Loading article...
Loading article...
Stream/Area:
-
Subject:
-
Paper ID:
10.55041/IJSREM35538
Volume:
8 |
6 |
Jun 2024
Pages:
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
The simple, rapid, precise, accurate, robust and economical analytical method has been developed for estimation of Ranolazine in bulk and pharmaceutical dosage form. This study describes the validation of an UV Spectrophotometric method for quantitative determination of Ranolazine in pharmaceutical dosage form using acetate buffer (pH 4.4) as solvent. The maximum absorbance was found at 272 nm. The Linearity was found to be in range of 5 to 40µg/ml. The %RSD for Intraday and Interday precision studies was found to be 0.793 and 0.793 respectively. The % assay was found to be 99.6%±0.05. The average % recovery of ranoalazine was found to be in between 98.5-101.7%. LOD and LOQ was found to be 0.58 µg/ml and 1.75 µg/ml respectively. The results suggest that this method can be employed for routine analysis of Ranolazine in bulk and commercial pharmaceutical formulations.
KEYWORDS
Publication Date
5/5/2024
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
Documents
Article Views
0
Total views since publication
PDF Downloads
0
Total downloads since publication
Geographic Reach
5
Digital Preservation: This article is permanently archived on Zenodo and complies with all data preservation standards across major indexing platforms.
Plagiarism Screening
This manuscript has been checked for plagiarism using TurnitinPlagiarismChecker software.
Conflict of Interest
The authors declare no conflict of interest related to this research work.
Funding Information
No funding information available for this research.
Related research in the same subject area
Loading similar articles...