Compostions and methods for enhancing the topical application of an acidic benefit agent

US9468606B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9468606-B2
Application numberUS-201414230535-A
CountryUS
Kind codeB2
Filing dateMar 31, 2014
Priority dateMar 31, 2014
Publication dateOct 18, 2016
Grant dateOct 18, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A powder is disclosed including core/shell particles having an average particle size of less than 1000 microns, each particle contains a liquid core that is substantially free of water and includes A) a polar liquid having a percent surface polarity of at least 24%, an active ingredient, and C) from about 0.1% to about 20% by weight of at least one solubility enhancing agent that is not an active ingredient; and a shell comprising hydrophobic particles. The powder can be used to topically administer the active ingredient to a human or animal.

First claim

Opening claim text (preview).

We claim: 1. A powder comprising core/shell particles having an average particle size of less than 1000 microns, each particle comprising: a liquid core that is substantially free of water and comprises A) a polar liquid having a percent surface polarity of at least 24%, B) an acid active agent comprising from about 0.001% to about 20% ibuprofen by weight of the powder, and C) from about 0.1% to about 20% by weight of at least one basic solubility enhancing agent that is not an active ingredient; and a shell comprising hydrophobic particles. 2. The powder of claim 1 , wherein the hydrophobic particles comprise hydrophobic fumed silica. 3. The powder of claim 2 , wherein the polar liquid comprises a polyol selected from the group consisting of glycerols, polyglycerols, glycols, polyglycols, and mixtures thereof. 4. The powder of claim 3 , wherein the polyol is selected from the group consisting of glycerol, diglycerol, triglycerol, tetraglycerol, polyglycerols having more than 4 glycerol groups, and mixtures thereof. 5. The powder of claim 3 , wherein the polar liquid comprises at least about 50 percent by weight of a glycerol, polyglycerol, or mixture thereof. 6. The powder of claim 1 , wherein the acidic active agent comprises from about 0.01% to about 10% by weight of the powder. 7. The powder of claim 6 , wherein the acidic active agent comprises from about 0.1% to about 5% by weight of the powder. 8. The powder of claim 1 , wherein the basic solubility enhancer is selected from the group consisting of sodium hydroxide, potassium hydroxide, ammonium hydroxide, calcium hydroxide, magnesium hydroxide, potassium carbonate, sodium carbonate, calcium carbonate, magnesium carbonate, ethylamine, diethylamine, triethylamine, diisopropylethylamine, ethanolamine, diethanolamine, triethanolamine, ethylenediamine, triisopropanolamine and mixtures thereof. 9. The powder of claim 1 , wherein the basic solubility enhancer is in an amount from about 1% to about 5% by weight of the powder. 10. A method for enhancing the topical application of a benefit agent which comprises topically administering to the skin of a human or animal the powder composition according to claim 1 . 11. The method of claim 10 , wherein the active agent comprises from about 0.01% to about 10% by weight of the powder. 12. The method of claim 11 , wherein the active agent comprises from about 0.1% to about 5% by weight of the powder. 13. The method of claim 10 , wherein the basic solubility enhancer is selected from the group consisting of sodium hydroxide, potassium hydroxide, ammonium hydroxide, calcium hydroxide, magnesium hydroxide, potassium carbonate, sodium carbonate, calcium carbonate, magnesium carbonate, ethylamine, diethylamine, triethylamine, diisopropylethylamine, ethanolamine, diethanolamine, triethanolamine, ethylenediamine, triisopropanolamine and mixtures thereof. 14. The method of claim 13 , wherein the basic solubility enhancer is in an amount from about 1% to about 5% by weight of the powder.

Assignees

Inventors

Classifications

  • for baldness or alopecia · CPC title

  • Inorganic compounds · CPC title

  • Skin, i.e. galenical aspects of topical compositions (non-active ingredients are additionally classified in A61K47/00; A61K9/0009, A61K9/0021, A61K9/7015, A61K9/7023 take precedence; cosmetic preparations A61K8/00, A61Q; preparations for wound dressings or bandages A61L26/00) · CPC title

  • The particulate/core comprising organic material · CPC title

  • Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones · CPC title

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What does patent US9468606B2 cover?
A powder is disclosed including core/shell particles having an average particle size of less than 1000 microns, each particle contains a liquid core that is substantially free of water and includes A) a polar liquid having a percent surface polarity of at least 24%, an active ingredient, and C) from about 0.1% to about 20% by weight of at least one solubility enhancing agent that is not an acti…
Who is the assignee on this patent?
Johnson & Johnson Consumer Inc
What technology area does this patent fall under?
Primary CPC classification A61K9/501. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Oct 18 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 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).