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Fast Disintegrating Combination Tablet of Taste Masked Levocetrizine Dihydrochloride and Montelukast Sodium: Formulation Design, Development, and Characterization.

Gupta MM, Gupta N, Chauhan BS, Pandey S - J Pharm (Cairo) (2014)

Bottom Line: An ion exchange resin complex was prepared by the batch technique and various parameters; namely, resin activation, drug: resin ratio, pH, temperature, and stirring time, and swelling time were optimized to successfully formulate the tasteless drug resin complex (DRC).The tablets were prepared using microcrystalline cellulose (MCC) PH 102 as diluent along with crospovidone (CP), croscarmellose sodium (CCM), and sodium starch glycolate (SSG) as a superdisintegrants.The stability studies were carried out for the optimized batch for three months and it showed acceptable results.

View Article: PubMed Central - PubMed

Affiliation: School of Pharmacy, Faculty of Medical Sciences, The University of the West Indies, St. Augustine, Trinidad and Tobago ; Department of Pharmaceutics, Jaipur College of Pharmacy, Sitapura, Tonk Road, Jaipur, Rajasthan 302022, India.

ABSTRACT
The aim of this study was to prepare fast disintegrating combination tablet of taste masked Levocetrizine dihydrochloride and Montelukast sodium by using direct compression method. To prevent bitter taste and unacceptable odour of the Levocetrizine dihydrochloride drug, the drug was taste masked with ion exchange resins like Kyron-T-104 and Tulsion-412. Among the two resins, Kyron-T-104 was selected for further studies because of high drug loading capacity, low cost, and better drug release profile. An ion exchange resin complex was prepared by the batch technique and various parameters; namely, resin activation, drug: resin ratio, pH, temperature, and stirring time, and swelling time were optimized to successfully formulate the tasteless drug resin complex (DRC). The tablets were prepared using microcrystalline cellulose (MCC) PH 102 as diluent along with crospovidone (CP), croscarmellose sodium (CCM), and sodium starch glycolate (SSG) as a superdisintegrants. The tablets were evaluated for weight variation, hardness, friability, wetting time, water absorption ratio, disintegration time (DT), and dissolution study and it was concluded that the tablet formulation prepared with 2% SSG + CCS showed better disintegration time in comparison with other formulation and good drug release. The stability studies were carried out for the optimized batch for three months and it showed acceptable results.

No MeSH data available.


Related in: MedlinePlus

Comparison of in vitro drug release study of Montelukast sodium in K4 and K5 batch in phosphate buffer (pH 6.8).
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Related In: Results  -  Collection


getmorefigures.php?uid=PMC4590803&req=5

fig10: Comparison of in vitro drug release study of Montelukast sodium in K4 and K5 batch in phosphate buffer (pH 6.8).

Mentions: The results of dissolution are shown in Tables 15 and 16 and Figures 9 and 10.


Fast Disintegrating Combination Tablet of Taste Masked Levocetrizine Dihydrochloride and Montelukast Sodium: Formulation Design, Development, and Characterization.

Gupta MM, Gupta N, Chauhan BS, Pandey S - J Pharm (Cairo) (2014)

Comparison of in vitro drug release study of Montelukast sodium in K4 and K5 batch in phosphate buffer (pH 6.8).
© Copyright Policy - open-access
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC4590803&req=5

fig10: Comparison of in vitro drug release study of Montelukast sodium in K4 and K5 batch in phosphate buffer (pH 6.8).
Mentions: The results of dissolution are shown in Tables 15 and 16 and Figures 9 and 10.

Bottom Line: An ion exchange resin complex was prepared by the batch technique and various parameters; namely, resin activation, drug: resin ratio, pH, temperature, and stirring time, and swelling time were optimized to successfully formulate the tasteless drug resin complex (DRC).The tablets were prepared using microcrystalline cellulose (MCC) PH 102 as diluent along with crospovidone (CP), croscarmellose sodium (CCM), and sodium starch glycolate (SSG) as a superdisintegrants.The stability studies were carried out for the optimized batch for three months and it showed acceptable results.

View Article: PubMed Central - PubMed

Affiliation: School of Pharmacy, Faculty of Medical Sciences, The University of the West Indies, St. Augustine, Trinidad and Tobago ; Department of Pharmaceutics, Jaipur College of Pharmacy, Sitapura, Tonk Road, Jaipur, Rajasthan 302022, India.

ABSTRACT
The aim of this study was to prepare fast disintegrating combination tablet of taste masked Levocetrizine dihydrochloride and Montelukast sodium by using direct compression method. To prevent bitter taste and unacceptable odour of the Levocetrizine dihydrochloride drug, the drug was taste masked with ion exchange resins like Kyron-T-104 and Tulsion-412. Among the two resins, Kyron-T-104 was selected for further studies because of high drug loading capacity, low cost, and better drug release profile. An ion exchange resin complex was prepared by the batch technique and various parameters; namely, resin activation, drug: resin ratio, pH, temperature, and stirring time, and swelling time were optimized to successfully formulate the tasteless drug resin complex (DRC). The tablets were prepared using microcrystalline cellulose (MCC) PH 102 as diluent along with crospovidone (CP), croscarmellose sodium (CCM), and sodium starch glycolate (SSG) as a superdisintegrants. The tablets were evaluated for weight variation, hardness, friability, wetting time, water absorption ratio, disintegration time (DT), and dissolution study and it was concluded that the tablet formulation prepared with 2% SSG + CCS showed better disintegration time in comparison with other formulation and good drug release. The stability studies were carried out for the optimized batch for three months and it showed acceptable results.

No MeSH data available.


Related in: MedlinePlus