FORMULATION AND EVALUATION OF MONTELUKAST SODIUM ORO DISPERSIBLE TABLETS
Nagineni Sudarshan Rao* and Padira Priyanka
.
Abstract
The main aim of the present study is to design and develop oro
dispersible tablets of Montelukast sodium. Montelukast is used to treat
and prevent asthma. It will decrease the symptoms and the number of
acute asthma attacks. Montelukast is also used to prevent exerciseinduced
bronchoconstriction (EIB), and treat symptoms of seasonal
(short-term) or perennial (long-term) allergies, such as sneezing, runny
nose, itching, or wheezing. Montelukast is an orally active compound
that binds with high affinity and selectivity to the CysLT1, receptor (in
preference to other pharmacologically important airway receptors, such
as the prostanoid, cholinergic, or β-adrenergic receptor). Montelukast
inhibits physiologic actions of LTD4 at the CysLT1, receptor without
any agonist activity. Montelukast sodium is prepared by using sublimation method.
Croscarmellosesodium(S1-S3), Sodium starch glycolate(S4-S6), and Cross povidone(S5-S9)
are used as super disintegrants. The formulation which contain crosscarmellose sodium
exhibits rapid disintegration time, when compared with other disintegrants. But the
formulation S9 which contain crosspovidone as super disintegrant has shown the maximum
drug release with time, when compared with other super disintegrants. the order of selection
of super disintegrents is cross povidone>cross carmellose sodium>sodium starch glycolate.
Keywords: Oro dispersible tablets, Montelukast sodium, Croscarmellose sodium, sodium starch glycolate, crospovidone.
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