Hydrogel adapted for treatment of acute dermal wounds

A hydrogel and gelation technology, which can be used in skin diseases, medical preparations with non-active ingredients, prostheses, etc., and can solve problems such as limiting function or aesthetics.

Inactive Publication Date: 2016-04-20
HALSCION
View PDF22 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are other wound healing events that can limit the resulting function or aesthetics

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Hydrogel adapted for treatment of acute dermal wounds
  • Hydrogel adapted for treatment of acute dermal wounds
  • Hydrogel adapted for treatment of acute dermal wounds

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0104] In preparing the compositions of the present disclosure, the polymer components can be mixed together with sufficient water (or other solvent) such that the polymers interact as discussed herein to form the hydrogel matrix. The polymers can be added to a mixing vessel for drying and then hydrated together, or separate solutions of each polymer (e.g., stock solutions, which can be provided in various concentrations to dilute to form a hydrogel composition) are prepared and then mixed in Together. Buffers or titrants may be added to adjust pH and ionic strength. The combination of components can then be mixed under heating (eg, to a temperature above the liquid transition temperature discussed herein) to form a homogeneous hydrogel composition. This mode of preparation allows for hydrogel matrices suitable for certain uses in which the therapeutic benefit depends on the properties of the components of the composition but not on the overall structure of the hydrogel itsel...

Embodiment 1

[0252] Example 1. Preparation of Gelatin / Dextran Compositions

[0253] Compositions according to one embodiment of the present disclosure were prepared by sequentially adding liquid and powdered materials (Table 1 ) at elevated temperatures at specific time points while mixing to maintain a homogeneous state of the liquid. The solution is then sterile filtered, dispensed aseptically into vials, sealed, and stored at refrigerated temperature.

[0254] Table 1

[0255]

[0256]

[0257] Glucose and Medium 199 (1.17 mM phosphate ion concentration) were measured and transferred to a preheated water-jacketed (50° C.) glass vessel and mixed using a stir bar. Allow the mixture to equilibrate to 50 °C before distributing L-cysteine, L-alanyl-L-glutamine, L-glutamic acid, L-lysine, and disodium EDTA into containers containing medium 199 middle. After equilibration time, dextran powder was added and the components were mixed. Once the dextran appears to be in solution, the g...

Embodiment 2

[0260] Example 2. Preparation of Gelatin / Dextran Compositions Containing Phosphate Buffer

[0261] Compositions were prepared by sequentially adding liquid and powdered materials (Table 2) at elevated temperatures while mixing to maintain liquid homogeneity.

[0262] Table 2

[0263]

[0264]

[0265] Different from the composition of Example 1, the composition formulation of this example was prepared using phosphate buffered saline (PBS) with a phosphate ion concentration of 65 mM. Also, no L-alanyl-L-glutamine or 50% glucose was added in this example. Specifically, the composition of this example was prepared by first placing 2,282 ml of PBS in a preheated water-jacketed (50° C.) glass vessel and mixing using a stir bar. The mixture was allowed to equilibrate to 50°C, then 375 μl L-cysteine, 6.9 ml L-glutamic acid, 13.8 ml L-lysine and 24.2 ml disodium EDTA were dispensed into vessels containing PBS. After equilibration time, 137.5 g of dextran powder was added an...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
molecular weightaaaaaaaaaa
molecular weightaaaaaaaaaa
molecular weightaaaaaaaaaa
Login to view more

Abstract

The present invention provides compositions and methods useful in the treatment of wounds, particularly in reducing or preventing scar formation, particularly hypertrophic scar or keloid formation. The invention thus further provides methods of treatment, including methods useful in hypertrophic scar or keloid revision as well as prophylactic, scar inhibiting methods.

Description

field of invention [0001] The present invention relates to compositions suitable for the treatment of dermal wounds, methods for such treatment and methods of making the compositions. In particular, the composition may be defined by a hydrogel stabilization factor, according to which the composition may be particularly effective for application to skin wounds, preferably to be effective in promoting healing and reducing scarring (in particular scarring tumor formation). Background of the invention [0002] There are many situations in medicine where wounds do not heal properly, such as compromised wound healing that delays or prevents wound resolution. However, there are other wound healing events that can limit the resulting function or aesthetics. Exemplary undesirable outcomes include hyperplastic reactions producing extensive scarring, keloids, or trauma contractures that compromise function and mobility. [0003] Hypertrophic scarring occurs when the body overproduce...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): A61L27/26A61L27/52A61L31/04A61L31/14A61L15/22
CPCA61L27/26A61L27/52A61L31/041A61L31/145A61L15/225A61P17/02C08L89/06C08L5/02A61K47/36A61K47/42
Inventor T.古延K.普鲁多姆R.亚马莫托A.G.洛A.M.格林
Owner HALSCION
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products