Sentence examples for mean absorption time from inspiring English sources

Mean absorption time was 1988.7 min and bioavailability was 95%.

Mean absorption time (MAT) after s.c. dosing was also prolonged (p = 0.006).

Pharmacokinetic characteristics (absolute bioavailability, Tmax, Cmax and mean absorption time) were determined by compartmental and non-compartmental analysis.

On the other hand, no significant differences were observed between the two formulations with regard to the mean residence time, the mean absorption time, and the rate of absorption.

For IND and BSP, their observed permeation profiles were comparable and their MAT (mean absorption time) showed no significant difference, which both demonstrated these two drugs achieved the synchronous skin permeation in their compound patch by the dual-directional regulation strategy of combining the technique of ion-pair complexation with chemical enhancers.

Similarly, Forbes et al. (Forbes et al. 2015) noted a clear correlation between solubility and mean absorption time in man for these compounds.

In our derivations of sojourn and mean absorption times, we assumed QLE.

As expected, the approximate mean absorption times based on the assumption of p0 small (t ¯ ˜ QLE and t ¯ ˜ QLE, ρ ≫ 0 ) deviate further from their exact conterparts (t ¯ QLE and t ¯ QLE, ρ ≫ 0, respectively) as Ne increases from 100to1010. See also Table S6 and S7.

Parameter estimates were reliable with small RSEs (Table 2), except for the mean absorption transit time which displayed a high RSE (106%) as few samples were collected during the absorption phase.

Standard diffusion theory predicts that the mean absorption (extinction) time of C1 is approximately t ¯ ˜ neut = N e − 1 ∫ 1 / (2 N ) 1 n − 1 (1 − n ) 2 μ − 1 d n (Ewens 2004, pp. 171 175).

Oral panobinostat demonstrated rapid absorption (time to Cmax <2 h), with a mean Cmax of 71 ng/mL at 60 mg [ 17].