Date of Award

8-23-2024

Degree Type

Thesis

Degree Name

Master of Science (MS)

Department

Biomedical and Chemical Engineering

Advisor(s)

Zhen Ma

Keywords

biomaterial;cardiac organoids;embryotoxicity;human induced pluripotent stem cell;in vitro model

Abstract

Medication use during pregnancy presents complex considerations due to its potential for causing congenital malformations and its implications for maternal and fetal health. With approximately 90% of pregnant women consuming at least one pharmaceutical agent, there is a critical need for comprehensive developmental toxicity screening, particularly for cancer treatments during pregnancy. Pluripotent stem cell (PSC) models, specifically iPSC-derived organoids, offer promising approaches for assessing drug toxicity and efficacy during pregnancy. This study introduces an embryotoxicity screening platform using biomaterial-engineered 3D cardiac organoids created through micropatterning techniques. The platform aims to characterize the response of six pharmaceutical agents across pregnancy risk categories, focusing on four chemotherapeutic compounds, based on the measurements of cardiac physiology and tissue morphology. The engineered cardiac organoids serve as a model for characterizing embryonic cardiac development and physiology, holding the potential to enhance diagnostic capabilities for chemotherapy-induced cardiotoxicity. This well-defined 3D structure is proposed as a pre-validation model for early-stage cardiotoxicity assessment, potentially contributing to an updated pregnancy risk classification system.

Access

Open Access

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