Formulation and Evaluation of Mouth Dissolving Tablets of Salbutamol Sulphate Using Various Superdisintegrants

Abstract

The present was study to formulate the mouth dissolving tablets using super disintegrants and evaluating for its characteristics. To enhance the solubility of salbutamal sulphate by using superdisintegrants in the oral cavity. and to develop mouth dissolving drug delivery system and enhance the patient compliance.Asthma is defined as chronic inflammatory disorder of the airways in which many cells a mast cells, esinofils, T-lymphocytes, macrophage, neutrophils and epithelial cells and other cellular elements play role in susceptible individual recurrent episodes of wheezing breathless chest fight and coughing. Anti asthmatics are typically corticosteroids, leuckotriene cormones, antihistamines, beta two agonist theopylline. Salbutamol sulphate is B2 adrenergic agonist that stimulator receptors of smooth muscles in the lungs. Salbutamol is believed to work by adenylate cyclase, the enzyme responsible for generating cyclic Amp an intracellular mediator. Increased cylase Amp lead to activating of intra cellular ionized cyclic Amp prokinase A which inhibits phosphorylation of myosin and lowers the intracellular ionic calcium concentration, resulting in relaxation of bronchial and tracheal smooth muscles, which in turn relieves branchospasm, reducer airway resistance, facilitates mucous drainage and increases vital capacity

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