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  <title><![CDATA[MS Defense by Ayla Natalia Toney]]></title>
  <body><![CDATA[<p>Ayla Natalia Toney<br>BME MS Thesis Defense Presentation<br><strong>Date</strong>: 2026-03-31<br><strong>Time</strong>: 1:30 - 2:30 PM<br><strong>Location / Meeting Link</strong>: IBB 2316<br><br><strong>Committee Members:</strong><br>Todd Sulchek - School of Mechanical Engineering, Department of Biomedical Engineering (Advisor); Ankur Singh - School of Mechanical Engineering, Department of Biomedical Engineering; Julia Babensee - Department of Biomedical Engineering&nbsp;<br><br><br><strong>Title</strong>: Functionalization of hydrogel microparticles that mimic antigen presenting cell mechanics for T cell activation<br><br><strong>Abstract:</strong><br>As the prevalence of cancer rises globally, it is crucial to develop effective treatment methods that are noninvasive, limit harsh side effects, and decrease reoccurrence. Advanced T cell therapies offer a promising alternative to chemotherapy and radiation, but struggle to target solid tumor malignancies due to decreased expansion and persistence. There has been increasing exploration into polymer biomimetic platforms for T cell activation; however, these do not properly emulate the mechanical properties of natural antigen presenting cells (APCs). This presentation describes a methodology to develop hydrogel microparticles (MPs) that mimic APC size and viscoelasticity and present anti-CD3/28 for T cell activation. Poly(ethylene) glycol diacrylate (PEGDA) microparticles are formulated at 10.5 ± 1.8 µm with flow-focusing microfluidics and functionalized downstream with biotin-PEG-acrylate, streptavidin, and biotinylated antibodies.</p>]]></body>
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      <value><![CDATA[<p>Functionalization of hydrogel microparticles that mimic antigen presenting cell mechanics for T cell activation</p>]]></value>
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