PDA Liposome Sensor for Platelet Activation Monitoring

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current methods for monitoring platelet activation are cumbersome, costly, and often require laboratory access, making it difficult to accurately assess platelet function in patients, particularly those on antiplatelet medications, which can lead to hazardous bleeding complications.

Innovation Solution

Development of a PDA-based microarray sensor device that uses antibodies specific for activated platelets, allowing for the detection of platelet activation in whole blood samples without the need for separation or pretreatment, utilizing polydiacetylene (PDA) liposomes conjugated to antibodies like 9F9, which changes fluorescence signal intensity in response to antiplatelet drug concentrations.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If traditional methods such as aggregometry, cytometry, or atomic force microscope are used to monitor platelet function, then measurement precision is improved, but device complexity and loss of time increase significantly

Engineering Contradiction:
Improveplatelet function monitoring accuracyVSAvoidmonitoring system complexity
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The patent replaces complex mechanical and electronic monitoring systems with a simple optical sensing system. The PDA liposome-based sensor detects platelet activation through optical signal changes (fluorescence intensity) when platelets bind to the sensor surface, eliminating the need for complex aggregometry equipment, cytometers, or atomic force microscopes while maintaining measurement precision

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

Solution Approach 2:

The patent extracts and isolates the essential detection function from complex monitoring systems. By using PDA liposomes with specific antibodies that bind to activated platelets, the system extracts only the necessary components (sensor surface, binding specificity, optical detection) to achieve accurate platelet activation monitoring without requiring elaborate experimental setups

Inventive Principle:
Principle #2Taking out (Extraction)

2Measurement precision

If laboratory-based methods are used for platelet monitoring, then measurement precision is improved, but loss of time and ease of operation deteriorate

Engineering Contradiction:
Improveplatelet activation detection accuracyVSAvoidexamination time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The PDA liposome sensor performs self-detection without requiring external laboratory equipment or complex operational procedures. The sensor automatically detects platelet activation through optical signal changes when blood samples are applied, eliminating the need for specialized laboratory instruments and reducing examination time while maintaining precision

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent utilizes changes in optical parameters (fluorescence intensity) of the PDA liposome sensor to detect platelet activation. When platelets bind to the sensor surface, the optical properties of the PDA liposome change, providing a rapid and direct measurement that eliminates time-consuming laboratory procedures

Inventive Principle:
Principle #35Parameter changes

3Reliability

If antiplatelet medication is administered to prevent blood clotting, then patient safety is improved, but object-affected harmful factors increase due to hazardous bleeding

Engineering Contradiction:
Improvepatient safetyVSAvoidbleeding risk
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent implements a feedback mechanism where the sensor continuously monitors platelet activation status in real-time. The optical signal changes detected by the PDA liposome provide immediate feedback on platelet function, allowing healthcare providers to adjust antiplatelet medication dosages to optimize patient safety while minimizing bleeding risks through data-driven decision-making

Inventive Principle:
Principle #23Feedback

4Ease of operation

If standard dose of antiplatelet drugs is advised without monitoring, then ease of operation is improved, but reliability deteriorates due to lack of accurate monitoring

Engineering Contradiction:
Improvemonitoring simplicityVSAvoidpatient outcome reliability
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The patent employs a simple, disposable PDA liposome sensor that can be easily applied to blood samples without requiring expensive laboratory equipment. The sensor's simplicity maintains ease of operation while its specific optical detection capability provides reliable monitoring data, bridging the gap between operational simplicity and monitoring reliability

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

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

Provides a rapid, cost-effective, and accurate method for monitoring platelet activation, enabling healthcare providers to determine appropriate antiplatelet drug dosages and adjust treatments accordingly, improving patient safety by facilitating continuous monitoring.

Implementation Method 1

The fluorescence signal intensity inversely related to the amount of Tirofiban, an inhibitor of platelet activated coagulation, added to whole blood samples

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Data Source

PatentUS20230067926A1Systems and methods for monitoring platelet activation
Publication Date: 2023.03.02 THE RGT UNIV OF MICHIGAN
  • US20230067926A1 patent drawing
  • US20230067926A1 patent drawing
  • US20230067926A1 patent drawing

AI summary

Provided herein are compositions, systems, and methods for monitoring platelet activation. In particular, provided herein are sensor devices for measuring platelet activation and uses thereof.