Drug – bio-affecting and body treating compositions – Extract – body fluid – or cellular material of undetermined... – Digestive system
Reexamination Certificate
1998-12-14
2002-02-26
Witz, Jean C. (Department: 1651)
Drug, bio-affecting and body treating compositions
Extract, body fluid, or cellular material of undetermined...
Digestive system
C424S520000, C514S012200, C514S021800
Reexamination Certificate
active
06350472
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention is directed to a method of treating human immuno-deficiency virus (HIV-1) infections and to the discovery that a mammalian liver extract is efficacious in treating such infections. The present invention is also directed to a method of treating HIV-1 infections with this same mammalian liver extract. The present invention is further directed to a method of preparing a colloidal dispersion for use with this same mammalian liver extract. The present invention is also directed to a method of using a transdermal colloidal dispersion delivery system to treat HIV-1 infections.
2. Brief Description of Prior Art
Acquired immune deficiency syndrome (AIDS) and AIDS-related complex (ARC) are caused by human immuno-deficiency virus (HIV-1), a retrovirus. The HIV-1 virus infects immune, neural, and other cells of its host. Eventually most people infected with HIV-1 become abnormally susceptible to a variety of serious opportunistic diseases as a result of the immune deficiency caused by the virus.
The current anti-HIV-1 drugs are either not effective or cause undesirable side effects. These drugs include AZT, 2′,3′-dideoxy cytidine (ddCyd), interferon (IFN), mismatched double stranded RNA (dsRNA) and amphotericin B. In particular, AZT, which has shown some promise in the treatment of AIDS, causes very serious side effects, such as bone marrow suppression, in a high proportion of patients. Also, the beneficial effects of AZT have been reported to abate in 12-18 months, and patients get new infections or develop toxic side effects. (Chase, “Doctors and Patients Hope AZT Will Help Stave Off AIDS,”
Wall Street Journal
, Apr. 28, 1988, p. 14, col. 1.)
One commercially available mammalian liver abstract useful for purposes of the present invention is sold under the trademark KUTAPRESSIN by Kremers-Urban Co., of Milwaukee, Wis. According to product literature, this extract exerts its action only with respect to tissues that have been injured, and particularly when inflammation and edema are present.
U.S. Pat. No. 5,055,296, filed by certain inventors common to the present application further discloses use of a particular heat stable, acetone-insoluble, water-soluble mammalian liver extract, designated as “KU 10,001” that was shown to be effective in the treatment of mammals infected with a non-dermatological virus and, in particular, chronic fatigue syndrome. The disclosure of this patent as to such extracts are incorporated herein by reference. This patent also discloses preliminary results of this extract as a protector of MT-2 cells using an in vitro test culture, when exposed to HIV-1.
U.S. Pat. No. 5,284,664, filed by certain inventors common to the present application, disclose a heat stable, acetone-insoluble, water-soluble mammalian liver extract, that is said to be effective in the treatment of symptoms of Alzheimer's Disease. The liver extract was also partially sequenced, and that sequence listing is incorporated herein by reference.
U.S. Pat. No. 5,316,775, filed by certain inventors common to the present application, discloses the same mammalian liver extract and demonstrates it to be effective in the treatment of Hepatitis B infections.
U.S. Pat. No. 5,334,395, filed by certain inventors common to the present application, discloses use of the same mammalian liver extract and demonstrates it to be effective in the treatment of Epstein-Barr viral infections.
U.S. Pat. No. 4,254,103, discloses a method of extracting Hepatoprotector Factor (HF) from bovine liver to be used in the treatment of cirrhosis of the liver and viral hepatitis.
U.S. Pat. No. 4,883,660, discloses gel bases for use in pharmaceutical compositions comprising a glycol solvent, and ethoxylated fatty alcohols or ethoxylated behenyl alcohol. The composition is suitable for topical, systemic and oral administration of pharmaceutical agents.
U.S. Pat. No. 5,492,937, discloses a composition which is a liquid at or below room temperature, and forms a highly viscous gel at body temperature. This composition is comprised of a cellulose ether, a surfactant, and other optional additives. It may be used for oral or local administration of a pharmaceutical to the skin, mucous membrane, eye, or body cavity.
U.S. Pat. No. 5,589,192, discloses a gel formulation for use with local anesthetics. A support of non-woven fabric with an impervious backing sheet is coated with a copolymer containing a local anesthetic. A polymer/drug matrix is formed, and an aqueous fluid is used to coat the surface of the matrix, converting the matrix into a gel with good percutaneous absorption.
U.S. Pat. No. 5,595,760, discloses a composition which includes a soluble, gelable salt of a peptide, and a pharmaceutical carrier. The composition forms a gel upon interacting with body fluids after injection, and the peptides are released continuously over a period of at least three days.
Against this background, the inventors have endeavored to discover a method to treat HIV-1 infections, using a heat stable, acetone-insoluble, water-soluble mammalian liver extract.
SUMMARY OF THE INVENTION
The present invention provides a method of treating HIV-1 infections involving administering to a mammal having said disease a therapeutically effective amount of mammalian liver extract, the extract being characterized by being heat stable, insoluble in acetone, and soluble in water. The terminology “heat stable” means that the liver extract does not lose appreciable activity at temperatures of about 100° C. in water over ten minutes. A preferred extract is specifically referred to as KUTAPRESSIN, which is further concentrated as disclosed herein. Also, this invention relates to a method of preparing a transdermal colloidal dispersion delivery system for use with said mammalian liver extract. This invention further relates to a method of using a transdermal colloidal dispersion delivery system to treat HIV-1 infections. One advantage of the above-mentioned colloidal dispersion delivery system is the improved ease of administration of the pharmaceutical composition by the patient. Another advantage of the above-mentioned colloidal dispersion delivery system is the ability to provide the pharmaceutical composition in a concentration high enough to be therapeutically effective in the treatment of HIV-1 infections.
Another advantage of the invention is the highly concentrated nature of the liver extract. The extracts of the prior art were more dilute and therefore administration of the liver extracts at dosages shown to be therapeutically effective herein for the treatment of HIV-1 viral infections was difficult and inefficient.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
The portion of mammalian liver extract that has been discovered to be effective in treating HIV-1 infection is the fraction which is heat stable, insoluble in acetone, and soluble in water. As disclosed in U.S. Pat. Nos. 5,284,664, 5,316,775, and 5,334,395, it is believed that these polysaccharides are present in KUTAPRESSIN in the form of proteoglycans or glycoproteins.
A transdermal delivery system has been discovered to be a particularly effective method of delivering a mammalian liver extract, such as KUTAPRESSIN, when further concentrated according to the present invention. Such a transdermal delivery system allows the concentrated liver extract to be absorbed into the blood in concentrations apparently adequate for the treatment of HIV-1 infection.
Preparation of a Transdermal Colloidal Dispersion Delivery System for Kutapressin
The transdermal colloidal dispersion employed in the present invention is one of the preferred methods for administering the liver extract.
A soy lecithin gel is prepared from 10 grams of soy lecithin, to which 11.7 ml of isopropyl palmitate and 0.2 g of sorbic acid are added. The gel is then allowed to meld for 24 hours. A 20% poly(oxypropylene)-poly(oxyethylene) copolymer gel, such as Pluronic 127 (BASF), is prepared by adding 0.2 g of potassium sorbate and 100 ml of distilled water
Hermann, Jr. William J.
Pylant Phillip R.
Steinbach Thomas
Fitzpatrick ,Cella, Harper & Scinto
Patten Patricia
Steinbach, Pylant, and Hermann, L.L.C.
Witz Jean C.
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