Formulation and in vitro evaluation of esomeprazole delayed release multi particulate capsules

  • Sirisha K.V.R JNTUA, Anantapur, Andhra Pradesh, India
  • Vijayasri K Malla Reddy College of Pharmacy, Secunderabad, Andhra Pradesh, India
  • Devanna N OTRI, JNTUA, Anantapur, Andhra Pradesh, India
  • Kamalakar reddy G Hetero Labs Ltd., Hyderabad, Andhra Pradesh, India


The present research was aimed to formulate and evaluate Esomeprazole magnesium dihydrate delayed release multi-particulate capsules. The delayed release multiple units were prepared by solution/suspension layering using fluid-bed Wurster (bottom-spray) technology, a well-recognized process for providing excellent coating uniformity and efficiency. The prepared multiparticulates consist of successive layers of seal coat, drug coat, barrier coat, enteric-polymer coat, over coat on existing inert seeds and finally filled into capsules. The finished pellets were evaluated for drug content, acid resistance test, in vitro drug release profile and compared with marketed product. The dissimilarity (f1) and similarity (f2) factors for optimized and marketed formulation were found to be 3.56 and 72.49, respectively. Accelerated stability study conducted as per ICH guide lines at 400C/75% RH for 6 months showed that the finalized formulation (E5 multiple units filled into capsules) was stable during the study period.


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Sirisha K.V.R, Vijayasri K, Devanna N, & Kamalakar reddy G. (2013). Formulation and in vitro evaluation of esomeprazole delayed release multi particulate capsules. International Journal of Research in Pharmaceutical Sciences, 4(3), 1-6.
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