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Method of Making Perfluorocarbon Emulsions With Non-Fluorinated Surfactants

a technology of fluorinated surfactants and emulsions, which is applied in the direction of halogenated hydrocarbon active ingredients, hair cosmetics, transportation and packaging, etc., can solve the problems of low stability, low reactivity, low stability, etc., and achieve the effect of simple and low energy methods

Inactive Publication Date: 2006-08-31
THEROX
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides stable fluorocarbon emulsions using non-fluorinated emulsifying agents and stabilizing agents that reduce the ability of the fluorocarbon droplets to move within the continuous phase of the emulsion. The emulsifying agents and stabilizing agents can be hydrogenated phospholipids or other non-fluorinated compounds. The emulsions can be made using a simple mixing process and can have a broad range of droplet sizes. The invention also provides methods for making the emulsions without the need for a solid emulsifying agent. The emulsified fluorocarbon droplets can be used in various applications such as industrial cleaning, coating, and delivery of oxygen.

Problems solved by technology

These compounds are clear, colorless, odorless, nonflammable, biocompatible, and have low reactivity.
One of the shortcomings of existing emulsions is their low stability.
These storage requirements seriously limit the field of application of such fluorocarbon emulsions.
However, most conventional emulsifying agents have a low affinity for fluorocarbons.
However, this method involves a complex multi-step procedure and requires high pressure homogenization or sonically-induced cavitations to effectively disperse fluorocarbons in water.
Fluorinated surfactants have been shown to improve the stability of FC emulsions (U.S. Pat. No. 6,113,919) However, this class of surfactants has also been shown to have a negative environmental impact that led to the withdrawal of some previously commercially available fluorinated surfactants.
However, the environmental concerns associated with such fluorinated compounds have greatly limited their use and availability in recent years.
Microemulsions, while stable thermodynamically, require a substantial amount of surfactants in their formulations, which may lead to bioincompatibiltiy for medical applications.
However, it is not clear whether such microemulsions are suitable for biomedical and cosmetic applications.
Still another group of FC emulsions limit the size of the FC droplets and do not provide an optimal therapeutic effect in topical applications.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

[0108]

Preparation of the FC emulsionIngredients% (wt / wt)A Water42B Glycerin12C Hydrogenated Phospholipid4.5D Cetyl alcohol0.6E Stearyl alcohol0.6F Polysorbate 600.5G Perfluorodecalin39.5H Tocopheryl acetate0.4

A is mixed into B. The mixture is heated to 70° C. in a reaction vessel with agitation. When the temperature reaches 70° C., C is added to the mixture at 70° C. with agitation. An overhead stirrer is used to conduct this step. After C is uniformly dispersed in the mixture, D, E and F are added with continued agitation. When all of the above ingredients are uniformly dispersed, G is added slowly at a controlled rate with agitation. When all G has been added, H is added while maintaining the temperature at 70° C. The mixture is cooled slowly to room temperature. Alternatively, prior to cooling, the mixture may be subjected to homogenization and then cooled slowly to room temperature.

example 2

[0109]

Preparation of alternate FC emulsionIngredients% (wt / wt)AWater42.5BPropylene Glycol30CHydrogenated Phospholipid4.4DCetyl alcohol0.3EStearyl alcohol0.3FPolysorbate 600.2GGlyceryl stearate, PEG-75 stearate,0.8ceteth-20, steareth-20(Emulium Delta, Gattefosse, France)HPerfluorodecalin20ITocopheryl acetate0.5JDimethicone0.7KBenzyl alcohol0.4LMethyl paraben0.1MPropyl paraben0.05NHyaluronic acid1

A is mixed into B. The mixture is heated to 70° C. in a reaction vessel with agitation. When the temperature reaches 70° C., C is added to the mixture at 70° C. with agitation. An overhead stirrer is used to conduct this step. After C is uniformly dispersed in the mixture, D, E, F and G are added with continued agitation. When all of the above ingredients are uniformly dispersed, H is added slowly at a controlled rate with agitation. When all H has been added, I and J are added while maintaining the temperature at 70° C. The mixture is cooled slowly to room temperature. While the mixture is ...

example 3

[0110]

Preparation of alternate FC emulsionIngredients% (wt / wt)AWater48BPropylene Glycol34CHydrogenated Phospholipid4DCetyl alcohol0.4EStearyl alcohol0.4FPolysorbate 600.3GGlyceryl stearate, PEG-75 stearate,1ceteth-20, steareth-20(Emulium Delta, Gattefosse, France)HPerfluorodecalin10ITocopheryl acetate0.8JDimethicone0.5KBenzyl alcohol0.4LMethyl paraben0.1MPropyl paraben0.05

A is mixed into B. The mixture is heated to 70° C. in a reaction vessel with agitation. When the temperature reaches 70° C., C is added to the mixture at 70° C. with agitation. An overhead stirrer is used to conduct this step. After C is uniformly dispersed in the mixture, D, E, F and G are added with continued agitation. When all of the above ingredients are uniformly dispersed, H is added slowly at a controlled rate with agitation. When all H has been added, I and J are added while maintaining the temperature at 70° C. The mixture is cooled slowly to room temperature. While the mixture is cooling, K, L and M are...

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Abstract

The present invention provides a method of making a FC emulsion. The method comprises mixing an FC immiscible hydrophilic liquid and a solid emulsifying agent by agitation at a temperature elevated above the phase transition temperature of the emulsifying agent and below the boiling temperature of the FC immiscible hydrophilic liquid, and adding FC to the mixture of step (a) and agitating at the elevated temperature to disperse droplets of FC in the FC immiscible hydrophilic liquid to form the FC emulsion. The invention also provides another method of making an FC emulsion, which does not require a solid emulsifying agent. The method comprises mixing an FC immiscible hydrophilic liquid and an emulsifying agent to form a first mixture; mixing a stabilizing agent with the first mixture to form a second mixture; and mixing FC with the second mixture to form a third mixture to disperse droplets of FC in the FC immiscible hydrophilic liquid and to form the FC emulsion, wherein the stabilizing agent reduces ability of the droplets to move within a continuous phase of the FC emulsion.

Description

CROSS-REFERENCE TO THE RELATED APPLICATIONS [0001] This application is a divisional of U.S. patent application Ser. No. 10 / 253,572, filed Sep. 24, 2002, which is incorporated herein by reference.FIELD OF THE INVENTION [0002] The invention relates generally to stable emulsions capable of gas-supersaturation, and methods of their preparation and use. Specifically, the present invention relates to stable fluorocarbon emulsions prepared with non-fluorinated emulsifying and stabilizing agents and methods of their preparation utilizing conventional mixing equipment. BACKGROUND OF THE INVENTION [0003] Fluorocarbons (fluorine substituted hydrocarbons) and perfluorocarbons (fluorocarbons in which all of the hydrogen atoms have been replaced with fluorine) have numerous applications in the biomedical field because of their unique chemical and biological properties. These compounds are clear, colorless, odorless, nonflammable, biocompatible, and have low reactivity. In addition, they are capab...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K8/30A61K8/06A61K8/70A61K9/00A61K9/107A61K31/03A61L9/04A61Q19/00C09K23/00C09K23/14C09K23/42C09K23/56
CPCA61K8/06A61K8/70A61K9/0014A61K9/107A61K31/03A61K2800/22A61Q19/00B01F3/0807B01F7/00633B01F7/16B01F13/1027B01F17/0028B01F17/0064B01F17/0085B01F17/0092B01F23/41B01F27/191B01F27/80B01F33/821C09K23/14C09K23/018C09K23/017C09K23/34
Inventor CREECH, JEFFREY L.HSU, LI-CHIENKIVINSKI, MARGARET A.ZALESKY, PAUL J.
Owner THEROX
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