Studies on Sustained Release II: in Vivo Performance of the Inert Matrix Sulfamethizole Tablet, Employing Polymethylmethacrylate
- 1 January 1986
- journal article
- research article
- Published by Taylor & Francis in Drug Development and Industrial Pharmacy
- Vol. 12 (3) , 423-430
- https://doi.org/10.3109/03639048609026622
Abstract
The in vivo performance of the developed sustained release preparation was assessed on eight subjects. Based upon urinary excretion rates, in vivo data supported previous in vitro dissolution test results. An overall release/excretion rate of 32.6 mg/hr was obtained. The blood levels were assayed for intact drug and were fit to a three exponential equation employing the program AUTOAN. First order release rate constant of 1.33 hr was calculated, but the fits were not very satisfactory Although the blood levels were in an acceptable range, it is concluded that a faster releasing dosage form would be more appropriate This might require however, switching to another dosage form.This publication has 3 references indexed in Scilit:
- Comparison of Bioavailabilities and Dissolution Characteristics of Commercial Tablet Formulations of SulfamethizoleJournal of Pharmaceutical Sciences, 1972
- Kinetics of plasma drug levels after sustained release dosageBiochemical Pharmacology, 1960
- A NEW COUPLING COMPONENT FOR SULFANILAMIDE DETERMINATIONJournal of Biological Chemistry, 1939