US2021052668A1PendingUtilityA1
Honey-based gel composition
Est. expiryApr 7, 2030(~3.7 yrs left)· nominal 20-yr term from priority
Inventors:Fatma Bilge Thompson
A61K 31/7028A61K 35/644A61K 31/23A61K 9/06A61K 9/0014A61L 26/0057A61P 17/02
45
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Claims
Abstract
A honey based composition is described. The composition includes a mixture of honey, a short chain fatty alcohol and a fatty ester or wax. The composition has applications for use in wound dressings and in one embodiment may be a gel. The composition has a higher than expected storage stability, remaining stable for many weeks when held at elevated temperatures and retains all of the other desirable characteristics including anti-microbial activity.
Claims
exact text as granted — not AI-modified1 . A composition for treating a patient wherein the composition comprises:
a. 70-90 wt % honey; b. 2-10 wt % caprylyl/capryl glucoside; and c. 2-15 wt % myristyl myristate;
wherein the composition has been subjected to a sterilization effective dosage of radiation and is storage stable for a time period of at least 24 hours at 40° C.
2 . The composition as claimed in claim 1 , wherein the composition is stable for at least 8 days when stored at 40° C.
3 . The composition as claimed in claim 1 , wherein the composition is stable for at least 21 days when stored at 40° C.
4 . The composition as claimed in claim 1 , wherein the composition is stable for at least 15 weeks when stored at 40° C.
5 . The composition as claimed in claim 1 , wherein the composition is a gel.
6 . The composition as claimed in claim 1 , wherein the composition has a viscosity of 50×10 3 to 600×10 3 cPs at 25° C.
7 . The composition as claimed in claim 1 , wherein the myristyl myristate has a melting point of about 37° C. or greater.
8 . The composition as claimed in claim 1 , wherein the honey has both peroxide and non-peroxide activity.
9 . The composition as claimed in claim 1 , wherein the pH is between 3.0 and 6.0 for the duration of storage.
10 . The composition as claimed in claim 1 , wherein the pH is between 4.0 and 5.0 for the duration of storage.
11 . The composition as claimed in claim 1 , wherein the sterilization effective dosage of radiation is greater than 10 kGy.
12 . The composition as claimed in claim 1 , wherein the sterilization effective dosage of radiation is greater than 20 kGy.
13 . The composition as claimed in claim 1 , wherein the sterilization effective dosage of radiation is 25 kGy.
14 . The composition as claimed in claim 1 , wherein the composition has an antibacterial activity >10% phenol equivalent or >10 unique manuka factor activity over the shelf life.
15 . The composition as claimed in claim 1 , wherein the honey is manuka honey.
16 . The composition as claimed in claim 15 , wherein the composition is stable for at least 8 days when stored at 40° C.
17 . The composition as claimed in claim 15 , wherein the composition is stable for at least 21 days when stored at 40° C.
18 . The composition as claimed in claim 15 , wherein the composition is stable for at least 15 weeks when stored at 40° C.
19 . The composition as claimed in claim 15 , wherein the composition has a viscosity of 50×10 3 to 600×10 3 cPs at 25° C.
20 . The composition as claimed in claim 15 , wherein the pH is between 4.0 and 5.0 for the duration of storage.
21 . A composition for treating a patient consisting essentially of:
a. 70-90 wt % honey; b. 2-10 wt % caprylyl/capryl glucoside; and c. 2-15 wt % myristyl myristate;
wherein the composition has been subjected to a sterilization effective dosage of radiation and is storage stable for a time period of at least 24 hours at 40° C.Join the waitlist — get patent alerts
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