The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs

Advanced tissue culture platforms harness microfabrication techniques and properties of biocompatible materials to create tunable and physiologically-relevant microenvironments. Traditional in vitro tissue models are restricted to flat, static culture plates, which allow for high-throughput experime...

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Main Author: Spencer, Abigail June
Language:en_US
Published: 2017
Subjects:
Online Access:https://hdl.handle.net/2144/23682
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spelling ndltd-bu.edu-oai-open.bu.edu-2144-236822019-01-08T15:42:16Z The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs Spencer, Abigail June Mechanical engineering Advanced tissue culture platforms harness microfabrication techniques and properties of biocompatible materials to create tunable and physiologically-relevant microenvironments. Traditional in vitro tissue models are restricted to flat, static culture plates, which allow for high-throughput experimentation but do not support physiological tissue function. Early research investigates cell response to physiological mechanical cues[1–3], but these devices are largely confined to materials like PDMS[4] or have too low throughput for industry use. The next generation of platforms will combine mechanical cues and integrated sensing with materials that are biologically inert and compatible with high throughput assays and large scale manufacturing, while remaining in an industry-standard footprint. This work represents the design, process development, manufacturing, and characterization of such a system. A microfluidic device manufacturing process was developed to translate the Draper PDMS bilayer microfluidic device[5–7] into a next generation system entirely made of hard plastic. Cyclic olefin copolymer (COC) and polycarbonate thermoplastics were characterized and chosen for their compatibility with drug development applications and large scale manufacturing processes. Hot embossing and thermal bonding procedures were developed that resulted in minimal feature deformation and a robust bond between material layers. Integrated electrical sensors were fabricated in microfluidic channels to quantify transepithelial electrical resistance (TEER) in real time. The sensor design and complex trace routing were demonstrated to be continuous, conductive and fully integrated in the next generation system. The culmination of these design decisions resulted in a hard plastic, bilayer microfluidic device with integrated sensors that is compatible with the industry-standard footprint suited for applications in drug development and disease modeling. 2017-08-28T15:36:12Z 2017-08-28T15:36:12Z 2017 2017-07-10T01:16:24Z Thesis/Dissertation https://hdl.handle.net/2144/23682 en_US
collection NDLTD
language en_US
sources NDLTD
topic Mechanical engineering
spellingShingle Mechanical engineering
Spencer, Abigail June
The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
description Advanced tissue culture platforms harness microfabrication techniques and properties of biocompatible materials to create tunable and physiologically-relevant microenvironments. Traditional in vitro tissue models are restricted to flat, static culture plates, which allow for high-throughput experimentation but do not support physiological tissue function. Early research investigates cell response to physiological mechanical cues[1–3], but these devices are largely confined to materials like PDMS[4] or have too low throughput for industry use. The next generation of platforms will combine mechanical cues and integrated sensing with materials that are biologically inert and compatible with high throughput assays and large scale manufacturing, while remaining in an industry-standard footprint. This work represents the design, process development, manufacturing, and characterization of such a system. A microfluidic device manufacturing process was developed to translate the Draper PDMS bilayer microfluidic device[5–7] into a next generation system entirely made of hard plastic. Cyclic olefin copolymer (COC) and polycarbonate thermoplastics were characterized and chosen for their compatibility with drug development applications and large scale manufacturing processes. Hot embossing and thermal bonding procedures were developed that resulted in minimal feature deformation and a robust bond between material layers. Integrated electrical sensors were fabricated in microfluidic channels to quantify transepithelial electrical resistance (TEER) in real time. The sensor design and complex trace routing were demonstrated to be continuous, conductive and fully integrated in the next generation system. The culmination of these design decisions resulted in a hard plastic, bilayer microfluidic device with integrated sensors that is compatible with the industry-standard footprint suited for applications in drug development and disease modeling.
author Spencer, Abigail June
author_facet Spencer, Abigail June
author_sort Spencer, Abigail June
title The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
title_short The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
title_full The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
title_fullStr The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
title_full_unstemmed The design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
title_sort design and characterization of a next generation microfluidic device for in vitro modeling of bilayer tissue constructs
publishDate 2017
url https://hdl.handle.net/2144/23682
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