Liver-on-a-chip |
iPSCs derived liver organoids |
Drug induced acute hepatotoxicity |
Acetaminophen (APAP) |
Liver on a chip for the generation and in situ
differentiation of liver organoids |
Cell viability |
Wang et al.
20
|
iPSCs derived liver organoids |
Nonalcoholic fatty liver disease |
Free fatty acids |
Cell viability, lipid accumulation and metabolism, oxidative
stress, inflammatory responses, and fibrosis |
Wang et al.
21
|
iPSCs derived hepatocytes and EA.hy926, LX-2, and THP-1 |
Drug induced acute hepatotoxicity |
Terfenadine, Tolcapone, Trovafloxacin, Troglitazone,
Rosiglitazone, Pioglitazone, and caffeine |
Nortis Bio™ microfluidic liver on a chip |
Cell viability, albumin, urea, lactate dehydrogenase (LDH),
tumor necrosis factor (TNF)-α, and fraction unbound for each
drug |
Sakolish et al.
22
|
iPSCs derived hepatocytes, THP-1, and HMEC-1 |
Drug induced acute hepatotoxicity |
Troglitazone |
OrganoPlate LiverTox™, 3D microfluidic liver on a
chip |
Albumin and urea production, hepatocyte nuclear
size, and viability. |
Bircsak et al.
23
|
159 compounds from the SCREEN-WELL library |
Dose-response study TC50 values for viability and
albumin assays |
Kidney-on-a-chip |
iPSCs derived kidney podocytes |
Albuminuria and podocyte injury |
Adriamycin |
Kidney glomerulus on a chip |
Cell adhesion, uptake of exogenous albumin, glomerular
filtration of albumin and inulin |
Musah et al.
24
and Jain
25
|
iPSCs derived kidney podocytes and endothelial cells |
Podocyte injury and delamination, urinary clearance of
albumin |
Jain
25
|
Gut-on-a-chip |
iPSCs derived intestinal organoids |
Inflammatory bowel disease |
Tumor necrosis factor (TNF)-α and interferon (IFN)-γ |
Intestine on a chip |
Cell viability, permeability, intestinal epithelial
response |
Workman et al.
26
|
iPSCs derived intestinal organoid tubules |
Inflammatory bowel disease |
IL-1β, IFN-γ and TNF-α |
Organo Plate™ for the in situ differentiation of intestinal-like
cells |
Cytokine responsiveness of interleukins |
Naumovska et al.
27
|
Heart-on-a-chip |
iPSCs derived cardiac spheroids |
Influence of compounds on cardiac cell growth |
Doxorubicin, Endothelin-1, Acetylsalicylic acid, Isoproterenol,
Phenylephrine, Amiodarone |
Cardiac spheroid on a chip |
Cell number |
Christoffersson et al.28,29
|
iPSCs derived cardiomyocytes |
Low blood pressure and heart failure |
Norepinephrine |
Heart-on-a-chip platform with integrated interpenetrating
sensors arrays for contractility and electrophysiology
recording |
Contractile force and electrical conductivity |
Qian et al.
30
|
miPSC derived cardiomyocytes |
Bradycardia or heart block |
Isoprenaline |
Heart-on-a-chip platform with an integrated pneumatic actuation
system for the induction of homogeneous uniaxial cyclic strains
to the 3D cell construct |
Contraction rate |
Marsano et al.
31
|
iPSC derived cardiomyocytes and human umbilical vein
endothelial cells HUVECs |
Drug induced cardiotoxicity |
Dexorubicin |
Endothelialized myocardium on a chip based on HUVECs
encapsulated inside the bioprinted microfibrous hydrogel
scaffold and cardiomyocytes seeded into the interstitial spaces
of the scaffold |
Beating rate and levels of secreted von Willebrand (vWF) |
Zhang et al.
32
|
iPSC derived cardiomyocytes |
Drug-induced changes in heart rate |
Isoproterenol |
Heart-on-a-chip device featuring micromolded gelatin multi
electrode arrays (MEA) |
Beating rate and rate correlated field potential duration |
Kujala et al.
33
|
iPSC derived cardiomyocytes |
Drug-induced changes in heart rate |
Isoproterenol |
Heart-on-a-chip platform, scaffold free, centrifugally assisted
cell loading procedure |
Beating rate and beating kinetics by optical mean |
Schneider et al.
34
|
iPSC derived cardiomyocytes and human umbilical vein
endothelial cells HUVECs |
Alteration in vascular permeability, Bradycardia and drug
induced cardiotoxicity |
TNF-α, Isoproterenol, TNF-α + Isoproterenol |
Microfluidic device with integrated TEER electrodes and multi
electrodes array (MEA) |
TEER measure in the endothelial layer, cardiac beat rate and
corrected field potential duration (cFPD) |
Maoz et al.
35
|
Cardiac microtissue composed of iPSC derived cardiomyocytes,
vascular endothelial and mural cells |
Drug-induced changes in heart rate |
Isoproterenol |
Heart-on-a-chip device with microelectromechanical system
(MEMS)-based microfluidic chips |
Beating rate, particle displacement in the presence of changes
in pulsation frequency |
Abulaiti et al.
36
|