Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai
Reexamination Certificate
2000-11-28
2003-05-20
Weber, Jon P. (Department: 1651)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Peptide containing doai
C514S002600, C514S008100
Reexamination Certificate
active
06566331
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to the treatment of collagen related diseases in mammals. More specifically, there is provided the treatment of interstitial cystitis, scleraderma, rheumatoid arthritis, and the like with serine protease inhibitors.
BACKGROUND OF THE INVENTION
Interstitial cystitis (IC) is characterized by a symptom complex which includes chronic, irritative and painful voiding symptoms that are associated with histological nonspecific chronic inflammation and cystoscopic finds of glomerulation and/or ulcers. It occurs primarily in women (10:1, female-to-male ratio), however, it has been diagnosed in children and adolescents. It is now believed that this clinical syndrome is multifactorial and involved several mechanisms. The hypothesized causes include infection, alternations in the glycosaminoglycan layer, lymphovascular obstruction, neurogenic disorders, endocrinologic disturbances, psychoneuroses, autoimmune disorders and nonspecific and nonspecific or immune-mediated inflammation. The disease is considered by many as being related to the collagen diseases.
Scleroderma is characterized by a thickening of the collagen. Telangrectase can appear on the face, chest, fingers and the tongue. In the gastrointestinal tract, Barrett's metaplasia of the esophagus occurs in about one third of all patients. Pneumatosis cytoides intestinalis may occur following degeneration of muscularis mucosa.
Briefly, the collagen diseases are characterized by a compaction or thickening of connective tissues which is generally treated by administration of corticosteroids alone or with immunosuppressive drugs. Inflammation is usually not present.
Many references disclose the concept of polyethylene glycol (PEG) derivatization of proteins such as alpha-1-proteinase inhibitor, asparaginase, uricase, superoxide dismutase, streptokinase, plasminogen activator, IgG, albumin, lipoprotein lipase, horseradish peroxidase, catalase, arginase and asparaginase, as well as peptides. Such derivatization through lysines was reported as improving half-life, decreasing immunogenicity, increasing solubility, and in general, increasing efficacy (which permitted less frequent dosing). In most cases, the proteins required multiple modifications per molecule to achieve improved performance in vivo, and the activity in vitro was significantly decreased by such modification.
Patents and patent publications that disclose use of polyvinyl alcohol (PVA) in protein conjugation reactions include U.S. Pat. Nos. 4,296,097 and 4,430,260, relating to conjugation of benzylpenicillin and PVA, U.S. Pat. No. 4,496,689 (EP No. 147,761), relating to conjugation of alpha-1-proteinase inhibitor with a polymer such as heparin,. PVA or PEG, EP No. 142,125 published May 22, 1985, disclosing non-covalent bonding of hemoglobin to PVA as a carrier, DE No. 2,312,615, relating to cross linked, water-insoluble PVA coupled to a protein, and DE No. 3,340,592 published May 23, 1985, relating to conjugates of PVA with human hemoglobin A, all of which are herein incorporated by reference.
Alpha
1
-antitrypsin (
∝1
-AT) belongs to serpin superfamily of serine protease inhibitor. It is a small glycoprotein which is mostly synthesized in the liver and has a molecular weight of 53,000 daltons. Human
∝1
-proteinase inhibitors are involved in the regulation of proteolysis, such as the coagulation pathway, fibrinolysis, tissue destruction by endogenous serine proteinases and inflammation.
U.S. Pat. No. 5,492,889 to Lezdey et al, which is herein incorporated by reference, discloses the treatment of mast cell tumors by the administration of alpha 1-antitrypsin alone or in combination with other serine protease inhibitors.
SUMMARY OF THE INVENTION
The present invention provides a method of treating collagen related diseases including diffuse connective tissue diseases, pulmonary fibrosis, splenomegaly, interstitial cystitis, scleroderma and vasculitis.
According to one embodiment of the invention, there is provided the treatment of interstitial cystitis by the intravesical instillation of a serine protease inhibitor. More specifically, the treatment provides instilling into the bladder a composition containing an effective amount of a serine protease inhibitor selected from the group consisting of alpha 1-antitrypsin, alpha-2-macroglobulin, secretory leucocyte protease inhibitor (SLPI) and mixtures thereof, their derivative, analogs or conjugates.
Furthermore, there is provided the treatment of urinary incontinence in individuals who have interstitial cystitis or symptoms thereof.
It is a general object of the invention to provide a composition and method for treating collagen diseases.
It is a further object of the invention to provide a composition for treating individuals having the symptoms of interstitial cystitis.
It is another object of the invention to treat an incontinent individual wherein the incontinence is caused as a result of interstitial cystitis.
It is yet another object of the invention to treat scleraderma.
It is still a further object to provide a method and composition for treating rheumatoid arthritis which is characterized by compaction of collagen at the joints.
It is a still further object of the invention to treat animals which also develop collagen related diseases, especially canine and horses.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
In accordance with one embodiment of the invention, there is provided a method for the treatment of individuals suffering from interstitial cystitis or symptoms thereof by the intravesical instillation of a serine protease inhibitor. The method consists of the administration an effective therapeutic amount of a protease inhibitor selected from the group consisting of alpha 1-antitrypsin, alpha 2-macroglobulin, secretory leucocyte, protease inhibitor or mixtures thereof and analogs or derivatives or conjugates thereof. The preferred conjugate is that with polyethylene glycol or an amphiphilic molecule.
Accordingly, a composition containing at least about 10 mg of protease inhibitor in a suitable pharmaceutical vehicle is instilled into the bladder.
Preferably, about 20 to 40 mg of the protease inhibitor in its natural, transgenic or recombinant form is dissolved in an aqueous medium, such as a saline or buffer solution, and instilled into the bladder. A corticosteroid may be included in the treating composition. The treatment provides immediate relief of pain since the kinins and kallikreins can be controlled together with healing of lesions or ulcers.
A cocktail of protease inhibitors is particularly effective which includes alpha 1-antichymotrypsin because it can control basophil infiltration.
Serine protease inhibitors have been found to play a major role in the direct controlling elastase activity which may also be present in arthritis. The almost immediate disappearance of pain indicates that there can be a control of the kinins as well. A cocktail of serine protease inhibitors their analogs, salts, derivatives or appears to provide the quickest healing when used in combination with a corticosteroid.
According to another embodiment of the invention, there is provided a method for topically treating skin and joints effected by compaction of collagen by use in combination with a penetrating agent such as dimelthylsulfoxide (DMSO) or insulin or some other penetrating agent which is known in the art.
The method provides the topical, oral, parental or suppository administration of a protease inhibitor selected from the group consisting of alpha 1-antitrypsin, alpha 2-macroglobulin, secretory leucocyte protease inhibitor or mixtures thereof, their derivatives.
The drug can be administered in unit dosage form containing about 10 to 20 mg per day depending on the severity of the disease. The use of controlled release substances, for example, liposomes, diketopyperazine microparticles as disclosed by U.S. Pat. Nos. 5,620,708 and 5,503,852 which are herein incorporated by reference, and the delivery systems of U.S. Pat. No. 5,620,708 which is herein incorporat
Kronis K. Anne
Lezdey Darren
Lezdey John
Alphamed Pharmaceutical Corp
Lezdey John
Weber Jon P.
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