Supersaturated controlled release matrix using amorphous dispersions of glipizide

Author:

Lu Zheng,Yang Yonglai,Covington Rae-Ann,Bi Yunxia (Vivian),Dürig Thomas,Ilies Marc A.,Fassihi Reza

Funder

Ashland Specialty Ingredient R&D Pharma

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference32 articles.

1. Center for Drug Evaluation and Research (CDER), 1995. Guidance for Industry: Immediate Release Solid Oral Dosage Forms Scale-up and Postapproval Changes: Chemistry, Manufacturing, and Controls. In Vitro Dissolution Testing and in Vivo Bioequivalence Documentation. http://www.fda.gov/downloads/Drugs/%E2%80%A6/Guidances/UCM070636.pdf. Accessed Nov 1995.

2. Guidance for Industry: Waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a biopharmaceutics classification system;Center for Drug Evaluation and Research,2015

3. A comparison of spray drying and milling in the production of amorphous dispersions of sulfathiazole/polyvinylpyrrolidone and sulfadimidine/polyvinylpyrrolidone;Caron;Mol. Pharm.,2011

4. Amorphous solid dispersions of sulfonamide/Soluplus® and sulfonamide/PVP prepared by ball milling;Caron;AAPS PharmSciTech,2013

5. Guar-based monolithic matrix systems: effect of ionizable and non-ionizable substances and excipients on gel dynamics and release kinetics;Dürig;J. Control. Release,2002

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