Title of article
Industrial perspective in ocular drug delivery
Author/Authors
Ali، نويسنده , , Yusuf and Lehmussaari، نويسنده , , Kari، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2006
Pages
11
From page
1258
To page
1268
Abstract
In the development of a commercial drug product, the formulator must consider various perspectives. The bioavailability of the active drug substance is often the major hurdle to overcome. In the past it has been common to add viscosity-enhancing agents or mucoadhesive polymers into formulations to improve ocular bioavailability. In addition to these conventional approaches, non-conventional technologies such as nanotechnology, microspheres and prodrugs could be considered to optimize the product.
with bioavailability, the formulator must also consider the tolerability and stability of the final drug product. Quite often, the final formulation is the ideal compromise between the three.
ities in different parts of the world have set strict requirements and guidelines for development and approval of drug products. In order to secure an expeditious development process and the shortest possible review and approval time, the formulator should be familiar with the current requirements and regulations.
Keywords
Ocular drug delivery , suspensions , Ointments , Gels , Eye drops , Mucoadhesives , New drug application , Marketing authorization application , Clinical trial application , Investigational new drugs , Dosage Forms , Regulatory requirements
Journal title
Advanced Drug Delivery Reviews
Serial Year
2006
Journal title
Advanced Drug Delivery Reviews
Record number
1761883
Link To Document