Antibacterial Compound Sensitizing Multidrug-Resistant Bacteria to Oxidative Stress

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Solution Overview

Problem

Bacterial infections, particularly those caused by multidrug-resistant strains, pose a significant challenge due to the bacteria's ability to evade host defense mechanisms and develop resistance to oxidative stress, necessitating a new therapeutic approach.

Innovation Solution

A novel antibacterial chemical compound with a specific chemical structure that targets bacterial resistance to oxidative stress, inhibiting intracellular bacterial growth and enhancing the effectiveness of antibiotics against multidrug-resistant bacteria.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional antibiotics are used to treat bacterial infections, then bacterial growth is inhibited, but bacteria develop multidrug resistance

Engineering Contradiction:
Improveantibacterial efficacyVSAvoidbacterial resistance
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The compound acts as an intermediary that blocks bacterial efflux pumps, preventing the expulsion of antibiotics and oxidative stress agents from bacterial cells. This mediator function restores the effectiveness of conventional antibiotics by stopping the resistance mechanism without directly killing bacteria, thereby addressing multidrug resistance while maintaining existing therapeutic approaches

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The compound changes the physiological parameters of bacterial cells by inhibiting efflux pump activity, which alters the intracellular concentration of antibiotics and oxidative stress agents. This parameter change (increased intracellular drug retention) sensitizes multidrug-resistant bacteria to oxidative stress and restores antibiotic efficacy without requiring new antibiotic mechanisms

Inventive Principle:
Principle #35Parameter changes

2Reliability

If efflux pumps are blocked to enhance antibiotic effectiveness, then bacterial resistance is reduced, but the complexity of treatment increases

Engineering Contradiction:
Improveantibiotic effectivenessVSAvoidtreatment complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The compound can be combined with conventional antibiotics in a single pharmaceutical formulation or treatment regimen, merging the efflux pump inhibition function with existing antibiotic therapy. This combination approach enhances antibiotic effectiveness against multidrug-resistant bacteria while maintaining a relatively simple treatment protocol that does not require separate administration steps

Inventive Principle:
Principle #5Merging (Combining)

3Reliability

If oxidative stress is enhanced to kill intracellular bacteria, then bacterial viability is reduced, but host cell damage may occur

Engineering Contradiction:
Improvebacterial killing efficiencyVSAvoidhost cell toxicity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The compound exhibits selective action by specifically targeting bacterial efflux pumps while sparing host cell mechanisms. By blocking bacterial efflux pumps locally, the compound enables oxidative stress agents to accumulate selectively within bacterial cells rather than throughout the entire host-bacteria system, thereby enhancing bacterial killing efficiency while minimizing host cell exposure and potential damage

Inventive Principle:
Principle #3Local quality

Data Source

PatentUS11925650B2Antibacterial chemical compound, its manufacturing method and its use thereof
Publication Date: 2024.03.12 NAT TAIWAN UNIV
  • US11925650B2 patent drawing
  • US11925650B2 patent drawing
  • US11925650B2 patent drawing

AI summary

The present invention provides an antibacterial chemical compound, its manufacturing method and its use thereof which acts as antibacterial agents being useful for treating a disease or condition characterized by infectious disease, such as gastroenteritis and invasive non-typhoidal Salmonellosis, and also providing a new therapeutic option for patients infected by the bacteria with the resistance to antibiotics.