Purpose . General use of nucleoside analogues in the treatment of viral infections and cancer is often limited by poor oral absorption. Valacyclovir, a water soluble amino acid ester prodrug of acyclovir has been reported to increase the oral bioavailability of acyclovir but its absorption mechanism is unknown. This study characterized the intestinal absorption mechanism of 5′-amino acid ester prodrugs of the antiviral drugs and examined the potential of amino acid esters as an effective strategy for improving oral drug absorption.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/41466/1/11095_2004_Article_303953.pd
A major challenge in drug development is the optimization of intestinal absorption and cellular upta...
The purpose is to identify transporters for drug absorption evaluation, prodrug design and in vivo/i...
5'-O-Dipeptide ester prodrugs of antiviral zidovudine (AZT) were designed to target the human intest...
Objectives. Peptide transporters have broad substrate specificity and could be a good target for che...
AbstractNucleoside analogues are first line chemotherapy in various severe diseases: AIDS (acquired ...
Nucleoside analogues are first line chemotherapy in various severe diseases: AIDS (acquired immunode...
The transport of valacyclovir, the L-valyl ester of acyclovir, has been suggested to be mediated by ...
Peramivir was a novel and highly potent neuraminidase (NA) inhibitor for the treatment of influenza ...
While active against Herpesviridae, oral aciclovir is limited by low and inconsistent bioavailabilit...
While active against Herpesviridae, oral aciclovir is limited by low and inconsistent bioavailabilit...
The primary objective of this study was to determine the in vivo absorption properties of valacyclov...
The purpose of this study was to quantitatively determine the contribution of PepT1 [peptide transpo...
Purpose . This study characterized the cellular uptake mechanism and hydrolysis of the amino acid es...
Poor systemic concentrations of lopinavir (LPV) following oral administration occur due to high cell...
ABSTRACT Despite peptide transporter 1 (PEPT1) being responsible for the bioavailability for a varie...
A major challenge in drug development is the optimization of intestinal absorption and cellular upta...
The purpose is to identify transporters for drug absorption evaluation, prodrug design and in vivo/i...
5'-O-Dipeptide ester prodrugs of antiviral zidovudine (AZT) were designed to target the human intest...
Objectives. Peptide transporters have broad substrate specificity and could be a good target for che...
AbstractNucleoside analogues are first line chemotherapy in various severe diseases: AIDS (acquired ...
Nucleoside analogues are first line chemotherapy in various severe diseases: AIDS (acquired immunode...
The transport of valacyclovir, the L-valyl ester of acyclovir, has been suggested to be mediated by ...
Peramivir was a novel and highly potent neuraminidase (NA) inhibitor for the treatment of influenza ...
While active against Herpesviridae, oral aciclovir is limited by low and inconsistent bioavailabilit...
While active against Herpesviridae, oral aciclovir is limited by low and inconsistent bioavailabilit...
The primary objective of this study was to determine the in vivo absorption properties of valacyclov...
The purpose of this study was to quantitatively determine the contribution of PepT1 [peptide transpo...
Purpose . This study characterized the cellular uptake mechanism and hydrolysis of the amino acid es...
Poor systemic concentrations of lopinavir (LPV) following oral administration occur due to high cell...
ABSTRACT Despite peptide transporter 1 (PEPT1) being responsible for the bioavailability for a varie...
A major challenge in drug development is the optimization of intestinal absorption and cellular upta...
The purpose is to identify transporters for drug absorption evaluation, prodrug design and in vivo/i...
5'-O-Dipeptide ester prodrugs of antiviral zidovudine (AZT) were designed to target the human intest...