DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR SIMULTANEOUS ESTIMATION OF BRINZOLAMIDE AND TIMOLOL BY HPLC FROM OPHTHALMIC PREPARATION
AbstractA fast, sensitive and accurate reverse phase liquid chromatographic method has been developed and validated for the simultaneous determination of Brinzolamide and Timolol maleate from ophthalmic preparation. Chromatographic separation of these two drugs were achieved on Zorbax Eclipse Plus, Agilent Technology (150mm x 4.6mm, 5μm) as stationary phase with a mobile phase comprising of triethylamine phosphate buffer : Acetonitrile : Methanol (70:20:10(v/v) at a flow rate of 1.0ml / min and PDA detection was set at 274 nm. Injection volume was 10 µl. Column oven temperature was maintained at 40°C. The retention time of timolol, and brinzolamide were 4.0 (±0.5) min, and 10.5 (±0.5) min respectively. Theoretical plate for Brinzolamide and Timolol were 5832 and 4876 respectively. The tailing factor was 1.09 and 1.21 for Brinzolamide and Timolol respectively. Resolution between the two compounds was 16.12. The developed method was validated according to the ICH guidelines and the proposed method can be applied for the routine quality control analysis of Brinzolamide and Timolol maleate from combined dosage form.
Article Information
43
1001-1007
452KB
2292
English
IJPSR
Rahima Khatun* and S.M. Ashraful Islam
Department of Pharmacy, University of Asia Pacific, Bangladesh
rahima676bph@gmail.com
25 October, 2013
31 December, 2013
16 February, 2014
http://dx.doi.org/10.13040/IJPSR.0975-8232.5(3).1001-07
01March2014
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