Chemically Treated Sample Collector for Biomarker Stabilization

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Solution Overview

Problem

Current diagnostic methods for infectious diseases like Ebola Virus Disease (EVD) are inadequate for decentralized healthcare settings with limited infrastructure, requiring improved sample collection and handling to enable rapid, safe, and effective testing and research.

Innovation Solution

A multiple format sample collection device using a cellulose fibre matrix with chemically treated areas for DNA, RNA, and protein stabilization, allowing for safe storage and analysis without extensive biosafety requirements, and incorporating UV light treatment for viral inactivation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If molecular assays and laboratory testing are used for EVD diagnosis, then diagnostic accuracy is improved, but infrastructure requirements and complexity increase

Engineering Contradiction:
Improvediagnostic accuracyVSAvoidinfrastructure requirements
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The sample collection device is divided into distinct functional zones: a first area for DNA collection/stabilization, a second area for RNA collection/stabilization, and a third area for protein collection/stabilization. This segmentation allows different biomarkers to be collected and stabilized independently on the same device, enabling comprehensive diagnostic testing without requiring complex separate collection systems for each biomarker type.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The sample collection device serves multiple functions: it collects, stabilizes, and preserves multiple types of biomarkers (DNA, RNA, proteins) simultaneously. The chemically treated areas provide stabilization properties that allow the device to function as both a collection tool and a sample preservation system, reducing the need for complex cold chain infrastructure and enabling use in resource-limited settings.

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

2Measurement precision

If venous blood sampling is used for diagnosis, then sample quality is improved, but patient safety and infection risk worsen

Engineering Contradiction:
Improvesample qualityVSAvoidinfection risk
Core Design Contradiction:
Measurement precisionVSObject-affected harmful factors

Solution Approach 1:

The device incorporates chemically treated areas with specific stabilization properties tailored for different biomarker types. Each treated area is optimized for its specific function (DNA stabilization, RNA stabilization, or protein stabilization), allowing effective sample preservation from simple finger-prick samples without requiring large-volume venous draws, thereby reducing patient exposure risk while maintaining diagnostic quality.

Inventive Principle:
Principle #3Local quality

3Reliability

If extensive sample preparation is required, then diagnostic reliability is improved, but time consumption and operational complexity increase

Engineering Contradiction:
Improvediagnostic reliabilityVSAvoidsample preparation time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The chemically treated areas are pre-prepared with stabilization agents during device manufacturing. When a sample is applied to the device, the stabilization occurs automatically without requiring additional preparation steps by the user. This preliminary action ensures sample integrity is maintained from the moment of collection, providing reliable diagnostic samples while minimizing preparation time and operational complexity.

Inventive Principle:
Principle #10Preliminary action

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

Facilitates early diagnosis, reduces infection risks during sample handling, and provides stable biological samples for research, enabling efficient analysis and understanding of infectious diseases.

Implementation Method 1

The solid support includes plural discrete areas which are chemically treated, or untreated. In this case the areas of the solid support include a first area chemically coated to aid in the stabilisation of DNA, a second area chemically coated to aid in the stabilisation of RNA, and a third area chemically coated to aid in the stabilisation of proteins

Methodology Applied
Scientific EffectChemical stabilization: Chemical Bonding

Implementation Method 2

incorporating UV light treatment for viral inactivation

Methodology Applied
Scientific EffectUV light inactivation: Photodissociation

Data Source

PatentEP3277426B1Improvements in and relating to biological sample collectors and handling thereof
Publication Date: 2022.12.28 GLOBAL LIFE SCI SOLUTIONS OPERATIONS UK LTD
  • EP3277426B1 patent drawingFigure 1~2a
  • EP3277426B1 patent drawingFigure 2b~2c
  • EP3277426B1 patent drawingFigure 3a~3c

AI summary

Disclosed is a biological sample collector 500 comprising a solid support 12 having plural discrete areas (22, 24, 26, 28 Fig 1) for accepting a biological sample, each area being chemically differentiated, for example by having a different chemical treatment sorbed onto the solid support. An envelope 530 encloses the solid support. A cover portion 520 can cover the biological sample after collection to prevent infection. UV light can be applied to the collected sample to reduce the risk of infection.