شماره ركورد كنفرانس :
5310
عنوان مقاله :
Recent developments of Organ-on-a-Chip platforms: A mini review
پديدآورندگان :
Mansoori Roghayeh Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran , Ghasemi Pouya Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran , Jaberi Ansari Farshid Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran , Ghanbari Hossein Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran. Research Center for Advanced Technologies in Cardiovascular Medicine, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran. Institute of Biomaterials, University of Tehran Tehran University of Medical Sciences, Tehran, Iran. hghanbari@tums.ac.ir
كليدواژه :
Keywords: Organ , on , a , chip , Microfluidic chip , Physiological model , Human organs
عنوان كنفرانس :
چهارمين كنفرانس بين المللي نانو پزشكي و نانو ايمني
چكيده فارسي :
Organ-on-a-chip (OOAC) is a cutting-edge technology and refers to a microengineered biomimetic system based on microfluidic chip and in vitro cell culture. The numerous advantages of this technology over conventional platforms make it highly popular in the healthcare industry. OOAC permits the study of human physiology in an organ-specific context. Such platforms can generate responses similar to those observed in vivo which enable development of novel in vitro disease models, and could potentially serve as replacements for animals used in drug development and toxin testing. For data collection, articles containing one of the words “Organ-on-a-chip”, “Microfluidic chip” and “Physiological model”, were searched and studied in Thomson Reuters, PubMed, Scopus and Science databases. Biomimetic microsystems representing different organs can be integrated into a single microdevice and linked by a microfluidic circulatory system in a physiologically relevant manner to model a complex, dynamic process of drug absorption, distribution, metabolism, excretion, evaluate drug efficacy and toxicity. Several tissues have been used so far such as liver, lung, kidney, gut, bone, breast, brain and heart. Reports show that microfluidic chips have a good similarity in the function with real organs in vivo therefore these tools were suitable for simulation of organs and drugs screening in laboratories.