Modified dosage forms are pharmaceutical formulations that have been altered from the conventional dosage forms to provide specific drug delivery profiles, improve patient compliance, or enhance therapeutic outcomes. Here are some different types of modified dosage forms:
It’s important to note that the development and availability of modified dosage forms may vary depending on the specific drug and the regulatory approval in different countries.
Brief:
SR, CR, DR, and ER are abbreviations used to describe different types of controlled-release or extended-release dosage forms. Here’s an overview of the differences between these terms:
Sustained-release dosage forms are designed to release the drug slowly and consistently over an extended period. They deliver a steady concentration of the drug in the body, reducing the frequency of dosing. SR formulations typically maintain therapeutic levels of the drug within a desired range over a specified duration.
Controlled-release dosage forms are also designed to release the drug in a controlled manner, but the release profile may be more complex or varied compared to sustained-release formulations. CR formulations may incorporate different mechanisms, such as diffusion or osmosis, to control drug release. They aim to achieve a specific release rate or maintain drug levels within a therapeutic window for an extended period.
Delayed-release dosage forms are specifically designed to release the drug at a predetermined time after administration or at a specific site in the gastrointestinal tract. They typically have an enteric coating that resists dissolution in the stomach but dissolves in the intestines, allowing for targeted drug delivery.
Extended-release dosage forms are designed to release the drug gradually over an extended period, often with the goal of maintaining therapeutic drug concentrations for a longer duration. ER formulations may utilize various release mechanisms, such as matrix systems, reservoirs, or layered coatings, to achieve the desired extended-release profile.
The dissolution profile refers to the rate at which a dosage form releases its active ingredient(s) in a specific dissolution medium. Here’s a summary of the dissolution profiles for each dosage form:
Dissolution Profile: SR dosage forms typically exhibit a slower and sustained release of the drug over an extended period. The dissolution curve shows a gradual increase in drug concentration over time, maintaining therapeutic levels for an extended duration.
Dissolution Profile: CR dosage forms are designed to provide controlled and consistent drug release. The dissolution curve demonstrates a controlled release rate, ensuring that the drug levels are maintained within a therapeutic window over a specified time period.
Dissolution Profile: DR dosage forms have a specific release pattern where the drug release is delayed until a specific time or site in the gastrointestinal tract is reached. The dissolution curve shows minimal drug release initially, followed by a rapid increase at the target location.
Dissolution Profile: ER dosage forms provide an extended and sustained release of the drug over an extended period. The dissolution curve demonstrates a gradual increase in drug concentration over time, maintaining therapeutic levels for an extended duration.
Below Table is sort description of Different types of Modified Dosage Forms:
Read More:
This website uses cookies.