Infusion Pump Sealing and Valve Design for Leak-Free Dosing

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Solution Overview

Problem

Existing portable infusion devices lack a reliable mechanism to ensure safe and accurate administration of liquid medications, particularly in the presence of pressure differentials, and are prone to leaks and malfunctions due to fluctuating container quality and friction issues.

Innovation Solution

The device incorporates a centred membrane valve with centring aids, a sealing mechanism using hydrophobic materials, and a drive mechanism with force sensing to prevent leaks and ensure accurate dosing, while maintaining air pressure equilibrium.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If a threaded rod with nut is used to advance the plug in the carpoule, then the drug can be expelled continuously, but the device becomes complex and prone to leakage due to pressure differentials

Engineering Contradiction:
Improvecontinuous drug expulsionVSAvoidthreaded rod mechanism complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The patent removes the threaded rod and nut mechanism from the infusion device, replacing it with a simpler plug advancement system. The plug is advanced directly by a drive mechanism without requiring threading components, thereby eliminating the complexity associated with threaded connections while maintaining continuous drug expulsion capability.

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent divides the infusion system into separate functional modules: a replaceable carpoule unit, a drive mechanism, and a control unit. This segmentation allows the complex drive mechanism to be isolated from the carpoule, reducing the complexity within each individual component while maintaining overall system functionality for continuous drug delivery.

Inventive Principle:
Principle #1Segmentation

2Length of moving object

If the electric motor is arranged next to the carpoule to limit length, then the device becomes compact, but the plug advancement mechanism becomes more difficult to implement reliably

Engineering Contradiction:
Improveinfusion apparatus lengthVSAvoidplug advancement reliability
Core Design Contradiction:
Length of moving objectVSReliability

Solution Approach 1:

The patent nests the drive mechanism within the housing structure, positioning the electric motor and plug advancement components in a nested arrangement. The motor is integrated into the housing with the plug advancement mechanism, creating a compact configuration that maintains reliability by ensuring proper mechanical coupling and alignment within the nested structure.

Inventive Principle:
Principle #7Nested doll (Nesting)

3Ease of manufacture

If standard sealing materials are used, then the manufacturing is simpler, but leaks occur due to pressure differentials between inside and outside of the device

Engineering Contradiction:
Improvesealing material selectionVSAvoidleak prevention
Core Design Contradiction:
Ease of manufactureVSReliability

Solution Approach 1:

The patent employs composite sealing structures combining multiple materials with complementary properties. The sealing system integrates elastomeric materials for flexibility with rigid components for structural support, creating a composite seal that can withstand pressure differentials while maintaining manufacturability through standard fabrication processes.

Inventive Principle:
Principle #40Composite materials

4Duration of action of moving object

If the carpoule is frequently exchanged, then continuous drug administration is maintained, but the risk of contamination and malfunction increases

Engineering Contradiction:
Improvecontinuous drug administrationVSAvoidcontamination risk
Core Design Contradiction:
Duration of action of moving objectVSReliability

Solution Approach 1:

The patent implements preliminary sealing and sterilization of the carpoule before use. The carpoule is pre-sealed with a protective cap and sterilized during manufacturing, allowing for safe exchange without exposing the internal components to contamination. The connection interface is designed with pre-positioned sealing elements that engage automatically upon attachment.

Inventive Principle:
Principle #10Preliminary action

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

The solution provides a safe and reliable infusion system that prevents leaks, ensures accurate dosing, and maintains air pressure balance, enhancing the safety and efficacy of medication administration.

Implementation Method 1

The sealing device or at least one sealing element (54, 54a, 54b, 54c) is made from a material which is permeable for air and impermeable for liquids or water, in particular from a hydrophobic material

Methodology Applied
Scientific EffectHydrophobic effect: Hydrophobe

Implementation Method 2

a membrane valve (35) which is arranged in the liquid path and comprises an inlet and an outlet, wherein the membrane valve (35) comprises a valve space (34), which is limited by walls, and a valve membrane (35)

Methodology Applied
Scientific EffectElastic deformation: Elasticity

Data Source

PatentEP3569270B1Device for administering a fluid product
Publication Date: 2026.01.28 MYLIFE DIABETES CARE AG
  • EP3569270B1 patent drawingFigure 1a~1b
  • EP3569270B1 patent drawingFigure 2
  • EP3569270B1 patent drawingFigure 3a~3f

AI summary

An infusion apparatus for the administration of a medication from a reservoir with a plug moveable along a central axis in a distal direction for ejection, the apparatus comprising a housing, a drive mechanism; an electronic controller, control module, or processor (80), a graphical code generator, preferably being included in or being part of the electronic controller, control module, or processor a display means , preferably a touch-sensitive or a touch display (20). The display means is able to display code data, preferably comprising a data matrix code (21), wherein the code data is generated by the graphical code generator using input information, and wherein the input information can be selected from a group consisting of configuration data, device data, system state data, device history data, infusion history data, device alarm data and malfunction data.