Formulation and Evaluation of Taste Masked Mouth Dissolving Tablets of Levocetirizine Hydrochloride

Aim of this research work was to develop mouth dissolving tablet that disintegrates rapidly in mouth by using tasteless complex of levocetirizine and tulsion-335. effect of different parameters such as swelling time, resin activation, drug resin ratio as well as stirring time was optimized by taste and percentage drug loading. formulated drc (drug resin complex) was characterized by infrared spectroscopy, thermal analysis and x-ray diffraction pattern. tablets were formulated by wet granulation with pvp as binder, sodium starch glycolate (ssg) and crospovidone as super disintegrants. in these batches optimum hardness was achieved but disintegration time was found to be very high as ≥ 70 second, so further trials were planned by using different superdisintegrants such as croscarmellose sodium, sodium starch glycolate (ssg) as well as crospovidone by wet granulation method. tablets formulated with 7.5% crospovidone showed comparatively low disintegration time (25 sec), wetting time (20 sec) and friability (0.60 %) than the other batches. in present study we optimized the conditions required for maximum drug loading of levocetirizine with tulsion-335. among different superdisintergants, crospovidone was found suitable with drug-resin complex to get the low disintegration time, wetting time and friability of tablets