Two-Film Biodegradable Bone Augmentation Bag for Stable Placement

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Solution Overview

Problem

Existing bone augmentation techniques using resorbable barrier membranes are not user-friendly, as they require complex intraoral operations to fix the bone substitute, leading to reduced bone augmentation and prolonged surgery times, and existing single-sheet membranes allow the bone substitute to move, halving the augmentation amount.

Innovation Solution

A biodegradable bag composed of two films with different degradation times, where the first film has a longer degradation time than the second, allowing for easy identification and placement, eliminating the need for complex fixation procedures by ensuring the bone substitute remains in place during bone augmentation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If a single-sheet resorbable barrier membrane is used, then the membrane can be easily placed, but the bone substitute moves during surgery reducing augmentation effectiveness

Engineering Contradiction:
Improveease of membrane placementVSAvoidstability of bone substitute
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The barrier membrane is divided into multiple sheets (first sheet and second sheet) that are stacked together. The first sheet has through-holes that allow the bone substitute to pass through and be anchored, while the second sheet provides additional barrier function. This segmentation enables the bone substitute to be securely held without requiring complex fixation procedures.

Inventive Principle:
Principle #1Segmentation

2Reliability

If barrier membrane fixation pins or sutures are used to stabilize the membrane, then the bone substitute stability improves, but the surgical complexity and time increase

Engineering Contradiction:
Improvestability of bone substituteVSAvoidcomplexity of fixation procedure
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The barrier membrane structure itself provides the fixation function through its design features (through-holes in the first sheet that receive and anchor the bone substitute). This eliminates the need for separate fixation pins or sutures, as the membrane serves both as a barrier and as a fixation device, reducing surgical complexity and time.

Inventive Principle:
Principle #25Self-service

3Reliability

If fixation pins are used to secure the barrier membrane, then the membrane stability improves, but the surgery time is prolonged

Engineering Contradiction:
Improvestability of barrier membraneVSAvoidsurgery time
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The barrier membrane and fixation function are merged into a single integrated structure. The first sheet's through-holes serve dual purposes: allowing bone substitute placement and providing anchorage points for stabilization. This combination eliminates the need for separate fixation steps, reducing surgery time while maintaining stability.

Inventive Principle:
Principle #5Merging (Combining)

4Reliability

If a non-resorbable barrier membrane or titanium frame is used, then the bone substitute stability is maintained, but the biocompatibility and resorbability are reduced

Engineering Contradiction:
Improvestability of bone substituteVSAvoidbiocompatibility issues
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The barrier membrane is designed to be resorbable, with its mechanical properties changing over time as it degrades. The first sheet provides initial structural support and fixation, then gradually resorbs as bone regenerates. This parameter change (from rigid to resorbable) maintains stability when needed while improving biocompatibility as the healing progresses.

Inventive Principle:
Principle #35Parameter changes

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 biodegradable bag provides user-friendly bone augmentation by maintaining the bone substitute in position, reducing surgery complexity and time, while ensuring effective bone regeneration without the need for additional fixation methods.

Implementation Method 1

an in vivo degradation time of the first film is equal to or longer than an in vivo degradation time of the second film

Methodology Applied
Scientific EffectBiodegradation: Decomposition (biological)

Data Source

PatentUS20250318929A1Bone Augmentation Bag and Manufacturing Method Therefor
Publication Date: 2025.10.16 NIHONBASHI IMPLANT CENTER CO LTD
  • US20250318929A1 patent drawing
  • US20250318929A1 patent drawing
  • US20250318929A1 patent drawing

AI summary

A bag 1 is used for bone augmentation, includes a first film 2a and a second film 2b each made of a biodegradable component, and has an opening 3 between the first film 2a and the second film 2b superimposed and bonded with each other. An in vivo degradation time of the first film 2a is equal to or higher than an in vivo degradation time of the second film 2b, and if the in vivo degradation times of the first film 2a and the second film 2b are different from each other, the first film 2a and the second film 2b are different from each other so as to be visually or tactilely identifiable.