About 60-70% of the drugs synthesized are poorly soluble and comes under BCS Class-II&IV. Now it is a challenging situation during the development of different dosage forms for pharmaceutical industries because solubility of the drug is the rate limiting step. Based on the solubility, the dissolution, bioavailability & therapeutic effect is dependent. To overcome this consequence a novel technique -Liquisolid compact is used by dissolving the poorly soluble drug in a non-volatile solvent that improves wettability & decreases the surface tension and ensures drug molecular dispersion in the formulation to increase the solubility of the drug. This admixture of drug loaded solution is blended with carrier adsorption & coating ma...
The current article aims with the introduction of newer solubility enhancing technique as Liquisolid...
The majority of the novel medication candidates are lipophilic and water-insoluble. The pharmaceutic...
AbstractMost of the newly developed drug candidates are lipophilic and poorly water-soluble. Enhanci...
The challenge faced by the majority of the pharmaceutical products is the poor solubility of the dru...
At present 40% of the drugs within the development pipelines, and approximately 60 % of the drugs co...
The poor dissolution rate of water-insoluble drugs is still a substantial problem confronting the ph...
The liquisolid technique is a novel approach for delivery of drugs through the oral route. This tech...
This technique is based upon the admixture of drug loaded solutions with appropriate carrier and coa...
In the drug development enhancement of oral bioavailability of poorly water soluble drugs is one of ...
Solubility plays a key role to achieve desired concentration of drug in systemic circulation and sho...
Liquisolid technique is also known as powder solution technology. It is the technique which deals wi...
Liquisolid formulations have attracted substantial interest as an efficient means of improving the d...
With the advent of high throughput screening, drugs are emerging to be more lipophilic and less hydr...
Solubility & dissolution rate enhancement from solid oral dosage form is a key issue for current...
Many modern drugs are poorly water soluble substances, which causes difficulties in the development ...
The current article aims with the introduction of newer solubility enhancing technique as Liquisolid...
The majority of the novel medication candidates are lipophilic and water-insoluble. The pharmaceutic...
AbstractMost of the newly developed drug candidates are lipophilic and poorly water-soluble. Enhanci...
The challenge faced by the majority of the pharmaceutical products is the poor solubility of the dru...
At present 40% of the drugs within the development pipelines, and approximately 60 % of the drugs co...
The poor dissolution rate of water-insoluble drugs is still a substantial problem confronting the ph...
The liquisolid technique is a novel approach for delivery of drugs through the oral route. This tech...
This technique is based upon the admixture of drug loaded solutions with appropriate carrier and coa...
In the drug development enhancement of oral bioavailability of poorly water soluble drugs is one of ...
Solubility plays a key role to achieve desired concentration of drug in systemic circulation and sho...
Liquisolid technique is also known as powder solution technology. It is the technique which deals wi...
Liquisolid formulations have attracted substantial interest as an efficient means of improving the d...
With the advent of high throughput screening, drugs are emerging to be more lipophilic and less hydr...
Solubility & dissolution rate enhancement from solid oral dosage form is a key issue for current...
Many modern drugs are poorly water soluble substances, which causes difficulties in the development ...
The current article aims with the introduction of newer solubility enhancing technique as Liquisolid...
The majority of the novel medication candidates are lipophilic and water-insoluble. The pharmaceutic...
AbstractMost of the newly developed drug candidates are lipophilic and poorly water-soluble. Enhanci...