Ion Mobility Spectrometer Shifting Reagent Drift Time Separation

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Solution Overview

Problem

Ion mobility spectrometers face challenges in resolving interfering chemical and biological molecules due to limited resolution, which leads to false positives and difficulties in detecting low levels of targeted molecules, especially as molecular complexity increases, as they rely primarily on ion mobility without effectively utilizing molecular geometry for differentiation.

Innovation Solution

The use of shifting reagents that selectively interact with targeted functional groups of molecules, altering their drift times and ion mobility characteristics, allowing for structure-selective based separation and reducing interference by adding energy to the sample components, thereby enhancing resolution beyond traditional ion mobility differences.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If traditional ion mobility separation is used, then device complexity is reduced, but the ability to differentiate molecules with similar ion mobilities deteriorates

Engineering Contradiction:
Improvespectrometer structureVSAvoidmolecular differentiation capability
Core Design Contradiction:
Device complexityVSMeasurement precision

Solution Approach 1:

The patent adds a spatial dimension (drift tube length) to the separation process. By extending separation in the drift direction rather than increasing mobility tube complexity, the system achieves better differentiation with minimal additional structural complexity.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

Solution Approach 2:

The patent utilizes changes in drift time as a separability parameter. By measuring and comparing drift times of ions through the drift tube, the system differentiates molecules with similar ion mobilities without requiring complex structural modifications to the spectrometer.

Inventive Principle:
Principle #35Parameter changes

2Adaptability or versatility

If molecules with high molecular complexity are analyzed, then the range of detectable analytes is expanded, but the number of possible conformations increases making separation more difficult

Engineering Contradiction:
Improveanalyte rangeVSAvoidseparation resolution
Core Design Contradiction:
Adaptability or versatilityVSMeasurement precision

Solution Approach 1:

The patent uses the drift tube to provide an additional separation dimension that handles conformational complexity. While the mobility tube separates based on ion mobility, the drift tube further separates conformers based on their drift characteristics, enabling analysis of complex molecules with multiple conformations.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

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

This approach significantly improves the separation and identification of chemical and biological molecules by shifting their drift times, reducing interference and enhancing detection sensitivity, allowing for more accurate analysis of complex samples.

Implementation Method 1

shifting reagents that selectively interact with targeted functional groups of molecules, altering their drift times and ion mobility characteristics

Methodology Applied
Scientific EffectChemical bonding: Chemical Bonding

Implementation Method 2

adding energy to the sample components, thereby enhancing resolution beyond traditional ion mobility differences

Methodology Applied
Scientific EffectThermal energy: Heating

Data Source

PatentUS8618477B2Method and apparatus for chemical and biological sample separation
Publication Date: 2013.12.31 EXCELLIMS CORP
  • US8618477B2 patent drawing
  • US8618477B2 patent drawing
  • US8618477B2 patent drawing

AI summary

The present invention involves a series of shifting reagents that selectively interact with a targeted functional group of biological molecules, pharmaceutical drugs, small molecules, chemicals, chemical agents, or explosives resulting in a structure selective based drift time shift in the IMS. Additional energy is used to enhance the mobility based separation; in particular, the energy level can be tuned.