MRS Meetings and Events

 

SB01.03.11 2023 MRS Spring Meeting

Manufacturing a Three-Dimensional Bioprinted and Oriented Electrospinning Dual-Scale Scaffold to Promote Cellular Alignment and Enhance Structural Elasticity for Muscular Functioning

When and Where

Apr 13, 2023
5:00pm - 7:00pm

Moscone West, Level 1, Exhibit Hall

Presenter

Co-Author(s)

Evan Fair1,Elizabeth Ricci1,Eliza Hogan1,Ryan jaworski1,Naser Haghbin1,Isaac Macwan1,Shelley Phelan1

Fairfield University1

Abstract

Evan Fair1,Elizabeth Ricci1,Eliza Hogan1,Ryan jaworski1,Naser Haghbin1,Isaac Macwan1,Shelley Phelan1

Fairfield University1
Every day, at least 22 people pass away while waiting for a vital organ donation. Biomanufacturing artificial organs have the potential to address the organ scarcity crisis and save lives. This study investigates muscle tissue engineering by combining 3D bioprinting and electrospinning methods to create a dual-scale scaffold (a porous block of 10 mm × 10 mm × 3.5 mm). The dual-scale scaffold contains multiple layers of 3D bioprinted microstructures and an integrated polycaprolactone (PCL) electrospun nanofiber matrix. The most significant limitation of using 3D-printed scaffolds relates to the ineffectiveness of cellular elongation resulting in resistance to the adsorption of muscle bundles. Synthetic nanofibers used in this study have the potential to influence the alignment of the cells in a specific direction, which improves the effectiveness of holistic muscle functioning through cooperative contraction and relaxation of the muscle cells. The 3D bioprinted microstructures serve as a gap collector and a flexible structure to allow extension and contraction of the cellular structure. Electrospun nanofibers form aligned mesh networks within the 3D printed scaffold's pores and are deposited perpendicular to the direction of the 3D bioprinted scaffold layer lines. The three-dimensional dual scaffold will be manufactured, characterized, sterilized, and then used as a scaffold for muscle cell culturing. The attachment, growth, viability, proliferation, and alignment of muscle cells are examined using fluorescence microscopy, scanning electron microscopy, and cellular assays to verify these characteristics.

Keywords

biological | biomaterial | tissue

Symposium Organizers

Marie-Eve Aubin-Tam, TU Delft
Maneesh Gupta, U.S. Air Force Research Laboratory
Srikanth Singamaneni, Washington University
Taylor Ware, Texas A&M University

Session Chairs

Marie-Eve Aubin-Tam
Srikanth Singamaneni

In this Session

SB01.03.02
Tissue-Attachable Intestinal Organoids as Injectable Therapeutics for Reconstruction of Intestinal Injuries

SB01.03.03
Tissue Extracellular Matrix-based Microribbon Scaffolds for Bone Regeneration via Immunomodulation

SB01.03.04
Sensory Artificial Octopus Suckers with Highly Adaptive Soft Micro-Denticles

SB01.03.05
Graphically-Encoded Biodegradable Microspheres with Hydrogel Shell for Sustained Release of Drugs at Controlled Rates

SB01.03.06
Nutrient Transport for Increasing the Active Lifespan of Engineered Living Materials

SB01.03.09
Enhancing Microbially-Induced Calcite Precipitation (MICP) Using Protein and Peptide Additives

SB01.03.10
Controlling Shape Morphing and Cell Release in Engineered Living Materials

SB01.03.11
Manufacturing a Three-Dimensional Bioprinted and Oriented Electrospinning Dual-Scale Scaffold to Promote Cellular Alignment and Enhance Structural Elasticity for Muscular Functioning

SB01.03.12
3D Bioprinting Human Blood Vessel Using a Collagen Bioink to Optimize Growth Conditions of Two Primary Cell Lines of HUVEC and HASMC

SB01.03.15
Engineered Extracellular Vesicles for Safe and Efficient Chemo-Sonodynamic Cancer Therapy via Stimuli-Responsive Drug Release

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Publishing Alliance

MRS publishes with Springer Nature