Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors.
Next generation bioreactors are being developed to generate multiple human cell-based tissue analogs within the same fluidic system, to better recapitulate the complexity and interconnection of human physiology [1, 2]. The effective development of these devices requires a solid understanding of thei...
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doaj-86566301b72244aaaaed3b96417a7e502020-11-25T01:48:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01119e016277410.1371/journal.pone.0162774Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors.Laura IannettiGiovanna D'UrsoGioacchino ConoscentiElena CutrìRocky S TuanManuela T RaimondiRiccardo GottardiPaolo ZuninoNext generation bioreactors are being developed to generate multiple human cell-based tissue analogs within the same fluidic system, to better recapitulate the complexity and interconnection of human physiology [1, 2]. The effective development of these devices requires a solid understanding of their interconnected fluidics, to predict the transport of nutrients and waste through the constructs and improve the design accordingly. In this work, we focus on a specific model of bioreactor, with multiple input/outputs, aimed at generating osteochondral constructs, i.e., a biphasic construct in which one side is cartilaginous in nature, while the other is osseous. We next develop a general computational approach to model the microfluidics of a multi-chamber, interconnected system that may be applied to human-on-chip devices. This objective requires overcoming several challenges at the level of computational modeling. The main one consists of addressing the multi-physics nature of the problem that combines free flow in channels with hindered flow in porous media. Fluid dynamics is also coupled with advection-diffusion-reaction equations that model the transport of biomolecules throughout the system and their interaction with living tissues and C constructs. Ultimately, we aim at providing a predictive approach useful for the general organ-on-chip community. To this end, we have developed a lumped parameter approach that allows us to analyze the behavior of multi-unit bioreactor systems with modest computational effort, provided that the behavior of a single unit can be fully characterized.http://europepmc.org/articles/PMC5036894?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Laura Iannetti Giovanna D'Urso Gioacchino Conoscenti Elena Cutrì Rocky S Tuan Manuela T Raimondi Riccardo Gottardi Paolo Zunino |
spellingShingle |
Laura Iannetti Giovanna D'Urso Gioacchino Conoscenti Elena Cutrì Rocky S Tuan Manuela T Raimondi Riccardo Gottardi Paolo Zunino Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors. PLoS ONE |
author_facet |
Laura Iannetti Giovanna D'Urso Gioacchino Conoscenti Elena Cutrì Rocky S Tuan Manuela T Raimondi Riccardo Gottardi Paolo Zunino |
author_sort |
Laura Iannetti |
title |
Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors. |
title_short |
Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors. |
title_full |
Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors. |
title_fullStr |
Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors. |
title_full_unstemmed |
Distributed and Lumped Parameter Models for the Characterization of High Throughput Bioreactors. |
title_sort |
distributed and lumped parameter models for the characterization of high throughput bioreactors. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2016-01-01 |
description |
Next generation bioreactors are being developed to generate multiple human cell-based tissue analogs within the same fluidic system, to better recapitulate the complexity and interconnection of human physiology [1, 2]. The effective development of these devices requires a solid understanding of their interconnected fluidics, to predict the transport of nutrients and waste through the constructs and improve the design accordingly. In this work, we focus on a specific model of bioreactor, with multiple input/outputs, aimed at generating osteochondral constructs, i.e., a biphasic construct in which one side is cartilaginous in nature, while the other is osseous. We next develop a general computational approach to model the microfluidics of a multi-chamber, interconnected system that may be applied to human-on-chip devices. This objective requires overcoming several challenges at the level of computational modeling. The main one consists of addressing the multi-physics nature of the problem that combines free flow in channels with hindered flow in porous media. Fluid dynamics is also coupled with advection-diffusion-reaction equations that model the transport of biomolecules throughout the system and their interaction with living tissues and C constructs. Ultimately, we aim at providing a predictive approach useful for the general organ-on-chip community. To this end, we have developed a lumped parameter approach that allows us to analyze the behavior of multi-unit bioreactor systems with modest computational effort, provided that the behavior of a single unit can be fully characterized. |
url |
http://europepmc.org/articles/PMC5036894?pdf=render |
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