Ten compounds having different solubilities and molecular weights were evaluated for incorporation into Eudragit microspheres using the spherical crystallization technique, and the effects of drug-related factors on the properties of Eudragit microspheres were investigated. The entrapment of the active compound within the microspheres was highly dependent on the acidic or basic characteristics of the drug. Structural changes were also observed on the microsphere surface prepared at different pH values. Microspheres prepared with slightly and very slightly soluble drugs such as salicylic acid, naproxen, piroxicam, indomethacin, and methylprednisolone indicated controlled-release properties. Generally, drug release from microspheres followed ...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
Ketoprofen controlled release microspheres were prepared, by emulsion/solvent evaporation, at 15 deg...
In this work we developed pH‐sensitive microspherical dosage forms for poorly water soluble flavonoi...
Abstract: Ketoprofen microspheres were prepared by a solvent diffusion technique using Aerosil as an...
The aim was to prepare theophylline-loaded Eudragit RS 100 microsphere to achieve sustained release ...
The aim of this study was to prepare and evaluate Eudragit (RS and RL) microspheres containing aceta...
The present study aimed to improve solubility and prolong the release duration of a poorly soluble d...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
Eudragit E 100 and polycaprolactone (PCL) floating microspheres for enhanced gastric retention and d...
Drugs with different water-solubility and molecular weights were microencapsulated in cellulose acet...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release ...
Emulsion–solvent evaporation is an established method to fabricate amorphous drug-loaded micropartic...
Dipyridamole alginate-Eudragit microspheres were prepared by the emulsification technique of Monship...
The objective of this study was to encapsulate ibuprofen in microspheres based on a co-polymer of Eu...
The aim of this present work was to formulate microspheres of BCS Class II drug Celecoxib. The drug ...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
Ketoprofen controlled release microspheres were prepared, by emulsion/solvent evaporation, at 15 deg...
In this work we developed pH‐sensitive microspherical dosage forms for poorly water soluble flavonoi...
Abstract: Ketoprofen microspheres were prepared by a solvent diffusion technique using Aerosil as an...
The aim was to prepare theophylline-loaded Eudragit RS 100 microsphere to achieve sustained release ...
The aim of this study was to prepare and evaluate Eudragit (RS and RL) microspheres containing aceta...
The present study aimed to improve solubility and prolong the release duration of a poorly soluble d...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
Eudragit E 100 and polycaprolactone (PCL) floating microspheres for enhanced gastric retention and d...
Drugs with different water-solubility and molecular weights were microencapsulated in cellulose acet...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release ...
Emulsion–solvent evaporation is an established method to fabricate amorphous drug-loaded micropartic...
Dipyridamole alginate-Eudragit microspheres were prepared by the emulsification technique of Monship...
The objective of this study was to encapsulate ibuprofen in microspheres based on a co-polymer of Eu...
The aim of this present work was to formulate microspheres of BCS Class II drug Celecoxib. The drug ...
Purpose: The aim of this study was to formulate and evaluate microencapsulated controlled release pr...
Ketoprofen controlled release microspheres were prepared, by emulsion/solvent evaporation, at 15 deg...
In this work we developed pH‐sensitive microspherical dosage forms for poorly water soluble flavonoi...