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Original Research Article | OPEN ACCESS

Colorimetric Determination of Cefadroxil and Ceftriazone in Pharmaceutical Dosage Forms

Aswani Ch Kumar, B M Gurupadayya , Navya S Sloka, R S Chandan, J C Thejaswini

Department of Pharmaceutical Analysis, JSS College of Pharmacy, JSS University, Mysore 570 015, (KA), India;

For correspondence:-  B Gurupadayya   Email: bmguru2004@yahoo.co.in   Tel:+919242886136

Received: 5 July 2010        Accepted: 7 December 2010        Published: 14 February 2011

Citation: Kumar AC, Gurupadayya BM, Sloka NS, Chandan RS, Thejaswini JC. Colorimetric Determination of Cefadroxil and Ceftriazone in Pharmaceutical Dosage Forms. Trop J Pharm Res 2011; 10(1):81-88 doi: 10.4314/tjpr.v10i1.13

© 2011 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To develop a simple, rapid and selective method for the spectrophotometric determination of cefadroxil and ceftriaxone using 1, 2- napthaquinone-4- sulfonic acid sodium.
Methods: The method was based on the derivatization of cefadroxil and ceftriaxone with 1, 2- naphthaquinone-4- sulfonic acid sodium in alkaline medium to yield orange-colored products.                                                                    
Results: The reaction products of cefadroxil and ceftriaxone at their respective λ max of 475 and 480 nm showed linearity in the concentration range of 10 - 100 and 25 - 175 µg/ml, respectively. Relative standard deviations of 0.82 % for cefadroxil and 0.95 % for ceftriaxone were obtained. Recoveries of cefadroxil tablets and ceftriaxone injection were in the range of 100.66 ± 0.98 and 99.38 ± 0.84 %, respectively.
Conclusion: Recovery studies gave satisfactory results indicating that none of the major additives/excipients interfered with the assay method. Therefore, the proposed method is simple, rapid, precise and convenient for the assay of cefadroxil and ceftriaxone in commercial preparations.

Keywords: Cephalosporins, Derivatization, 1, 2- Naphthaquinone 4- sulfonic acid sodium, Colorimetry, Pharmaceutical formulation

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Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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