Translational Roadmap for the Organs-on-a-Chip Industry toward Broad Adoption
Organs-on-a-Chip (OOAC) is a disruptive technology with widely recognized potential to change the efficiency, effectiveness, and costs of the drug discovery process; to advance insights into human biology; to enable clinical research where human trials are not feasible. However, further development...
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| Vydáno v: | Bioengineering (Basel) Ročník 7; číslo 3; s. 112 |
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| Jazyk: | angličtina |
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Switzerland
MDPI AG
16.09.2020
MDPI |
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| ISSN: | 2306-5354, 2306-5354 |
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| Abstract | Organs-on-a-Chip (OOAC) is a disruptive technology with widely recognized potential to change the efficiency, effectiveness, and costs of the drug discovery process; to advance insights into human biology; to enable clinical research where human trials are not feasible. However, further development is needed for the successful adoption and acceptance of this technology. Areas for improvement include technological maturity, more robust validation of translational and predictive in vivo-like biology, and requirements of tighter quality standards for commercial viability. In this review, we reported on the consensus around existing challenges and necessary performance benchmarks that are required toward the broader adoption of OOACs in the next five years, and we defined a potential roadmap for future translational development of OOAC technology. We provided a clear snapshot of the current developmental stage of OOAC commercialization, including existing platforms, ancillary technologies, and tools required for the use of OOAC devices, and analyze their technology readiness levels. Using data gathered from OOAC developers and end-users, we identified prevalent challenges faced by the community, strategic trends and requirements driving OOAC technology development, and existing technological bottlenecks that could be outsourced or leveraged by active collaborations with academia. |
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| AbstractList | Organs-on-a-Chip (OOAC) is a disruptive technology with widely recognized potential to change the efficiency, effectiveness, and costs of the drug discovery process; to advance insights into human biology; to enable clinical research where human trials are not feasible. However, further development is needed for the successful adoption and acceptance of this technology. Areas for improvement include technological maturity, more robust validation of translational and predictive in vivo-like biology, and requirements of tighter quality standards for commercial viability. In this review, we reported on the consensus around existing challenges and necessary performance benchmarks that are required toward the broader adoption of OOACs in the next five years, and we defined a potential roadmap for future translational development of OOAC technology. We provided a clear snapshot of the current developmental stage of OOAC commercialization, including existing platforms, ancillary technologies, and tools required for the use of OOAC devices, and analyze their technology readiness levels. Using data gathered from OOAC developers and end-users, we identified prevalent challenges faced by the community, strategic trends and requirements driving OOAC technology development, and existing technological bottlenecks that could be outsourced or leveraged by active collaborations with academia. Organs-on-a-Chip (OOAC) is a disruptive technology with widely recognized potential to change the efficiency, effectiveness, and costs of the drug discovery process; to advance insights into human biology; to enable clinical research where human trials are not feasible. However, further development is needed for the successful adoption and acceptance of this technology. Areas for improvement include technological maturity, more robust validation of translational and predictive in vivo-like biology, and requirements of tighter quality standards for commercial viability. In this review, we reported on the consensus around existing challenges and necessary performance benchmarks that are required toward the broader adoption of OOACs in the next five years, and we defined a potential roadmap for future translational development of OOAC technology. We provided a clear snapshot of the current developmental stage of OOAC commercialization, including existing platforms, ancillary technologies, and tools required for the use of OOAC devices, and analyze their technology readiness levels. Using data gathered from OOAC developers and end-users, we identified prevalent challenges faced by the community, strategic trends and requirements driving OOAC technology development, and existing technological bottlenecks that could be outsourced or leveraged by active collaborations with academia.Organs-on-a-Chip (OOAC) is a disruptive technology with widely recognized potential to change the efficiency, effectiveness, and costs of the drug discovery process; to advance insights into human biology; to enable clinical research where human trials are not feasible. However, further development is needed for the successful adoption and acceptance of this technology. Areas for improvement include technological maturity, more robust validation of translational and predictive in vivo-like biology, and requirements of tighter quality standards for commercial viability. In this review, we reported on the consensus around existing challenges and necessary performance benchmarks that are required toward the broader adoption of OOACs in the next five years, and we defined a potential roadmap for future translational development of OOAC technology. We provided a clear snapshot of the current developmental stage of OOAC commercialization, including existing platforms, ancillary technologies, and tools required for the use of OOAC devices, and analyze their technology readiness levels. Using data gathered from OOAC developers and end-users, we identified prevalent challenges faced by the community, strategic trends and requirements driving OOAC technology development, and existing technological bottlenecks that could be outsourced or leveraged by active collaborations with academia. |
| Author | McLean, John A. Viswanathan, Priyalakshmi Allwardt, Vanessa Haddrick, Malcolm Pensabene, Virginia Ainscough, Alexander J. Sherrod, Stacy D. |
| AuthorAffiliation | 3 Medicines Discovery Catapult, Alderley Park, Alderley Edge, Macclesfield SK10 4TG, UK; priya.viswanathan@md.catapult.org.uk (P.V.); malcolm.haddrick@md.catapult.org.uk (M.H.) 5 School of Electronic and Electrical Engineering, School of Medicine, Leeds Institute of Medical Research at St. James’s, University of Leeds, Leeds LS2 9JT, UK 1 Center for Innovative Technology, Department of Chemistry, Vanderbilt University, Nashville, TN 37212, USA; vanessa.allwardt@Vanderbilt.Edu (V.A.); stacy.d.sherrod@vanderbilt.edu (S.D.S.); john.a.mclean@Vanderbilt.Edu (J.A.M.) 2 National Heart and Lung Institute, Imperial College London, London SW3 6LY, UK; alex.ainscough14@imperial.ac.uk 4 Vanderbilt Institute of Chemical Biology, Vanderbilt-Ingram Cancer Center, Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt University, Nashville, TN 37235, USA |
| AuthorAffiliation_xml | – name: 1 Center for Innovative Technology, Department of Chemistry, Vanderbilt University, Nashville, TN 37212, USA; vanessa.allwardt@Vanderbilt.Edu (V.A.); stacy.d.sherrod@vanderbilt.edu (S.D.S.); john.a.mclean@Vanderbilt.Edu (J.A.M.) – name: 5 School of Electronic and Electrical Engineering, School of Medicine, Leeds Institute of Medical Research at St. James’s, University of Leeds, Leeds LS2 9JT, UK – name: 2 National Heart and Lung Institute, Imperial College London, London SW3 6LY, UK; alex.ainscough14@imperial.ac.uk – name: 3 Medicines Discovery Catapult, Alderley Park, Alderley Edge, Macclesfield SK10 4TG, UK; priya.viswanathan@md.catapult.org.uk (P.V.); malcolm.haddrick@md.catapult.org.uk (M.H.) – name: 4 Vanderbilt Institute of Chemical Biology, Vanderbilt-Ingram Cancer Center, Vanderbilt Institute for Integrative Biosystems Research and Education, Vanderbilt University, Nashville, TN 37235, USA |
| Author_xml | – sequence: 1 givenname: Vanessa surname: Allwardt fullname: Allwardt, Vanessa – sequence: 2 givenname: Alexander J. surname: Ainscough fullname: Ainscough, Alexander J. – sequence: 3 givenname: Priyalakshmi surname: Viswanathan fullname: Viswanathan, Priyalakshmi – sequence: 4 givenname: Stacy D. surname: Sherrod fullname: Sherrod, Stacy D. – sequence: 5 givenname: John A. surname: McLean fullname: McLean, John A. – sequence: 6 givenname: Malcolm surname: Haddrick fullname: Haddrick, Malcolm – sequence: 7 givenname: Virginia orcidid: 0000-0002-3352-8202 surname: Pensabene fullname: Pensabene, Virginia |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32947816$$D View this record in MEDLINE/PubMed |
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| Copyright | 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2020 by the authors. 2020 |
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