Effect of Formulation Variables on the Preparation and in Vitro-in Vivo evaluation of Cimetidine Release from Ethyl Cellulose Micropellets
- 1 January 1990
- journal article
- research article
- Published by Taylor & Francis in Drug Development and Industrial Pharmacy
- Vol. 16 (2) , 283-293
- https://doi.org/10.3109/03639049009114886
Abstract
Ethyl cellulose embedded prolonged release microparticles containing cimetidine was designed by dispersing the drug-ethyl cellulose mixture in acetone, into a medium of mineral oil and subsequent rigidization of the ethyl cellulose matrix. Significant reproducibility of the manufacturing process was observed. In vitro-in vivo correlation revealed the the dissolution process is the rate determining step in drug absorption and the significant in vivo efficiency of the dosage form is well expected.This publication has 11 references indexed in Scilit:
- Simulation of Physiological pH - Time Profile in In Vitro Dissolution Study: Relationship Between Dissolution Rate and Bioavailability of Controlled Release Dosage FormDrug Development and Industrial Pharmacy, 1988
- Design and in Vitro Evaluation of a Controlled Release Drug Delivery System of SulfasomidineDrug Development and Industrial Pharmacy, 1985
- High-Pressure Liquid Chromatographic Analysis of Cimetidine, a Histamine H2-Heceptor Antagonist, in Blood and UrineJournal of Pharmaceutical Sciences, 1977
- Use of Rabbits for GI Drug Absorption StudiesJournal of Pharmaceutical Sciences, 1977
- Controlled Release: Mechanisms and RatesPublished by Springer Nature ,1974
- Complication in Using Rabbits for the Study of Oral Drug AbsorptionCHEMICAL & PHARMACEUTICAL BULLETIN, 1969
- Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matricesJournal of Pharmaceutical Sciences, 1963
- A New Oral Gelatinized Sustained-Release Dosage FormJournal of Pharmaceutical Sciences, 1963