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机构地区:[1]华中科技大学同济医学院附属同济医院药学部,湖北武汉430030
出 处:《华西药学杂志》2006年第6期577-579,共3页West China Journal of Pharmaceutical Sciences
摘 要:目的 建立开胸顺气滴丸中厚朴酚与和厚朴酚含最的测定方法。方法 采用RP—HPLC法,色谱柱为VPC18(150mm×4.6mm,5μm);流动相为甲醇-乙腈-水(50:20:40);流速1.0ml·min^-1;柱温25℃;检测波长294nm。结果 厚朴酚的线件范围为0.2961~2.9610μg(r=0.9996);和厚朴酚的线性范围为0.1608—1.6080μg(r=0.9996)。厚朴酚的平均回收率为99.17%±1.66%,RSD=1.3%(n=6);和厚朴酚的平均回收率为99.04%±2.06%,RSD=1.7%(n=6)。结论 所用方法简便、准确,可用于开胸顺气滴丸中厚朴酚与和厚朴酚的含量测定。OBJECTIVE To establish a method for determination of magnolol and isomagnololin in Kaixiong Shunqi drops. METH- ODS An RP - HPLC method was adopted. The analysis was carried out on an analytical column C18 ( 150 mm × 4. 6 mm,5 μm). The mobile phase consisted of methanol -acetonitrile -water (50 : 20 : 40 ) and the flow rate was 1.0 ml·min^-1, The detective wavelength was set at 294 nm with column temperature of 25℃. RESULTS The lienar range was 0. 2961 - 2. 9610 μg ( r = 0. 9996) and the average recovery was 99.17%±1.66% with the RSD of 1.3% (n = 6) for magnolol, respectively. The linear range was 0, 1608 - 1. 6080 μg( r = 0. 9996 ) and the average recovery was 99.04%± 2.06% with the RSD of 1.7% ( n = 6 ) for isomagnololin, respectively. CONCLUSION The method is simple,reproducible and suitable for determination of magnolol and isomagnololin in Kaixinng Shunqi drops.
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