A simple model for the simultaneous passive membrane transport and bioconversion of a drug, which may be a weak electrolyte or a neutral molecule, is mathematically described. It includes an aqueous diffusion layer and an operational aqueous pore pathway. The applicability of the model is shown for the in situ rat intestinal transport of prostaglandin F2a.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/21678/1/0000066.pd
Oral drug administration remains the most popular route of drug delivery. Absorption of the dissolve...
A reasonably realistic physical model has been described for the simultaneous longitu-dinal spreadin...
A model analysis of the process of carrier mediated membrane transport is presented, wherein the car...
Ph.D.PharmacologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue...
A computational approach has been presented for modeling simultaneous diffusion and metabolism in bi...
PhDPharmacologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.l...
A physical model is described for the simultaneous enzymatic bioconversion of a nonelectrolyte solut...
A reasonably realistic physical model has been described for the simultaneous longitudinal spreading...
Some general physical models are described for the diffusional transport of drugs across membranes o...
This study aimed to construct a new local pharmacokinetic model of gastrointestinal absorption, the ...
To describe quantitatively the peritoneal transport of drugs, the kinetic model, which involves chan...
A reasonably realistic physical model has been described for the simultaneous longitudinal spreading...
The single-pass intestinal perfusion technique has been used extensively to estimate the wall permea...
PhDPharmacologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.l...
Passive movement of lipids through a membrane-embedded pore is analysed with kinetic equations of tr...
Oral drug administration remains the most popular route of drug delivery. Absorption of the dissolve...
A reasonably realistic physical model has been described for the simultaneous longitu-dinal spreadin...
A model analysis of the process of carrier mediated membrane transport is presented, wherein the car...
Ph.D.PharmacologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue...
A computational approach has been presented for modeling simultaneous diffusion and metabolism in bi...
PhDPharmacologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.l...
A physical model is described for the simultaneous enzymatic bioconversion of a nonelectrolyte solut...
A reasonably realistic physical model has been described for the simultaneous longitudinal spreading...
Some general physical models are described for the diffusional transport of drugs across membranes o...
This study aimed to construct a new local pharmacokinetic model of gastrointestinal absorption, the ...
To describe quantitatively the peritoneal transport of drugs, the kinetic model, which involves chan...
A reasonably realistic physical model has been described for the simultaneous longitudinal spreading...
The single-pass intestinal perfusion technique has been used extensively to estimate the wall permea...
PhDPharmacologyUniversity of Michigan, Horace H. Rackham School of Graduate Studieshttp://deepblue.l...
Passive movement of lipids through a membrane-embedded pore is analysed with kinetic equations of tr...
Oral drug administration remains the most popular route of drug delivery. Absorption of the dissolve...
A reasonably realistic physical model has been described for the simultaneous longitu-dinal spreadin...
A model analysis of the process of carrier mediated membrane transport is presented, wherein the car...