Fenofibrate is more effective drug as compared to other fibrates. But low bioavailability of it is due to its poor aqueous solubility. The purpose of present study was to improve fenofibrate dissolution through its formulation into liquisolid tablets and then to investigate in vitro performance of prepared liquisolid systems. By use of this technique, liquid medications such as solutions or suspensions of water insoluble drugs in suitable non-volatile liquid vehicles can be easily converted into powders with acceptable flow properties and compression behavior by using suitable powder excipients. X-ray powder diffraction and Differential Scanning Calorimetry were used for evaluation of physicochemical properties of Fenofibrate in liquisolid ...
Most of the newly developed drug candidates are lipophilic and poorly water-soluble. Enhancing the d...
The in-vitro dissolution property of poorly water soluble Carvedilol was improved by exploring the p...
This technique is based upon the admixture of drug loaded solutions with appropriate carrier and coa...
Fenofibrate is more effective drug as compared to other fibrates. But low bioavailability of it is d...
The present work deals with the comparison of in vitro dissolution profiles of fenofibrate liquisoli...
A liquisolid system has the ability to improve the dissolution properties of poorly water soluble d...
This project report is submitted in partial fulfilment of the requirements for the degree of Bachelo...
Numerous methods have been applied to improve drug release of pharmaceuticals, among which the liqui...
Liquisolid system is a novel concept of drug delivery via oral route. This technique is applied to w...
In this study the effect of liquisolid technique on the dissolution profile of spironolactone was ev...
ABSTRACT: Fenofibrate is a drug of the fibrate class. It is a widely used hypolipidemic drug. The po...
The in vitro dissolution property of poorly water soluble Tamoxifen citrate was improved by explorin...
A liquisolid system has the ability to improve the dissolution properties of poorly water-soluble dr...
In the drug development enhancement of oral bioavailability of poorly water soluble drugs is one of ...
According to the liquisolid methodology, liquid medications in solutions or suspension form of water...
Most of the newly developed drug candidates are lipophilic and poorly water-soluble. Enhancing the d...
The in-vitro dissolution property of poorly water soluble Carvedilol was improved by exploring the p...
This technique is based upon the admixture of drug loaded solutions with appropriate carrier and coa...
Fenofibrate is more effective drug as compared to other fibrates. But low bioavailability of it is d...
The present work deals with the comparison of in vitro dissolution profiles of fenofibrate liquisoli...
A liquisolid system has the ability to improve the dissolution properties of poorly water soluble d...
This project report is submitted in partial fulfilment of the requirements for the degree of Bachelo...
Numerous methods have been applied to improve drug release of pharmaceuticals, among which the liqui...
Liquisolid system is a novel concept of drug delivery via oral route. This technique is applied to w...
In this study the effect of liquisolid technique on the dissolution profile of spironolactone was ev...
ABSTRACT: Fenofibrate is a drug of the fibrate class. It is a widely used hypolipidemic drug. The po...
The in vitro dissolution property of poorly water soluble Tamoxifen citrate was improved by explorin...
A liquisolid system has the ability to improve the dissolution properties of poorly water-soluble dr...
In the drug development enhancement of oral bioavailability of poorly water soluble drugs is one of ...
According to the liquisolid methodology, liquid medications in solutions or suspension form of water...
Most of the newly developed drug candidates are lipophilic and poorly water-soluble. Enhancing the d...
The in-vitro dissolution property of poorly water soluble Carvedilol was improved by exploring the p...
This technique is based upon the admixture of drug loaded solutions with appropriate carrier and coa...