Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Compound lidocaine gel patch

A technology of prilocaine gel patch and lidocaine, which is applied in antiviral agents, pharmaceutical formulas, medical preparations of non-active ingredients, etc., to improve release and absorption in the body, improve stability, and improve the efficacy of use Effect

Active Publication Date: 2021-09-17
THE EYE HOSPITAL OF WENZHOU MEDICAL UNIV
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] At present, the compound lidocaine / prilocaine gel patch with stable and controllable quality and good analgesic effect has not been reported yet.

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
  • Compound lidocaine gel patch

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0052] Embodiment 1 Compound lidocaine / prilocaine gel patch P1 of the present invention

[0053] Fully dissolve 24.98g of chicory-derived fructooligosaccharides in 30ml of water, then add 5g of lidocaine hydrochloride, 5g of prilocaine hydrochloride, 30g of D-sorbitol, 0.01g of disodium edetate, 2g of calcium hydroxide, and 8g of micropowder Silica gel was added to the fructooligosaccharide aqueous solution to obtain a phase A solution; 4g sodium polyacrylate NP-700, 2g sodium carboxymethylcellulose, 4g polyvinylpyrrolidone K90, 2g camphor, 2g eucalyptus oil, 0.01g ethylparaben Dissolve in a mixture consisting of 8g propylene glycol and 2g glycerin to obtain a phase B solution; pass the phase A solution through an 80 mesh sieve, mix it with the phase B solution, and then add a 10% aqueous solution containing 0.5g citric acid and 0.5g malic acid , mix well, spread on non-woven fabric, dry at 50°C for 8 hours, cut into pieces of 70cm each 2 Gel patch, the gel patch contains 5mg...

Embodiment 2

[0054] Embodiment 2 Compound lidocaine / prilocaine gel patch P2 of the present invention

[0055] Adjust the type of transdermal absorption accelerator, replace the composition of 2g camphor and 2g eucalyptus oil with 4g camphor in embodiment 1, and all the other prescriptions and preparation processes are the same as in embodiment 1 to obtain compound lidocaine / prilocaine of the present invention Because of the gel patch P2.

Embodiment 3

[0056] Embodiment 3 Compound lidocaine / prilocaine gel patch P3 of the present invention

[0057] Adjust transdermal absorption accelerator kind, the composition of 2g camphor and 2g eucalyptus oil in embodiment 1 is replaced with 4g eucalyptus oil, and all the other prescriptions and preparation technology are identical with embodiment 1, obtain compound recipe lidocaine of the present invention / Prilocaine gel patch P3.

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

No PUM Login to View More

Abstract

The invention relates to a compound lidocaine / prilocaine gel patch. The gel patch is prepared from following components in percentage by weight: 4%-8% of lidocaine hydrochloride, 4%-8% of prilocaine hydrochloride, 2%-5% of a framework material, 5%-10% of a filler, 20%-30% of an adhesive, 3%-9% of a tackifier, 1%-5% of a cross-linking agent, 2%-4% of a transdermal absorption enhancer, 30%-50% of a humectant, 0.005%-0.02% of a preservative, 0.005%-0.02% of a complexing agent and 0.5%-2% of a stabilizer. The compound lidocaine / prilocaine gel patch is stable in quality, good in treatment effect, simple in preparation process and capable of realizing industrial production.

Description

technical field [0001] The invention relates to the field of medicines, in particular to an analgesic gel patch. Background technique [0002] Pain is listed as the "fifth vital sign" of the human body and is a common adverse human experience. Epidemiological surveys show that the incidence of chronic pain in adults is 20%-60%, and the incidence of pain with neuropathic features is 6.9%-10% in the population, of which local neuropathic pain accounts for 60%. Chronic pain can lead to reduced ability to work, and its accompanying emotional and sleep disturbances have a serious impact on quality of life. However, pain management is complex and often requires a combination of multiple treatments, and many patients are not satisfied with pain treatment outcomes. Treatment of neuropathic pain is particularly suboptimal, with patients often relapsing and half suffering from inadequate pain relief. [0003] Herpes zoster is an acute central nervous system infection that primarily...

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): A61K9/70A61K31/167A61K47/10A61K47/12A61K47/32A61K47/44A61P25/00A61P31/22
CPCA61K31/167A61K9/703A61K47/32A61K47/10A61K47/44A61K47/12A61P25/00A61P31/22A61K2300/00
Inventor 李军花赵云娥
Owner THE EYE HOSPITAL OF WENZHOU MEDICAL UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products