Portable Fluidic Cartridge for Real-Time Analyte Detection

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Solution Overview

Problem

Current point-of-care testing methods lack an integrated solution for sample acquisition, testing, analysis, and communication of results, leading to inefficiencies in pharmacokinetic and pharmacodynamic parameter determination and adverse drug reaction monitoring, with patients often failing to comply with scheduled drug dosing and resulting in improper drug levels and adverse effects.

Innovation Solution

A portable fluidic device with a cartridge containing a sample collection unit and assay assembly that collects, meters, and dilutes bodily fluid samples, using reactants to detect analytes and transmit results for real-time monitoring and communication of pharmacological parameters.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If patients visit clinics multiple times to provide blood samples for pharmacokinetic and pharmacodynamic parameter determination, then comprehensive drug monitoring can be achieved, but patient compliance deteriorates and data response time increases

Engineering Contradiction:
Improvepharmacokinetic and pharmacodynamic parameter determinationVSAvoiddata response time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The system enables patients to self-monitor their drug levels at home using a portable fluidic device, eliminating the need to visit clinics for sample collection. The device automatically performs sample processing, reactant delivery, and analyte detection, allowing patients to conduct their own pharmacokinetic monitoring without requiring clinic visits.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The monitoring system is divided into separate functional modules: a sample collection unit, a fluidic processing cartridge with reactant chambers, a detection assembly, and a communication system. This segmentation allows the system to be portable while maintaining comprehensive monitoring capabilities through coordinated operation of independent components.

Inventive Principle:
Principle #1Segmentation

2Measurement precision

If blood samples are pre-processed in laboratories before analysis, then accurate pharmacokinetic and pharmacodynamic parameters can be determined, but measurement time increases and physiological variability increases

Engineering Contradiction:
Improvetarget analyte and biomarker concentration determinationVSAvoidsample processing time
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The system combines multiple functions that were previously performed separately in different locations (sample collection, sample processing, reactant delivery, analyte detection, and result communication) into a single integrated portable device. The fluidic cartridge merges sample processing steps with the detection assay, eliminating the time delay between sample collection and analysis.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

Reagents and reactants are pre-loaded into the fluidic cartridge in controlled amounts, and sample processing steps are prepared in advance. When a sample is introduced, the system automatically executes pre-programmed processing steps including dilution, mixing, and reactant delivery, eliminating the need for manual laboratory pre-processing.

Inventive Principle:
Principle #10Preliminary action

3Reliability

If multiple combination therapies are used to treat patients, then treatment efficacy improves, but the complexity of monitoring pharmacokinetic and pharmacodynamic parameters increases

Engineering Contradiction:
Improvetreatment efficacyVSAvoidmonitoring system complexity
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The portable fluidic device is designed to monitor multiple analytes and pharmacological parameters simultaneously using a single integrated system. The device can detect different drug concentrations and biomarkers in the same sample, providing comprehensive monitoring for patients on combination therapies without requiring multiple separate monitoring systems.

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

Solution Approach 2:

The system uses digital communication to transmit monitoring data to electronic health records and communication assemblies, creating digital copies of the monitoring information. This allows complex multi-parameter data from combination therapy monitoring to be stored, analyzed, and shared electronically, reducing the operational complexity of managing multiple monitoring systems.

Inventive Principle:
Principle #26Copying

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

Enables real-time detection and monitoring of analytes, improving patient compliance and reducing adverse drug reactions by providing a portable, efficient system for pharmacokinetic and pharmacodynamic parameter assessment and adverse drug reaction detection.

Implementation Method 1

the assay assembly comprises at least one reaction site containing a reactant that reacts with the analyte to yield a signal indicative of the presence of the analyte

Methodology Applied
Scientific EffectChemical reaction: Chemical Bonding

Data Source

PatentUS20230035908A1Systems and Methods of Sample Processing and Fluid Control in a Fluidic System
Publication Date: 2023.02.02 GOLDEN DIAGNOSTICS CORP
  • US20230035908A1 patent drawing
  • US20230035908A1 patent drawing
  • US20230035908A1 patent drawing

AI summary

This invention is in the field of medical devices. Specifically, the present invention provides portable medical devices that allow real-time detection of analytes from a biological fluid. The methods and devices are particularly useful for providing point-of-care testing for a variety of medical applications.