17-allylaminogeldanamycin (NSC-330507D) toxicity in rats”, Proc Annu Am Assoc Cancer Res, 38:A2067 1997 (Abstract only).
Eiseman et al., “Plasma pharmacokinetics and tissue distribution of 17-allylaminogeldanamycin (NSC-330507), a prodrug for geldanamycin, in DC2F1 mice and Fisher 344 rats”, Proc Annu Am Assoc Cancer Res, 38:A2063 1977 (Abstract only).
Larroque et al., “Serum albumin as a vehicle for zinc phthalocyanine: photodynamic activities in solid tumour models”, Br J Cancer, 1996, 74(12):1886-90 (Abstract only).
Merisko-Liversidge et al., “Formulation and antitumor activity evaluationof nanocrystalline suspensions of poorly soluble anticancer drugs”, Pharm Res, 13(2):272-8 1996 (Abstract only).
Son, “Intravenous delivery of water-insoluble drugs”, Diss Absr Int [B], 52(5):2518 1991 (Abstract only).
Zuidam et al., “Sterilization of liposomes by heat treatment”, Pharm Res, 10(11):1591-6 1993 (Abstract only).
Tiurin-Kuz'Min et al., “Vliianie davleniia metabolicheski ine

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Water-insoluble drug delivery system does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Water-insoluble drug delivery system, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Water-insoluble drug delivery system will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3437586

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.