Multicomponent Composition for Alzheimer's Neuroprotection

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Solution Overview

Problem

Current treatments for neurodegenerative diseases like Alzheimer's disease are ineffective, as they primarily target single pathways, failing to address the complex biological processes involved, leading to limited therapeutic success.

Innovation Solution

Development of a pharmaceutical composition comprising nicotinamide mononucleotide (NMN), nicotinamide riboside (NR), phenethyl isothiocyanate (PEITC), and other natural compounds that modulate multiple upstream cellular pathways associated with Alzheimer's disease, protecting neurons from cell death and regulating microglia phagocytic activity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If single pathway targeting is used in current AD treatments, then treatment simplicity is maintained, but therapeutic effectiveness is limited

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

Solution Approach 1:

The patent combines multiple natural compounds (NAD+, NADH, PEITC, and other antioxidants) into a single pharmaceutical composition that simultaneously targets multiple upstream cellular pathways involved in AD pathology, including mitochondrial dysfunction, oxidative stress, and neuroinflammation, thereby achieving enhanced therapeutic effectiveness without requiring multiple separate treatments

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The pharmaceutical composition is designed to perform multiple therapeutic functions simultaneously: it acts as an antioxidant, anti-inflammatory agent, and mitochondrial enhancer, making the treatment versatile and effective against the complex, multifactorial nature of Alzheimer's disease pathology

Inventive Principle:
Principle #6Universality (Multi-functionality)

2Reliability

If multiple upstream cellular pathways are targeted with pharmaceutical composition, then therapeutic effectiveness is improved, but composition complexity increases

Engineering Contradiction:
Improvetherapeutic effectivenessVSAvoidcomposition complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent segments the complex task of targeting multiple AD pathways into distinct functional components, each natural compound in the composition being responsible for specific pathway modulation (e.g., NAD+ for mitochondrial function, PEITC for anti-inflammatory effects), allowing for systematic design and optimization of the multi-component composition

Inventive Principle:
Principle #1Segmentation

3Reliability

If natural compounds are used to modulate multiple pathways, then neuroprotective effects are achieved, but development time increases

Engineering Contradiction:
Improveneuroprotective effectVSAvoiddevelopment time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The patent utilizes naturally occurring compounds that have already been shown to have beneficial biological activities in other contexts, performing preliminary validation of their safety and efficacy before combining them for AD treatment, thereby reducing the need for extensive de novo testing and accelerating development

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent leverages existing knowledge about the biological activities of natural compounds from previous research and clinical use in other conditions, copying proven mechanisms of action and applying them to AD treatment, which reduces development time compared to creating entirely new therapeutic mechanisms

Inventive Principle:
Principle #26Copying

Data Source

PatentUS20240156846A1Compositions and methods for treating neurodegenerative disorders
Publication Date: 2024.05.16 THE TRUSTEES OF COLUMBIA UNIV IN THE CITY OF NEW YORK
  • US20240156846A1 patent drawing
  • US20240156846A1 patent drawing
  • US20240156846A1 patent drawing

AI summary

This invention relates generally to neurodegenerative diseases and conditions (e.g., Alzheimer's disease) characterized with dysfunctional energetic function, unregulated microglia phagocytic activity and other related de-regulated biological functions. This invention further relates to methods and compositions for treating such neurodegenerative diseases and conditions with pharmaceutical compositions capable of protecting neurons from cell death and unregulated microglia phagocytic activity.