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|Title: ||Novel selective kinetic spectrophotomeric method for determination of norfloxacin|
|Authors: ||A. Darwish, Ibrahim.|
A. Sultan, Maha.
A. Al-Arfaj, Hessa.
|Keywords: ||Amlodipine, Atorvastatin, capillary electrophoresis.|
|Issue Date: ||2009 |
|Citation: ||Talanta, 78, 1383-1388.|
|Abstract: ||A simple, accurate, precise, and sensitive capillary electrophoresis (CE) technique coupled to a diode array detector (DAD) has been developed for the separation and simultaneous determination of amlodipine (AM) and atorvastatin (AT) from their combination formulations. The proposed method utilized fused silica capillary (50 cm_75 mm ID) and background electrolyte (BGE) composed of phosphate buffer (pH 6.5, 25 mM)-methanol, (80:20, v=v). The separation was achieved at 15KV applied voltage and 25_C. Losartan was chosen as the internal standard to guarantee a high level of quantitative performance. The two drugs were subjected to thermal, photolytic, hydrolytic, and oxidative stress conditions and the stressed samples were analyzed by the proposed method. The method has
shown adequate separation for AM and AT from its main degradation products (UK-55-410) & (PD 0162910-00), respectively, which demonstrated the specificity of the assay. The described method was linear over the range of 1 – 50 mg=mL (r¼0.9998) for both drugs (2.4_10_6_1.2_10_4M for AM and 1.8_10_6 _8.6_10_5M for AT). Intra- and inter-day RSD (n¼6) was _2.2%. The limits of detection for AM and AT were 0.5 mg=mL. The percentage recoveries (n¼6) of the two drugs from their tablet formulations were 99.97_1.84 and 100.96_ 1.12, respectively. Degradation products produced as a result of stress studies did not interfere with the detection of AM and AT and the assay can thus be
considered stability indicating.those obtained by a reference spectrophotometric method showed excellent agreement between the accuracy and precision of the two methods.|
|Appears in Collections:||College of Pharmacy|
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