Cured PGS Microparticles via Sol-Gel Transition

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Solution Overview

Problem

Current methods for forming poly(glycerol sebacate) (PGS) microparticles are limited by the need for thermal processing, which causes them to melt and lose their spherical conformation, and often require photo-induced crosslinkers that can be harmful in biological systems.

Innovation Solution

A method for forming cured PGS microparticles without the use of molds or photo-induced crosslinkers, involving the combination of PGS resin with a phase-incompatible liquid that undergoes a reversible sol-gel transition, allowing for microwave or thermal curing to maintain spherical shape and prevent melting.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If thermal processing is used to cure PGS microparticles, then the PGS is cured and forms a solid structure, but the microparticles melt and lose their spherical conformation

Engineering Contradiction:
Improvecuring of PGSVSAvoidspherical conformation
Core Design Contradiction:
ReliabilityVSShape

Solution Approach 1:

The patent utilizes the phase transition of a liquid support medium from liquid to gel state at a specific transition temperature. The PGS microparticles are formed in this liquid medium, then the medium is heated above its transition temperature to gelify, providing structural support during thermal curing. This allows the PGS to be cured thermally without the microparticles deforming, as the gelified medium maintains their spherical shape throughout the curing process.

Inventive Principle:
Principle #36Phase transitions

2Reliability

If photo-induced crosslinkers are used to cure PGS microparticles, then the microparticles can be cured without thermal processing, but toxic by-products are generated that are harmful in biological systems

Engineering Contradiction:
Improvecuring of PGSVSAvoidtoxicity
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent removes photo-induced crosslinkers and initiators from the system entirely. Instead, it uses thermal curing of PGS combined with a liquid support medium that undergoes sol-gel transition. This extraction of harmful photo-initiators eliminates the generation of toxic by-products while maintaining effective curing capability through the thermal crosslinking of PGS alone.

Inventive Principle:
Principle #2Taking out (Extraction)

3Reliability

If a mold is used to hold PGS resin shape during crosslinking, then the thermoset structure can be formed, but the process becomes complex and cannot produce spherical microparticles

Engineering Contradiction:
Improveformation of thermoset structureVSAvoidmolding process
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent introduces a liquid support medium as an intermediary that temporarily holds the PGS microparticles in their spherical form. This medium acts as a sacrificial matrix that provides mechanical support during the crosslinking process. After curing is complete, the liquid medium can be removed or degraded, leaving behind the cured spherical microparticles without requiring complex molding equipment or processes.

Inventive Principle:
Principle #24Intermediary (Mediator)

4Ease of manufacture

If fillers are added to solidify PGS resin, then the resin can be processed without molding, but the elastomeric properties and biodegradability are compromised

Engineering Contradiction:
Improveprocessing without moldVSAvoidbiodegradability
Core Design Contradiction:
Ease of manufactureVSStability of the object's composition

Solution Approach 1:

Instead of adding fillers to solidify the PGS resin, the patent uses a liquid support medium that undergoes phase transition from liquid to gel. This gelified medium provides the necessary structural support during processing without requiring solid fillers. The medium can be chosen to be biocompatible and removable, preserving the biodegradability and elastomeric properties of the PGS while enabling mold-free processing of spherical microparticles.

Inventive Principle:
Principle #36Phase transitions

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

Enables the creation of biodegradable, elastomeric microparticles with tunable degradation kinetics and controlled release properties, suitable for biomedical applications without the toxicity concerns of photo-induced initiators.

Implementation Method 1

combining the PGS resin composition with a phase-incompatible liquid that undergoes a reversible sol-gel transition

Methodology Applied
Scientific EffectSol-gel transition: Gel

Implementation Method 2

curing the plurality of uncured microparticles to form the plurality of cured microparticles

Methodology Applied
Scientific EffectThermal curing: Heating

Implementation Method 3

To create a PGS thermoset/solid structure, neat PGS resin must be crosslinked/cured at elevated temperatures

Methodology Applied
Scientific EffectCrosslinking: Chemical Bonding

Data Source

PatentUS11602721B2Cured biodegradable microparticles and scaffolds and methods of making and using the same
Publication Date: 2023.03.14 SECANT GROUP LLC
  • US11602721B2 patent drawing
  • US11602721B2 patent drawing
  • US11602721B2 patent drawing

AI summary

A method of forming cured microparticles includes providing a poly(glycerol sebacate) resin in an uncured state. The method also includes forming the composition into a plurality of uncured microparticles and curing the uncured microparticles to form the plurality of cured microparticles. The uncured microparticles are free of a photo-induced crosslinker. A method of forming a scaffold includes providing microparticles including poly(glycerol sebacate) in a three-dimensional arrangement. The method also includes stimulating the microparticles in the three-dimensional arrangement to sinter the microparticles, thereby forming the scaffold having a plurality of pores. A scaffold is formed of a plurality of microparticles including a poly(glycerol sebacate) thermoset resin in a three-dimensional arrangement. The scaffold has a plurality of pores.