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. 2021 Feb 1;157:105639. doi: 10.1016/j.ejps.2020.105639

Table 1.

Population pharmacokinetic parameters describing QDs disposition characteristics in blood (CL: clearance; V1: volume of distribution in central compartment; V2: volume of distribution in peripheral compartment; Q: the inter-compartmental clearance, CV: coefficient of variation, T1/2: elimination half-life).

Parameters Final model estimate % CV
CL (L/h) 0.0416 12
V1 (L) 0.0027 9
Q (L/h) 0.498 21
V2 (L) 0.068 17
Proportional error 0.0686 8
Additive error (ng/L) 0.05 (38%) 12
T1/2 (min) 28 -