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

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

JETIREXPLORE- Search Thousands of research papers



WhatsApp Contact
Click Here

Published in:

Volume 6 Issue 3
March-2019
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:
JETIR1903518


Registration ID:
200109

Page Number

139-157

Share This Article


Jetir RMS

Title

“FORMULATION AND IN-VITRO DISSOLUTION ENHANCEMENT OF BLONANSERIN USING LIQUISOLID COMPACTS” Tit

Abstract

The present study was to carried out pre-formulation studies for possible drug and excipients interactions and to formulate liquid solid complex using different carriers and disintegrants and to identify Physico-chemical characterization and In vitro drug release study of prepared liquid solid complex. The solubility studies of Blonanserin in presence of PEG were high when compared with Propylene Glycol and glycerine. The liquisolid technique was found to be a promising approach for improving the dissolution of poorly soluble drugs like Blonanserin. The Dissolution of Blonanserin was significantly increased in liquisolid Formulation compared to the marketed product. The IR spectra indicate there was no interaction between the drug and excipients. The increased dissolution rate may be due to increased wetting and increased surface area of the particles. From the XRD, FT-IR, Drug content & In Vitro dissolution studies of Blonanserin liquisolid compacts it was concluded that the formulation F9 is the best formulation. The powder blend was subjected to various physical characteristics such as bulk density, tapped density, Hausner’s ratio, compressibility index. The powder was compressed and the core tablets were evaluated for weight variation, hardness, disintegration time, drug content, dissolution studies, powder analysis like XRD and FT-IR studies is concluded the best formulation is F9.

Key Words

Blonanserin, XRD, FT-IR

Cite This Article

"“FORMULATION AND IN-VITRO DISSOLUTION ENHANCEMENT OF BLONANSERIN USING LIQUISOLID COMPACTS” Tit", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.6, Issue 3, page no.139-157, March-2019, Available :http://www.jetir.org/papers/JETIR1903518.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 IN-VITRO DISSOLUTION ENHANCEMENT OF BLONANSERIN USING LIQUISOLID COMPACTS” Tit", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.6, Issue 3, page no. pp139-157, March-2019, Available at : http://www.jetir.org/papers/JETIR1903518.pdf

Publication Details

Published Paper ID: JETIR1903518
Registration ID: 200109
Published In: Volume 6 | Issue 3 | Year March-2019
DOI (Digital Object Identifier):
Page No: 139-157
Country: Dhanap ,Gandhinagar, Gujarat, India .
Area: Pharmacy
ISSN Number: 2349-5162
Publisher: IJ Publication


Preview This Article


Downlaod

Click here for Article Preview

Download PDF

Downloads

0002933

Print This Page

Current Call For Paper

Jetir RMS