海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2015年
7期
37-38
,共2页
八珍益母胶囊%槲皮素%山奈素%HPLC
八珍益母膠囊%槲皮素%山奈素%HPLC
팔진익모효낭%곡피소%산내소%HPLC
Bazhenyimu capsules%Quercetin%HPLC
目的:建立八珍益母胶囊中槲皮素的HPLC的测定方法,为制定该制剂质量标准中定量测定方法及限度提供依据。方法色谱柱:Sun-fire-C18(4.6mm ×150mm,5μm);流动相:以甲醇-0.4%磷酸溶液(50∶50);流速:1.0mL? min -1,检测波长:360nm,柱温:25℃,进样量:10μL。结果槲皮素的线性范围分别为34.35~429.43μg,平均加样回收率(n=6)分别为99.26%,RSD分别为0.26%。结论该方法简单、快速、结果准确,重现性好,为八珍益母胶囊中槲皮素的测定提供可靠的方法。
目的:建立八珍益母膠囊中槲皮素的HPLC的測定方法,為製定該製劑質量標準中定量測定方法及限度提供依據。方法色譜柱:Sun-fire-C18(4.6mm ×150mm,5μm);流動相:以甲醇-0.4%燐痠溶液(50∶50);流速:1.0mL? min -1,檢測波長:360nm,柱溫:25℃,進樣量:10μL。結果槲皮素的線性範圍分彆為34.35~429.43μg,平均加樣迴收率(n=6)分彆為99.26%,RSD分彆為0.26%。結論該方法簡單、快速、結果準確,重現性好,為八珍益母膠囊中槲皮素的測定提供可靠的方法。
목적:건립팔진익모효낭중곡피소적HPLC적측정방법,위제정해제제질량표준중정량측정방법급한도제공의거。방법색보주:Sun-fire-C18(4.6mm ×150mm,5μm);류동상:이갑순-0.4%린산용액(50∶50);류속:1.0mL? min -1,검측파장:360nm,주온:25℃,진양량:10μL。결과곡피소적선성범위분별위34.35~429.43μg,평균가양회수솔(n=6)분별위99.26%,RSD분별위0.26%。결론해방법간단、쾌속、결과준학,중현성호,위팔진익모효낭중곡피소적측정제공가고적방법。
OBJECTIVE To establish a method for determing quercetin in Bazhenyimu capsules by HPLC.METHODS The HPLC method was carried out on Agilent C 18 column(4.6mm ×150mm,5μm),The mo-bile phase was methanol-0.5%phosphate(50∶50);The flow rate was 1.0mL? min-1,The detection wavelength was at 360nm,The column temperature was set at 25℃,and 10μL injection volumn. RESULTS There was a good lin-ear relationship when quercetin were in the range of 34.35~429.43μg.The average recoveries were 99.26%, re-spective RSD were 0.26%.CONCLUSION The method is simple in operation ,high in sensitivity and good in re-producibility ,and can be used for the determination the quercetin in Bazhenyimu capsules by HPLC .