International Journal For Multidisciplinary Research
E-ISSN: 2582-2160
•
Impact Factor: 9.24
A Widely Indexed Open Access Peer Reviewed Multidisciplinary Bi-monthly Scholarly International Journal
Home
Research Paper
Submit Research Paper
Publication Guidelines
Publication Charges
Upload Documents
Track Status / Pay Fees / Download Publication Certi.
Editors & Reviewers
View All
Join as a Reviewer
Reviewer Referral Program
Get Membership Certificate
Current Issue
Publication Archive
Conference
Publishing Conf. with IJFMR
Upcoming Conference(s) ↓
WSMCDD-2025
GSMCDD-2025
Conferences Published ↓
RBS:RH-COVID-19 (2023)
ICMRS'23
PIPRDA-2023
Contact Us
Plagiarism is checked by the leading plagiarism checker
Call for Paper
Volume 7 Issue 1
January-February 2025
Indexing Partners
Design And Evaluation of Fexofenadine Orally Disintegrating Tablets For Rapid Dissolution
Author(s) | Naveen Yadhav.J.K, Christopher Vimalson.D, Alagarraja.M, Gowrishankar.T, Nivetha.A, Krishnakanth.R, Rajaregam.K, Jannathul Firthosh.S |
---|---|
Country | India |
Abstract | Abstract: This study aims to formulate and evaluate Fexofenadine Oral Disintegration Tablets (ODTs), focusing on overcoming patient compliance issues related to taste and swallowing difficulties, especially in elderly and pediatric patients. Fexofenadine, a first-line treatment for type 2 diabetes, is used to enhance rapid dissolution, absorption, and bioavailability. Objectives included preparing tablets using direct compression and evaluating formulations through in-vitro tests such as weight variation, thickness, hardness, friability, drug content, wetting time, dispersion time, disintegration time, and dissolution studies. FTIR spectral analysis confirmed the presence of principal peaks and interactions between drugs and polymers. Results indicated a strong correlation (r = 0.998) between fexofenadine concentration and absorbance values. Tablets exhibited weight and thickness within pharmacoeial limits, with hardness, friability, and drug content meeting acceptable standards. Wetting time and water absorption ratio varied among formulations, with Cross povidone and Croscarmellose sodium showing superior performance. Disintegration times ranged from 17.66±0.51 to 171.83±1.16 seconds, with tablet formulations containing Cross povidone or combinations of super disintegrants (CP + CCS, CP + SSG) demonstrating rapid disintegration. In-vitro dispersion and dissolution studies reaffirmed these findings, suggesting these ODT formulations can significantly improve patient adherence, providing a quick onset of action and enhanced drug bioavailability. Further studies are recommended to establish extended in vivo performance and safety profiles, supporting the efficacy of fexofenadine ODTs in clinical settings. |
Keywords | Keywords: Fexofenadine, Oral disintegration tablets (ODTs), Direct compression technique, In-vitro evaluation, and Patient compliance. |
Field | Medical / Pharmacy |
Published In | Volume 7, Issue 1, January-February 2025 |
Published On | 2025-01-28 |
Cite This | Design And Evaluation of Fexofenadine Orally Disintegrating Tablets For Rapid Dissolution - Naveen Yadhav.J.K, Christopher Vimalson.D, Alagarraja.M, Gowrishankar.T, Nivetha.A, Krishnakanth.R, Rajaregam.K, Jannathul Firthosh.S - IJFMR Volume 7, Issue 1, January-February 2025. DOI 10.36948/ijfmr.2025.v07i01.35894 |
DOI | https://doi.org/10.36948/ijfmr.2025.v07i01.35894 |
Short DOI | https://doi.org/g829ps |
Share this
E-ISSN 2582-2160
doi
CrossRef DOI is assigned to each research paper published in our journal.
IJFMR DOI prefix is
10.36948/ijfmr
Downloads
All research papers published on this website are licensed under Creative Commons Attribution-ShareAlike 4.0 International License, and all rights belong to their respective authors/researchers.