December 13th 2024
The partners will aim to establish a platform that enables rapid development of DPI products.
The Importance of Leachables and Extractables Testing for a Successful Product Launch
January 2nd 2008FDA’s May 1999 container-closure guidance has accelerated the requirements for extractable and leachable testing of container-closure packaging components. Since that date, additional recommendations have been made by industry groups to clarify how these issues should be addressed.
The Disintegration and Dissolution of Nabumetone Dispersible Tablets
December 2nd 2007The authors analyzed the effects of complexation as well as the levels of ammonium bicarbonate and crospovidone on tablet wetting time (WT), disintegration time (DT), and percent dissolution efficiency at 60 min (%DE60).
Topical delivery of oily actives using solid lipid particles
December 1st 2007Lipid-based drug delivery systems - such as liposomes, micro-and nanoemulsions, self-emulsified drug delivery systems, and solid lipid micro-and nanoparticles - are becoming more popular because lipid materials are easily characterized, contain a high range of well-defined/tolerated surfactant molecules and can be developed for several administration routes.
King and Acura to Develop Immediate-Release Pain Medicines
November 8th 2007King Pharmaceuticals, and Acura Pharmaceuticals have entered into a license, development and commercialization agreement for the United States, Canada, and Mexico, encompassing a potentially wide range of opioid analgesic products utilizing Acura?s patented Aversion (abuse-deterrent) Technology platform.
Converting Intravenous Dosing to Subcutaneous Dosing With Recombinant Human Hyaluronidase
October 2nd 2007The preferred route of administration for an injected therapeutic agent is subcutaneous (SC), but SC injections are generally limited to no more than 1-2 mL in volume, representing a major challenge, especially for large protein biologics.