IP Library › Granted Patent US 11,110,195
Granted Patent B2
US 11,110,195 · App. 16/912,944 · Granted Sep 7, 2021

Esculentin 1a derivatives and uses thereof

Inventors: Alison McDermott (Bellaire, TX); Maria Luisa Mangoni (Rome, IT)
Assignees: UNIVERSITY OF HOUSTON SYSTEM; UNIVERSITA' DEGLI STUDI DI ROMA LA SAPIENZA
A61L12/14A61K38/04A61P27/02B29D11/00096B29D11/00865A61K9/0048G02B1/043
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Quick Facts
Patent No.
US 11,110,195
App. No.
16/912,944
Granted
Sep 7, 2021
Kind
B2
Abstract

Provided herein are synthetic antibacterial peptides that have a sequence at least 80% identical to a sequence shown in SEQ ID NO: 2 or the diastereomer thereof with a sequence shown in SEQ ID NO: 3 or pharmaceutical compositions thereof. Also provided are methods for stimulating wound healing via the synthetic antibacterial peptides and for forming an antimicrobial coating on contact lenses. In addition a device is provided that has a surface with a coating of the synthetic antibacterial peptides.

Claims (8)

1. A method for stimulating wound healing, comprising the step of contacting a wound with an antimicrobial component comprising an antibacterial peptide with a sequence at least 80% identical to the sequence of SEQ ID NO: 2 or a diastereomer thereof with a sequence at least 80% identical to the sequence of SEQ ID NO: 3.

2. The method of claim 1 , wherein the step of contacting the wound with the antimicrobial component induces closure of the wound.

3. The method of claim 1 , wherein the step of contacting the wound with the antimicrobial component comprises complete coverage of the wound with the antimicrobial component.

4. The method of claim 1 , wherein the antimicrobial component is in the form of a solid, an ointment, a gel, a liquid, an aerosol, a mist, a polymer, a film, an emulsion, or a suspension.

5. The method of claim 1 , wherein the antimicrobial component further comprises a sustained-release carrier.

6. The method of claim 5 , wherein the sustained-release carrier is a sustained release polymer, a nanoparticle, a nanosuspension, a liposome or a microcapsule.

7. The method of claim 1 , wherein the antimicrobial component comprises the antibacterial peptide in a concentration of 0.005 μM to 256 μM.

8. The method of claim 1 , wherein the wound is contacted with the antimicrobial component for a period of time between three hours and twenty-four hours.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2020
From: MCDERMOTT, ALISON
To: UNIVERSITY OF HOUSTON SYSTEM
Reel/Frame 053047/0347 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2020
From: MANGONI, MARIA LUISA
To: UNIVERSITA' DEGLI STUDI DI ROMA LA SAPIENZA
Reel/Frame 053047/0403 →
Continuity (4)
Division 16112741 · Aug 26, 2018
Continuation In Part 14506383 · Oct 3, 2014
Provisional Application 61890521 · Oct 14, 2013
Related Publication 20200324014A1 · Oct 15, 2020
Cited By (1)
US 12,544,336