MRI Contrast Agents with Aptamer Oligonucleotides for In Vivo Detection

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Solution Overview

Problem

Current aptamer sensors face challenges in vivo applications due to difficulties with light penetration through skin and signal interference from cellular components, limiting their effectiveness in human imaging and diagnostics.

Innovation Solution

Development of MRI contrast agents comprising MRI contrast agent particles and oligonucleotides, where the oligonucleotides are attached to the particles and form aggregates or disaggregate in response to specific molecules, enhancing contrast in MRI images by altering T1 and T2 relaxation times, and utilizing aptamers, enzymes, and substrates to detect biomolecular markers.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If fluorescent, colorimetric, or electrochemical aptamer sensors are used, then high sensitivity and selectivity in detecting biomolecular markers are achieved, but light penetration through skin and signal interference from cellular components prevent effective in vivo applications

Engineering Contradiction:
Improvedetection sensitivityVSAvoidlight penetration limitation and cellular interference
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The patent replaces optical detection systems (fluorescent, colorimetric sensors) with magnetic resonance imaging (MRI) detection. This substitution eliminates the harmful effects of light penetration limitations and cellular interference by using magnetic fields instead of light for detection, enabling effective in vivo applications while maintaining high detection sensitivity through the use of aptamer-functionalized contrast agents

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

2Reliability

If aptamers are used for molecular recognition, then high affinity and selectivity binding is achieved, but the complexity of converting aptamers into functional sensors for in vivo use increases

Engineering Contradiction:
Improvebinding affinityVSAvoidsensor system complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent merges the molecular recognition function of aptamers with the imaging function of MRI contrast agents into a single integrated system. By conjugating aptamers to contrast agent particles, the invention combines high affinity binding with non-invasive imaging capability, simplifying the overall sensor system while maintaining reliable molecular detection in vivo

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The patent creates a universal platform where aptamer-contrast agent conjugates can detect multiple different biomolecular markers by simply changing the aptamer sequence while maintaining the same contrast agent core. This multi-functional approach reduces system complexity by using a standardized detection mechanism for various therapeutic applications

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

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enables non-invasive, high-sensitivity detection of biomolecular markers and pathologies like tumors through enhanced MRI contrast, overcoming previous limitations of light penetration and cellular interference.

Implementation Method 1

enhancing contrast in MRI images by altering T1 and T2 relaxation times

Methodology Applied
Scientific EffectMagnetic relaxation (T1 and T2): Magnetic Field

Data Source

PatentUS8568690B2MRI contrast agents and high-throughput screening by MRI
Publication Date: 2013.10.29 THE BOARD OF TRUSTEES OF THE UNIV OF ILLINOIS
  • US8568690B2 patent drawing
  • US8568690B2 patent drawing
  • US8568690B2 patent drawing

AI summary

The present invention provides an MRI contrast agent, comprising: MRI contrast agent particles, and oligonucleotides, attached to the particles.