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机构地区:[1]广西壮族自治区人民医院,南宁530021 [2]广西万寿堂药业有限公司,南宁530219
出 处:《海峡药学》2006年第5期65-67,共3页Strait Pharmaceutical Journal
摘 要:目的建立清咽胶囊中穿心莲内酯和脱水穿心莲内酯的含量测定方法。方法应用HPLC法,选用ReliesilCls色谱柱(250×4.6mm,5μm),流动相为甲醇-水(65:35),流速为:1ml·min^-1,检测波长为250nm。结果本品中穿心莲内酯含量测定线性范围为0.084-0.756μg(r=0.9999),平均回收率为97.5%(RSD=2.26%,n=5);脱水穿心莲内酯含量测定线性范围为0.036~0.324μg(r=0.9998),平均回收率为100.1%(RSD=0.86%,n=5)。结论含量测定方法准确可行,重复性好,作为药品标准可有效地控制清咽胶囊的质量。OBJECTIVE To establish a determination of Andrographolide and Dehyandro grapholide in Qingyan Capsules. METHODS Reliesil C18 column (5μm, 250 × 4.6mm) was used. The mobile phase was consisted of methanol-water (65 : 35) and the measuring wavelength was 250nm. RESULTS Linear range of Andrographolide was 0. 084 to 0. 756ttg(r=0. 9999),The average recovery was 97.5% (RSD= 2.26% n= 5); and the dehydroandrographolide was 0. 036 to 0. 324 μg(r=0. 9998),The average recovery was 100.1% (RSD =0. 86% n= 5). CONCLUSION The method of quantification were accurate, realizible and reproductable. It can be used effectively for the quality control of Qingyan Capsules.
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