The objective of this study was to improve the dissolution rate of a poor water soluble drug, piroxicam, by solid dispersion technique. Solid dispersions were prepared by three different methods depending on the type of carrier. The dissolution rate of piroxicam was markedly increased in solid dispersion of myrj 52, Eudragit E100 and mannitol. Solubility studies revealed a marked increase in the solubility of piroxicam with an increase in myrj 52 and Eudragit E100 concentrations. Data from the X-ray diffraction and FT-IR spectroscopy showed that piroxicam was amorphous in the solid dispersions prepared with dextrin and Eudragit E100
This investigation aimed to enhance the solubility and bioavailability of the BCS class II poorly wa...
Piroxicam is a nonsteroidal anti-inflammatory drug with low aqueous solubility which exhibits polymo...
The potential of liquisolid systems to improve the dissolution properties of a water-insoluble agent...
The objective of this study was to improve the dissolution rate of a poor water soluble drug, piroxi...
Introduction: The main objective of this study was preparation and characterization of solid dispers...
Background and purpose: Piroxicam is a non-steroidal anti- inflammatory drug that is characterized b...
Development and characterization of solid dispersion of piroxicam for improvement of dissolution rat...
The solid dispersion technique is one of the most effective methods for improving the dissolution ra...
Improving oral bioavailability of drugs those given as solid dosage forms remains a challenge for th...
ABSTRACT Piroxicam is a long acting potent NSAID with inflammatory potency and good analgesic-antipy...
\ud \ud It is hoped that solid dispersion and recrystalization can solve the problem of low solubili...
Several biologically relevant phospholipids were assessed as potential carriers/additives for rapidl...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
Objective: This research was aimed to increase the intrinsic dissolution rate (IDR) of piroxicam wi...
This investigation aimed to enhance the solubility and bioavailability of the BCS class II poorly wa...
This investigation aimed to enhance the solubility and bioavailability of the BCS class II poorly wa...
Piroxicam is a nonsteroidal anti-inflammatory drug with low aqueous solubility which exhibits polymo...
The potential of liquisolid systems to improve the dissolution properties of a water-insoluble agent...
The objective of this study was to improve the dissolution rate of a poor water soluble drug, piroxi...
Introduction: The main objective of this study was preparation and characterization of solid dispers...
Background and purpose: Piroxicam is a non-steroidal anti- inflammatory drug that is characterized b...
Development and characterization of solid dispersion of piroxicam for improvement of dissolution rat...
The solid dispersion technique is one of the most effective methods for improving the dissolution ra...
Improving oral bioavailability of drugs those given as solid dosage forms remains a challenge for th...
ABSTRACT Piroxicam is a long acting potent NSAID with inflammatory potency and good analgesic-antipy...
\ud \ud It is hoped that solid dispersion and recrystalization can solve the problem of low solubili...
Several biologically relevant phospholipids were assessed as potential carriers/additives for rapidl...
Solid dispersions have been employed as a method to improve the dissolution rate and hence the bioav...
Objective: This research was aimed to increase the intrinsic dissolution rate (IDR) of piroxicam wi...
This investigation aimed to enhance the solubility and bioavailability of the BCS class II poorly wa...
This investigation aimed to enhance the solubility and bioavailability of the BCS class II poorly wa...
Piroxicam is a nonsteroidal anti-inflammatory drug with low aqueous solubility which exhibits polymo...
The potential of liquisolid systems to improve the dissolution properties of a water-insoluble agent...