Response surface based optimization of system variables for liquid chromatographic analysis of candesartan cilexetil
Autor: | Dipak D. Kumbhar, Rajesh G Jadhao, Shreyas D. Jogdand, Snehal S. Vispute, Jagdish V. Manwar, Ravindra L. Bakal, Rahul S. Manmode |
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Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Detection limit
Chromatography Correlation coefficient Chemistry 010401 analytical chemistry Analytical chemistry Linearity 02 engineering and technology Factorial experiment 021001 nanoscience & nanotechnology 01 natural sciences High-performance liquid chromatography Standard deviation Candesartan cilexetil 0104 chemical sciences Volumetric flow rate Response surface methodology Factorial design HPLC 0210 nano-technology lcsh:Science (General) lcsh:Q1-390 |
Zdroj: | Journal of Taibah University for Science, Vol 11, Iss 1, Pp 159-172 (2017) |
ISSN: | 1658-3655 |
Popis: | A statistical optimization method was successfully employed to study the effect of system variables on the chromatographic analysis of candesartan cilexetil. The effect of simultaneously varying the flow rate, temperature and concentration of acetonitrile in the mobile phase in water (0.05% O-phosphoric acid (0.05% OPA)) was studied to optimize the method to obtain excellent chromatographic responses. The optimum conditions were determined with the help of response surface methodology (RSM) using Plackett–Burman designs. From the response surface graphs, the optimum regions were selected to be −1, +1 and +1 for flow rate (0.8 ml/min), temperature (25 °C) and concentration of acetonitrile in water (0.05% OPA) (80%, v/v), respectively. Pareto ranking indicated that the most important variable affecting the selected responses was temperature. Linearity was found in the range of 10 of 50 μg/ml, with a significantly high correlation coefficient ( r 2 = 0.9989). The limits of detection and quantitation were 0.12 and 0.33 μg/ml, respectively. The developed method was validated for accuracy, precision, linearity, range, and specificity. The method was successfully used to analyze a tablet formulation to assess the chromatographic performance, and it was found to be 99.03%, with a standard deviation of ±0.04. |
Databáze: | OpenAIRE |
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