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. 2021 Mar 17;117(14):2742–2754. doi: 10.1093/cvr/cvab088

Table 1.

Summary of the heart-on-chip platforms.

Aspects of human cardiac physiology and disease in organs-on-chips
Cardiac physiology Defined 3D tissue organization 43 , 48 , 61 , 62 , 64 , 135
Force of contraction 51 , 54 , 130 , 135
Electrophysiology 43 , 46 , 57 , 62 , 64 , 65 , 67 , 135
Cardiac-vascular interactions 44 , 46 , 62 , 135
Body-on-chip approach 54 , 130 , 135
Cardiac disease and toxicity Hypertrophy 61
Arrhythmia 47 , 49
Ischaemia 67
Fibrosis (e.g. fibroblast proliferation, collagen deposition, and valve calcification) 47 , 49
Inflammation 46 , 135
Cardiotoxicity & Pharmacology 43 , 44 , 46 , 51 , 54 , 61 , 62 , 64 , 65 , 130 , 135

The selection criteria employed in this table were that the devices used in the study could be considered a heart-on-a-chip device, i.e. a microfluidic device where the microenvironment of the cells or tissue in culture can be controlled and/or be stimulated mechanically and/or electrically. Platforms where constructs are cultured in well-plates or make use of spheroid technology were not considered due to the lack of their microfluidic character, which is seen as a requirement for organs-on-chips.