The repeatability of the developed UPLC method was checked by a six-fold analysis

of the Metoclopramide sample spiked with the four impurities. The RSD of peak area was calculated for each impurity. Inter and Intra-day variation and analyst variation were studied to determine the intermediate precision of the developed method. The RSD of the area of Metoclopramide related compound ACETYLMETO, ACMA, CLEE and ACME was within 0.3%. The RSD of results obtained selleck kinase inhibitor in intermediate precision studies was within 0.9% (Table 2). Limit of detection (LOD) and limit of quantification (LOQ) values were determined using the signal to noise ratio method. The LOD of Metoclopramide and its impurities were found to be in the

range of 0.001–0.004 μg/mL (of analyte concentration 1 mg/mL). The LOQ of Metoclopramide and its impurities were found to be in the range of 0.07–0.1 μg/mL. The precision for Metoclopramide and its impurities at LOQ level was below 3.0% RSD (Table 3). The linearity of the test method was established from the LOQ to 150% of the test concentration for Metoclopramide and its related substances. The correlation coefficients obtained were greater than 0.9999. The result showed that an excellent correlation existed between the peak area and concentration of the analyte (Table 4). The accuracy of an analytical procedure expresses the closeness of agreement between the reference value and the value found. The percentage recovery of ACETYLMETO, ACMA, CLEE and ACME ranged from 99 to 105% (Table 5). Chromatograms of Antidiabetic Compound Library datasheet spiked samples at 0.2% level of all four impurities in a Metoclopramide sample are shown in Fig. 3. The robustness of an analytical procedure is a measure of its capacity to remain unaffected Adenylyl cyclase by small but deliberate variations in chromatographic method parameters and provided an indication of its reliability during normal usage. In all the varied chromatographic conditions (flow rate, pH of the mobile phase and column temperature), the resolution between impurities and analyte was found to be more than 2.0 (Table 6).

The %RSD values of the four impurities during solution stability and mobile phase stability experiments were within 1.0%. No significant change was observed in the content of impurities during solution stability and mobile phase stability experiments confirm that sample solutions and mobile phase used during the study were stable up to 48 h. The simple UPLC method developed for the quantitative determination of related compounds of Metoclopramide and its possible degradation products is precise, accurate and specific for the analysis of bulk material and formulation samples. The method was fully validated, showing satisfactory results for all the parameters tested. The developed method is stability indicating and can be used for the routine analysis of production samples. All authors have none to declare.