3D Printed Scaffolds with Electrospun Nanofiber Coatings

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Solution Overview

Problem

Current methods for fabricating scaffolds for tissue regeneration, such as 3D printing, lack biomimetic surface nanotopography and limited biomolecule presenting capacity, which hinders effective cell adhesion and proliferation, especially for critical-sized tissue defects.

Innovation Solution

A method involving surface modification of 3D printed scaffolds with electrospun nanofiber segments, specifically bioactive glass and PLGA-collagen-gelatin nanofibers, combined with plasma treatment and crosslinking, to create a biomimetic nanofibrous structure that enhances cell adhesion and proliferation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If 3D printing is used to fabricate scaffolds, then manufacturing precision and structural control are improved, but surface nanotopography and biomolecule presenting capacity deteriorate

Engineering Contradiction:
Improvepore size controlVSAvoidsurface nanotopography
Core Design Contradiction:
Manufacturing precisionVSEase of manufacture

Solution Approach 1:

The patent combines 3D printing technology with electrospinning technology to create hybrid scaffolds. The 3D printed scaffold provides the macroscopic structure with controlled pore size, while the electrospun nanofiber coating provides the biomimetic surface nanotopography. This merging of two fabrication techniques allows both manufacturing precision and surface quality to be achieved simultaneously.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The 3D printed scaffold is first fabricated with precise pore size control, then subsequently coated with electrospun nanofibers to add surface nanotopography. This sequential approach where the base structure is prepared first and then enhanced with surface modification allows each technique to optimize its contribution without interfering with the other.

Inventive Principle:
Principle #10Preliminary action

2Ease of manufacture

If conventional scaffold fabrication methods are used, then ease of manufacture is improved, but pore size precision and interconnectivity deteriorate

Engineering Contradiction:
Improvefabrication processVSAvoidpore size control
Core Design Contradiction:
Ease of manufactureVSManufacturing precision

Solution Approach 1:

The patent merges conventional electrospinning (easy to manufacture) with 3D printing (precise pore control) to create a composite scaffold system. The electrospun nanofibers are applied as a coating on the 3D printed scaffold, combining the ease of nanofiber fabrication with the precision of 3D printed architecture.

Inventive Principle:
Principle #5Merging (Combining)

3Reliability

If scaffold surface is modified with nanofibers, then cell adhesion and proliferation are improved, but device complexity increases

Engineering Contradiction:
Improvecell adhesionVSAvoidsurface modification process
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent utilizes the porous structure of electrospun nanofibers to create a biomimetic extracellular matrix environment on the scaffold surface. The nanofibrous porous structure naturally promotes cell adhesion and proliferation by mimicking natural tissue architecture, achieving improved reliability through material structure rather than complex surface chemistry modifications.

Inventive Principle:
Principle #31Porous materials

Solution Approach 2:

The patent creates a composite material system where electrospun nanofibers (containing biomolecules like gelatin, collagen, or chitosan) are combined with the 3D printed scaffold material. This composite approach enhances cell adhesion through the nanofiber's inherent biomimetic properties and embedded biomolecules, reducing the need for additional complex surface modification steps.

Inventive Principle:
Principle #40Composite materials

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 modified scaffolds promote significant adhesion and proliferation of pre-osteoblasts and bone marrow mesenchymal stem cells, and immobilization of BMP-2 mimicking peptides enhances osteogenic differentiation, improving the efficacy of scaffolds for tissue engineering.

Implementation Method 1

The method may further comprise plasma treating the scaffold prior to coating the surface of the scaffold

Methodology Applied
Scientific EffectPlasma treatment: Plasma

Implementation Method 2

In certain embodiments, the nanofiber segments are electrospun nanofiber segments

Methodology Applied
Scientific EffectElectrospinning: Electrohydrodynamics

Implementation Method 3

the crosslinking comprises contacting the coated scaffold with a chemical crosslinker such as glutaraldehyde

Methodology Applied
Scientific EffectChemical crosslinking: Chemical Bonding

Data Source

PatentUS20230390456A1Surface modified scaffolds and methods of use thereof
Publication Date: 2023.12.07 BOARD OF RGT UNIV OF NEBRASKA
  • US20230390456A1 patent drawing
  • US20230390456A1 patent drawing
  • US20230390456A1 patent drawing

AI summary

Surface modified scaffolds are provided as well as methods of use thereof and methods of making.