Pipette Tip Nucleic Acid Extraction for Fast High-Sensitivity Purification

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Solution Overview

Problem

Current nucleic acid extraction methods are time-consuming, complex, and often yield crude samples with insufficient sensitivity, requiring adaptation based on sample type and target cells, complicating integration with downstream processes.

Innovation Solution

A method involving lysis of cells to release nucleic acids, binding to a substrate using non-orbital movement, washing with multiple buffers, and eluting with a high-pH elution buffer in a pipette tip to enhance efficiency and sensitivity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If current sample preparation methods are used, then nucleic acids can be extracted, but the process takes long time and involves complex purification steps

Engineering Contradiction:
Improveextraction speedVSAvoidpurification steps
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent combines multiple extraction steps (lysis, binding, washing, elution) into a single integrated pipette tip system, eliminating the need for separate purification devices and reducing overall process complexity while maintaining high extraction efficiency

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The pipette tip is designed as a universal platform that can process various sample types (blood, sputum, urine) and perform all extraction functions within a single device, replacing multiple specialized devices with one multi-functional tool

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

2Loss of time

If rapid sample preparation methods are used, then turnaround time is reduced, but the extract becomes crude with insufficient detection sensitivity

Engineering Contradiction:
Improveturnaround timeVSAvoiddetection sensitivity
Core Design Contradiction:
Loss of timeVSMeasurement precision

Solution Approach 1:

The patent optimizes critical parameters including using high-pH elution buffer (pH 8.0-9.5), controlling incubation temperature (65-95°C), and adjusting buffer compositions to achieve both rapid processing and high sensitivity, allowing fast extraction without sacrificing detection quality

Inventive Principle:
Principle #35Parameter changes

3Productivity

If sample preparation methods are adapted for different sample types, then extraction efficiency improves, but the process becomes more complex and harder to integrate with downstream steps

Engineering Contradiction:
Improveextraction efficiencyVSAvoidsample type adaptation
Core Design Contradiction:
ProductivityVSAdaptability or versatility

Solution Approach 1:

The pipette tip system is designed as a universal platform with standardized protocols that can efficiently process various sample types (blood, sputum, urine, swabs) without requiring different devices or complex adaptation procedures, enabling seamless integration with downstream PCR and sequencing workflows

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

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 rapid, universal, and automatable nucleic acid extraction with high yield and sensitivity, suitable for various samples, facilitating quick integration with downstream diagnostics.

Implementation Method 1

introducing the released nucleic acids to a substrate, where the nucleic acids bind to the substrate

Methodology Applied
Scientific EffectAdsorption: Adsorption

Implementation Method 2

eluting the nucleic acids from the substrate

Methodology Applied
Scientific EffectDesorption: Desorption

Data Source

PatentUS20260028615A1Extraction method for nucleic acids
Publication Date: 2026.01.29 SIEMENS HEALTHCARE DIAGNOSTICS INC
  • US20260028615A1 patent drawing
  • US20260028615A1 patent drawing
  • US20260028615A1 patent drawing

AI summary

A method (100) of extracting nucleic acids is disclosed. The method includes receiving a sample containing nucleic acids to be extracted. The method (100) includes lysing cells in the sample to release the nucleic acids. The method (100) also includes introducing the released nucleic acids to a substrate, wherein the nucleic acids bind to the substrate. The method (100) includes washing the substrate bound to the nucleic acids and eluting the nucleic acids from the substrate. The introducing of the released nucleic acids to the substrate. the washing of the substrate bound to the nucleic acids, and the eluting of the nucleic acids are performed in a pipette tip.