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

Multidrug-Resistant Gram-Positive Bacteria Antibacterial Agent and Topical Agent

a multi-drug-resistant, topical technology, applied in the direction of antibacterial agents, drug compositions, aerosol delivery, etc., can solve the problem of increasing the difficulty of countermeasures

Inactive Publication Date: 2016-10-20
Q P CORP
View PDF1 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides a new substance that can kill multidrug-resistant bacteria that are resistant to traditional antibiotics. Additionally, an external agent containing this substance is also available.

Problems solved by technology

Multidrug resistant bacteria resistant to a number of medical agents raise an issue.
However, the use of antibiotics generates a new resistant bacteria, and there is a possibility that countermeasures become more difficult.

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
  • Multidrug-Resistant Gram-Positive Bacteria Antibacterial Agent and Topical Agent
  • Multidrug-Resistant Gram-Positive Bacteria Antibacterial Agent and Topical Agent
  • Multidrug-Resistant Gram-Positive Bacteria Antibacterial Agent and Topical Agent

Examples

Experimental program
Comparison scheme
Effect test

embodiments

Example 1

[0075]Firstly, an antibacterial agent in Example 1 was prepared. In Example 1, as the amphiphilic compound, which is the active ingredient of the antibacterial agent, lyso phosphatidylcholine derived from egg yolk (manufactured by Kewpie Corporation, egg yolk lysolecithin LPC-1) was used. The lyso phosphatidylcholine in Example 1 had the HLB value of 14 and the iodine value of 9. Table 2 shows substance names, derived sources, and HLB values in Examples and Comparative Examples, respectively.

TABLE 2Ingredient ofDerivedHLBantibacterial agentfromvalueEx. 1lysoegg yolk14phosphatidylcholineEx. 2lysophospholipidssoybeans11 to 20Ex. 3sucrose fatty acidsynthesized15esterEx. 4sucrose fatty acidsynthesized19esterComp. Ex. 1lyso phosphatidylsoybeans22glycerolComp. Ex. 2sucrose fatty acidsynthesized1esterComp. Ex. 3glycerin fatty acidsynthesized4.3esterComp. Ex. 4sucrose fatty acidsynthesized6esterComp. Ex. 5glycerin fatty acidsynthesized7esterComp. Ex. 6sucrose fatty acidsynthesized9...

example 2

[0078]In Example 2, as the amphiphilic compound, hydrogenated soybean lysophospholipid (manufactured by Nikko Chemicals Co., Lecinol LL-20) was used. It is conceivable that a plurality of phospholipids may be mixed to provide the soybean lysophospholipid in Example 2, and it confirms that the soybean lysophospholipid had an HLB value of 11 to 20. The iodine value was 20 or less. The soybean lysophospholipid is represented by the above formula 1. The soybean lysophospholipid was prepared in the same manner as in Example 1, and the test solution having a concentration of 5000 ppm (5000 μg / mL), 1250 ppm (1250 μg / mL), or 313 ppm (313 μg / mL) was prepared. When the soybean lysophospholipid was not easily dissolved in purified water, it was heated to about 70° C.

example 3

[0097]In Example 3, as the amphiphilic compound, sucrose fatty acid ester (manufactured by Dai-ichi Kogyo Seiyaku Co., Ltd., DK ester F-160) was used (see Table 2). The sucrose fatty acid ester in Example 3 had the HLB value of 15. The sucrose fatty acid ester was prepared in the same manner as in Example 1, and the test solution having a concentration of 5000 ppm (5000 μg / mL), 1250 ppm (1250 μg / mL), or 313 ppm (313 μg / mL) was prepared. When the sucrose fatty acid ester was not easily dissolved in purified water, it was heated to about 70° C.

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
iodine valueaaaaaaaaaa
concentrationaaaaaaaaaa
resistanceaaaaaaaaaa
Login to View More

Abstract

To provide a multidrug-resistant Gram positive bacteria antibacterial agent containing as an active ingredient a novel component to which multidrug-resistant bacteria are not resistant, and an external agent containing the same. The multidrug resistant Gram-positive bacteria antibacterial agent according to the present invention contains an amphipathic compound having an HLB value of greater than 9.5 and 20 or less and an acyl group as an active ingredient. The external agent according to the present invention contains the multidrug resistant Gram-positive bacteria antibacterial agent.

Description

TECHNICAL FIELD[0001]The present invention relates to an antibacterial agent against multidrug-resistant Gram-positive bacteria, and an external agent containing the same.BACKGROUND ART[0002]Multidrug resistant bacteria resistant to a number of medical agents raise an issue. In particular, methicillin-resistant Staphylococcus aureus (MRSA) among the multidrug resistant bacteria is Staphylococcus aureus resistant to methicillin that is an antibiotic, and may be resistant to a plurality of antibiotics including methicillin. MRSA infections often are seen in nosocomial infections. As there may be serious infectious cases, sufficient countermeasures are required.[0003]As the countermeasures for multidrug resistant bacterial infections, it is considered to use an antibiotic that does not acquire resistance. However, the use of antibiotics generates a new resistant bacteria, and there is a possibility that countermeasures become more difficult.[0004]Meanwhile, there is a substance other t...

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(United States)
IPC IPC(8): A61K31/685A61K9/12A61K9/00A61K31/7024A61K9/06
CPCA61K31/685A61K31/7024A61K9/12A61K9/0014A61K9/06A61K9/08A61K31/683A61K47/10A61K47/12A61K47/14A61P17/00A61P31/04A61P43/00A61K47/16A61K47/22A61K47/24A61K47/44
Inventor KOZONO, MARIEYOSHIDA, HIDETO
Owner Q P CORP
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