Hemant Kumar Jain

A simple, selective and rapid reverse phase high performance liquid chromatographic (RP-HPLC) method for the analysis of Gliclazide in bulk and in tablet dosage form has been developed and validated. Sample was analysed on a Enable C18 (250mm X 4.6 mm i.d, particle size 5μm) column. The mobile phase consist of Methanol: Water (pH 3.5) in the ratio of 85:15v/v which was sonicated to degased and delivered at a flow rate of 1ml/min at ambient temperature. The retention time of Gliclazidewas 3.7+0.02 minutes. Studies were performed using an HPLC system equipped with a UV detector; the response was monitored at 230 nm.The calibration curve was linear over the concentration range of 20-70 μg/ml (r2=0.999). The limit of detection for Gliclazide was found to be 0.2438 μg/ml and the limit of quantification limit was about 0.7388 μg/ml. The accuracy of the method was established based on the recovery studies. The proposed method can be applied to the routine analysis of Gliclazide in bulk and in tablet dosage form.

The present work was defined to develop area under curve method for antipsychotic drug by UV spectrophotometric analysis which was economical, precise and an accurate method for estimation of Quetiapine fumarate. This method was based on area under curve of UV spectrum between 287 to 297 nm and validated as per ICH guideline Q2 (R1). The linearity in the range was found to be 4-14 μg/ml. The result of correlation coefficient was 0.999. The results of percent relative standard deviation for the intra-day and inter-day precision indicated that method is precise. The values of the recovery studies (99.65 % to 101.04 %) showed good accuracy of the method. LOD and LOQ were calculated as 0.3806 and 1.153μg/ml, respectively. The developed method can be applied for routine estimation of Quetiapine fumarate in bulk and tablet dosage forms.

The aim of present work was to develop an accurate, precise, reproducible and economical UV spectrophotometric method for estimation of Loratadine. This method was based on area under curve of UV spectrum between 241 to 251 nm and validated as per ICH guideline Q2 (R1). The method has followed linearity in the range of 5-30µg/ml. The value of correlation coefficient was 0.999. Satisfactory values of Percent relative standard deviation for the intra-day and inter-day precision indicated that method is precise. Results of the recovery studies (99.66 % to 99.95 %) showed accuracy of the method. LOD and LOQ were calculated as 0.581 µg/ml and 1.935 µg/ml, respectively. The developed method can be used for routine estimation of Loratadine in bulk and tablet dosage forms.