Emerging microfluidics-enabled platforms for osteoarthritis management: From benchtop to bedside

Osteoarthritis (OA) is a prevalent debilitating age-related joint degenerative disease. It is a leading cause of pain and functional disability in older adults. Unfortunately, there is no cure for OA once the damage is established. Therefore, it promotes an urgent need for early detection and interv...

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Bibliographic Details
Main Authors: Chen, Z. (Author), Luo, X. (Author), Wen, C. (Author), Zhang, Y.S (Author), Zou, Z. (Author)
Format: Article
Language:English
Published: Ivyspring International Publisher 2022
Subjects:
Online Access:View Fulltext in Publisher
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008 220420s2022 CNT 000 0 und d
020 |a 18387640 (ISSN) 
245 1 0 |a Emerging microfluidics-enabled platforms for osteoarthritis management: From benchtop to bedside 
260 0 |b Ivyspring International Publisher  |c 2022 
300 |a 19 
856 |z View Fulltext in Publisher  |u https://doi.org/10.7150/thno.62685 
520 3 |a Osteoarthritis (OA) is a prevalent debilitating age-related joint degenerative disease. It is a leading cause of pain and functional disability in older adults. Unfortunately, there is no cure for OA once the damage is established. Therefore, it promotes an urgent need for early detection and intervention of OA. Theranostics, combining therapy and diagnosis, emerges as a promising approach for OA management. However, OA theranostics is still in its infancy. Three fundamental needs have to be firstly fulfilled: i) a reliable OA model for disease pathogenesis investigation and drug screening, ii) an effective and precise diagnostic platform, and iii) an advanced fabrication approach for drug delivery and therapy. Meanwhile, microfluidics emerges as a versatile technology to address each of the needs and eventually boost the development of OA theranostics. Therefore, this review focuses on the applications of microfluidics, from benchtop to bedside, for OA modelling and drug screening, early diagnosis, and clinical therapy. We first introduce the basic pathophysiology of OA and point out the major unfilled research gaps in current OA management including lack of disease modelling and drug screening platforms, early diagnostic modalities and disease-modifying drugs and delivery approaches. Accordingly, we then summarize the state-of-the-art microfluidics technology for OA management from in vitro modelling and diagnosis to therapy. Given the existing promising results, we further discuss the future development of microfluidic platforms towards clinical translation at the crossroad of engineering and biomedicine. © The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. 
650 0 4 |a animal 
650 0 4 |a Animals 
650 0 4 |a Biosensing Techniques 
650 0 4 |a Biosensor 
650 0 4 |a disease model 
650 0 4 |a Disease Models, Animal 
650 0 4 |a Drug Evaluation, Preclinical 
650 0 4 |a genetic procedures 
650 0 4 |a human 
650 0 4 |a Humans 
650 0 4 |a Intra-articular injection 
650 0 4 |a microfluidics 
650 0 4 |a Microfluidics 
650 0 4 |a Microfluidics 
650 0 4 |a Organ-on-a-chip 
650 0 4 |a osteoarthritis 
650 0 4 |a Osteoarthritis 
650 0 4 |a Osteoarthritis 
650 0 4 |a pathophysiology 
650 0 4 |a personalized medicine 
650 0 4 |a point of care system 
650 0 4 |a Point-of-Care Systems 
650 0 4 |a Precision Medicine 
650 0 4 |a preclinical study 
700 1 0 |a Chen, Z.  |e author 
700 1 0 |a Luo, X.  |e author 
700 1 0 |a Wen, C.  |e author 
700 1 0 |a Zhang, Y.S.  |e author 
700 1 0 |a Zou, Z.  |e author 
773 |t Theranostics