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

ISSN: 2349-5162 | ESTD Year : 2014
Volume 12 | Issue 9 | September 2025

JETIREXPLORE- Search Thousands of research papers



WhatsApp Contact
Click Here

Published in:

Volume 5 Issue 12
December-2018
eISSN: 2349-5162

UGC and ISSN approved 7.95 impact factor UGC Approved Journal no 63975

7.95 impact factor calculated by Google scholar

Unique Identifier

Published Paper ID:
JETIR1812667


Registration ID:
193663

Page Number

499-509

Share This Article


Jetir RMS

Title

SOLUBILITY ENHANCEMENT STUDIES OF FEBUXOSTAT BY EMPLOYING GELUCIRE 50/13

Abstract

ABSTRACT Aim: Febuxostat (FBX) is a non purine selective inhibitor of xanthine oxidase/xanthine reductase. It belongs to BCS class II with low solubility and high permeability. Because of low solubility the bioavailability of the drug is hampered, food also interferes with the absorption of drug and decreases the Cmax by 38-49%. The bioavailability of a drug is a function of dissolution rate of the drug which is controlled by the surface area of the drug. In the category of poorly soluble drugs the change in surface area of the drug will show considerable changes in the solubility and dissolution of the drug. Materials and methods: In the present study, attempts were made to improve the bioavailability of FBX by solid dispersions technique by employing Gelucire 50/13 as carrier molecule. Different ratios on weight basis viz (1:1, 1:2, 2:1, 3:1, 4:1, 5:1, 6:1) coded as (FBXG1, FBXG2, FBXG3, FBXG4, FBXG5, FBXG6, FBXG7) with Gelucire 50/13 were prepared. Results and Discussion: The drug release studies were characterized in liquid state by phase solubility studies and in solid state by Fourier transform infrared spectroscopy (FTIR), Differential scanning calorimetry (DSC), Powdered X ray diffraction studies (PXRD) and Scanning electron microscopy (SEM). The aqueous solubility of FBX was favored by the presence of carriers. Solid state characterization indicated that FBX was present as fine amorphous form in the carrier polymeric molecules. Conclusion: In contrast to the solution rate of pure FBX the drug in carriers considerably improved the dissolution rate, this can be attributed to the increased wettability and dispersibility as well as decreased crystallinity and increased amorphous fraction of drug.

Key Words

KEYWORDS: Febuxostat, solid dispersions, Gelucire 50/13, Phase solubility, drug release studies.

Cite This Article

"SOLUBILITY ENHANCEMENT STUDIES OF FEBUXOSTAT BY EMPLOYING GELUCIRE 50/13", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.5, Issue 12, page no.499-509, December-2018, Available :http://www.jetir.org/papers/JETIR1812667.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

"SOLUBILITY ENHANCEMENT STUDIES OF FEBUXOSTAT BY EMPLOYING GELUCIRE 50/13", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.5, Issue 12, page no. pp499-509, December-2018, Available at : http://www.jetir.org/papers/JETIR1812667.pdf

Publication Details

Published Paper ID: JETIR1812667
Registration ID: 193663
Published In: Volume 5 | Issue 12 | Year December-2018
DOI (Digital Object Identifier):
Page No: 499-509
Country: hyderabad, telangana, India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


Preview This Article


Downlaod

Click here for Article Preview

Download PDF

Downloads

0003019

Print This Page

Current Call For Paper

Jetir RMS