Staircase Microstructure Scaffold for Tissue Engineering

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Solution Overview

Problem

Current scaffolds for tissue engineering face challenges in controlling fine structure, leading to insufficient surface area for cell attachment and low medium diffusion, which restricts the regeneration of complex tissues, and the traditional production process of poly(glycerol sebacate) requires high temperature and low pressure, limiting its application.

Innovation Solution

A scaffold with a staircase microstructure made of light-curable and biodegradable poly(glycerol sebacate acrylate) is developed, featuring stacked layers with regular polygon-shaped through holes for enhanced cell seeding efficiency and medium diffusivity, allowing for tissue integration after implantation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If traditional preparing method is used for cell culture scaffolds, then the scaffold structure is simple to manufacture, but the fine structure control is insufficient resulting in excessive pores and insufficient surface area for cell attachment

Engineering Contradiction:
Improvefine structure controlVSAvoidscaffold structure complexity
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The scaffold is divided into multiple layers (first layer, second layer, third layer) with distinct through-hole patterns. Each layer contains through holes at different positions and orientations, allowing independent optimization of each layer's structure while maintaining overall manufacturing simplicity through repetitive stacking processes.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The scaffold employs a nested hierarchical structure where through holes exist at multiple levels (first layer through holes, second layer through holes, third layer through holes) that interconnect vertically. This nesting approach enables fine structure control at each level while maintaining a relatively simple overall manufacturing process through layer-by-layer construction.

Inventive Principle:
Principle #7Nested doll (Nesting)

2Adaptability or versatility

If traditional PGS production process is used, then the material has good biocompatibility, but the high temperature and low pressure environment limits its application in tissue engineering

Engineering Contradiction:
Improveapplication suitability for tissue engineeringVSAvoidproduction temperature
Core Design Contradiction:
Adaptability or versatilityVSTemperature

Solution Approach 1:

The production parameters of PGS are fundamentally changed by introducing photopolymerization chemistry. Instead of requiring high temperature and low pressure for traditional PGS synthesis, the invention uses photopolymerizable monomers that cure under UV light at ambient temperature and pressure, making the material suitable for tissue engineering applications while maintaining biocompatibility.

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention utilizes the phase transition properties of photopolymerizable monomers to PGS. The monomers remain in liquid state during handling and casting, then undergo phase transition to solid polymer network upon UV irradiation. This allows low-temperature processing while achieving the structural integrity needed for tissue engineering scaffolds.

Inventive Principle:
Principle #36Phase transitions

3Area of stationary object

If scaffolds with high surface area are designed, then cell attachment is improved, but medium diffusion becomes restricted

Engineering Contradiction:
Improvesurface area for cell attachmentVSAvoidmedium diffusion
Core Design Contradiction:
Area of stationary objectVSQuantity of substance

Solution Approach 1:

The scaffold implements local quality differentiation by creating distinct through-hole regions that serve different functions. Some through holes are optimized for cell attachment (providing high local surface area), while interconnected vertical channels provide dedicated pathways for medium diffusion. This spatial differentiation allows simultaneous optimization of both cell attachment and medium transport.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The invention transitions from two-dimensional surface optimization to three-dimensional structured design. Through holes are positioned at different vertical levels (first layer, second layer, third layer) and interconnected to create vertical diffusion pathways. This dimensional approach allows high surface area for cell attachment on layer surfaces while maintaining open vertical channels for medium penetration throughout the scaffold depth.

Inventive Principle:
Principle #17Another dimension (Dimensionality change)

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 scaffold promotes efficient cell seeding, medium diffusion, and tissue integration by increasing the surface area to volume ratio, facilitating the regeneration of defective tissues and vascularization, as demonstrated by improved cell differentiation and vascularization in both in vitro and in vivo tests.

Implementation Method 1

The scaffold is made of a light-curable and biodegradable polymer, poly(glycerol sebacate) acrylate (PGSA), which is an acrylation-modified PGS and can be produced by light-curing technology

Methodology Applied
Scientific EffectPhotopolymerization: Photopolymerisation

Data Source

PatentUS20230183641A1Scaffold for cell or tissue culture, the preparing method and use thereof in tissue engineering and regenerative medicine
Publication Date: 2023.06.15 NATIONAL HEALTH RESEARCH INSTITUTE
  • US20230183641A1 patent drawing
  • US20230183641A1 patent drawing
  • US20230183641A1 patent drawing

AI summary

The present disclosure relates to a scaffold with staircase microstructure for cell or tissue culture, comprising multiple layers. Each layer defines a plurality of through holes, and the through holes of each layer is in communication with a corresponding through holes of an adjacent layer. A method for culturing cell and tissue regeneration is also provided.