Extrusion: An Enabling Technology for Controlled-Release Hydrophilic Matrix Systems

Author:

Tewari Divya,Dürig Thomas

Publisher

Springer New York

Reference33 articles.

1. Lapidus H, Lordi NG. Some factors affecting the release of a water-soluble drug from a compressed hydrophilic matrix. J Pharm Sci. 1966;55(8):840–3.

2. Dürig T, Fassihi R. Mechanistic evaluation of binary effects of magnesium stearate and talc as dissolution retardants at 85 % drug loading in an experimental extended‐release formulation. J Pharm Sci. 1997;86(10):1092–8.

3. Dürig T, Venkatesh GM, Fassihi R. An Investigation into the erosion behaviour of a high drug‐load (85 %) particulate system designed for an extended‐release matrix tablet. Analysis of erosion kinetics in conjunction with variations in lubrication, porosity and compaction rate. J Pharm Pharmacol. 1999;51(10):1085–92.

4. Dürig T, Harcum WW, Tewari D, Kinsey BR, Divi M. Development of a controlled release coating system for highly soluble drug matrix tablets. Ashland pharmaceutical technology report. PTR, 73-1. 2009 (Presented at annual meeting of the association of American pharmaceutical scientists, Nov 8–12, 2009, Los Angeles).

5. Mollan M. Historical overview. In: Ghebre-Sellassie I, Martin C, editors. Pharmaceutical extrusion technology, drugs and the pharmaceutical sciences, vol. 133. New York: Dekker; 2003. p. 1.

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