Drug – bio-affecting and body treating compositions – Extract – body fluid – or cellular material of undetermined... – Derived from musculoskeletal system – other than cardiac muscle
Reexamination Certificate
1999-12-10
2002-04-30
Tate, Christopher R. (Department: 1651)
Drug, bio-affecting and body treating compositions
Extract, body fluid, or cellular material of undetermined...
Derived from musculoskeletal system, other than cardiac muscle
C514S021800, C530S400000
Reexamination Certificate
active
06379709
ABSTRACT:
FIELD OF INVENTION
This invention relates to a process for obtaining angiogenesis activators and angiogenesis inhibitors from shark cartilage, the angiogenesis activator and inhibitor products of the process, compositions comprising them, and methods of using them, particularly for the control of biological processes such as wound healing and tumour formation and growth.
BACKGROUND
Angiogenesis (or neovascularization) is the formation of new blood vessels. Many biological processes, over which control is desired, may depend on the activation of angiogenesis or on the inhibition of angiogenesis. For example, as new blood vessel formation is required by solid tumours for growth, angiogenesis inhibition is an attractive strategy for the treatment of cancer. It has been demonstrated that cartilage extracts inhibit angiogenesis when implanted adjacent to tumours.
Furthermore, the oral consumption of dried powdered shark cartilage has been widely promoted as a natural health remedy for the treatment of cancer. Powdered whole cartilage from bovine trachea and soluble bovine cartilage extracts have also been used to treat a variety of diseases which involve angiogenesis, such as psoriasis and rheumatoid arthritis.
It is known that shark cartilage is comprised principally of calcium salts, protein and polysaccharide material. It is further known that a substantial portion of the polysaccharide material is in the form of glycosaminoglycans (GAGs). The principal GAG in cartilage is chondroitin sulphate.
It has been disputed whether any angiogenesis controlling component of shark cartilage can cross the gut lining of an animal following oral ingestion. It is thought that most of the protein found in shark cartilage would be digested into smaller peptides in the gut. However, GAGs present in cartilage have been shown to be absorbed from the gut largely intact when orally ingested.
Previous studies linking cartilage with the control of angiogenesis have been concerned with angiogenesis inhibition. However, activation of angiogenesis also has therapeutic potential. For example, the promotion of angiogenesis is desirable for expediting biological processes such as wound healing, collateral circulation, and organ transplantation.
It is known to prepare an angiogenesis inhibiting substance from “wet” shark cartilage by extracting it with water to give a solid residue and a lyophilisate. Cartilage described as “wet” is not treated, for example by lyophilisation, to remove water. The solid residue and the lyophilisate were both found to exhibit angiogenesis inhibition.
In addition, there is some evidence that consumption of shark cartilage prepared by conventional processes, especially long term consumption, may cause liver damage. One or more hepatotoxic substances may be present in such cartilage.
SUMMARY OF INVENTION
It is therefore an object of this invention to enable improved control of angiogenesis or to at least provide a useful alternative to known angiogenesis inhibitors and activators by providing a process for obtaining an angiogenesis activator and an angiogenesis inhibitor from dried shark cartilage.
According to first aspect of this invention, there is provided a process for obtaining an angiogenesis activating product and an angiogenesis inhibiting product from shark cartilage comprising the steps of:
drying the shark cartilage so that it is free or substantially free of water,
mixing the dried shark cartilage with water to give an aqueous extract and an insoluble residue, and
separating the aqueous extract from the insoluble residue,
wherein the aqueous extract is an angiogenesis activator and the insoluble residue is an angiogenesis inhibitor.
The water used in the mixing step may contain dissolved salts or electrolytes. For example, it may be a phosphate buffered saline solution. Also, the water may contain one or more water-miscible organic solvents such as ethanol, acetone, or dimethyl sulphoxide, provided to proportion of organic solvent is low, for example, less than 50% v/v, preferably less than 10% v/v.
It is preferred that the shark cartilage is ground, milled, pulverised or powdered to granules having a particle size in the range of less than approximately 500 microns, preferably less than approximately 300 microns.
The separation of the aqueous extract from the insoluble residue may be according to any commonly used separation procedure, for example, filtration including ultrafiltration or dialysis, decantation or centrifugation.
In a preferred embodiment of the invention, the aqueous extract may be dried, for example, via freeze drying, to give a solid product. A solid product may also be obtained from the aqueous extract by the addition of an organic solvent, such as ethanol or acetone, to cause precipitation of a solid followed by filtration and drying.
The shark cartilage may be obtained from one or a mixture of shark species.
In a second aspect of this invention, there is provided an angiogenesis activating product obtained from shark cartilage by a process comprising the steps of:
drying the shark cartilage so that it is free or substantially free of water,
mixing the dried shark cartilage with water to give an extract and an insoluble residue, and
separating the aqueous extract from the insoluble residue,
wherein the aqueous extract is an angiogenesis activator.
In a third aspect of this invention, there is provided an angiogenesis inhibiting product obtained from shark cartilage by a process comprising the steps of:
drying the shark cartilage so that it is free or substantially free of water,
mixing the dried shark cartilage with water to give an aqueous extract and an insoluble residue, and
separating the aqueous extract from the insoluble residue,
wherein the insoluble residue is an angiogenesis inhibitor.
In a preferred embodiment of this aspect of the invention, the insoluble residue exhibits increased angiogenesis inhibition in comparison with the angiogenesis inhibition activity exhibited by the shark cartilage prior to the extraction step.
In a further preferred embodiment of this aspect of the invention, the insoluble residue leads to reduced serum alanine-lactate aminotransferase activity relative to the serum alanine-lactate aminotransferase activity resulting from the use of the shark cartilage not subjected to the extraction step.
In another aspect of this invention, there is provided a composition containing a therapeutically effective amount of an angiogenesis inhibiting product obtained by the process of this invention together with an acceptable carrier.
In a further aspect of this invention, there is provided a composition containing a therapeutically effective amount of an angiogenesis activating product obtained by the process of this invention together with an acceptable carrier.
Yet another aspect of this invention is a method of controlling angiogenesis in an animal comprising administering an effective amount of an angiogenesis activating product obtained by the process of this invention or an angiogenesis inhibiting product obtained by the process of this invention.
In another aspect of this invention, there is provided a use of an angiogenesis activating product or an angiogenesis inhibiting product for the preparation of an agent for controlling angiogenesis.
DETAILED DESCRIPTION
The cartilage used in this invention may be obtained from a mixture of shark species, principally blue shark (
Prionace glauca
), but may include other species such as school shark (
Galeorhinus galeus
), rig or smooth dogfish (
Mustelus lenticulatus
) and spiky dog fish (
Squalus acanthias, Squalus mitsukurii
). The meat adhering to the cartilage may first be removed by any suitable means known to a person skilled in the art such as manual scraping, mild protease treatment or high pressure water treatment. The cartilage may then be dried by freeze drying, air drying or any other suitable means.
The cartilage is preferably milled, ground or pulverised to provide a powder having a particle size of less than approximately 500 microns, preferably less than 300 m
Davis Paul Frank
He Yi
Slim George Charles
Xu Bei
Flood Michele
Industrial Research Limited
Merchant & Gould P.C.
Tate Christopher R.
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