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作 者:金伟华[1] 范开华[1] 于波涛[1] 陈华[1] 易荣[1]
出 处:《药学服务与研究》2013年第6期460-462,共3页Pharmaceutical Care and Research
摘 要:目的:制备氯诺昔康乳膏剂,建立HPLC法测定乳膏剂中氯诺昔康的含量。方法:用水包油型基质制备含氯诺昔康0.2%的乳膏剂,HPLC法所用色谱柱为Eclipse XDB-C18柱,流动相为0.05 mo1/L乙酸钠溶液(pH 6.5)-甲醇(50∶50),流速1 ml/min,检测波长378 nm,柱温30 ℃。结果:氯诺昔康在0.01~0.10 mg/ml范围内呈良好线性关系,标准曲线方程为:A=4.85×104 c-29.69(r=0.999 5)。低、中、高浓度(0.02、0.06、0.10 mg/ml)氯诺昔康的加样回收率分别为(99.10±1.37)%、(101.47±0.37)%和(99.25%±1.89)%(n=3),日内和日间精密度良好。结论:制备的氯诺昔康乳膏剂质量合格,建立的含量测定方法简便、准确、可靠。Objective:To prepare lornoxicam cream and establish a HPLC method for the determination of the content of lornoxicam. Methods:The cream containing 0.2% lornoxicam was prepared by using oil in-water matrix. HPLC was applied on an Eclipse XDB-C18 column with the mobile phase consisting of 0.05 mol/L sodium acetate solution (pH 6.5)-methanol(50 : 50). The flow rate was i ml/min and detection wavelength was 378 nm and the column temperature was 30 C. Results:Lornoxi cam was of good linearity within the range of 0.01-0. 10 mg/ml. The standard curve equation was A = 4.85 × 101 c 29.69(r=0. 999 5). The recovery rates of low-,middle and high concentrations(0.02,0. 06,0. 10 mg/ml) were (99.10±1. 37)%, (101.47±0.37) % and (99.25± 1.89)% (n = 3). The precision of intra-day and interday was also good. Conclusion.. The prepared lornoxieam cream met with specified quality and the HPLC method for content determination was simple,accurate and reliable.
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