西北药学杂志
西北藥學雜誌
서북약학잡지
2013年
5期
492-494
,共3页
陈勇%蒋慧莲%周建良%盛燕
陳勇%蔣慧蓮%週建良%盛燕
진용%장혜련%주건량%성연
盆炎净胶囊%芍药苷%HPLC
盆炎淨膠囊%芍藥苷%HPLC
분염정효낭%작약감%HPLC
Penyanjing Capsules%paeoniflorin%HPLC
目的建立 HPLC法测定盆炎净胶囊中芍药苷的含量测定方法。方法采用Kromasil KR100-5 C18色谱柱(250 mm ×4.6 mm ,5μm);以乙腈-0.5 mL · L -1三乙胺溶液(用磷酸调节pH值至2.5)(14∶86)为流动相;流速为1.0 mL · min-1;检测波长为230 nm。结果芍药苷的线性范围为68~1692 ng ,回归方程为Y=1.3424 X+0.2891,r=1.000;平均回收率为100.3%, RSD为1.8%(n=9)。结论该方法结果准确,灵敏度高,重复性好,可用于盆炎净胶囊的质量控制。
目的建立 HPLC法測定盆炎淨膠囊中芍藥苷的含量測定方法。方法採用Kromasil KR100-5 C18色譜柱(250 mm ×4.6 mm ,5μm);以乙腈-0.5 mL · L -1三乙胺溶液(用燐痠調節pH值至2.5)(14∶86)為流動相;流速為1.0 mL · min-1;檢測波長為230 nm。結果芍藥苷的線性範圍為68~1692 ng ,迴歸方程為Y=1.3424 X+0.2891,r=1.000;平均迴收率為100.3%, RSD為1.8%(n=9)。結論該方法結果準確,靈敏度高,重複性好,可用于盆炎淨膠囊的質量控製。
목적건립 HPLC법측정분염정효낭중작약감적함량측정방법。방법채용Kromasil KR100-5 C18색보주(250 mm ×4.6 mm ,5μm);이을정-0.5 mL · L -1삼을알용액(용린산조절pH치지2.5)(14∶86)위류동상;류속위1.0 mL · min-1;검측파장위230 nm。결과작약감적선성범위위68~1692 ng ,회귀방정위Y=1.3424 X+0.2891,r=1.000;평균회수솔위100.3%, RSD위1.8%(n=9)。결론해방법결과준학,령민도고,중복성호,가용우분염정효낭적질량공제。
Objective To establish a method for determination of paeoniflorin in Penyanjing Capsules by HPLC .Methods The Kro-masil KR100-5 C18 (250 mm × 4 .6 mm ,5 μm) was used ,and the mobile phase was consisted of acetonitrile and 0 .5 mL · L -1 triethylamine (adjusting to pH2 .5 with phosphoric acid) (14∶86) at the flow rate of 1 .0 mL · min-1 .The detection wavelength was 230 nm .Results A good linear correlation of paeoniflorin was observed within the range of 68-1 692 ng (r= 1 .000) .The average recovery was 100 .3% with RSD 1 .8% (n=9) .Conclusion The method is accurate ,sensitive and repeatable ,and can be used for the quality control of Penyanjing Capsules .