Ambient Pressure Ionization Interface for DMS Analysis

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Solution Overview

Problem

Conventional methods for sample preparation in differential mobility spectrometry (DMS) are limited in analyzing non-volatile and semi-volatile substances, as they often result in fragmentation and are not suitable for high molecular weight compounds, and require operation under high vacuum, making them unsuitable for portable and field-deployable devices.

Innovation Solution

An interface assembly that utilizes ambient pressure matrix-assisted laser desorption ionization (AP-MALDI) and electrospray ionization (ESI) techniques to ionize and introduce samples into a DMS, allowing for the analysis of high molecular weight biological and non-biological molecules without fragmentation, and operates at ambient pressure, enabling portable and field-deployable systems.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional sample preparation methods are used in DMS, then the system can operate under high vacuum, but it results in fragmentation of high molecular weight compounds and is not suitable for portable devices

Engineering Contradiction:
Improvechemical integrityVSAvoidvacuum system requirement
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The invention changes the operating pressure parameter from high vacuum to ambient pressure, enabling the use of AP-MALDI and ESI ionization techniques that preserve chemical integrity of high molecular weight compounds while eliminating the need for complex vacuum systems, making the device portable and field-deployable

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention replaces the mechanical vacuum system with an ambient pressure operation mode, substituting the need for vacuum pumps and seals with ionization techniques (AP-MALDI and ESI) that function effectively at atmospheric pressure, thereby simplifying the device structure and enabling portability

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

2Manufacturing precision

If conventional ionization methods are used, then the system is simpler to operate, but it causes fragmentation and is not suitable for high molecular weight compounds

Engineering Contradiction:
ImproveresolutionVSAvoidionization method complexity
Core Design Contradiction:
Manufacturing precisionVSEase of operation

Solution Approach 1:

The invention changes the ionization method from conventional electron impact to AP-MALDI and ESI techniques, which use softer ionization mechanisms that deposit less energy on analyte molecules, thereby preventing fragmentation and improving resolution for high molecular weight compounds while maintaining operational simplicity through automated sample introduction

Inventive Principle:
Principle #35Parameter changes

3Measurement precision

If the drift tube length is increased to improve resolution in TOF spectrometry, then better separation is achieved, but the device size increases and sensitivity decreases due to ion loss

Engineering Contradiction:
ImproveresolutionVSAvoidion abundance
Core Design Contradiction:
Measurement precisionVSQuantity of substance

Solution Approach 1:

The invention introduces a reflectron as an intermediary component in the flight path that reflects ions back toward the detector, effectively increasing the flight path length and resolution without proportionally increasing the physical device size, while minimizing ion loss through the use of electrostatic mirrors that efficiently reflect ions back into the detection region

Inventive Principle:
Principle #24Intermediary (Mediator)

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 the analysis of high molecular weight molecules up to 100,000 Da, preserving chemical integrity and improving resolution, and facilitates the development of portable and field-deployable systems for detecting biological and chemical agents.

Implementation Method 1

an ionization source for producing ionized analyte from the sample, the ionization source including an ambient pressure matrix-assisted laser desorption ionization apparatus

Methodology Applied
Scientific EffectLaser desorption ionization: Laser Ablation

Implementation Method 2

a laser for providing energy to desorb and ionize the analyte in the presence of the ionization-assisting matrix

Methodology Applied
Scientific EffectPhotoionisation: Photoionisation

Implementation Method 3

electrospray ionization (ESI) techniques to ionize and introduce samples into a DMS

Methodology Applied
Scientific EffectElectrospray ionization: Electrohydrodynamics

Implementation Method 4

an ion flow generator that draws the ionized analyte from the ionization apparatus into the interface assembly and through the capillary tube

Methodology Applied
Scientific EffectPressure gradient: Pressure Gradient

Implementation Method 5

a gas manifold assembly through which a carrier gas flows, the gas manifold assembly disposed in relation to the capillary tube to allow infusion of the ionized analyte into the carrier gas and delivery of the resulting gas stream into the ion mobility spectrometer

Methodology Applied
Scientific EffectGas flow: Convection

Data Source

PatentUS7968842B2Apparatus and systems for processing samples for analysis via ion mobility spectrometry
Publication Date: 2011.06.28 THE CHARLES STARK DRAPER LABORATORY INC
  • US7968842B2 patent drawing
  • US7968842B2 patent drawing
  • US7968842B2 patent drawing

AI summary

The invention provides an interface assembly for delivering an ionized analyte from an ionization apparatus into an ion mobility spectrometer. This allows analysis of biological and non-biological samples, even non-volatile solids, via differential mobility spectrometry, without fragmentation of molecules. The invention also provides portable sample analysis systems that operate at ambient pressure. Systems of the invention may be used for high molecular weight species detection, for example, drinking water contaminants, pathogenic biological agents, bio-organic substances, non-biological material, peptides, proteins, oligonucleotides, polymers, bacteria, and hydrocarbons.