Fluorine Contrast Agent Nitroxide Relaxation Optimization

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Solution Overview

Problem

Conventional contrast agents for magnetic resonance imaging using fluorine as a detection nucleus fail to achieve high-sensitivity MRI images.

Innovation Solution

A fluorine-containing compound with two nitroxide radical-containing groups and one to three fluorine atom-containing groups, where the nitroxide radicals are bound to the fluorine atoms through a chain structure, is used as a contrast agent to enhance the 19F spin-lattice relaxation time and signal intensity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If conventional contrast agents are used for 19F-MRI diagnosis, then the diagnostic imaging function is provided, but high-sensitivity MRI images cannot be obtained

Engineering Contradiction:
ImproveMRI sensitivityVSAvoidimage quality
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The patent changes the chemical structure parameters of the contrast agent by introducing specific fluorine-containing groups (CF3, CF2, or F) and controlling their数量和 positions. This structural parameter optimization directly improves the 19F spin-lattice relaxation time and signal intensity, achieving high-sensitivity MRI images while maintaining diagnostic reliability

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent creates a composite molecular structure combining nitroxide radical-containing groups with fluorine atom-containing groups through chain structures. This composite design synergistically enhances both the relaxation properties and signal intensity, resolving the contradiction between sensitivity and image quality

Inventive Principle:
Principle #40Composite materials

2Measurement precision

If the 19F spin-lattice relaxation time is optimized for high signal intensity, then MRI sensitivity improves, but the spin-spin relaxation time must be maintained appropriately

Engineering Contradiction:
Improvesignal intensityVSAvoidrelaxation time balance
Core Design Contradiction:
Measurement precisionVSStability of the object's composition

Solution Approach 1:

The patent optimizes the spin-lattice relaxation time parameter through specific molecular design while simultaneously controlling the spin-spin relaxation time. By adjusting the fluorine group composition and chain structure, both relaxation parameters are tuned to achieve optimal signal intensity and image quality balance

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent introduces different fluorine-containing groups (CF3, CF2, or F) at specific positions in the molecular structure to locally enhance relaxation properties. This localized optimization allows independent tuning of spin-lattice and spin-spin relaxation times to achieve the desired balance

Inventive Principle:
Principle #3Local quality

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

The compound achieves high-sensitivity magnetic resonance images by optimizing the 19F spin-lattice relaxation time and maintaining appropriate 19F spin-spin relaxation time, resulting in improved signal intensity and diagnostic quality.

Implementation Method 1

two nitroxide radical-containing groups... bound to the fluorine atom-containing groups... to enhance the 19F spin-lattice relaxation time and signal intensity

Methodology Applied
Scientific EffectParamagnetic relaxation enhancement:

Data Source

PatentUS20230293734A1Fluorine-containing compound and contrast agent
Publication Date: 2023.09.21 TDK CORP
  • US20230293734A1 patent drawing
  • US20230293734A1 patent drawing
  • US20230293734A1 patent drawing

AI summary

The fluorine-containing compound includes: two nitroxide radical-containing groups represented by Formula (1) (R1, R2, R3, and R4 are each independently a C1-10 alkyl group unsubstituted or substituted with a substituent containing no fluorine atoms); and one to three —O—C(CF3)3 groups, in which the nitroxide radical-containing groups are bound to the —O—C(CF3)3 groups through a chain structure with 2 to 17 atoms.