Solid dispersions of artemether and polyethylene glycol 6000 (PEG6000) were prepared in ratio 12 : 88 (group-1). Self-emulsified solid dispersions of artemether were prepared by using polyethylene glycol 6000, Cremophor-A25, olive oil, Transcutol, and hydroxypropyl methylcellulose (HPMC) in ratio 12 : 75 : 5 : 4 : 2 : 2, respectively (group-2). In third group, only Cremophor-A25 was replaced with Poloxamer 188 compared to group-2. The solid dispersions and self-emulsified solid dispersions were prepared by physical and freeze dried methods, respectively. All samples were characterized by X-ray diffraction, attenuated total reflectance Fourier transform infrared spectroscopy, differential scanning calorimeter, scanning electron microscopy, a...
ABSTRACTObjective: This study was undertaken to devise the best way to incorporate artemether-lumefa...
AbstractThe aim of this study was to investigate and characterize different crystal forms of arteeth...
The main objective of the present work was to enhance the solubility and dissolution rate of poorly ...
Copyright © 2015 Muhammad Tayyab Ansari et al. This is an open access article distributed under the ...
Introduction: Artemether, a BCS class IV drug (poorly water soluble and poorly permeable, less bioav...
Artemether (ARM) is a poorly water soluble and poorly permeable drug effective against acute and sev...
AbstractArtemether (ARM) is a poorly water soluble and poorly permeable drug effective against acute...
Purpose: To investigate experimentally the inclusion of artemether into the cavity of hydroxypropyl...
The aim of this study was to investigate the industrial feasibility of developing a co-formulated so...
The purpose of this work was to develop rapidly disintegrating tablet (RDT) of artemether-lumefantri...
Aim: The objective of the current study is to increase the dissolution rate of cefuroxime axetil (CA...
Artemether and lumefantrine are anitmalarial drugs used in the management of malaria. The objective ...
Poor aqueous solubility is often linked with a poor dissolution rate and ultimately, limited bioavai...
This study was aimed to fabricate and evaluate a combination of Artemether and Lumefantrine as table...
Objective: The aim of this study was to formulate and evaluate a taste-masked formulation using hot ...
ABSTRACTObjective: This study was undertaken to devise the best way to incorporate artemether-lumefa...
AbstractThe aim of this study was to investigate and characterize different crystal forms of arteeth...
The main objective of the present work was to enhance the solubility and dissolution rate of poorly ...
Copyright © 2015 Muhammad Tayyab Ansari et al. This is an open access article distributed under the ...
Introduction: Artemether, a BCS class IV drug (poorly water soluble and poorly permeable, less bioav...
Artemether (ARM) is a poorly water soluble and poorly permeable drug effective against acute and sev...
AbstractArtemether (ARM) is a poorly water soluble and poorly permeable drug effective against acute...
Purpose: To investigate experimentally the inclusion of artemether into the cavity of hydroxypropyl...
The aim of this study was to investigate the industrial feasibility of developing a co-formulated so...
The purpose of this work was to develop rapidly disintegrating tablet (RDT) of artemether-lumefantri...
Aim: The objective of the current study is to increase the dissolution rate of cefuroxime axetil (CA...
Artemether and lumefantrine are anitmalarial drugs used in the management of malaria. The objective ...
Poor aqueous solubility is often linked with a poor dissolution rate and ultimately, limited bioavai...
This study was aimed to fabricate and evaluate a combination of Artemether and Lumefantrine as table...
Objective: The aim of this study was to formulate and evaluate a taste-masked formulation using hot ...
ABSTRACTObjective: This study was undertaken to devise the best way to incorporate artemether-lumefa...
AbstractThe aim of this study was to investigate and characterize different crystal forms of arteeth...
The main objective of the present work was to enhance the solubility and dissolution rate of poorly ...