摘要
目的:建立乙美片中乙水杨胺、咖啡因和美索巴莫的含量测定方法。方法:采用 HPLC 法测定,C_(18)柱(150 mm×4.6 mm,5μm),以甲醇-水-冰醋酸(39:61:1)为流动相,流速为1 mL·min^(-1),紫外检测波长为280 nm,柱温:室温;进样量:20μL。结果:乙水杨胺、咖啡因和美索巴莫线性范围分别为0.16~1.48μg,0.0163~0.1465μg,0.275~2.475μg;平均回收率(n=9)分别为99.5%(RSD 为0.78%),99.7%(RSD 为0.95%),100.6%(RSD 为0.98%)。结论:本方法简便、准确,可为评价乙美片中乙水杨胺、咖啡因和美索巴莫的含量提供依据。
Objective: To establish a method for the determination of ethenzamide, caffeine and methocarbamol in compound methocarbamol tablets. Methods:The HPLC column was C18 (150 mm ×4. 6 mm,5 μm);the mobile phase was methanol - water - acetic acid (39:61 : 1 ) ; the flow rate was 1 mL · min^ - 1, the UV detection wavelength was 280 nm, room temperature for column. Loaded volume was 20 μL. Results:The calibration curves of ethenzamide, caffeine and methocarbamol were linear in the range of 0. 16 - 1.48 μg,0. 0163 - 0. 1465 μg,0. 275 - 2. 475 μg respectively ; The average recoveries ( n = 9 ) were 99.5% ( RSD 0. 78% ) , 99. 7% ( RSD 0. 95% ) and 100. 6% (RSD 0. 98% )respectively. Conclusion: The method is rapid , accurate and reliable.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2007年第3期345-347,共3页
Chinese Journal of Pharmaceutical Analysis