License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The main objectives of this study were (a) to evaluate the in vitro performance of the rapid disintegration tablets as a way to improve the solid dispersions and (b) to study the in vivo pharmacokinetics of the albendazole modified formulation in dogs. Rapid disintegration of tablets seems to be a key factor for efficiency of solid dispersions with regard to improvement of the albendazole bioavailability. The in vivo assays performed on dogs showed a marked increase in drug plasma exposure when albendazole was given in solid dispersions incorporated into rapid disintegration tablets compared with conventional ...
Abstract: The aim of the study has been evaluation of the pharmacokinetics of fenbendazole molecule,...
Poor aqueous solubility of drugs results in poor absorption and bioavailability. The objective...
Name: Ivan Vokřál Title: On pharmacokinetic of single administration of albendazole in mouflon (Ovis...
The main objectives of this study were (a) to evaluate the in vitro performance of the rapid disinte...
Albendazole is an oral broad spectrum anthelmintic, antiparasitic agent generally prescribed for the...
New therapeutic strategies based on the search of alternative formulations of albendazole (ABZ) and ...
Background: Flubendazole, originally developed to treat infections with intestinal nematodes, has be...
Fenbendazole was administered to dogs at a dose rate of 20 mg/kg body weight on a single occasion in...
The plasma disposition of fenbendazole (FBZ), oxfendazole (OFZ) and albendazole (ABZ); and the enant...
Benzimidazole (BZD) and pro-BZD drugs are used widely produced by oxidation and hydrolysis, are all ...
BackgroundFlubendazole, originally developed to treat infections with intestinal nematodes, has been...
Tinidazole mouth dissolving tablet were prepared to achieve quick onset of action and for maximum bi...
Hydatid disease occurs in most areas of the world and currently affects about one million people. Al...
ABSTRACT: The purpose of the study was to prepare orally disintegrating tablets (ODTs) of mosapride ...
Low solubility and dissolution rate are the primary challenges in the drug development which substan...
Abstract: The aim of the study has been evaluation of the pharmacokinetics of fenbendazole molecule,...
Poor aqueous solubility of drugs results in poor absorption and bioavailability. The objective...
Name: Ivan Vokřál Title: On pharmacokinetic of single administration of albendazole in mouflon (Ovis...
The main objectives of this study were (a) to evaluate the in vitro performance of the rapid disinte...
Albendazole is an oral broad spectrum anthelmintic, antiparasitic agent generally prescribed for the...
New therapeutic strategies based on the search of alternative formulations of albendazole (ABZ) and ...
Background: Flubendazole, originally developed to treat infections with intestinal nematodes, has be...
Fenbendazole was administered to dogs at a dose rate of 20 mg/kg body weight on a single occasion in...
The plasma disposition of fenbendazole (FBZ), oxfendazole (OFZ) and albendazole (ABZ); and the enant...
Benzimidazole (BZD) and pro-BZD drugs are used widely produced by oxidation and hydrolysis, are all ...
BackgroundFlubendazole, originally developed to treat infections with intestinal nematodes, has been...
Tinidazole mouth dissolving tablet were prepared to achieve quick onset of action and for maximum bi...
Hydatid disease occurs in most areas of the world and currently affects about one million people. Al...
ABSTRACT: The purpose of the study was to prepare orally disintegrating tablets (ODTs) of mosapride ...
Low solubility and dissolution rate are the primary challenges in the drug development which substan...
Abstract: The aim of the study has been evaluation of the pharmacokinetics of fenbendazole molecule,...
Poor aqueous solubility of drugs results in poor absorption and bioavailability. The objective...
Name: Ivan Vokřál Title: On pharmacokinetic of single administration of albendazole in mouflon (Ovis...