西北药学杂志
西北藥學雜誌
서북약학잡지
2013年
5期
486-488
,共3页
反相高效液相色谱法%金钱草%广金钱草%绿原酸%槲皮素%山柰酚
反相高效液相色譜法%金錢草%廣金錢草%綠原痠%槲皮素%山柰酚
반상고효액상색보법%금전초%엄금전초%록원산%곡피소%산내분
RP-HPLC%Herba lysimachiae%Desmodium styracifolium%chlorogenic acid%quercetin%kaempferol
目的建立同时测定金钱草和广金钱草中绿原酸、槲皮素和山柰酚含量的RP-HPLC方法。方法色谱柱为Dikma Dia-monsilTM C18柱(250 mm ×4.6 mm ,5μm);流动相为甲醇-4 mL · L -1甲酸,梯度洗脱;流速为1.0 mL · min-1;检测波长360 nm。结果绿原酸、槲皮素和山柰酚的线性范围分别为42.08~84.16 ng ( r=0.9998),19.13~382.68 ng ( r=0.9995)和16.96~339.20 ng(r=0.9995),平均加样回收率分别为99.91%,97.92%和99.31%,方法精密度 RSD分别为1.6%,1.4%和1.6%(n=6)。结论该方法快速、简便、准确度高、重复性好、专属性强,可用于金钱草和广金钱草的质量控制。
目的建立同時測定金錢草和廣金錢草中綠原痠、槲皮素和山柰酚含量的RP-HPLC方法。方法色譜柱為Dikma Dia-monsilTM C18柱(250 mm ×4.6 mm ,5μm);流動相為甲醇-4 mL · L -1甲痠,梯度洗脫;流速為1.0 mL · min-1;檢測波長360 nm。結果綠原痠、槲皮素和山柰酚的線性範圍分彆為42.08~84.16 ng ( r=0.9998),19.13~382.68 ng ( r=0.9995)和16.96~339.20 ng(r=0.9995),平均加樣迴收率分彆為99.91%,97.92%和99.31%,方法精密度 RSD分彆為1.6%,1.4%和1.6%(n=6)。結論該方法快速、簡便、準確度高、重複性好、專屬性彊,可用于金錢草和廣金錢草的質量控製。
목적건립동시측정금전초화엄금전초중록원산、곡피소화산내분함량적RP-HPLC방법。방법색보주위Dikma Dia-monsilTM C18주(250 mm ×4.6 mm ,5μm);류동상위갑순-4 mL · L -1갑산,제도세탈;류속위1.0 mL · min-1;검측파장360 nm。결과록원산、곡피소화산내분적선성범위분별위42.08~84.16 ng ( r=0.9998),19.13~382.68 ng ( r=0.9995)화16.96~339.20 ng(r=0.9995),평균가양회수솔분별위99.91%,97.92%화99.31%,방법정밀도 RSD분별위1.6%,1.4%화1.6%(n=6)。결론해방법쾌속、간편、준학도고、중복성호、전속성강,가용우금전초화엄금전초적질량공제。
Objective To simultaneously determine chlorogenic acid ,quercetin and kaempferol in Herba lysimachiae and desmodi-um styracifolium ,an RP-HPLC method was developed .Methods The separation was performed on a C18 (250 mm × 4 .6 mm , 5 μm) column with a gradient elution system of methanol and 4 mL · L -1 formic acid at the flow rate of 1 .0 mL · min-1 .The detection wave length was set at 360 nm .Results The linear ranges of determination for chlorogenic acid ,quercetin and kaempfer-ol were 42 .08-84 .16 ng (r=0 .999 8) ,19 .13-382 .68 ng (r=0 .999 5) and 16 .96-339 .20 ng (r=0 .999 5) ,respectively .The av-erage recoveries were 99 .91% ,97 .92% and 99 .31% ,respectively .The relative standard deviation of precision of the method were 1 .6% ,1 .4% and 1 .6% (n=6) ,respectively .Conclusion The method is rapid ,simple ,and with high accuracy ,good re-peatability ,strong specificity ,and can be used for the Herba lysimachiae and Desmodium styracifolium quality monitoring .