880 and 1.857 and 2.151, Pfizer Licensed Compound Library solubility dmso 1.543 and 1.542 at HQC, MQC and LQC levels respectively. The experimentally determined accuracy of the proposed method was presented in Table 2. Typical LC/MS/MS chromatograms for standard and test were presented in Fig. 4 and Fig. 5. LOD and LOQ can be expressed as a concentration at a specified signal: noise ratio
usually between 3:1 and 10:1 respectively. In the present study the LOD was determined to be 5 ng/mL with a signal:noise ratio of 3.1. The LOQ was 10 ng/mL with a signal:noise ratio of 10.2. The percent of RSD for six replicate injections of the LOQ solution was found to be less than 2.0%. The LOD and LOQ values were given in Table 3. To study the response of the instrument as a function of concentration of analyte (linear calibration curve), a series of different concentration solutions from 5 to 2000 ng/mL were prepared in triplicate and chromatograms were obtained by injecting 10 μL of each solution by LC-ESI HRMS. The calibration curve (Fig. 6) was plotted for the mean peak area of the chromatogram against Vismodegib the concentration of the MMF. The developed method showed linearity from 10 to 2000 ng/mL. The range of an analytical procedure is the interval between the upper and lower concentration of analyte in the sample for which it has been demonstrated
the analytical procedure has a suitable level of precision, accuracy and linearity. The range of this analytical method was found to be 10 to 2000 ng/mL. The linear regression coefficient (r2) was found to be 0.9999 for all the analyte. The results were presented in Table 4. In the present investigation study of robustness was demonstrated with the following changes (a linearity crotamiton and three concentrations range batch performed with the small changes in the method, there is a) one change pH of the mobile phase ±0.1 and mobile phase composition ±10% of Acetonitrile. These changes may not affect or alter the entire or end result of the method. In the study of robustness, linearity and three concentrations range batch performed with the changes in chromatographic conditions and found there was no change in the end result of the
study. The results were presented in Table 5. Study of ruggedness was found by making changes in the analytical column or change in the analyst it may not affect the end result of the analytical method. In the study of ruggedness, linearity and three concentrations range batch performed with the change in the different lot analytical column usage, there is no change in the end result of the study. Different pharmaceutical formulations were analysed by the developed method and the percent of drug content present in these formulations were reported. MMF tablets of 20 mg or 40 mg dosage were purchased from local market. Weight of each tablet was accurately determined by using high precision analytical balance and average weight of five 20 mg (or 40 mg) tablets was calculated and then these tablets finely powdered in a mortar.
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