Thermal Inkjet Reagent Injection into Single Cells

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Solution Overview

Problem

Current cell transfection methods often introduce contamination, are costly, lack control over material transfer, and cannot handle microscopic fluid injections into single cells.

Innovation Solution

A system utilizing a thermal inkjet resistor to generate a synthetic jet for direct reagent injection into cells, accompanied by a sensor and feedback loop for controlled operation and successful injection verification.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If conventional cell transfection methods are used, then cells can be transfected with foreign material, but contamination is introduced and costs increase

Engineering Contradiction:
Improvetransfection successVSAvoidcontamination
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent replaces conventional mechanical transfection methods (such as microinjection needles, electroporation cuvettes, or viral vectors) with a thermal inkjet-based synthetic jet system. This substitution eliminates physical contact between the reagent delivery system and the cell, thereby preventing contamination while maintaining transfection efficacy. The synthetic jet creates a controlled fluid dynamic environment that delivers reagents directly into the cell without introducing external contaminants.

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

Solution Approach 2:

The patent introduces a liquid bridge as an intermediary medium between the thermal inkjet nozzle and the cell. The liquid bridge serves as a controlled interface that transfers reagents from the synthetic jet to the cell membrane without direct contact between the nozzle and cell. This intermediary approach enables precise reagent delivery while maintaining sterility and preventing contamination pathways.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If conventional transfection methods are used, then cells can be transfected, but control over material transfer is insufficient

Engineering Contradiction:
Improvetransfection controlVSAvoidmaterial transfer precision
Core Design Contradiction:
ReliabilityVSQuantity of substance

Solution Approach 1:

The patent employs parameter changes in the thermal inkjet system to achieve precise control over material transfer. By adjusting parameters such as heating pulse duration, temperature, and synthetic jet frequency, the system can precisely control the volume, velocity, and timing of reagent delivery to single cells. This level of parameter control enables accurate dosing of transfection reagents, ensuring consistent and reproducible transfection outcomes.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent implements a feedback mechanism using sensors to detect cell presence and position in real-time. The sensor signals are fed back to the thermal inkjet controller, which adjusts the synthetic jet activation timing and parameters accordingly. This closed-loop feedback system ensures that reagents are delivered only when a cell is properly positioned, maximizing material transfer precision and preventing wasted reagent on empty space or misplaced cells.

Inventive Principle:
Principle #23Feedback

3Reliability

If conventional methods are used, then transfection can be performed, but microscopic fluid injections into single cells are not possible

Engineering Contradiction:
Improvesingle cell transfectionVSAvoidmicroscopic fluid injection capability
Core Design Contradiction:
ReliabilityVSManufacturing precision

Solution Approach 1:

The patent segments the transfection process to operate at the single-cell level rather than treating cell populations collectively. The thermal inkjet system is designed to address individual cells sequentially, with the synthetic jet capable of delivering picoliter-scale reagent volumes to single targets. This segmentation approach, combined with sensor-based cell detection and positioning, enables precise microscopic fluid injection into individual cells, which is not achievable with conventional bulk transfection methods.

Inventive Principle:
Principle #1Segmentation

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

This method ensures precise and contamination-free transfection of cells with microscopic amounts of reagents, improving control and reducing costs by using a synthetic jet for poration and injection.

Implementation Method 1

The energy source may create local vapor bubbles that may burst to create the synthetic jet in a direction towards the cell

Methodology Applied
Scientific EffectVapor bubble generation and bursting: Cavitation

Implementation Method 2

The apparatus may use an energy source, such as a thermal inkjet (TIJ) resistor that can generate a synthetic jet

Methodology Applied
Scientific EffectJoule heating: Joule Heating

Data Source

PatentUS20230174908A1Reagent injections into cells
Publication Date: 2023.06.08 HEWLETT PACKARD DEVELOPMENT COMPANY LP
  • US20230174908A1 patent drawing
  • US20230174908A1 patent drawing
  • US20230174908A1 patent drawing

AI summary

In example implementations, an apparatus is provided. The apparatus includes a channel, a reagent chamber, a synthetic jet channel, and an energy source. The channel is to hold a cell. The reagent chamber is coupled to the channel and stores a reagent. The synthetic jet channel is coupled to the channel and the reagent chamber. The energy source is located in the synthetic jet channel to heat a liquid in the synthetic jet channel to create a synthetic jet that carries the reagent through towards the cell to inject the reagent into the cell.