Nanofiber Microspheres via Electrospinning Electrospraying

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Solution Overview

Problem

Existing methods for fabricating nanofiber microspheres are limited by polymer chemistry and composition, making it difficult to achieve uniform-sized microspheres with controllable porosity and functionality for drug delivery and tissue regeneration.

Innovation Solution

A method combining electrospinning and electrospraying is used to fabricate nanofiber microspheres, allowing for the production of various morphologies and compositions independent of polymer chemistry, using electrospun nanofiber segments that are crosslinked and thermally treated, and can include therapeutic agents, cells, or tissue.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If conventional microsphere fabrication methods are used, then microspheres can be produced, but uniform size and controllable porosity are difficult to achieve

Engineering Contradiction:
Improvemicrosphere size uniformityVSAvoidfabrication complexity
Core Design Contradiction:
Manufacturing precisionVSEase of manufacture

Solution Approach 1:

The invention changes physical parameters (electrospraying voltage, flow rate, collection distance) to precisely control microsphere size and porosity. By adjusting these parameters, uniform microspheres with controlled pore structures can be fabricated without complex multi-step processes

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention utilizes phase transition of the polymer solution during electrospraying, where the solution transitions from liquid jet to solidified microsphere upon contact with the collection surface. This phase transition enables precise size control and porosity formation through parameter optimization

Inventive Principle:
Principle #36Phase transitions

2Adaptability or versatility

If polymer chemistry-specific methods are used, then nanofiber microspheres can be fabricated, but the method is limited to specific polymer compositions

Engineering Contradiction:
Improvepolymer composition flexibilityVSAvoidmicrosphere morphology control
Core Design Contradiction:
Adaptability or versatilityVSManufacturing precision

Solution Approach 1:

The electrospraying method serves as a universal fabrication approach that can process various polymer compositions (natural polymers like gelatin and chitosan, synthetic polymers like PLGA and PCL) without requiring chemistry-specific procedures. The same equipment and parameter ranges work across different material systems

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

By adjusting electrospraying parameters (voltage, flow rate, distance) based on polymer properties, the method maintains morphology control versatility across different polymer compositions, enabling uniform microspheres regardless of material type

Inventive Principle:
Principle #35Parameter changes

3Device complexity

If solid microspheres are used, then simple structure is achieved, but cell carrier efficiency is reduced

Engineering Contradiction:
Improvemicrosphere structureVSAvoidcell carrier efficiency
Core Design Contradiction:
Device complexityVSReliability

Solution Approach 1:

The invention creates porous nanofiber microspheres that maintain structural simplicity while dramatically improving cell carrier efficiency. The porous structure provides increased surface area and internal volume for cell attachment and nutrient transport, enhancing biological performance without complex multi-component construction

Inventive Principle:
Principle #31Porous materials

4Reliability

If 3D porous scaffolds are used, then tissue regeneration capability is improved, but minimally invasive injection is not achieved

Engineering Contradiction:
Improvetissue regeneration capabilityVSAvoidinjection capability
Core Design Contradiction:
ReliabilityVSEase of operation

Solution Approach 1:

The invention segments the 3D scaffold structure into microsphere-sized units that can be injected minimally invasively. Each microsphere contains nanofiber structures that provide tissue regeneration capability, combining the benefits of injectability with 3D scaffold functionality

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The invention nests nanofiber structures within microsphere shells, creating a hierarchical structure where the outer microsphere enables injection while the inner nanofiber network provides tissue regeneration. This nested design integrates multiple functions across different scales

Inventive Principle:
Principle #7Nested doll (Nesting)

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 method enables the production of injectable nanofiber microspheres with improved cell carrier efficiency, promoting tissue regeneration and drug delivery, and can form microtissue-like structures in situ, enhancing wound healing and tissue regeneration.

Implementation Method 1

electrospinning and electrospraying is used to fabricate nanofiber microspheres

Methodology Applied
Scientific EffectElectrostatic forces: Electrostatics

Implementation Method 2

electrospinning and electrospraying is used to fabricate nanofiber microspheres

Methodology Applied
Scientific EffectElectrospraying: Electrostatic Deposition

Implementation Method 3

using electrospun nanofiber segments that are crosslinked and thermally treated

Methodology Applied
Scientific EffectCrosslinking: Chemical Bonding

Implementation Method 4

using electrospun nanofiber segments that are crosslinked and thermally treated

Methodology Applied
Scientific EffectThermal treatment: Heat Treatment

Data Source

PatentUS20250205159A1Nanofiber microspheres and methods os use thereof
Publication Date: 2025.06.26 BOARD OF RGT UNIV OF NEBRASKA
  • US20250205159A1 patent drawing
  • US20250205159A1 patent drawing
  • US20250205159A1 patent drawing

AI summary

Nanofiber segments and nanofiber microspheres are provided as well as methods of use thereof and methods of making.