FORMULATION AND EVALUATION OF DELAYED RELEASE TABLETS OF RABEPRAZOLE

The Rabeprazole sodium is a proton pump inhibitor which is used in the treatment of peptic ulcer. In this study Rabeprazole compression coated tablets were prepared by using HPMCK4M as a compression coating polymer. Nine formulations of compression coated tablets of Rabeprazole were developed by preparing core tablets using microcrystalline cellulose as diluent as in different proportions and varying the composition of compression coating using HPMCK4M, HPMCK15M and ethyl cellulose. The core tablets were prepared by direct compression method. Among all the formulations, F1 was found to be best of all the formulations showing drug release matching the innovator product so to that formulation all the quality control tests were done for conformation. Stability study is carried out at 25°C; 60% RH and 40 °C; 75% RH according to ICH guidelines. The tablets were tested for acid release during the stability period and conformed that results were found within the limits.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-09-30
DOI
https://doi.org/10.5281/zenodo.17234980
Primary Topic
Agriculture, Water, and Health
Type
article
Field-Weighted Citation Impact
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article

FORMULATION AND EVALUATION OF DELAYED RELEASE TABLETS OF RABEPRAZOLE

Zenodo (CERN European Organization for Nuclear Research)
Agriculture, Water, and Health
article

FORMULATION AND EVALUATION OF DELAYED RELEASE TABLETS OF RABEPRAZOLE

article en

Abstract

The Rabeprazole sodium is a proton pump inhibitor which is used in the treatment of peptic ulcer. In this study Rabeprazole compression coated tablets were prepared by using HPMCK4M as a compression coating polymer. Nine formulations of compression coated tablets of Rabeprazole were developed by preparing core tablets using microcrystalline cellulose as diluent as in different proportions and varying the composition of compression coating using HPMCK4M, HPMCK15M and ethyl cellulose. The core tablets were prepared by direct compression method. Among all the formulations, F1 was found to be best of all the formulations showing drug release matching the innovator product so to that formulation all the quality control tests were done for conformation. Stability study is carried out at 25°C; 60% RH and 40 °C; 75% RH according to ICH guidelines. The tablets were tested for acid release during the stability period and conformed that results were found within the limits.

Zenodo (CERN European Organization for Nuclear Research)
Kakatiya University (IN)
Openalex Percentile: Top 50%
Agriculture, Water, and Health
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