Uronic Acid Polysaccharide Composition for Automated Nucleic Acid Isolation

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Solution Overview

Problem

Current nucleic acid extraction methods are lengthy and not easily amenable to automation, requiring extensive sample processing and often include components that inhibit polymerase activity, making them unsuitable for rapid and accurate molecular diagnostics.

Innovation Solution

A method involving the use of an aqueous composition containing polysaccharides with uronic acid units to isolate nucleic acids by precipitation or concentration on a solid support, utilizing agents like modified pectins and carrageenan for efficient nucleic acid isolation compatible with automated detection methods.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional nucleic acid extraction methods are used, then nucleic acids can be isolated, but the process is lengthy and not easily amenable to automation

Engineering Contradiction:
Improvespeed of nucleic acid isolationVSAvoidcomplexity of extraction process
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent changes the chemical parameters of the extraction system by using polysaccharides with uronic acid units instead of conventional reagents. This parameter change enables rapid nucleic acid isolation while maintaining compatibility with automated systems, resolving the contradiction between speed and process complexity

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent extracts only the essential function of nucleic acid isolation from complex conventional methods by using a simplified aqueous polysaccharide composition. This extraction of the core function enables automation while maintaining isolation effectiveness, addressing the contradiction between productivity and device complexity

Inventive Principle:
Principle #2Taking out (Extraction)

2Reliability

If conventional extraction reagents are used, then nucleic acids can be isolated, but components inhibit polymerase activity

Engineering Contradiction:
Improvequality of isolated nucleic acidVSAvoidinhibition of polymerase activity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent converts the potential harm of polysaccharide interference into a benefit by selecting specific polysaccharides with uronic acid units that do not inhibit polymerase activity. This transforms the challenge of reagent compatibility into an advantage, ensuring both reliable nucleic acid isolation and subsequent amplification

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Solution Approach 2:

The polysaccharide acts as an intermediary that facilitates nucleic acid isolation without transferring harmful properties to the isolated product. The specific structure of polysaccharides with uronic acid units mediates the isolation process while remaining compatible with downstream polymerase-based detection methods

Inventive Principle:
Principle #24Intermediary (Mediator)

3Manufacturing precision

If extensive sample processing is performed, then nucleic acid quality is improved, but the method is not compatible with automated detection

Engineering Contradiction:
Improvequality of nucleic acid preparationVSAvoidautomatability of detection process
Core Design Contradiction:
Manufacturing precisionVSExtent of automation

Solution Approach 1:

The polysaccharide composition performs multiple functions in a self-service manner: it facilitates nucleic acid isolation, ensures quality preparation, and remains compatible with automated detection without requiring additional processing steps. This self-service capability enables both high quality and automatability simultaneously

Inventive Principle:
Principle #25Self-service

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 rapid and efficient isolation of nucleic acids from various samples, compatible with automated systems, without inhibiting subsequent detection, allowing for high-quality nucleic acid analysis and detection methods such as PCR.

Implementation Method 1

concentrating the nucleic acid on a solid support thereby isolating the nucleic acid

Methodology Applied
Scientific EffectPrecipitation: Precipitation

Data Source

PatentUS12365891B2Methods and compositions for nucleic acid isolation
Publication Date: 2025.07.22 CEPHEID INC
  • US12365891B2 patent drawing
  • US12365891B2 patent drawing
  • US12365891B2 patent drawing

AI summary

Methods and compositions for isolation of nucleic acids from biological samples are provided.