Role ofin vitrorelease models in formulation development and quality control of parenteral depots-Reference-Cited by-同舟云学术

Role ofin vitrorelease models in formulation development and quality control of parenteral depots

Published:2009-11-26 Issue:12 Volume:6 Page:1283-1295
ISSN:1742-5247
Container-title:Expert Opinion on Drug Delivery
language:en
Short-container-title:Expert Opinion on Drug Delivery

Author:

Larsen Claus¹,Larsen Susan Weng²,Jensen Henrik²,Yaghmur Anan²,Østergaard Jesper²

Affiliation:

1. University of Copenhagen, Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, Universitetsparken 2, DK-2100 Copenhagen, Denmark ; ;

2. University of Copenhagen, Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, Universitetsparken 2, DK-2100 Copenhagen, Denmark

Publisher

Informa Healthcare

Subject

Pharmaceutical Science

Link

https://www.tandfonline.com/doi/pdf/10.1517/17425240903307431

Reference126 articles.

1. Intra‐articular depot formulation principles: Role in the management of postoperative pain and arthritic disorders

2. Macromolecule Release from Monodisperse PLG Microspheres: Control of Release Rates and Investigation of Release Mechanism

3. Assuring quality and performance of sustained and controlled release parenterals: Workshop report

4. Assuring quality and performance of sustained and controlled release parenterals

5. In vitro and in vivo considerations associated with parenteral sustained release products: A review based upon information presented and points expressed at the 2007 Controlled Release Society Annual Meeting

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