Titlebook: Microfluidics and Multi Organs on Chip; P. V. Mohanan Book 2022 The Editor(s) (if applicable) and The Author(s), under exclusive license t

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Futuristic Aspects of Human Organ on a Chip,al. Today, it is possible to keep 10–13 connected organs alive for 1–3 weeks without losing a significant function in most of the organs in the system. This number of organs is sufficient to model a large part of the basic physiology of an organism. Selecting which cell models to use and how to scal

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Multiorgans-on-a-Chip for Personalized Medicine,organs on chips. Multiorgan-on-a-chip devices have the potential to revolutionize how human health research is carried out. In theory, they can be “personalized” for reflection of individual physiology by including blood samples, primary human tissue, and cells derived from induced pluripotent stem

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Development and Application of Microfluidics in Organoid Formation,ers if not all during the recent decades. The studies have been successful with the help of animal models and cell culture models, conventionally. Though these numerous scientific advances have given greater insights, their applications in modelling human physiology and pathology are limited. Owing

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Liver-on-a-Chip,iology that affects interpretation in predicting clinical outcome. Organ-on-a-chip (OoC) is a cutting-edge technology that helps to mimic the microarchitecture and reproduce physiological functions of an organ in vitro cell-based model system. Organ-on-a-chip representing skin, brain, liver, lung, k

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Placenta on Chip: A Modern Approach to Probe Feto-Maternal Interface,e fetus. It also protects the fetus from maternal insults such as infections and exposure to toxicants, thereby minimizing any teratogenicity. Therefore, ensuring placental health is essential for a successful pregnancy. However, the development, differentiation, functions, and dysfunctions of the h

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Microfluidic Retina-on-Chip,rdination, in vitro replication of retinal functions has been a daunting task. Ex-vivo/in vivo animal retinal models are limited by their ethical concerns, cost, reproducibility, and prolonged experimental duration. Over the years, microfluidic perfusion devices have captured significant interest as

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Kidney-on-a-Chip,ovel drug discovery. For the advancement of kidney-on-a-chip models, there is a prime requirement to do rigorous validation. It could be determined whether kidney-on-a-chip models can predict clinical outcomes before the severe stage and represent human-relevant physiology. Recent advances in kidney

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J. Malcolm Wilkinson and biotic environments has justified the present triumvirate of specialized publications in this field: comprehensive reviews, rapidly published progress reports, and archival documentations. These three publications are integrated and scheduled to provide in international communication the cohere