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A two-compartment pharmacokinetic model with a dosing compartment was used to describe the plasma concentration profile of TFV after oral administration of TDF.
Set to zero after ndoses ; administered dosingperiod = if time < ndoses*dose_int-DT then 1 else 0 input = pulse(dose,0,dose_int)*dosingperiod d/dt(comp1)=-ka*comp1 +input ; dosing compartment d/dt blood)=+ka*comp1 -ke*blood ; blood compartment init comp1 = 0 init blood = 0 One may want to copy the code into an "Equation Window" in Berkeley Madonna and run it.
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This model assumes that the appearance of the drug in a dose compartment is described by a zero-order process over a fixed duration (D).
The delayed absorption of once daily tacrolimus was best described with three transit compartments: a first-order rate constant describing the transfer from the dose compartment into the transit compartments and finally into the central compartment (Fig. 1).
The delayed absorption of everolimus and tacrolimus was best described with a lag time, and the delayed absorption of cyclosporine was best described with a transit compartment, using a first-order rate constant describing the transfer from the dose compartment into the transit compartment and subsequently into the central compartment.
The variability in the delayed absorption of CsA could best be described with a transit compartment, using a first-order rate constant describing the transfer from the dose compartment into the transit compartment and subsequently into the central compartment (Fig. 1).
Begin filling the smaller compartment (the dosing tank) with incoming beer, and mix it with DE powder.
Topics covered include one compartment single dose administration (iv bolus, oral, short infusion), intravenous infusion, repeated doses, renal and hepatic clearance, nonlinear elimination, two compartment model, plasma protein binding and the relationship between pharmacokinetics and drug effect.
Thus, the computation of the compartment absorbed doses will require an accurate measure of the total delivered activity.
The 14C-labelled tested substance (0.1 µCi/ml) was only present in the donor compartment ("infinite dose assay" [23]), facing the internal surface of the skin; so the flux from body side to external medium was measured.
In a homogeneous cohort of 25 patients with metastatic colorectal carcinoma (mCRC), we found that the calculated absorbed doses to the tumour compartment (DT) and to the functional liver compartment (DFL-TOT) are significantly correlated with efficacy and toxicity.
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