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In Vitro Release from Semisolid Dosage Forms
| Content Provider | Scilit |
|---|---|
| Author | Shah, Vinod P. |
| Copyright Year | 2021 |
| Description | A key aspect of any new drug product is its safety and efficacy as demonstrated in controlled clinical trials. This chapter focuses on the application of in vitro release approaches in the documentation of the performance of semisolid dosage forms. In vitro approaches, such dissolution, are standard methods used to assess performance characteristics of a solid oral dosage formulation. It has evolved as a critical test method in the field of drug development. In vitro dissolution is used specifically to guide formulation development, monitor manufacturing process, ensure batch-to-batch quality, and possibly predict in vivo performance. A simple, reliable, reproducible, relevant, and generally acceptable in vitro method to assess drug release from a semisolid dosage form is highly valuable for the same reasons that such methodology has proved valuable in the development, manufacture, and batch-to-batch quality control of solid oral dosage forms. Book Name: Percutaneous Absorption |
| Related Links | https://api.taylorfrancis.com/content/chapters/edit/download?identifierName=doi&identifierValue=10.1201/9780429202971-18&type=chapterpdf |
| Ending Page | 272 |
| Page Count | 6 |
| Starting Page | 267 |
| DOI | 10.1201/9780429202971-18 |
| Language | English |
| Publisher | Informa UK Limited |
| Publisher Date | 2021-06-08 |
| Access Restriction | Open |
| Subject Keyword | Book Name: Percutaneous Absorption Biomedical Engineering Pharmacology and Pharmacy Efficacy Dosage Forms Semisolid Dosage Form Release From a Semisolid Dosage Safety |
| Content Type | Text |
| Resource Type | Chapter |
