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

Application of ethyl potassium sulfate in preparation of drugs for preventing or treating inflammatory diseases

A technology for inflammatory diseases and potassium sulfate, which is applied in the direction of sulfate ester preparation, diseases, skin diseases, etc., can solve the problems of undiscovered medical uses of potassium ethyl sulfate, and achieve good anti-inflammatory effects

Pending Publication Date: 2019-02-26
JIANGZI QINGFENG PHARMACEUTICALS INC
View PDF7 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Potassium ethyl sulfate has not been found to have medicinal uses

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
  • Application of ethyl potassium sulfate in preparation of drugs for preventing or treating inflammatory diseases
  • Application of ethyl potassium sulfate in preparation of drugs for preventing or treating inflammatory diseases
  • Application of ethyl potassium sulfate in preparation of drugs for preventing or treating inflammatory diseases

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Embodiment 1: the preparation of potassium ethyl sulfate

[0044] Add a certain amount of ethanol to the reaction kettle, slowly add 6 times the amount of sulfuric acid ethanol solution dropwise under stirring, control the temperature of the reaction kettle at 38°C, and continue stirring for 24 hours for the esterification reaction. Add ethanol, stir well, adjust the pH to 7.0 with 10% KOH, add 95% ethanol to make the alcohol content reach more than 85%, recover ethanol under reduced pressure, and separate the aqueous solution through adsorption resin column chromatography, and use water: ethanol gradient elution, The eluate was collected and potassium ethyl sulfate was crystallized.

Embodiment 2

[0045] Embodiment 2: Potassium ethyl sulfate is to the influence of phorbol ester-induced mouse auricle swelling

[0046] experimental method

[0047]ICR mice, half male and half female, aged 6-8 weeks, weighing 18-22 g, were randomly divided into 6 groups (model group, five dose groups of potassium ethylsulfate). Use a 20 μL pipette to evenly apply 20 μL of TPA solution to the right ear of each mouse. Potassium ethyl sulfate was injected intravenously at a volume of 0.1 mL / 10 g 1 hour after modeling, and the dosages were 12.5, 25, 50, 100, and 200 mg / kg, respectively. After 6 hours of modeling, the mice were sacrificed by dislocation of the cervical vertebrae, and round ears were punched in the same part of the two auricles with a punch with a diameter of 8 mm, weighed with an electronic balance, and the swelling degree and swelling inhibition rate of the auricles were calculated according to the following formula. Degree of swelling (%)=(right ear mass−left ear mass) / left ...

Embodiment 3

[0056] Example 3: Effect of Potassium Ethyl Sulfate on Rat Paw Swelling Caused by Carrageenan

[0057] experimental method

[0058] Wistar rats, 200-220g, were randomly divided into 6 groups (normal group, model group, four dose groups of potassium ethyl sulfate). After chloral hydrate anesthesia, in addition to the normal group given the same amount of normal saline, the rats in other groups were injected subcutaneously with 0.1 mL of sterile 1% carrageenan normal saline suspension on the right hind paw to cause inflammation, and 0.5 hours after inflammation Different doses of potassium ethyl sulfate or normal saline were administered intravenously, and the administration volume was 1 mL / 100 g. The water volume method was used to measure the volume of the right hind paw before inflammation and 1, 3, 5, and 7 hours after inflammation, and the swelling rate and swelling inhibition rate were calculated. Swelling rate (%), expressed as (Vt-Vn) / Vn*100, Vn and Vt represent the pa...

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 discloses an application of ethyl potassium sulfate in the preparation of drugs for treating inflammations, fever, diarrhea, and cough as a NF-[kappa]B inhibitor, and a preparation method and a composition of ethyl potassium sulfate.

Description

technical field [0001] The invention relates to the application of potassium ethyl sulfate in the preparation of medicines for preventing or treating inflammatory diseases. Background technique [0002] Ethyl sulfuric acid is also called ethylbisulfate or ethyl-sulfuric acid. The boiling point is 280°C (decomposition). The relative density is 1.316. When heated or boiled in concentrated solution, it decomposes into toxic sulfur oxide (SOx) fumes, which are highly irritating and corrosive to skin, eyes and mucous membranes. The product is etherified with ethanol to obtain anesthesia ether; neutralized with potassium carbonate to obtain potassium ethyl sulfate. [0003] Potassium ethyl sulfate has not been found to have medicinal uses. Contents of the invention [0004] The applicant unexpectedly discovered the new application of potassium ethyl sulfate for the preparation of inflammatory diseases, antipyretic, diarrhea or NF-κB inhibitor drugs, the compound preparation ...

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
IPC IPC(8): A61K31/255A61P29/00A61P1/12A61P11/14A61P1/00A61P5/14A61P19/02A61P1/02A61P17/00A61P11/00A61P15/02A61P13/10C07C303/24C07C305/06
CPCA61K31/255C07C303/24C07C305/06
Inventor 李志勇蒋春红刘尧奇王章伟邓双炳黄冰峰周鹏
Owner JIANGZI QINGFENG PHARMACEUTICALS INC
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com