Dermal Patch Fluidics for Low-Discomfort Sample Collection

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing dermal patches for collecting physiological samples face challenges such as low sensitivity and specificity, discomfort, and difficulty in obtaining samples, especially from children, and lack of capability for complex sample processing without user intervention.

Innovation Solution

A dermal patch with a housing containing a sample collection chamber, fluidic channels, and a pin that generates negative pressure for sample collection, coupled with a processing fluid reservoir and a detector for in-situ analysis, allowing for the collection and analysis of physiological samples with minimal user intervention.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Object-affected harmful factors

If a dermal patch is used to collect physiological samples, then the invasiveness is reduced and subject comfort is improved, but the sensitivity and specificity of sample detection deteriorates

Engineering Contradiction:
Improveinvasiveness and discomfortVSAvoidsensitivity and specificity
Core Design Contradiction:
Object-affected harmful factorsVSMeasurement precision

Solution Approach 1:

The device segments the sample collection and processing functions into distinct modules: a collection chamber for receiving the physiological sample, a separate processing fluid reservoir, and a detection chamber. This segmentation allows each component to be optimized independently, maintaining minimal invasiveness while enabling sophisticated sample processing to preserve detection precision.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A processing fluid acts as an intermediary between the collected physiological sample and the detection system. The processing fluid facilitates sample preparation, concentration, and conditioning within the sealed patch environment, enabling high-sensitivity detection without requiring invasive sample collection methods.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Ease of operation

If a dermal patch allows self-use collection, then ease of operation is improved, but the capability to perform complex sample processing deteriorates

Engineering Contradiction:
Improveself-use capabilityVSAvoidsample processing capability
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The processing fluid is pre-loaded into a sealed reservoir within the patch before use. The reservoir includes a frangible barrier that automatically breaks when the sample is introduced, initiating the processing sequence without user intervention. This preliminary preparation enables complex processing to occur automatically after simple sample application.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The device performs self-service through automated mechanisms: the frangible barrier breaks automatically upon sample introduction, releasing the processing fluid which then automatically mixes with and processes the sample in the collection chamber, eliminating the need for user intervention in complex processing steps.

Inventive Principle:
Principle #25Self-service

3Ease of operation

If a pin is used to generate negative pressure for sample collection, then ease of operation is improved, but device complexity increases

Engineering Contradiction:
Improvesample collection easeVSAvoidmechanism complexity
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The pin is designed as a removable component that can be extracted from the device after use. This extraction capability simplifies the overall device structure by eliminating the need for complex integrated pin deployment mechanisms, while still enabling easy negative pressure generation during operation.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The mechanical pin system replaces more complex automated pump or vacuum mechanisms. By using a simple removable pin that creates negative pressure through its removal action, the device achieves effective sample collection with minimal mechanical complexity.

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

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 easy and comfortable collection of physiological samples, enabling in-situ analysis and storage, with improved sensitivity and specificity for various analytes, including biomarkers and pathogens, suitable for use in diverse environments.

Implementation Method 1

The pin is configured to seal the receptacle when in the undeployed position and is further configured to facilitate generation of a negative pressure in the sample fluidic channel when the pin is moved from the undeployed to the deployed position

Methodology Applied
Scientific EffectNegative pressure generation: Pressure Gradient

Implementation Method 2

When the processing fluid and the physiological sample enter the collection chamber, they mix and interact to form a processed physiological sample

Methodology Applied
Scientific EffectFluid mixing: Diffusion

Data Source

PatentUS20260041343A1Dermal Patch for Collecting a Physiological Sample
Publication Date: 2026.02.12 SATIO INC
  • US20260041343A1 patent drawing
  • US20260041343A1 patent drawing
  • US20260041343A1 patent drawing

AI summary

A dermal patch device for acquisition and analysis of a physiological sample from a subject can include, a lancet port configured to receive a lancet to pierce the skin of the subject and thereby obtain the physiological sample, a sensor disposed in a sensor chamber, and a plurality of fluid pathways. The dermal patch device can further include a first fluid-filled ampoule, a second fluid-filled ampoule, and a third fluid-filled ampoule. The first fluid-filled ampoule can be actuated to release calibration fluid into the sensor chamber via a first group of the fluid pathways. The second fluid-filled ampoule can be actuated to evacuate the calibration fluid from the sensor chamber via a second group of the fluid pathways among the plurality of fluid pathways. The third fluid-filled ampoule can be actuated to draw the physiological sample into the sensor chamber via a third group of the fluid pathways.