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      Organ-on-a-chip: recent breakthroughs and future prospects

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          Abstract

          The organ-on-a-chip (OOAC) is in the list of top 10 emerging technologies and refers to a physiological organ biomimetic system built on a microfluidic chip. Through a combination of cell biology, engineering, and biomaterial technology, the microenvironment of the chip simulates that of the organ in terms of tissue interfaces and mechanical stimulation. This reflects the structural and functional characteristics of human tissue and can predict response to an array of stimuli including drug responses and environmental effects. OOAC has broad applications in precision medicine and biological defense strategies. Here, we introduce the concepts of OOAC and review its application to the construction of physiological models, drug development, and toxicology from the perspective of different organs. We further discuss existing challenges and provide future perspectives for its application.

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          Microfluidics: Fluid physics at the nanoliter scale

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            Advantages and challenges of microfluidic cell culture in polydimethylsiloxane devices.

            Culture of cells using various microfluidic devices is becoming more common within experimental cell biology. At the same time, a technological radiation of microfluidic cell culture device designs is currently in progress. Ultimately, the utility of microfluidic cell culture will be determined by its capacity to permit new insights into cellular function. Especially insights that would otherwise be difficult or impossible to obtain with macroscopic cell culture in traditional polystyrene dishes, flasks or well-plates. Many decades of heuristic optimization have gone into perfecting conventional cell culture devices and protocols. In comparison, even for the most commonly used microfluidic cell culture devices, such as those fabricated from polydimethylsiloxane (PDMS), collective understanding of the differences in cellular behavior between microfluidic and macroscopic culture is still developing. Moving in vitro culture from macroscopic culture to PDMS based devices can come with unforeseen challenges. Changes in device material, surface coating, cell number per unit surface area or per unit media volume may all affect the outcome of otherwise standard protocols. In this review, we outline some of the advantages and challenges that may accompany a transition from macroscopic to microfluidic cell culture. We focus on decisive factors that distinguish macroscopic from microfluidic cell culture to encourage a reconsideration of how macroscopic cell culture principles might apply to microfluidic cell culture.
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              Development of an enhanced human gastrointestinal epithelial culture system to facilitate patient-based assays.

              The technology for the growth of human intestinal epithelial cells is rapidly progressing. An exciting possibility is that this system could serve as a platform for individualised medicine and research. However, to achieve this goal, human epithelial culture must be enhanced so that biopsies from individuals can be used to reproducibly generate cell lines in a short time frame so that multiple, functional assays can be performed (ie, barrier function and host-microbial interactions).
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                Author and article information

                Contributors
                wuqirui@shu.edu.cn
                Perpethere@shu.edu.cn
                wxh0201@t.shu.edu.cn
                lingyanfeng@t.shu.edu.cn
                jinbowu@t.shu.edu.cn
                xiaolizhu@shu.edu.cn
                phwen@ust.hk
                gongxiuqing@shu.edu.cn
                Journal
                Biomed Eng Online
                Biomed Eng Online
                BioMedical Engineering OnLine
                BioMed Central (London )
                1475-925X
                12 February 2020
                12 February 2020
                2020
                : 19
                : 9
                Affiliations
                [1 ]ISNI 0000 0001 2323 5732, GRID grid.39436.3b, Materials Genome Institute, , Shanghai University, ; Shanghai, 200444 China
                [2 ]ISNI 0000 0001 2323 5732, GRID grid.39436.3b, School of Life Sciences, , Shanghai University, ; Shanghai, 200444 China
                Author information
                http://orcid.org/0000-0001-8519-1317
                Article
                752
                10.1186/s12938-020-0752-0
                7017614
                32050989
                ce9685b6-7d02-4ab5-96f3-537aef8dc2fe
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 11 November 2019
                : 5 February 2020
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 21775101
                Award Recipient :
                Funded by: Shanghai Pujiang Program
                Award ID: 17PJ1402800
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2020

                Biomedical engineering
                organ-on-a-chip,microfluidic chip,physiological model,human organs,stem cell

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