US2019290736A1PendingUtilityA1
Topical composition for improved healing of open wounds
Est. expiryOct 19, 2037(~11.2 yrs left)· nominal 20-yr term from priority
A61K 9/06A61K 9/0014A61K 38/28A61K 9/006A61P 17/02A61K 47/36A61P 3/10
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Claims
Abstract
The present disclosure is concerned with compositions comprising insulin and a pharmaceutically acceptable topical carrier. The present disclosure is also concerned with methods of using these compositions for the treatment of a skin ailment such as a diabetic ulcer. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A topical composition comprising insulin and a mucoadhesive polymer carrier, wherein the carrier is not a cyanoacrylate polymer carrier.
2 . The composition of claim 1 , wherein the composition consists essentially of the mucoadhesive polymer carrier and insulin.
3 . The composition of claim 1 , wherein the mucoadhesive polymer carrier comprises pullulan, sodium hyaluronate, tamarind xyloglucan, and Zea mays starch.
4 . The composition of claim 1 , wherein the mucoadhesive polymer carrier is a gel.
5 . The composition of claim 1 , wherein the mucoadhesive polymer carrier is MucoLox™.
6 . The composition of claim 1 , wherein the mucoadhesive polymer carrier is present in amount of from about 90 wt % to about 99 wt %.
7 . The composition of claim 1 , wherein the mucoadhesive polymer carrier comprises at least two polysaccharide polymers.
8 . The composition of claim 7 , wherein the polysaccharide polymers are selected from pullulan, sodium hyaluronate, tamarind xyloglucan, and amylopectin.
9 . The composition of claim 1 , wherein the insulin is selected from Humalog®, Humilin® R, Novolog®, Novolin® R, Lantus®, and Levemir®.
10 . The composition of claim 1 , wherein the insulin is present in an amount of from about 1 wt % to about 10 wt %.
11 . A method for treating a skin ailment in a subject, the method comprising the step of topically administering to the skin ailment an effective amount of the topical composition of claim 1 .
12 . The method of claim 11 , wherein the skin ailment is a diabetic ulcer.
13 . The method of claim 11 , wherein the effective amount is an amount effective to decrease blood sugar levels of the subject by at least about 50%.
14 . A method for treating a skin ailment having an outer edge in a subject, the method comprising managing the wound via administration of an antibiotic, debridement, off-loading, revascularization, hyperbaric oxygen therapy, administration of a wound care product, negative-pressure wound therapy, advanced moist wound therapy, or a combination thereof, wherein the subject was previously identified as being in need of treatment of the skin ailment by the steps of:
(a) obtaining a biological sample from the skin ailment or from a surrounding tissue, wherein the surrounding tissue is within about one inch of the outer edge; and (b) measuring the subject's blood sugar levels in the biological sample.
15 . The method of claim 14 , wherein the subject has been diagnosed with diabetes prior to the administering step.
16 . The method of claim 14 , wherein the skin ailment is a diabetic ulcer.
17 . The method of claim 14 , wherein managing the wound is via administration of a wound care product.
18 . The method of claim 17 , wherein the wound care product comprises a topical composition comprising insulin and a pharmaceutically acceptable topical carrier.
19 . The method of claim 18 , wherein the pharmaceutically acceptable topical carrier is a mucoadhesive polymer carrier comprising at least two polysaccharide polymers.
20 . The method of claim 18 , wherein the mucoadhesive polymer carrier is not a cyanoacrylate polymer carrier.Join the waitlist — get patent alerts
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