Development and validation of RP-HPLC and UV spectroscopy method for the determination of diroximel fumarate in bulk drug and pharmaceutical dosage form (Record no. 22104)

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003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250109161851.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250109b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 25057
Author Patil, Jayesh D.
245 ## - TITLE STATEMENT
Title Development and validation of RP-HPLC and UV spectroscopy method for the determination of diroximel fumarate in bulk drug and pharmaceutical dosage form
250 ## - EDITION STATEMENT
Volume, Issue number Vol.14(3), Jul-Sep
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Raipur
Name of publisher, distributor, etc. Asian Pharma Press
Year 2024
300 ## - PHYSICAL DESCRIPTION
Pagination 147-150p.
520 ## - SUMMARY, ETC.
Summary, etc. Two new, simple, specific, precise and accurate UV-spectrophotometric and one reverse phase high performance liquid chromatography methods have been developed for the estimation of Diroximel Fumarate in Pharmaceutical dosage form. First UV-spectrophotometric methods show absorption maxima at 253nm for the Diroximel Fumarate. Percentage mean recovery obtained was 100.00%; coefficient of variance was found to be less than 2% and linearity coefficient was 0.9998. Linear response obtained for Diroximel Fumarate was in the concentration range of 0.5-2.5?g/ml. The limit of detection and limit of quantification for Diroximel was found to be 0.049?g/ml and 0.149?g/ml, respectively, and Second RP-HPLC method, chromatography analysis is carried out using Methanol: 10mm of KH2PO4 buffer solution (pH 3.1) (70:30%, v/v) as the mobile phase and C18 Waters (4.6mm x 150mm), 5.0µ column as stationery phase with detection wavelength of 272nm linearity was obtained in the concentration range of 5-25µg/ml for Diroximel Fumarate. Both UV-spectrophotometric and reverse phase high performance liquid chromatography methods were statistically validated according to I.C.H. Guidelines.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4642
Topical term or geographic name entry element Humanities and Applied Sciences
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 24937
Co-Author Dhankani, Amitkumar R.
773 0# - HOST ITEM ENTRY
Title Asian journal of pharmaceutical analysis
Place, publisher, and date of publication Raipur A & V Publications
International Standard Serial Number 2231-5667
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://ajpaonline.com/AbstractView.aspx?PID=2024-14-3-7
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
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          School of Pharmacy School of Pharmacy Archieval Section 2025-01-09 2025-0020 2025-01-09 2025-01-09 Articles Abstract Database
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