Objectives: To prepare and evaluate sustained release artemether-loaded SLMs based on SRMS Material and methods: SRMS, consisting of mixtures of Phospholipon® 90H (P90H) and Softisan® 154 (1:1, 2:1 and 1:2) were formulated and characterized using differential scanning calorimetry (DSC). The SRMS were used to formulate artemether-loaded SLMs by melt homogenization. The SLMs were characterized based on particle size and morphology, pH stability, encapsulation efficiency (EE%) and loading capacity. In vitro release was carried out in simulated intestinal fluid (SIF, pH 7.5). Results: Thermograms of the SRMS (1:1, 2:1 and 1:2) showed sharp endothermic peaks at 65.5, 64.4 and 62.3 oC respectively. Maximum EE% of 70.00 ± 1.50 % was obtained fo...
Purpose: To formulate and determine the release profile of zidovudine (AZT)-loaded solidified lipid ...
rtemether (ART) is second to artesunate in being the most widely used derivatives of artemisinin in ...
Objective: The poor water solubility of the drug presents a great challenge for the formulatio...
Purpose: To formulate and evaluate sustained-release indomethacin tablets based on solidified revers...
Highly lipophilic antimalarial drugs, artemether and lumefantrine, whilst an effective fixed-dose co...
For preparing nebivolol loaded solid lipid microparticles (SLMs) by the solvent evaporation microenc...
The objective of the present investigation was to formulate self-microemulsifying drug delivery syst...
Objective: Nasal delivery provides a route of entry of drug to the brain that circumvents the obstac...
Nanoparticle has emerged as a promising strategy for the efficient delivery of drugs used for the tr...
The objective of the present investigation was to explore the potential of nanostructured lipid carr...
β-Arteether, an effective artemisinin derivative, is used in the treatment of malaria but available ...
The aim of current work to develop and evaluate sustained release mucoadhesive (SRM) microspheres of...
The controlled release of drugs for pulmonary, delivery is a research field which has been so far ra...
Background: Artemether and lumefantrine display low aqueous solubility leading to poor release profi...
NLC topical formulation as an alternative to oral and parenteral (IM) delivery of artemether (ART), ...
Purpose: To formulate and determine the release profile of zidovudine (AZT)-loaded solidified lipid ...
rtemether (ART) is second to artesunate in being the most widely used derivatives of artemisinin in ...
Objective: The poor water solubility of the drug presents a great challenge for the formulatio...
Purpose: To formulate and evaluate sustained-release indomethacin tablets based on solidified revers...
Highly lipophilic antimalarial drugs, artemether and lumefantrine, whilst an effective fixed-dose co...
For preparing nebivolol loaded solid lipid microparticles (SLMs) by the solvent evaporation microenc...
The objective of the present investigation was to formulate self-microemulsifying drug delivery syst...
Objective: Nasal delivery provides a route of entry of drug to the brain that circumvents the obstac...
Nanoparticle has emerged as a promising strategy for the efficient delivery of drugs used for the tr...
The objective of the present investigation was to explore the potential of nanostructured lipid carr...
β-Arteether, an effective artemisinin derivative, is used in the treatment of malaria but available ...
The aim of current work to develop and evaluate sustained release mucoadhesive (SRM) microspheres of...
The controlled release of drugs for pulmonary, delivery is a research field which has been so far ra...
Background: Artemether and lumefantrine display low aqueous solubility leading to poor release profi...
NLC topical formulation as an alternative to oral and parenteral (IM) delivery of artemether (ART), ...
Purpose: To formulate and determine the release profile of zidovudine (AZT)-loaded solidified lipid ...
rtemether (ART) is second to artesunate in being the most widely used derivatives of artemisinin in ...
Objective: The poor water solubility of the drug presents a great challenge for the formulatio...