Ultraviolet spectrophotometric quantitation of anticancer drug alectinib hydrochloride in pharmaceutical formulation using green solvent (Record no. 22066)

MARC details
000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250108120711.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250108b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 25003
Author Koradia, Shaileshkumar K.
245 ## - TITLE STATEMENT
Title Ultraviolet spectrophotometric quantitation of anticancer drug alectinib hydrochloride in pharmaceutical formulation using green solvent
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 119-121p.
520 ## - SUMMARY, ETC.
Summary, etc. The developed ultraviolet spectrophotometric method allows simple, eco- friendly, accurate and precise determination of anti-cancer agent alectinib hydrochloride in bulk and its pharmaceutical formulation. Alectinib hydrochloride standard drug was dissolved and quantitatively diluted in methanol to produced a solution of 8.0 µg/mL concentration and absorbance was measured at its detection wavelength 339 nm against methanol as reagent blank. The calibration curve obeyed Beer’s law in the concentration range of 2 - 12 µg/mL with correlation co-efficient of 0.9996. The detection limits and quantitation limits were found to be 0.57 µg/mL and 1.71 µg/mL, respectively which indicates method is sensitive. Precision experiment was for intra-day, inter-day and repeatability and %RSD was found to be within the specified limits. The percent recovery studies was performed at three different levels and was observed between 99.56 - 101.43 %, indicating insignificant interference from the other ingredients present in the capsule formulation. The robustness study was performed by deliberately variations in the method parameters and % RSD was calculated and found within the limits indicates that the method is robust. The method validation parameters such as accuracy, precision, linearity, detection limit and quantitation limit of were validated as per international council for harmonization guidelines Q2-R1 and successfully applied for the quantitative analysis of alectinib hydrochloride from its pharmaceutical formulation.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 25004
Co-Author Thakkar, Rushik P.
773 0# - HOST ITEM ENTRY
International Standard Serial Number 2231-5667
Place, publisher, and date of publication Raipur A & V Publications
Title Asian journal of pharmaceutical analysis
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://ajpaonline.com/AbstractView.aspx?PID=2024-14-3-1
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Dewey Decimal Classification
Koha item type Articles Abstract Database
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 08/01/2025   2025-0006 08/01/2025 08/01/2025 Articles Abstract Database
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