Microfluidic-Chip-Integrated Biosensors for Lung Disease Models
Lung diseases (e.g., infection, asthma, cancer, and pulmonary fibrosis) represent serious threats to human health all over the world. Conventional two-dimensional (2D) cell models and animal models cannot mimic the human-specific properties of the lungs. In the past decade, human organ-on-a-chip (OO...
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2021
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oai:doaj.org-article:421e8c23c4bc42b89a793bf825a0372e2021-11-25T16:55:38ZMicrofluidic-Chip-Integrated Biosensors for Lung Disease Models10.3390/bios111104562079-6374https://doaj.org/article/421e8c23c4bc42b89a793bf825a0372e2021-11-01T00:00:00Zhttps://www.mdpi.com/2079-6374/11/11/456https://doaj.org/toc/2079-6374Lung diseases (e.g., infection, asthma, cancer, and pulmonary fibrosis) represent serious threats to human health all over the world. Conventional two-dimensional (2D) cell models and animal models cannot mimic the human-specific properties of the lungs. In the past decade, human organ-on-a-chip (OOC) platforms—including lung-on-a-chip (LOC)—have emerged rapidly, with the ability to reproduce the in vivo features of organs or tissues based on their three-dimensional (3D) structures. Furthermore, the integration of biosensors in the chip allows researchers to monitor various parameters related to disease development and drug efficacy. In this review, we illustrate the biosensor-based LOC modeling, further discussing the future challenges as well as perspectives in integrating biosensors in OOC platforms.Shuang DingHaijun ZhangXuemei WangMDPI AGarticlebiosensormicrofluidicsorgan-on-a-chiplung modellung-on-a-chipBiotechnologyTP248.13-248.65ENBiosensors, Vol 11, Iss 456, p 456 (2021) |
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biosensor microfluidics organ-on-a-chip lung model lung-on-a-chip Biotechnology TP248.13-248.65 |
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biosensor microfluidics organ-on-a-chip lung model lung-on-a-chip Biotechnology TP248.13-248.65 Shuang Ding Haijun Zhang Xuemei Wang Microfluidic-Chip-Integrated Biosensors for Lung Disease Models |
description |
Lung diseases (e.g., infection, asthma, cancer, and pulmonary fibrosis) represent serious threats to human health all over the world. Conventional two-dimensional (2D) cell models and animal models cannot mimic the human-specific properties of the lungs. In the past decade, human organ-on-a-chip (OOC) platforms—including lung-on-a-chip (LOC)—have emerged rapidly, with the ability to reproduce the in vivo features of organs or tissues based on their three-dimensional (3D) structures. Furthermore, the integration of biosensors in the chip allows researchers to monitor various parameters related to disease development and drug efficacy. In this review, we illustrate the biosensor-based LOC modeling, further discussing the future challenges as well as perspectives in integrating biosensors in OOC platforms. |
format |
article |
author |
Shuang Ding Haijun Zhang Xuemei Wang |
author_facet |
Shuang Ding Haijun Zhang Xuemei Wang |
author_sort |
Shuang Ding |
title |
Microfluidic-Chip-Integrated Biosensors for Lung Disease Models |
title_short |
Microfluidic-Chip-Integrated Biosensors for Lung Disease Models |
title_full |
Microfluidic-Chip-Integrated Biosensors for Lung Disease Models |
title_fullStr |
Microfluidic-Chip-Integrated Biosensors for Lung Disease Models |
title_full_unstemmed |
Microfluidic-Chip-Integrated Biosensors for Lung Disease Models |
title_sort |
microfluidic-chip-integrated biosensors for lung disease models |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/421e8c23c4bc42b89a793bf825a0372e |
work_keys_str_mv |
AT shuangding microfluidicchipintegratedbiosensorsforlungdiseasemodels AT haijunzhang microfluidicchipintegratedbiosensorsforlungdiseasemodels AT xuemeiwang microfluidicchipintegratedbiosensorsforlungdiseasemodels |
_version_ |
1718412833671086080 |