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Optimization and Development of Swellable Controlled Porosity Osmotic Pump Tablet for Theophylline
Purpose: To develop swellable controlled porosity osmotic pump tablet of theophylline and to define the formulation and process variables responsible for drug release by applying statistical optimization technique. Methods: Formulations were prepared based on Taguchi Orthogonal Array design and Frac...
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Published in: | Tropical journal of pharmaceutical research 2009-07, Vol.8 (3) |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Purpose: To develop swellable controlled porosity osmotic pump tablet
of theophylline and to define the formulation and process variables
responsible for drug release by applying statistical optimization
technique. Methods: Formulations were prepared based on Taguchi
Orthogonal Array design and Fraction Factorial design for core and
coating, respectively. The tablets were prepared by direct compression
and wet granulation methods; spray coated with ethyl cellulose solution
containing varying amounts of PEG 400 and plasdone. Drug release from
the osmotic drug delivery system was studied using USP Type I paddle
type apparatus. The membrane morphology of the delivery system was
determined by scanning electron microscopy (SEM). Results:
Optimization results indicated that the release rate of theophylline
from the swellable controlled porosity osmotic pump tablet is directly
proportional to the levels of osmotic agent, solubilizing agent and
pore former in the tablet core and the membrane, respectively. SEM
showed the formation of pores in the membrane through which drug
release occurred. The best formulation showed 98.2 % drug release and
complied with USP requirements. Conclusion: The results confirmed
that the factors responsible for drug release were osmotic agents
(core) and pore former (membrane). Also, the preparation of swellable
controlled porosity osmotic pump tablet was facilitated by coating the
core tablet with pore forming agent, thus eliminating the need for the
more expensive laser drilling. |
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ISSN: | 1596-5996 1596-9827 |
DOI: | 10.4314/tjpr.v8i3.44541 |