Defense Date

11-7-2023

Graduation Date

Fall 12-15-2023

Availability

One-year Embargo

Submission Type

thesis

Degree Name

MS

Department

Biomedical Engineering

School

School of Science and Engineering

Committee Chair

Bin Yang

Committee Member

Kimberly Williams

Committee Member

Kyle Selcer

Committee Member

Ipsita Banerjee

Keywords

Organoid, Pluripotent Stem Cell, Alginate, Air-jetting Bioprinting, Cell Encapsulation, Type-1 Diabetes, 3D Stem Cell Culture, Tissue Engineering, Droplet based Bioprinting, Hydrogel, Coaxial Air Channel

Abstract

Biomanufactured 3D-organoids show promise for modeling and treating various conditions, particularly insulin-dependent diabetes mellitus (type-1 diabetes). Pancreatic islet organoids serve as sustainable sources of insulin-producing β-cells, potentially restoring insulin regulation in patients and providing a long-term solution for diabetes. Hydrogel droplet printing is an emerging technique in regenerative medicine due to its advantageous tunability and biocompatibility; however, challenges of consistency, quality control, and scalability persist. To address these issues, we developed a novel air-jetting based droplet bioprinting system for the generation of monodispersed alginate micro-droplets. The objective of this project was to incorporate human induced pluripotent stem cells (hiPSCs) into these micro-droplets while maintaining uniformity, size, viability, and functionality. Comprehensive parametric studies led to the standardization of our process for the scalable production of spherical stem cell-laden micro-droplets within a customizable size range (300-650μm). Ongoing investigations into cell seeding density, aggregation, and pluripotency will enhance our role of cell encapsulation in the organoid generation pipeline. Herein, we aim to improve the scalability and quality control of bioprinting stem cell-laden micro-droplets to facilitate the manufacturing of suitable organoids for islet transplantation.

Language

English

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