DESIGN, IN VITRO EVALUATION AND IN VIVO STUDIES OF NOVEL DELAYED RELEASE TABLETS OF PANTOPRAZOLE

International Journal of Biomedical and Advance Research

piyush trivedi¹  Pooja Choudhry¹  Monika Arora¹  sandeep sinde¹  kuldeep singh patel¹  mayank nagar¹  Mona nagar¹  Prince kumar jain¹ 

关键词: Pantoprazole;    delayed release;    subcoating;    enteric coating;    acid uptake;    stability;    pharmacokinetic;    bioequivalence;   

DOI  :  10.7439/ijbar.v3i11.466

学科分类：药学、药理学、毒理学（综合）

来源: Scholar Science Journals

【 摘 要 】

In an effort to reduce production costs, a simple, direct compression delayed release formulation consisting of pantoprazole was investigated. Pantoprazole is a proton pump inhibitor belongs to group of benzimidazole. It is very efficient for the treatment of gastric and duodenum ulcers. Even in solid state pantoprazole is sensitive to heat, humidity, light and especially to substances containing an acidic group. For such types of drugs, enteric coating added to the formulation tends to avoid the stomach's acidic exposure, delivering them instead to a basic pH environment where they do not degrade, and give their desired action. Subcoating is desirable to protect the enteric coating. Opadry and Acryl-EZE systems have been utilized for subcoating and enteric coating respectively. Delayed-release tablets with good physical, mechanical and technological properties were obtained with use of different combinations of diluents, binders, superdisintegrants and lubricants. A comparative kinetic study of the present tablets and commercial tablets was established. The value for the similarity factor ( f 2 = 71.6) suggested that the dissolution profile of the present two delayed-release oral dosage forms are similar. Hixon???Crowell (erosion) kinetic profiles were achieved"

【 授权许可】

CC BY