Etizolam
Explore 2 research publications tagged with this keyword
Publications Tagged with "Etizolam"
2 publications found
2014
1 publicationMethod Development and Validation for the Simultaneous Estimation of Propranolol Hydrochloride and Etizolam by Reverse Phase High Performance Liquid Chromatography
RP-HPLC method has been developed for the quantitative estimation of Propranolol hydrochloride and Etizolam using C 18 column and a mobile phase consisting of Methanol and Water in the ratio 70:30. The mobile phase was pumped at a rate of 1ml/min and detection was carried out at 281.5 nm(iso-absorptive point). The linearity was found to be in range of 5-50µg/ml and 0.5-5µg/ml with regression coefficient (r2=0.999, and r2=0.997) for Propranolol hydrochloride and Etizolam respectively. The peaks obtained were sharp having baseline separation with a retention time of 2.35and 6.57min for Propranolol hydrochloride and Etizolam respectively.The LOD was found to be at the concentration of0.1µg/ml and 0.025µg/ml for Propranolol hydrochloride and Etizolam respectively. The percentage recovery was found to be 98.5% to 100.58% for Propranololhydrochloride and 95% to 106.6% for Etizolam. The method was validated statistically.
2012
1 publicationRP-HPLC Method for Simultaneous Estimation of Escitalopram oxalate and Etizolam in Bulk and Tablet Dosage Form
Present work describes a selective, precise and accurate Reverse Phase High Performance Liquid Chromatographic (RP-HPLC) method for simultaneous estimation of Escitalopram Oxalate (ESC) and Etizolam (ETI) on Kromasil 100 C18, 5µ(150×4.6 mm) Column using Acetonitrile:0.005 M Hexane Sulfonic Acid pH 3.0 (adjusted with o-phosphoric acid) (40:60 v/v) as mobile phase, at a flow rate of 1.0 ml/min and the detection wavelength was 254 nm. The retention time for ESC and ETI was found to be 3.66 and 8.07 min, respectively. The ion-pairing reagent improved the retention of polar ESC on Reverse-phase column. The method was validated for linearity, precision, accuracy, LOD, LOQ robustness, solution stability and specificity. The method was linear in the concentration range of 20-160µg/ml for ESC and 2-16 µg/ml for ETI with a correlation coefficient of 0.9994 and 0.9993 for respective drugs. The percent recovery was found in the range of 98.14-101.72% and 98.83-101.12 % for ESC and ETI, respectively. The specificity of method was established based on peak purity data. The proposed method was successfully applied for quantitative determination of escitalopram oxalate and Etizolam in combined tablet dosage form for routine analysis.
