Evaluation of Methodology for Assessing Release Characteristics of Thermosoftening Vehicles

Author:

Kopcha Michael1,Tojo Kakuji J2,Lordi Nicholas G3

Affiliation:

1. Schering-Plough Research, Kenilworth, NJ 07033, USA

2. Kyushu Institute of Technology, College of Computer Science and Systems Engineering, Lizuka, Fukuoka 820, Japan

3. Rutgers, The State University, College of Pharmacy, Piscataway, NJ 08854, USA

Abstract

Abstract Methodology has been devised for the testing and evaluation of the mechanistic release of drug or markers from thermosoftening materials, as represented by the Gelucire class of excipients, which could be predictive. Release of a drug (anhydrous theophylline) and a marker (D&C yellow No. 10) was determined using a calibrated stationary disc/rotating fluid system. Of the fourteen commercially available Gelucire excipients, six were investigated in detail (G46/07, G48/09, G50/02, G50/13, G53/10, G62/05) and found to have biphasic release profiles. Lipid soluble materials demonstrated predominantly diffusion-controlled release, while water-dispersible materials absorbed water and showed signs of swelling which led to erosion as an additional component of the release characteristics.

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

Reference10 articles.

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2. Drug release from a slowly hydrating semi-solid matrix;Dennis;J. Pharm. Pharmacol.,1987

3. Drug/polymer matrix swelling and dissolution;Harland;Pharm. Research,1988

4. Mechanism of sustained-action medication. Theoretical analysis of rate of release of solid drugs dispersed on solid matrices;Higuchi;J. Pharm. Sci.,1963

5. Drug release from thermosetting fatty vehicles filled into hard gelatin capsules;Howard;Drug Devel. Ind. Pharm.,1987

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