Use of an oleogel containing triterpene for healing wounds
View Patent ↗An oleogel comprising a non-polar liquid and a powder containing triterpene is provided as an oleogel that may be used for healing wounds.
1. A method for treating epidermolysis bullosa in a patient in need thereof, comprising topically administering to an area of epidermolysis bullosa of the patient an oleogel, wherein the oleogel comprises betulin as an active substance in a powder form, and wherein the fraction of betulin in the powder is greater than 50 weight-percent.
2. The method of claim 1 , wherein the area of epidermolysis bullosa comprises blisters.
3. The method of claim 1 , wherein the powder comprises betulin and lupeol.
4. The method of claim 3 , wherein the joint fraction of betulin and lupeol in the powder is greater than 80 weight-percent.
5. The method of claim 3 , wherein the joint fraction of betulin and lupeol in the powder is greater than 85 weight-percent.
6. The method of claim 1 , wherein the oleogel further comprises a nonpolar liquid.
7. The method of claim 6 , wherein the nonpolar liquid comprises a fraction of between 80 weight-percent and 99 weight-percent in relation to the total weight of the oleogel, and wherein the powder comprises a fraction of between 1 weight-percent and 20 weight-percent in relation to the total weight of the oleogel.
8. The method of claim 6 , wherein the nonpolar liquid is a plant, animal, mineral, or synthetic oil.
9. The method of claim 8 , wherein the plant oil is a vegetable oil which is selected from one of the following: sunflower oil, olive oil, avocado oil, and almond oil.
10. The method of claim 1 , wherein the fraction of betulin in the powder is greater than 60 weight-percent.
11. The method of claim 1 , wherein a mean particle size of the powder is between 20 nm and 50 μm.
12. The method of claim 1 , wherein a mean particle size of the powder is less than 10 μm.
13. The method of claim 1 , wherein the oleogel includes an additional wound healing substance.
14. The method of claim 1 , wherein the powder further comprises betulinic acid, oleanolic acid, and erythrodiol.
15. The method of claim 1 , wherein the patient is a human.