In vitro assessment of drug release rates from oil depot formulations intended for intra-articular administration

Author:

Larsen Susan Weng,Østergaard Jesper,Friberg-Johansen Henrik,Jessen Marit N.B.,Larsen Claus

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference21 articles.

1. Optimisation of drug delivery. 6. Modified-release parenterals;Benson;Aust. J. Hosp. Pharm.,1998

2. Assuring quality and performance of sustained and controlled release parenterals: workshop report, co-sponsored by FDA and USP;Burgess;Pharm. Res.,2002

3. Burgess, D.J., Crommelin, D.J.A., Hussain, A.S., Chen, M.-L., 2004. Assuring quality and performance of sustained and controlled release parenterals: EUFEPS workshop report. AAPS PharmSci. 6, article 11.

4. Long-acting parenteral drug formulations;Chien;J. Parenter. Sci. Technol.,1981

5. Possibilities for determinating the active substance release from hydrophobic carriers especially as suppositories;Dibbern;Pharm. Ind.,1983

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