![]() | Only 14 pages are availabe for public view |
Abstract Hepatitis C is an infectious disease caused by the hepatitis C virus (HCV) that until recently did not have effective treatments. A new class of oral antiviral drugs called direct-acting antivirals has, for the first time, provided an opportunity for widespread scale-up of curative treatment. These oral medications have been proven to be safe and effective in clearing hepatitis C from the body within 12 weeks of treatment. Daclatasvir is a direct-acting antiviral agent used to treat the hepatitis C virus. Daclatasvir has a bitter taste and poor solubility in water and ethanol at neutral pH. The drug product is manufactured by a standard manufacturing process. In-process controls include weight variation, friability, disintegration time, tablet weight and hardness during tablet compression and weight gain during film coating. The formulation technique plays an important role in overcoming the shortcoming of poorly water-soluble drugs and enhancing patient compliance. Oral disintegrating tablets offer several advantages over conventional tablets with reference to their stability, administration without water, accurate dosing, and easy manufacturing. Their simple administration within the population especially for paediatric, geriatric, or any people persons makes them a popular dosage form. They have preferable taste, enhanced stability, superior bioavailability, greater efficacy, allow for variable dosing and are more cost-effective and provide a rapid onset of action. |