<p>The directional transport of two drug analogues Imatinib (A) and INNO-406 (B) were determined in BBMEC. The apical-to-basolateral transport (A→B) (open circles) and basolateral-to-apical (B→A)(closed circles). The data are presented as percent transported as a function of time (means ± SD, n = 3). * Considered statistically significant (p<0.05).</p
Bidirectional transport studies were conducted using Caco-2, MDCK, and MDCK-MDR1 to determine P-gp i...
The bioavailability of orally administered imatinib is 90%, although the drug is monocationic under ...
The purpose of this work is to investigate several aspects of transporter-mediated interactions in a...
Transport of erlotinib, gefitinib, sorafenib, sunitinib, dasatinib and crizotinib can be active or p...
Purpose: This study aimed to characterize the transepithelial transport of miltefosine (HePC), the f...
<p>Transport was measured in the absence or presence of P-gp inhibitor zosuquidar or BCRP inhibitor ...
AbstractUnderstanding of the interactions between P-glycoprotein and multidrug resistance (MDR) reve...
The aim of this work was to conduct a comprehensive study about the transport properties of NSAIDs a...
Bidirectional transport studies were conducted using Caco-2, MDCK, and MDCK?MDR1 to determine P-gp ...
Receptor-mediated endocytosis (RME) has been extensively studied as a method for augmenting the tran...
Multidrug resistance (MDR) driven by ABC (ATP binding cassette) membrane transporters is one of the ...
The aim of this work was to conduct a comprehensive study about the transport properties of NSAIDs a...
<p>Comparison between the cleared volume vs. time graphs of internal standards for the transcellular...
Purpose: previous studies have shown that the rat small intestinal cell line IEC-18 provides a size-...
The kinetics of solute transport across cell monolayers is complex, and often consists of multiple a...
Bidirectional transport studies were conducted using Caco-2, MDCK, and MDCK-MDR1 to determine P-gp i...
The bioavailability of orally administered imatinib is 90%, although the drug is monocationic under ...
The purpose of this work is to investigate several aspects of transporter-mediated interactions in a...
Transport of erlotinib, gefitinib, sorafenib, sunitinib, dasatinib and crizotinib can be active or p...
Purpose: This study aimed to characterize the transepithelial transport of miltefosine (HePC), the f...
<p>Transport was measured in the absence or presence of P-gp inhibitor zosuquidar or BCRP inhibitor ...
AbstractUnderstanding of the interactions between P-glycoprotein and multidrug resistance (MDR) reve...
The aim of this work was to conduct a comprehensive study about the transport properties of NSAIDs a...
Bidirectional transport studies were conducted using Caco-2, MDCK, and MDCK?MDR1 to determine P-gp ...
Receptor-mediated endocytosis (RME) has been extensively studied as a method for augmenting the tran...
Multidrug resistance (MDR) driven by ABC (ATP binding cassette) membrane transporters is one of the ...
The aim of this work was to conduct a comprehensive study about the transport properties of NSAIDs a...
<p>Comparison between the cleared volume vs. time graphs of internal standards for the transcellular...
Purpose: previous studies have shown that the rat small intestinal cell line IEC-18 provides a size-...
The kinetics of solute transport across cell monolayers is complex, and often consists of multiple a...
Bidirectional transport studies were conducted using Caco-2, MDCK, and MDCK-MDR1 to determine P-gp i...
The bioavailability of orally administered imatinib is 90%, although the drug is monocationic under ...
The purpose of this work is to investigate several aspects of transporter-mediated interactions in a...