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首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >DEVELOPMENT AND VALIDATION OF REVERSE-PHASE HPLC METHOD FOR ESTIMATION OF HAMYCIN AND KETOCONAZOLE IN PHARMACEUTICAL CREAM
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DEVELOPMENT AND VALIDATION OF REVERSE-PHASE HPLC METHOD FOR ESTIMATION OF HAMYCIN AND KETOCONAZOLE IN PHARMACEUTICAL CREAM

机译:反相高效液相色谱法测定药物中的胰蛋白酶和酮康唑的开发与验证

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A simple, accurate rapid and precise RP-HPLC method has been developed and validated for determination of Hamycin and Ketoconazole in Pharmaceutical Cream. The RP-HPLC separation was achieved on Thermosil C-18, (250 mm, 4.6 mm, 5μm) using mobile phase 0.4 % ( v/v) diisopropylamine in methanol (v/v): 0.5% (w/v) Ammonium acetate in distilled water (90:10 % v/v) pH 6.5 adjusted with Glacial acetic acid at flow rate of 1.0 ml/min at ambient temperature. The retention times were 2.433 min. for Hamycin and 4.711 min. for Ketoconazole. Calibration plots were linear over the concentration range 50-250 μg/ml for Hamycin and 200-1000 μg/ml. Quantification was achieved with UV detection at 263 nm over the Beer-Lambert’s range.The method was validated statistically and applied successfully for the determination of Hamycin and Ketoconazole. Validation studies revealed that method is specific, rapid, reliable, and reproducible. The high recovery and low relative standard deviation confirm the suitability of the method for the routine determination of Hamycin and Ketoconazole in pharmaceutical cream. The proposed method was validated as per the ICH and USP guidelines.
机译:已开发出一种简单,准确,快速和精确的RP-HPLC方法,并已验证了该方法可用于测定药膏中的Hamycin和Ketoconazole。使用流动相0.4%(v / v)二异丙胺的甲醇溶液(v / v):0.5%(w / v)乙酸铵在Thermosil C-18(250 mm,4.6 mm,5μm)上进行RP-HPLC分离在室温下用冰醋酸调节的蒸馏水(90:10%v / v)pH 6.5中的溶液以1.0 ml / min的流速调节。保留时间为2.433分钟。为Hamycin和4.711分钟。用于酮康唑。校准曲线在Hamycin浓度范围为50-250μg/ ml和200-1000μg/ ml范围内是线性的。通过在Beer-Lambert范围内的263 nm处进行UV检测实现了定量。该方法经过统计学验证,成功地用于Hamycin和Ketoconazole的测定。验证研究表明该方法具有特异性,快速,可靠和可重现的特点。高回收率和低相对标准偏差证实了该方法适用于常规测定药用乳膏中的Hamycin和Ketoconazole的方法。根据ICH和USP指南对提出的方法进行了验证。

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