Post-Mortem Oral Fluid Drug Testing via ELISA and LC-MS/MS

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Solution Overview

Problem

Current post-mortem forensic drug analysis methods using blood, urine, and liver tissue are time-consuming, invasive, and often unsuitable due to autolysis and sample degradation, necessitating a faster and less invasive approach for drug detection and quantification.

Innovation Solution

A method utilizing oral fluid collected from post-mortem subjects for rapid and sensitive detection and quantification of drugs through enzyme-linked immunosorbent assay (ELISA) and liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS), allowing for qualitative and quantitative analysis within three hours.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional biological matrices (blood, urine, liver tissue) are used for post-mortem drug analysis, then drug detection can be performed, but the analysis is time-consuming and sample quality degrades due to autolysis

Engineering Contradiction:
Improvedrug detection sensitivityVSAvoidanalysis time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The patent applies preliminary action by collecting oral fluid samples immediately after death before autolysis can occur. This prevents sample degradation beforehand, ensuring high-quality samples are available for rapid analysis within 3 hours, thus resolving the contradiction between maintaining detection sensitivity and reducing analysis time.

Inventive Principle:
Principle #10Preliminary action

2Measurement precision

If traditional biological matrices are used for sample collection, then drug analysis can be conducted, but the collection process is invasive and requires protective gear

Engineering Contradiction:
Improvedrug concentration measurementVSAvoidsample collection invasiveness
Core Design Contradiction:
Measurement precisionVSEase of operation

Solution Approach 1:

The patent extracts the sampling process from invasive internal body matrices (blood, urine, liver tissue) and relocates it to a non-invasive external matrix (oral fluid). This extraction eliminates the need for protective gear and complex collection procedures while maintaining the ability to accurately measure drug concentrations, thus resolving the contradiction between measurement precision and ease of operation.

Inventive Principle:
Principle #2Taking out (Extraction)

3Adaptability or versatility

If multiple instrumentalities are employed for qualitative and quantitative analysis of traditional samples, then comprehensive drug screening is achieved, but the process becomes complex and time-consuming

Engineering Contradiction:
Improvedrug class detection rangeVSAvoidnumber of instrumentalities
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The patent applies universality by developing a single analytical platform (LC-MS/MS) that can perform both qualitative screening and quantitative analysis across multiple drug classes (opioids, stimulants, depressants, cannabinoids, etc.). This multi-functional approach eliminates the need for multiple separate instrumentalities while maintaining comprehensive detection capabilities, thus resolving the contradiction between adaptability and device complexity.

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

This method provides faster, more sensitive, and less invasive drug testing compared to traditional methods, with results obtained in as little as three hours, and is capable of detecting a wide range of drugs, including those not detectable in blood or other matrices.

Implementation Method 1

analyzing the oral fluid sample qualitatively to detect the presence of one or more non-naturally occurring drugs

Methodology Applied
Scientific EffectAntigen-antibody binding:

Implementation Method 2

analyzing the oral fluid sample quantitatively to determine concentration of the one or more non-naturally occurring drugs

Methodology Applied
Scientific EffectChromatography: Chromatography

Implementation Method 3

liquid chromatography-mass spectrometry/mass spectrometry (LC-MS/MS)

Methodology Applied
Scientific EffectMass spectrometry:

Data Source

PatentUS10267811B2Rapid and sensitive method of forensic toxicology in post-mortem subjects using oral fluid testing
Publication Date: 2019.04.23 REISINGER AMY J
  • US10267811B2 patent drawing
  • US10267811B2 patent drawing
  • US10267811B2 patent drawing

AI summary

The present invention provides a rapid, sensitive method for forensic drug testing in a post-mortem subject using oral fluid collected from the post-mortem subject. The method comprises collecting a sample of oral fluid from a post-mortem subject, analyzing the oral fluid sample qualitatively to detect the presence of one or more non-naturally occurring drugs, analyzing the oral fluid sample quantitatively to determine concentration of the one or more non-naturally occurring drugs in the post-mortem subject, and identifying the one or more non-naturally occurring drugs in the post-mortem subject. The detection and quantification in oral fluid is more sensitive and faster than detection and quantification of the non-naturally occurring drugs in blood, urine, bile, and liver tissue collected from the same post-mortem subject. Further, the qualitative and quantitative results are obtained in as little as three hours.