Method Development and Validation of Lorazepam by Using RP-HPLC in Pharmaceutical Formulation

J.R.V.Prasanna, D.Narendra, K.Susritha Reddy, A.Lakshmi Tulasi, A.Nikhitha, M.Krishna, Sowmya Sri
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Abstract

High pressure liquid chromatography (RP-HPLC) is a column chromatographic technique employing high pressure pump to pass both mobile phase and sample mixture through stationary phase column and perform efficient separation. A C-18 column with mobile phase containing Acetonitrile: methanol (80: 20) was used. The flow rate was 1.0ml/min. and were monitored at 210 nm. The retention time for Lorazepam was 1.3 min. The method was validated for linearity, accuracy, precision, limit of detection. The Mean percent recovery of Lorazepam from tablet formulation was found to be 94.80 %.
方法采用反相高效液相色谱法对劳拉西泮的处方进行开发和验证
高压液相色谱(RP-HPLC)是一种利用高压泵将流动相和样品混合物通过固定相柱进行高效分离的柱相色谱技术。采用C-18色谱柱,流动相为乙腈:甲醇(80:20)。流速1.0ml/min。并在210 nm处进行监测。劳拉西泮的保留时间为1.3 min。对方法进行了线性度、准确度、精密度、检出限的验证。劳拉西泮片剂的平均回收率为94.80%。
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