UGC Approved Journal no 63975(19)
New UGC Peer-Reviewed Rules

ISSN: 2349-5162 | ESTD Year : 2014
Volume 13 | Issue 3 | March 2026

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Published in:

Volume 12 Issue 5
May-2025
eISSN: 2349-5162

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Published Paper ID:
JETIR2505A55


Registration ID:
563393

Page Number

j601-j612

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Title

FORMULATION AND DEVELOPMENT OF METOPROLOL SUCCINATE TABLETS IN TERMS OF FLOATING DRUG DELIVERY SYSTEM

Abstract

The main goal of this study is to formulate and develop Metoprolol Succinate Floating tablet. To optimize Metoprolol Succinate floating tablet and carry out stability studies as per ICH guidelines. Metoprolol Succinate is classified as a BCS Class I medication, commonly prescribed for managing conditions like hypertension, angina pectoris, and heart attacks. It has a relatively short half-life, ranging from 3 to 7 hours, and its absorption can vary because of its poor solubility. Floating tablets of Metoprolol Succinate were formulated using hydrophilic polymers such as Hydroxypropyl Methylcellulose (HPMC), Carbopol, and swelling agents like calcium carbonate to create a buoyant matrix. Various formulations were developed by altering polymer content. Tablets were evaluated for parameters including hardness, thickness, weight variation, friability, drug content, floating lag time, total floating duration, swelling index, and in vitro drug release profile. The FTIR data indicates that there are no interactions of excipients with the drug. Among the formulations tested, formulation F5 exhibited the most beneficial qualities. It demonstrated a consistent drug release of 92.63% and maintained buoyancy for up to 16 hours. All key evaluation parameters such as floating lag time, swelling index, and in vitro drug release were optimized in F5 compared to other formulations. The stability study indicates that there are no significant differences in the physical parameters. The results indicate that a sustained-release floating drug delivery system for Metoprolol Succinate was successfully developed. The optimized formulation (F5) significantly improves gastric retention and drug release, making it a promising candidate for enhanced antihypertensive therapy.

Key Words

Metoprolol Succinate, Floating Drug Delivery System (FDDS), Hydrophilic Polymers, Sustained Release, In Vitro Drug Release

Cite This Article

"FORMULATION AND DEVELOPMENT OF METOPROLOL SUCCINATE TABLETS IN TERMS OF FLOATING DRUG DELIVERY SYSTEM", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.12, Issue 5, page no.j601-j612, May-2025, Available :http://www.jetir.org/papers/JETIR2505A55.pdf

ISSN


2349-5162 | Impact Factor 7.95 Calculate by Google Scholar

An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 7.95 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator

Cite This Article

"FORMULATION AND DEVELOPMENT OF METOPROLOL SUCCINATE TABLETS IN TERMS OF FLOATING DRUG DELIVERY SYSTEM", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.12, Issue 5, page no. ppj601-j612, May-2025, Available at : http://www.jetir.org/papers/JETIR2505A55.pdf

Publication Details

Published Paper ID: JETIR2505A55
Registration ID: 563393
Published In: Volume 12 | Issue 5 | Year May-2025
DOI (Digital Object Identifier): https://doi.org/10.56975/jetir.v12i5.563393
Page No: j601-j612
Country: North 24 Parganas, West Bengal, India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


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