TABLE II.
Select studies on multi-organ-on-a-chip platforms involving the gut.
Authors | Type of the chip | Example case study |
---|---|---|
Choe et al.142 | Gut-liver | First pass metabolism of apigenin |
Lee et al.143 | Gut-liver | Gut absorption and liver metabolism of fatty acids |
De Gregorio et al.144 | Intestine-liver | First pass metabolism of ethanol and the resulting hepatic damage |
Chen et al.145 | Intestine-liver | Urea and albumin metabolism and CYP enzyme activity |
Chen et al.146 | Gut-liver | Inflammatory inter-tissue crosstalk |
Maschmeyer et al.147 | Liver-intestine | Repeated dose administration of troglitazone |
Prot et al.148 | Intestine-liver | First pass metabolism of paracetamol |
Kim et al.149 | Gut-brain axis | Exosomes transport across the gut barrier toward the blood-brain barrier |
Lee et al.150 | Gut-kidney | Antibiotic treatment effect on hemolytic uremic syndrome in Shiga-producing E. coli infection |
Lee et al.151 | Gut-skin | The effect of gut-absorbed fatty acids on the skin upon gut inflammation |
Kimura et al.152 | Lung-intestine-liver | The pharmacokinetics studies of three anticancer drugs-epirubicine (EPI), irinotecan (CPT-11), cyclophosphamide (CPA) |
Ramme et al.153 | Intestine-liver-brain-kidney | Generation of four organs from induced pluripotent stem cells |
Vernetti et al.154 | Intestine-liver-kidney-blood brain barrier-skeletal muscle | Absorption, metabolism, and excretion of terfenadine, trimethylamine (TMA), and vitamin D3 |
Imura et al.155 | Intestine-liver-cancerous breast | Absorption, metabolism, and bioactivity of cyclophosphamide, epirubicin, 17-β estradiol, and soy isoflavone |