Method of treating topical angiogenesis-related disorders

Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Cosmetic – antiperspirant – dentifrice

Reexamination Certificate

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Details

C424S078020, C424S078050, C424S195110, C514S863000, C514S886000, C514S887000

Reexamination Certificate

active

06248341

ABSTRACT:

FIELD OF THE INVENTION
The invention relates to cosmetic and pharmaceutical treatment methods. More specifically, the invention relates to treatment of angiogenesis-related disorders, particularly skin disorders.
BACKGROUND OF THE INVENTION
Angiogenesis, which is the process of producing new capillaries from already existing blood vessels, is a tightly regulated event that does not normally occur in healthy adults, except for certain very specific occurrences such as wound-healing and the female reproductive cycle. It is a complex process that involves a number of steps, including basement membrane degradation, cellular proliferation, migration, and differentiation of endothelial cells, formation of a lumen, and deposition of a new basement membrane. The regulation of the process is also complex, involving a number of diverse factors, for example, enzymes such as collagenase and protein kinase C, growth factors and signaling molecules such as VEGF and cAMP, and by cell-matrix adhesion molecules. Angiogenesis is an integral part of the pathogenesis of certain conditions, such as tumor formation, and chronic inflammatory disorders such as rheumatoid arthritis. Angiogenesis has been associated with chronic inflammatory skin diseases characterized by the neogenesis of capillaries and post-capillary venules due to over-expression of VEGF in epidermal keratinocytes. New vessel growth exacerbates chronic inflammation by facilitating infiltration of monocytes and lymphocytes. In addition to the angiogenic growth factors VEGF and FGF, the cytokines TNFA and IL-1, as well as the lipid inflammatory mediators PGE
1
, PGE
2
, and PAF have also been implicated in inflammatory angiogenesis. Because there are so many stages in the pathway, however, this provides a number of points in the pathway at which its progress can be stopped. A number of different natural sources of angiogenesis inhibitors have previously been reported; the present invention now presents a new natural source for limiting the progress of angiocenesis.
SUMMARY OF THE INVENTION
The invention relates to a method of inhibiting angiogenesis in a mammalian tissue which comprises providing to the tissue an effective amount of epigallocatechin gallate(EGCG), epicatechin gallate(ECG), or a combination thereof. The method can be used to treat a number of conditions, such as chronic inflammatory conditions and cancerous tumors. In a particularly preferred embodiment, the EGCG and/or ECG are applied topically to inhibit or reduce angiogenesis associated with various skin conditions.
DETAILED DESCRIPTION OF THE INVENTION
EGCG and ECG are two of several polyphenols that occur naturally in green tea, among other natural sources. These two compounds, and green tea generally, have found numerous cosmetic and pharmaceutical uses, including free-radical scavenging, skin whitening, antiinflammatory, and hair coloring. It has now been unexpectedly discovered that these compounds are capable of inhibiting the process of angiogenesis. In particular, it had been initially observed in vitro that each of these compounds can inhibit both collagenase and protein kinase C, as well as VEGF-induced migration of endothelial cells, some of the many components that are involved in the angiogenesis pathway. The effect of these inhibitions on angiogenesis has subsequently been confirmed in vivo in the chick embryo chorioallantoic membrane assay.
Although several flavonoid compounds have previously been shown to be active in inhibiting angiogenesis(Fotsis et al., Cancer Research 5: 2916-2921, 1997), it has been expressly noted that catechin was inactive in this regard. It is therefore particularly surprising to observe that these specific green tea catechins have any effect on angiogenesis. The catechins employed in the invention may be a EGCG or ECG-enriched fraction of green tea, or it can be any substantially pure EGCG, ECG, or combinations thereof, “substantially pure” being defined as at least 75%, preferably at least 90% free of non-EGCG or ECG compounds.
The effect on angiogenesis of EGCG and ECG is dose-dependent. When evaluated in the chorioallantoic membrane assay, which measures the inhibition of migration of endothelial cells, concentrations of as low as 0.01 mg/ml has a substantial effect on inhibiting this migration, this effect increasing as the concentration is increased, and being most pronounced at a level of about 1 mg/ml. Thus, for practical application for treatment of angiogenesis related disorders, the effective amount of active compound employed will range from about 0.01% to about 10%, preferably about 0.05 to about 5%, most preferably about 0.05 to about 3%, by weight of the total composition. Each compound can be used alone, or in combination with the other.
The catechin component of the composition useful in the methods of the invention can be incorporated into any type of vehicle that is appropriate for the intended mode of administration, which will of course depend upon the condition to be treated. The catechins can be formulated for systemic, e.g., oral or parenteral delivery, or can be formulated for topical delivery. Formulation of these active ingredients is achieved by routine methods, such are described in Remington's Pharmaceutical Sciences, 18
th
ed., 1990, the contents of which are incorporated herein by reference.
The utility of the these green tea catechins in inhibiting angiogenesis makes them very useful in the treatment of a broad variety of conditions, the pathology of which is connected with proliferation of blood vessels, or the migration of blood cells. Such conditions include vascularized solid cancerous tumors, which, as proliferating tissues, are heavily reliant on blood vessels to support their growth. Thus, the EGCG/ECG compositions can be used in a method of treatment of neoplastic growth, either topically or systemically. Additionally, EGCG and/or ECG can be used to prevent angiogenesis caused by chronic inflammatory conditions such as rheumatoid arthritis and psoriasis. The EGCG/ECG compositions can also be used in the treatment of diabetic retinopathy.
In a preferred embodiment, the catechins are used topically to treat skin conditions that are angiogenesis-related. Examples of such conditions include inflammatory skin disorders, such as psoriasis, atopic dermatitis, contact dermatitis, skin cancers such as melanoma, or basal or squamous cell carcinoma, spider veins, and undereye circles. In topical application, the active catechin component is added to the chosen vehicle in the amounts indicated above, and typically applied to the skin in an amount of from about 0.1 &mgr;g/cm
2
to 2 mg/cm
2
of skin. Depending upon the condition, the composition may be applied on a temporary schedule, until such time as the condition is relieved, or, with chronic conditions, the compositions can be applied chronically, e.g., a safe and effective amount of a composition containing the mixture is applied to prevent development of the symptoms of the angiogenesis-related condition, or to relieve a recurring condition. In all cases, topical application of the composition can be performed from about once per week to about 4 or 5 times daily, preferably from about 3 times a week to about 3 times daily, most preferably about once or twice per day. By “chronic” application, it is meant herein that the period of topical application may be over the lifetime of the user, preferably for a period of at least about one month, more preferably from about three months to about twenty years, more preferably from about six months -to about ten years, more preferably still from about one year to about five years, which treatment can prevent development of conditions such as undereye shadows and circles, skin inflammation or spider veins.
It may also be desirable to combine other actives with the EGCG/ECG components of the compositions. Examples of other actives that may provide a particular beneficial effect in combination with EGCG or ECG are shark cartilage, phytosphingosine or sphingosine, each of which also has an effect o

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