Adhesive Patch Skin Sampling for Non-Invasive Cancer Diagnosis

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Solution Overview

Problem

Current methods for identifying skin diseases, such as skin cancers, are invasive, lack sensitivity, are costly, and often result in late-stage detection, necessitating the development of non-invasive methods for assessing skin disease risk and providing early treatment interventions.

Innovation Solution

Non-invasive gene expression analysis using adhesive patches to collect skin samples, followed by RNA-sequencing or RT-qPCR to analyze specific mRNA transcripts, applying classifiers like deep learning or cluster analysis to diagnose squamous cell carcinoma (SCC) and basal cell carcinoma (BCC), and providing targeted treatments.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If non-invasive sampling methods are used, then patient comfort and ease of operation are improved, but measurement precision and detection sensitivity deteriorate

Engineering Contradiction:
Improveease of samplingVSAvoiddetection sensitivity
Core Design Contradiction:
Ease of operationVSMeasurement precision

Solution Approach 1:

The patent segments the skin sample collection process by using multiple adhesive patches applied to different areas of the skin, allowing comprehensive sampling without requiring invasive procedures. This segmentation enables the system to gather sufficient molecular material through non-invasive means while maintaining detection sensitivity.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent introduces an intermediary approach by using adhesive patches as mediators between the skin and the analysis system. These patches collect skin cells and molecular material without direct tissue penetration, enabling non-invasive sampling while preserving the integrity and quality of the biological material for accurate detection.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Loss of time

If early detection methods are implemented, then treatment effectiveness is improved, but device complexity and analysis cost increase

Engineering Contradiction:
Improvedetection timingVSAvoidanalysis system complexity
Core Design Contradiction:
Loss of timeVSDevice complexity

Solution Approach 1:

The patent applies preliminary action by collecting skin samples using adhesive patches that can be applied and processed before the development of visible skin lesions or at early stages of skin disease. This enables early detection and intervention while using relatively simple, readily available sampling technology rather than complex invasive procedures.

Inventive Principle:
Principle #10Preliminary action

3Quantity of substance

If multiple adhesive patches are applied to different skin areas, then sampling comprehensiveness is improved, but device complexity and procedure time increase

Engineering Contradiction:
Improvesampling comprehensivenessVSAvoidprocedure complexity
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The patent employs universal adhesive patches that can be applied to multiple different skin areas with the same basic device. These multi-functional patches serve multiple sampling locations simultaneously, enhancing sampling comprehensiveness without requiring multiple specialized devices or significantly increasing procedure complexity.

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

Data Source

PatentUS20240191309A1Gene classifiers and uses thereof
Publication Date: 2024.06.13 DERMTECH LLC
  • US20240191309A1 patent drawing
  • US20240191309A1 patent drawing
  • US20240191309A1 patent drawing

AI summary

Described herein are methods, systems, and compositions for non-invasively diagnosing or detecting a skin disease or disorder. Diagnosing or detecting a non-melanoma skin cancer (e.g., squamous cell carcinoma or basal cell carcinoma) as provided herein comprises detecting and/or comparing gene expression levels of identified genes. Methods, systems, and compositions are also described for differentiation of non-melanoma skin cancer (NMSC) from other diseases, such as actinic keratosis (AK).