Nanoemulsion therapeutic compositions and methods of using the same

US9259407B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9259407-B2
Application numberUS-201514628886-A
CountryUS
Kind codeB2
Filing dateFeb 23, 2015
Priority dateSep 26, 2008
Publication dateFeb 16, 2016
Grant dateFeb 16, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present invention relates to therapeutic nanoemulsion compositions and to methods of utilizing the same. In particular, nanoemulsion compositions are described herein that find use in the treatment and/or prevention of infection (e.g., respiratory infection (e.g., associated with cystic fibrosis)), in burn wound management, and in immunogenic compositions (e.g., comprising a Burkholderia antigen) that generate an effective immune response (e.g., against a bacterial species of the genus Burkholderia ) in a subject administered the immunogenic composition. Compositions and methods of the present invention find use in, among other things, clinical (e.g. therapeutic and preventative medicine), industrial, and research applications.

First claim

Opening claim text (preview).

We claim: 1. A method of treating an infection of a wound comprising administering a composition comprising a therapeutically effective amount of a nanoemulsion, wherein the nanoemulsion comprises: 1. 30-90%, 60-80%, or 60-70% by volume oil; 2. 3-15% by volume solvent; wherein said solvent is selected from the group consisting of ethanol and glycerol; 3. 0.05-10.0% by volume non-ionic surfactant and 0.001-5.0% by volume cationic surfactant; 4. ethylenediaminetetraacetic acid (EDTA); and 5. water to said wound, wherein said composition kills or inhibits growth of bacteria within the wound infection in the absence of increased inflammation and edema at the site of the wound. 2. The method of claim 1 , wherein said wound infection comprises Staphylococcus aureus. 3. The method of claim 2 , wherein said Staphylococcus aureus are antibiotic resistant. 4. The method of claim 1 , wherein said wound infection comprises Pseudomonas aeruginosa. 5. The method of claim 1 , wherein said composition is co-administered with a bioactive agent. 6. The method of claim 1 , wherein said nanoemulsion comprises: a) water; b) polyoxyethylenesorbitan monolaurate; c) glycerol or ethanol; d) oil; e) dimethyl benzyl ammonium chloride; and f) ethylenediaminetetraacetic acid (EDTA). 7. The method of claim 1 , wherein said nanoemulsion comprises: a) water; b) a non-ionic surfactant selected from the group consisting of polyoxyethylenesorbitan monolaurate, polyoxyethylenesorbitan monooleate, and a poloxamer; c) glycerol or ethanol; d) oil; e) a cationic surfactant selected from the group consisting of cetylpyridinium chloride (CPC), benzalkonium chloride, and alkyl dimethyl benzyl ammonium chloride; and f) ethylenediaminetetraacetic acid (EDTA). 8. The method of claim 1 , wherein said nanoemulsion has a mean particle size of 0.2-0.8 microns. 9. The method of claim 1 , wherein said nanoemulsion has a mean particle size less than 0.5 microns. 10. The method of claim 1 , further comprising the step of co-administering an antimicrobial agent to said wound. 11. The method of claim 10 , wherein said antimicrobial agent is an antibiotic. 12. The method of claim 1 , wherein said nanoemulsion comprises: a) water; b) 0.05-10.0% polyoxyethylene sorbitan monolaurate; c) 3-15% glycerol; d) oil; e) 0.001-5.0% benzalkonium chloride; and f) ethylenediaminetetraacetic acid (EDTA).

Assignees

Inventors

Classifications

  • Antibacterial agents · CPC title

  • A61K31/198Primary

    Alpha-amino acids, e.g. alanine or edetic acid [EDTA] (betaine A61K31/205; proline A61K31/401; tryptophan A61K31/405; histidine A61K31/4172; peptides not degraded to individual amino acids A61K38/00) · CPC title

  • not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine · CPC title

  • Drugs for disorders of the respiratory system · CPC title

  • Quaternary ammonium compounds, e.g. edrophonium, choline (betaines A61K31/205) · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9259407B2 cover?
The present invention relates to therapeutic nanoemulsion compositions and to methods of utilizing the same. In particular, nanoemulsion compositions are described herein that find use in the treatment and/or prevention of infection (e.g., respiratory infection (e.g., associated with cystic fibrosis)), in burn wound management, and in immunogenic compositions (e.g., comprising a Burkholderia …
Who is the assignee on this patent?
Univ Michigan
What technology area does this patent fall under?
Primary CPC classification A61K31/198. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Feb 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).