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HPTLC Method Development and Validation of Cilnidipine and Metoprolol Succinate in Combined Dosage Form

机译:联合剂量形式西尼地平和琥珀酸美托洛尔的HPTLC方法开发和验证

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Introduction and Objectives: The present work involves developmentand validation of HPTLC method for simultaneous estimation of Cilnidipineand Metoprolol Succinate in their combined tablet dosage form. Method:In HPTLC method, Silica Gel G60 F254 TLC plate as the stationary phaseand a mobile phase of Toluene: Chloroform: Methanol: Glacial acetic acid(45: 25: 25: 5 v/v/v/v) was used to resolve CIL and METO. CIL and METOwere quantified at 231 nm. The proposed method weas validated accordingto International Conference on Harmonization. Result and Discussion:Two well-separated and sharp peak for CIL and METO were obtained at Rfvalues of 0.70 ± 0.01 and 0.34 ± 0.005 respectively. The linearity range obtainedfor HPTLC method were 100-500 ng/spot and 500-2500 ng/spot forCIL and METO respectively. Conclusion: Method validation was found tobe accurate, specific and precise.The developed method was successfullyapplied for estimation of CIL and METO in combined tablet formulation.
机译:引言和目的:本工作涉及HPTLC方法的开发和验证,该方法可同时估计西尼地平和琥珀酸美托洛尔的片剂组合剂量形式。方法:在HPTLC方法中,硅胶G60 F254 TLC板为固定相,流动相为甲苯:氯仿:甲醇:冰醋酸(45:25:25:5 v / v / v / v)和METO。 CIL和METO在231nm处定量。所提出的方法已根据国际协调会议进行了验证。结果与讨论:CIL和METO分别得到两个分离良好且尖锐的峰,Rf值分别为0.70±0.01和0.34±0.005。 HPTLC方法获得的线性范围分别为CIL和METO的100-500 ng / spot和500-2500 ng / spot。结论:方法验证准确,专一,准确。该方法已成功应用于组合片剂中CIL和METO的估算。

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