Medicine Administration Device with Grip Section for High Back Pressure

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Solution Overview

Problem

Existing drug administration devices face challenges when administering drugs to the skin's upper section due to high back pressure, leading to needle dislodgment and drug leakage, and are complicated in design with increased parts for high-pressure injection.

Innovation Solution

A drug administration device with a tubular section, a pusher section, and a grip section that allows for strong force application to prevent needle dislodgment, featuring a gasket and plunger system with a connection section for stable operation, reducing complexity and preventing drug leakage.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Stress or pressure

If a drug is administered to the skin upper section using an ordinary syringe, then the injection pressure increases to overcome high back pressure, but the needle comes off from the skin and the drug leaks

Engineering Contradiction:
Improveinjection pressureVSAvoidneedle retention
Core Design Contradiction:
Stress or pressureVSReliability

Solution Approach 1:

The pressing section is designed to apply pressing force to the skin in advance before and during the injection process. This preliminary action counteracts the high back pressure that would otherwise cause needle dislodgment, allowing the needle to remain securely in place while enabling drug delivery to the skin upper section.

Inventive Principle:
Principle #9Preliminary anti-action

2Stress or pressure

If a pressure syringe with release button and compression spring is used to generate high pressure, then the injection pressure increases, but the number of parts increases and the constitution becomes complicated

Engineering Contradiction:
Improveinjection pressureVSAvoidnumber of parts
Core Design Contradiction:
Stress or pressureVSDevice complexity

Solution Approach 1:

The invention merges the pressing function and injection function into a single integrated structure. The pressing section is formed as an integral part of the syringe body, eliminating the need for separate components like release buttons and compression springs. This integration maintains the capability to generate high injection pressure while significantly simplifying the overall device structure.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The pressing section is designed to be directly operable by the user's finger without requiring separate control mechanisms. The structure allows the user to apply pressing force directly to the skin through the pressing section, which automatically translates this force into the necessary injection pressure, eliminating the need for complex mechanical advantage systems.

Inventive Principle:
Principle #25Self-service

3Quantity of substance

If a small-sized syringe is used to administer small amount of drug (about 100 μL), then the drug amount is appropriate, but the syringe cannot strongly press against the skin to prevent drug leakage

Engineering Contradiction:
Improvedrug amountVSAvoidpressing force
Core Design Contradiction:
Quantity of substanceVSForce

Solution Approach 1:

The syringe is segmented into distinct functional sections: the tubular section for holding the drug, the pressing section for applying force to the skin, and the connection section for linking these functions. This segmentation allows the pressing section to be optimized for force application while the tubular section maintains appropriate size for small drug volumes, resolving the conflict between size and pressing capability.

Inventive Principle:
Principle #1Segmentation

Data Source

PatentEP2554199B1Medicine administration device and medicine injection device
Publication Date: 2020.10.14 TERUMO KK
  • EP2554199B1 patent drawingFigure 1
  • EP2554199B1 patent drawingFigure 2
  • EP2554199B1 patent drawingFigure 3

AI summary

A needle does not come off even if a high back pressure occurs at the skin upper section. Thus, the drug leakage from the skin can be prevented. A drug administration device 1 includes a tubular section 2 having a fluid chamber 7 capable of accommodating a drug and a discharge section 22, a pusher member 3 moving within the tubular section 2, a grip section 4, and a connection section 5. The pusher member 3 includes a rod-shape plunger 31 and a gasket 32. The grip section 4 is disposed along the outer periphery of the tubular section 2 and kept away from the tubular section 2, and the connection section 5 is formed between the tubular section 2 and the grip section 4.