The effects of binary and ternary systems of acetazolamide (ACZ) with hydroxypropyl-β-cyclodextrin (HP-β-CD) alone or with triethanolamine (TEA) on the crystalline properties, dissolution and intraocular pressure (IOP)-lowering effect were investigated. It was found that the crystal structure of ACZ powder could be modified by the processing conditions. Freeze-drying ACZ powder affected not only the particle morphology but also its polymorphic form and the starting ACZ was converted to pure form A upon freeze-drying treatment. Results provided by DSC/TGA, XRPD, SEM and FT-IR suggested the formation of inclusion complexes between ACZ with HP-β-CD alone or with TEA, obtained by the freeze-drying method and the conversion of the drug into the ...
The importance of polymorphism in pharmaceuticals makes its study relevant. The aim of this study wa...
Amorphization is a well-established strategy to enhance the dissolution properties of poorly water-s...
This study used actarit (ACT), an antirheumatic drug, to examine the molecular interaction of ACT an...
The present study is focused on the characterization of the interaction between trimethoprim, a dihy...
Triclabendazole is the first-line drug of choice to treat and control fasciolasis, a neglected paras...
The interaction of methotrexate (MTX) with beta-cyclodextrin (β-CD) in the presence of triethanolami...
Antiprotozoal tinidazole (TNZ) exhibits low aqueous solubility (Sw) and poor photochemical stability...
The main objective of this study was to investigate different manufacturing processes claimed to pro...
Triclabendazole belongs to the class II/IV of the Biopharmaceuticals Classification System, and its ...
Introduction: Cyclodextrins (CD), are known to form inclusion complexes with a variety of guest mole...
The aim of this study was to improve the solubility of chloramphenicol and reduce the production of ...
The purpose of this study was to improve the physicochemical and biological properties of chloramphe...
The rate-limiting step to drug absorption is often dissolution from the dosage form, especially for ...
A acetazolamida (ACZ) é um potente inibidor da anidrase carbônica, utilizado no tratamento de epilep...
Albendazole (ABZ) is a broad-spectrum antiparasitic drug used in the treatment of human or animal in...
The importance of polymorphism in pharmaceuticals makes its study relevant. The aim of this study wa...
Amorphization is a well-established strategy to enhance the dissolution properties of poorly water-s...
This study used actarit (ACT), an antirheumatic drug, to examine the molecular interaction of ACT an...
The present study is focused on the characterization of the interaction between trimethoprim, a dihy...
Triclabendazole is the first-line drug of choice to treat and control fasciolasis, a neglected paras...
The interaction of methotrexate (MTX) with beta-cyclodextrin (β-CD) in the presence of triethanolami...
Antiprotozoal tinidazole (TNZ) exhibits low aqueous solubility (Sw) and poor photochemical stability...
The main objective of this study was to investigate different manufacturing processes claimed to pro...
Triclabendazole belongs to the class II/IV of the Biopharmaceuticals Classification System, and its ...
Introduction: Cyclodextrins (CD), are known to form inclusion complexes with a variety of guest mole...
The aim of this study was to improve the solubility of chloramphenicol and reduce the production of ...
The purpose of this study was to improve the physicochemical and biological properties of chloramphe...
The rate-limiting step to drug absorption is often dissolution from the dosage form, especially for ...
A acetazolamida (ACZ) é um potente inibidor da anidrase carbônica, utilizado no tratamento de epilep...
Albendazole (ABZ) is a broad-spectrum antiparasitic drug used in the treatment of human or animal in...
The importance of polymorphism in pharmaceuticals makes its study relevant. The aim of this study wa...
Amorphization is a well-established strategy to enhance the dissolution properties of poorly water-s...
This study used actarit (ACT), an antirheumatic drug, to examine the molecular interaction of ACT an...