DEVELOPMENT AND EVALUATION OF DRDAS OF COMBINATION OF DIGOXIN AND PHENYTOIN SODIUM FOR CONGESTIVE HEART FAILURE
P. U. Parikh*, V. A. Pande, P. S. Kudi, S. R. Yadav and V. P. Patel
Abstract
Background & Objective: The purpose of this research was to
develop a Dual Release Drug Absorption System (DRDAS) that would
increase the therapeutic efficacy of digoxin for the treatment of
congestive heart failure while reducing side effects. To treat
Congestive Heart Failure and digoxin side effects, bilayer tablets
comprising a combination of two different cardiovascular drugs i.e.,
digoxin and phenytoin sodium were used. Method: In bilayer tablets
various superdisintegrants added, digoxin is utilized as an immediaterelease
layer, and phenytoin sodium is used as a prolonged-release
layer with addition HPMC K100M. The optimization method was used
to test bilayer tablets for immediate release Digoxin layer and
sustained release Phenytoin Sodium bilayer. Result: Digoxin's
immediate release layer demonstrated complete release in 20 minutes,
while phenytoin sodium release was prolonged to 6-8 hours. Conclusion: according to the
results of this study, Digoxin and phenytoin sodium bilayer pills were successfully prepared
for the treatment of congestive heart failure and digoxin side effects (Arrhythmic condition).
Keywords: Congestive Heart Failure, Dual Release Drug Absorption System (DRDAS), Digoxin, Phenytoin sodium, HPMC K 100M.
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