Objective: This present study aims to screen pharmaceutical cocrystal of Fenofibrate and coformers. Further the preparation and evaluation of fenofibrate-coformer cocrystal and In-Vitro drug release and Ex-Vivo Permeation study was done. Material and Methods: The coformers for Fenofibrate were screened using molecular docking. The cocrystals produced were characterized using Differential Scanning Calorimetry (DSC), X-ray diffraction (XRPD) study and Infrared spectroscopy. Results: Cocrystal of Fenofibrate with tartaric acid was successfully prepared. The cocrystals displayed enhanced dissolution rate by 2.36 fold, similarly the ex-vivo drug uptake through everted chicken intestine model was improved by 4.38 fold. The formation of cocr...
Acyclovir is an antiviral drug having potent activity against the virus of herpes family and varicel...
Objective: Most of the drugs are relevant BSC class II and class IV having solubility problem. Co-cr...
Potensi formulasi berasaskan sebaran pepejal menggunapakai Gelucire 44/14 sebagai pembawa untuk men...
The active moiety with poor solubility is posing a challenge in drug development which may reduce th...
Cocrystals are multicomponent system in which one component is Active Pharmaceutical Ingredient (API...
Water solubility and low bioavailability of active pharmaceutical ingredients are some of the main c...
In the current study, we attempted to improve the physicochemical properties of antiviral drug efavi...
Objective: Lansoprazole (LPZ) is a Biopharmaceutics Classification System Class II drug. It has low ...
Objective: Development of pharmaceutical co-crystals is an interesting area of research as co-crysta...
Objective: Cocrystals have been increasingly recognized as an attractive alternative for solid forms...
Objective: Cocrystallisation is a promising method in order to increase the solubility and dissoluti...
The present work deals with the development of cocrystal of ambrisentan (AMT) to improve its biophar...
In development of new product major constraints are poor aqueous solubility and low oral bioavailabi...
During drug research and development, improving the solubility of poorly water soluble drugs without...
Objective: The solubility of a drug in water plays an important role in the absorption of the drug a...
Acyclovir is an antiviral drug having potent activity against the virus of herpes family and varicel...
Objective: Most of the drugs are relevant BSC class II and class IV having solubility problem. Co-cr...
Potensi formulasi berasaskan sebaran pepejal menggunapakai Gelucire 44/14 sebagai pembawa untuk men...
The active moiety with poor solubility is posing a challenge in drug development which may reduce th...
Cocrystals are multicomponent system in which one component is Active Pharmaceutical Ingredient (API...
Water solubility and low bioavailability of active pharmaceutical ingredients are some of the main c...
In the current study, we attempted to improve the physicochemical properties of antiviral drug efavi...
Objective: Lansoprazole (LPZ) is a Biopharmaceutics Classification System Class II drug. It has low ...
Objective: Development of pharmaceutical co-crystals is an interesting area of research as co-crysta...
Objective: Cocrystals have been increasingly recognized as an attractive alternative for solid forms...
Objective: Cocrystallisation is a promising method in order to increase the solubility and dissoluti...
The present work deals with the development of cocrystal of ambrisentan (AMT) to improve its biophar...
In development of new product major constraints are poor aqueous solubility and low oral bioavailabi...
During drug research and development, improving the solubility of poorly water soluble drugs without...
Objective: The solubility of a drug in water plays an important role in the absorption of the drug a...
Acyclovir is an antiviral drug having potent activity against the virus of herpes family and varicel...
Objective: Most of the drugs are relevant BSC class II and class IV having solubility problem. Co-cr...
Potensi formulasi berasaskan sebaran pepejal menggunapakai Gelucire 44/14 sebagai pembawa untuk men...