Exploring cosolvency in analytical method development and validation of poorly aqueous soluble candesartan cilexetil in bulk and dosage forms (Record no. 23120)

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000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250718151203.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 250718b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 26771
Author Yadav, P. S.
245 ## - TITLE STATEMENT
Title Exploring cosolvency in analytical method development and validation of poorly aqueous soluble candesartan cilexetil in bulk and dosage forms
250 ## - EDITION STATEMENT
Volume, Issue number Vol.86(2), Mar-Apr
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Pharmacutical Association
Year 2024
300 ## - PHYSICAL DESCRIPTION
Pagination 195-201p.
520 ## - SUMMARY, ETC.
Summary, etc. The study was performed with a dual approach to develop and validate analytical method for poorly water soluble candesartan cilexetil by enhancing its solubility employing cosolvency technique. In order to enhance drug’s solubility based on its solubility characteristics, phosphate buffer (pH 6.8):ethanol (95 % v/v) mixture at 90:10 proportion was used along with Tween 80 (1 % v/v). Solubility of candesartan cilexetil in phosphate buffer (pH 6.8) enhanced due to the addition of co-solvent ethanol and Tween 80. Developed method obeyed Beer-Lambert’s law in the concentration range between 3-21 μg/ml. The regression coefficient at the wavelength 232 nm was 0.999. The analysis of tablets by the proposed method indicated a good correlation between estimated and label claims. Recovery studies showed that any small difference in drug concentration could be accurately determined. Low values of limit of detection and limit of quantitation indicated that the proposed method is sensitive, economic, accurate, precise, and robust for routine analysis of candesartan cilexetil in bulk and dosage forms.
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) 4538
Co-Author Hajare, Ashok A.
773 0# - HOST ITEM ENTRY
International Standard Serial Number 0250-474X
Title Indian journal of pharmaceutical sciences
Place, publisher, and date of publication New Delhi Indian Pharmaceutical Association
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijpsonline.com/articles/exploring-cosolvency-in-analytical-method-development-and-validation-of-poorly-aqueous-soluble-candesartan-cilexetil-in-.pdf
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942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 18/07/2025   2025-1036 18/07/2025 18/07/2025 Articles Abstract Database
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