Cell Delivery Syringe Loading to Prevent Needle Clogging

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Solution Overview

Problem

Existing methods for delivering high-density cell suspensions, such as those containing mesenchymal stem cells transiently-transfected by a polynucleotide encoding a Notch intracellular domain, face challenges like needle blockage and cell damage due to high viscosity, leading to inconsistent treatment results.

Innovation Solution

A method involving a syringe with a chemically inert polymeric plunger tip and a horizontal alignment for loading cell suspensions, followed by use of a cannula or needle to expel controlled droplets, ensuring uniform distribution and minimizing cell damage.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If a fine needle is used to deliver high-density cell suspensions, then precision of delivery is improved, but needle blockage occurs due to high viscosity

Engineering Contradiction:
Improvedelivery precisionVSAvoidneedle blockage
Core Design Contradiction:
Measurement precisionVSReliability

Solution Approach 1:

The syringe barrel is divided into multiple lumens (first lumen and second lumen) with different functions. The first lumen receives high-density cell suspension while the second lumen receives lower-density suspension, allowing segmented delivery that prevents blockage in the fine needle while maintaining delivery precision.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

A plunger with a porous tip acts as an intermediary between the lumens and the needle. The porous structure allows cell suspension to pass through while filtering out clumps that would cause blockage, enabling precise delivery without needle obstruction.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If high concentration of cells is administered, then treatment effectiveness is improved, but cell damage occurs due to needle blockage

Engineering Contradiction:
Improvetreatment effectivenessVSAvoidcell damage
Core Design Contradiction:
ProductivityVSObject-affected harmful factors

Solution Approach 1:

Cell suspension is segmented into multiple lumens with different cell densities. The first lumen contains high-density suspension for effectiveness, while the second lumen contains filtered suspension that prevents cell damage from blockage, allowing both effectiveness and safety to be achieved simultaneously.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The porous plunger tip serves as a protective intermediary that filters the cell suspension before it enters the needle. This prevents cell clumps from causing blockage and damaging the needle, thereby preserving cell viability and treatment effectiveness.

Inventive Principle:
Principle #24Intermediary (Mediator)

3Reliability

If high-density cell suspension is delivered, then treatment consistency is improved, but shear stress on cells increases

Engineering Contradiction:
Improvetreatment consistencyVSAvoidshear stress
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The system segments cell suspension delivery into multiple lumens, allowing the fine needle to receive only the filtered portion that causes minimal shear stress. This maintains treatment consistency through controlled delivery while reducing mechanical stress on cells.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The porous plunger tip acts as a gentle intermediary that filters cell suspension without applying excessive shear stress. This allows consistent delivery of therapeutic cells while minimizing mechanical damage from high-density suspension injection.

Inventive Principle:
Principle #24Intermediary (Mediator)

Data Source

PatentUS20260069790A1Cell delivery system and methods of operation thereof
Publication Date: 2026.03.12 SANBIO INC
  • US20260069790A1 patent drawing
  • US20260069790A1 patent drawing
  • US20260069790A1 patent drawing

AI summary

A method of preparing a syringe in connection with a therapeutic treatment is disclosed. The method can include removing a plunger of the syringe from a barrel of the syringe, aligning the barrel in a horizontal orientation, filling a lumen of the barrel with a viscous material through an opening at a proximal end of the barrel, and inserting a plunger tip into the lumen to seal the lumen. The method can also include attaching an implantation device to a hub coupled to the barrel at a distal end of the barrel. The method can also include depressing the plunger until the cell suspension fills the implantation device and a droplet of the cell suspension is expelled from a distal tip of the implantation device.