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Examines the history and recent developments in drug dosage forms for pharmaceutical sciences; Focuses on physicochemical aspects, prefomulation solid state properties and polymorphism
- Dosage Form Design Considerations
Dosage Form Design Parameters, Volume I, examines the...
- Dosage Form Design Considerations
The main objective of pre-formulation testing is to collect the information useful to develop stable, bioavailable dosage forms with safety consideration. Pre-formulation investigations are designed to collect all necessary data, especially physicochemical, physico-mechanical, and biopharmaceutical properties of drug substances, excipients, and ...
4 Dosage Form Design: Pharmaceutical and Formulation Considerations. After reading this chapter, the student will be able to: List reasons for the incorporation of drugs into various dosage forms. Compare and contrast the advantages/disadvantages of various drug dosage forms.
27 Ιουλ 2021 · A comprehensive textbook covering the design of dosage forms and all aspects of drug delivery systems. `Pharmaceutics' in its broadest sense is the `art of the apothecary' or, in simple terms, pharmaceutical preparations.
11 Αυγ 2020 · Pharmaceutics : the science of dosage form design. Publication date 1988 Topics Drugs -- Design, Drugs -- Dosage forms, Biopharmaceutics, Pharmaceutical technology, Pharmaceutical chemistry, Chemistry, ...
In this chapter, we will delve into the intricate world of dosage form design, where pharmaceutical scientists and engineers harness their expertise to create formulations that optimize drug absorption, bioavailability, stability, and patient compliance.
Dosage Form Design Parameters, Volume I, examines the history and current state of the field within the pharmaceutical sciences, presenting key developments. Content includes drug development issues, the scale up of formulations, regulatory issues, intellectual property, solid state properties and polymorphism.
