dc.creatorNegi, Bhawana
dc.creatorBansal, Ruchi
dc.creatorSingh, Dhirendra P.
dc.creatorSingh, Lokesh K.
dc.date2011
dc.date2012-02-03T03:00:00Z
dc.identifierhttp://sedici.unlp.edu.ar/handle/10915/8410
dc.identifierhttp://www.latamjpharm.org/resumenes/30/10/LAJOP_30_10_1_22.pdf
dc.descriptionA simple, economic and time-efficient, isocratic reverse-phase ultra performance liquid chromatographic (RP-UPLC) method has been developed to analyze aripiprazole in tablets. Successful chromatographic elution and quantification of the drug was achieved on a Waters Symmetry C18, 100 mm x 4.6mm, 3.5 μm column, UV detection at 220 nm with a isocratic mobile phase comprising a mixture of component A (pH 2.5, phosphate buffer) and component B (methanol and acetonitrile (1:1, v/v) in the ratio of 45:55 (v/v). The flow rate was 1.0 mL/min. The method was validated for specificity, precision, linearity, accuracy, range, stability in analytical solution, robustness and system suitability. The linearity concentration range was 5.4-67.8 μg/mL with the correlation coefficient of 0.9997. Total elution time was about 6 min which allowed quantification of more than 100 samples per day.
dc.descriptionColegio de Farmacéuticos de la Provincia de Buenos Aires
dc.formatapplication/pdf
dc.format2016-2023
dc.languageen
dc.relationLatin American Journal of Pharmacy
dc.relationvol. 30, no. 10
dc.subjectFarmacia
dc.titleNew validated RP-UPLC method for determination of aripiprazole assay in aripiprazole tablets
dc.typeArticulo
dc.typeArticulo


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