中国药业
中國藥業
중국약업
CHINA PHARMACEUTICALS
2015年
15期
32-33
,共2页
李庆德%郑锦坤%李旭桂%黄红雯%张毅%卞益民%罗启年
李慶德%鄭錦坤%李旭桂%黃紅雯%張毅%卞益民%囉啟年
리경덕%정금곤%리욱계%황홍문%장의%변익민%라계년
醒酒护肝口服液%槲皮素%高效液相色谱法
醒酒護肝口服液%槲皮素%高效液相色譜法
성주호간구복액%곡피소%고효액상색보법
Xingjiuhugan oral liquid%quercetin%HPLC
目的:建立测定醒酒护肝口服液中槲皮素含量的高效液相色谱(HPLC)法。方法色谱柱为 Kromasil C18柱(250 mm ×4.6 mm,5μm),以甲醇-0.4%磷酸溶液(50:50)为流动相,检测波长360 nm,柱温25℃。结果槲皮素进样量在0.1098~0.5490μg 范围内与峰面积呈良好的线性关系( r =0.9995)。平均回收率为98.26%,RSD 为0.61%( n =6)。结论该法操作简便、快速、重复性好,可用于醒酒护肝口服液的质量控制。
目的:建立測定醒酒護肝口服液中槲皮素含量的高效液相色譜(HPLC)法。方法色譜柱為 Kromasil C18柱(250 mm ×4.6 mm,5μm),以甲醇-0.4%燐痠溶液(50:50)為流動相,檢測波長360 nm,柱溫25℃。結果槲皮素進樣量在0.1098~0.5490μg 範圍內與峰麵積呈良好的線性關繫( r =0.9995)。平均迴收率為98.26%,RSD 為0.61%( n =6)。結論該法操作簡便、快速、重複性好,可用于醒酒護肝口服液的質量控製。
목적:건립측정성주호간구복액중곡피소함량적고효액상색보(HPLC)법。방법색보주위 Kromasil C18주(250 mm ×4.6 mm,5μm),이갑순-0.4%린산용액(50:50)위류동상,검측파장360 nm,주온25℃。결과곡피소진양량재0.1098~0.5490μg 범위내여봉면적정량호적선성관계( r =0.9995)。평균회수솔위98.26%,RSD 위0.61%( n =6)。결론해법조작간편、쾌속、중복성호,가용우성주호간구복액적질량공제。
Objective To investigate quantitative determination method of quercetin in Xingjiuhugan oral solution to provide identifiable ground for the foundation of quality standards. Methods Octadecylsilane chemically bonded silica column was adopted with methanol -0. 4% phosphate(50 : 50) as flowing phase, testing wave 360 nm, column temperature 25 ℃ . Results A good linear relationship of Quercetin showed between 0. 109 8 - 0. 549 0 μg( r = 0. 999 5). Lower limit of average recovery was 98. 26% ,RSD = 0. 61% ( n = 6). Conclusion This method is simple, rapid, reproducible and can be used for the quality control of Xingjiuhugan oral liquid.