Albendazole (ABZ) is an effective anthelmintic and an anticancer candidate. Due to the low oral bioavailability associated with its poor aqueous solubility, high doses are required, and dose-related side effects are reported. To enhance ABZ dissolution different formulation approaches were proposed, among others, its combination with cyclodextrins. In this work, co-precipitation of β-cyclodextrin and ABZ was performed by supercritical antisolvent technique as an alternative preparation technique. The operating temperature and pressure of the experiments were selected by thermodynamic modeling in order to obtain a miscible solution between solvent mixture (DMSO+acetone) and CO2. Precipitated microparticles were characterized by spectroscopic...
The aim of the present review is to summarize and discuss the main strategies for addressing the poo...
In this work, β-cyclodextrin (β-CD) was used as a carrier to produce inclusion complexes containing ...
The aim of this study was to enhance the apparent solubility and dissolution properties of flurbipro...
The main objective of this study was to investigate different manufacturing processes claimed to pro...
Novel complexes of two different solid forms of Albendazol and β-cyclodextrin were investigated in a...
Albendazole (ABZ) is a broad-spectrum antiparasitic drug used in the treatment of human or animal in...
The potential use of natural cyclodextrins and their synthetic derivatives have been studied extensi...
Albendazole, an effective broad-spectrum anthelmintic agent, showed unpredictable therapeutic respon...
peer reviewedPURPOSE: The aim of the study is to evaluate the effect of different acidic compounds o...
<p>Econazole is an imidazole antifungal drug used in the treatment of mycotic infections. It has a v...
The rate-limiting step to drug absorption is often dissolution from the dosage form, especially for ...
The main objective of this study was to investigate different manufacturing processes claimed to pro...
The purpose of this study was to evaluate a single-step, organic solvent-free supercritical fluid pr...
In this work, rutin (RUT)–β-cyclodextrin (β-CD) inclusion complexes are prepared by Supercritical An...
Triclabendazole is the first-line drug of choice to treat and control fasciolasis, a neglected paras...
The aim of the present review is to summarize and discuss the main strategies for addressing the poo...
In this work, β-cyclodextrin (β-CD) was used as a carrier to produce inclusion complexes containing ...
The aim of this study was to enhance the apparent solubility and dissolution properties of flurbipro...
The main objective of this study was to investigate different manufacturing processes claimed to pro...
Novel complexes of two different solid forms of Albendazol and β-cyclodextrin were investigated in a...
Albendazole (ABZ) is a broad-spectrum antiparasitic drug used in the treatment of human or animal in...
The potential use of natural cyclodextrins and their synthetic derivatives have been studied extensi...
Albendazole, an effective broad-spectrum anthelmintic agent, showed unpredictable therapeutic respon...
peer reviewedPURPOSE: The aim of the study is to evaluate the effect of different acidic compounds o...
<p>Econazole is an imidazole antifungal drug used in the treatment of mycotic infections. It has a v...
The rate-limiting step to drug absorption is often dissolution from the dosage form, especially for ...
The main objective of this study was to investigate different manufacturing processes claimed to pro...
The purpose of this study was to evaluate a single-step, organic solvent-free supercritical fluid pr...
In this work, rutin (RUT)–β-cyclodextrin (β-CD) inclusion complexes are prepared by Supercritical An...
Triclabendazole is the first-line drug of choice to treat and control fasciolasis, a neglected paras...
The aim of the present review is to summarize and discuss the main strategies for addressing the poo...
In this work, β-cyclodextrin (β-CD) was used as a carrier to produce inclusion complexes containing ...
The aim of this study was to enhance the apparent solubility and dissolution properties of flurbipro...