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Abstract

Development and validation of new RP-HPLC method for the determination of dexrazoxane

Author(s): MV Basaveswara Rao1, V Prasanthi1, G Venkata Rao2, BV Raman3
1Department of Chemistry, Krishna University, Andhra Jateeya Kalasala Campus, Machilipatnam-521 001, India 2Department of Chemistry, SRR and CVR Govt. Degree College, Machavaram, Vijayawada-520 004, India 3Department of Biotechnology, MITS School of Biotechnology, 2(P), Infocity, Patia, Bhubaneswar-751 024, India

Correspondence Address:
M V Basaveswara Rao Department of Chemistry, Krishna University, Andhra Jateeya Kalasala Campus, Rajupeta, Machilipatnam-521 001 India E-mail: [email protected]


A new sensitive, precise, rapid and linear RP-HPLC method was developed and validated for the determination of dexrazoxane in formulations and human serum samples. Good chromatographic separation of dexrazoxane was achieved by using Kromasil C 18 column. The system was operated at ambient temperature using a mobile phase consisting of methanol, 5% ortho phosphoric acid, 0.01M ammonium dihydrogen phosphate and tetrahydrofuran, pH 4.2 (10:40:30:20, v/v) isocratically at a flow rate of 1 ml/min. The method showed high sensitivity with good linearity (r 2=0.9998)] over the tested concentration range of 0.1 to 0.9 mg/ml. Detection was carried out at 272 nm and retention time was 7.005 min. The accuracy, formulation assay and percentage of RSD were 100.03, 97.48 and 0.03184, respectively with tailing factor (1.84)]. This method can be used for the routine quality control analysis.

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