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. Author manuscript; available in PMC: 2021 Mar 31.
Published in final edited form as: Nat Biomed Eng. 2020 Jan 27;4(4):421–436. doi: 10.1038/s41551-019-0498-9

Table 3.

Predictions of human PK parameters for oral nicotine (a) and intravenous cisplatin (b) obtained with the multi-Organ Chip IVIVT platform compared to clinical values and rodent clearance results.

a
Organ PK Parameters – Nicotine
PK Parameter Rodent
(in vivo)
Human
(Clinical
data)
In Silico Model
(Multi-Organ
Chips)
Gut Papp (10−6 m/s) NA 9.5 to 57.2 1.3 to 7.5 (δ=21-98%) ****
Liver Intrinsic Clearance, CLint (ml/min/kg.BW) 300 12.5 10.0 (δ=20 %)
8.004 (δ=36,0 %)
Secondary Intrinsic Clearance, CLint, sec (ml/min/kq.BW) NA 0.74 0.15 (δ=80,0 %)
Kidney Renal Clearance, CLR, (ml/min/kg.BW) 5.5 0.5 to 1.29 0.03 to 0.13 (δ=75-98%) ****
b
Organ PK Parameters - Cisplatin
PK Parameter Rodent
(in vivo)
Human
(Clinical
data)
In Silico Model
(Multi-Organ
Chips)
Liver Intrinsic Clearance, CLint (ml/min/kg.BW) 3.73 0.25 0.20=20,0 %)
Kidney Renal Clearance, CLR (ml/min/kg.BW) 0.19 1.39 0.008=99,4 %)

Comments for Table 3a.

*

In vivo data from Digard et al. 28 (human) and Yamazaki et al 35 (rodent)

**

AUC was computed for t=0 to 2hrs (i.e., times when clinical measurements were available) for both in vivo and in silico studies

Comments for Table 3b

*

In vivo data from Rajkumar et al. 39 (human) and Gong et al.69 (rodent) – where total cisplatin clearance was used for liver clearance and clearance out of tissue for kidney

****

Minimum to maximum % relative error in the interval