The anionic surfactant sodium dodecylsulfate (SDS) has improved the physical stability of flurbiprofen (FBP) suspension, which was suspended by 0.2% (w/v) hydroxypropylmethyl cellulose (HPMC, K4M). Therefore, the physical stability of FBP suspensions and the interaction of HPMC/SDS were studied, and a certain association between them was revealed. The anti-solvent precipitation method was used to prepare suspensions. The apparent drug concentration from different sites was evaluated to get the dispersion of drug actually. The process of flocculation and deflocculation with the addition of SDS was caught by analyzing the morphology of the suspended particles. The physical stability of the FBP suspensions was characterized mainly by measuring...
In order to investigate the effects of solid carriers on the crystalline properties, dissolution and...
Mixtures of polymers and surfactants are commonly found in a range of products of pharmaceutical,...
The poor aqueous solubility of hydrophobic drugs has always been a challenge for formulation scienti...
To develop a novel flurbiprofen-loaded solid dispersion without crystalline change, various flurbipr...
<div><p>ABSTRACT The intent of the current work is to study the effect of polyethylene glycol 8000 a...
ABSTRACT The intent of the current work is to study the effect of polyethylene glycol 8000 and polye...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
Many food, pharmaceutical, cosmetic and chemical products exist in the form of emulsions. A common p...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
The purpose of the PhD was to study the interactions of alkylpolyglycoside surfactants (APGs) with a...
The main purpose of this study was to evaluate the effect of a mixed drug solution containing a surf...
In order to investigate the effects of solid carriers on the crystalline properties, dissolution and...
Mixtures of polymers and surfactants are commonly found in a range of products of pharmaceutical,...
The poor aqueous solubility of hydrophobic drugs has always been a challenge for formulation scienti...
To develop a novel flurbiprofen-loaded solid dispersion without crystalline change, various flurbipr...
<div><p>ABSTRACT The intent of the current work is to study the effect of polyethylene glycol 8000 a...
ABSTRACT The intent of the current work is to study the effect of polyethylene glycol 8000 and polye...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
Many food, pharmaceutical, cosmetic and chemical products exist in the form of emulsions. A common p...
To evaluate the role of polymer-surfactant interactions in drug solubilisation/stabilisation during ...
The purpose of the PhD was to study the interactions of alkylpolyglycoside surfactants (APGs) with a...
The main purpose of this study was to evaluate the effect of a mixed drug solution containing a surf...
In order to investigate the effects of solid carriers on the crystalline properties, dissolution and...
Mixtures of polymers and surfactants are commonly found in a range of products of pharmaceutical,...
The poor aqueous solubility of hydrophobic drugs has always been a challenge for formulation scienti...