新疆医科大学学报
新疆醫科大學學報
신강의과대학학보
JOURNAL OF XINJIANG MEDICAL UNIVERSITY
2013年
8期
1094-1097
,共4页
高效液相色谱法%金雀花%槲皮素%山萘素%异鼠李素
高效液相色譜法%金雀花%槲皮素%山萘素%異鼠李素
고효액상색보법%금작화%곡피소%산내소%이서리소
HPLC%TCL%caragana altaica Kom .Pojark .%quercetin%kaempferol%isorhamnetin
目的研究金雀花的薄层色谱鉴别特征,建立HPLC法测定黄酮类化合物的方法。方法采用薄层色谱法对金雀花中槲皮素和山萘酚进行定性鉴别,槲皮素以甲苯-乙酸乙酯-甲酸=5∶2∶1为展开剂,山萘素以甲苯-乙酸乙酯-甲酸=5∶4∶1为展开剂;采用色谱柱:Shim-pack VP-ODS(150 mm ×4.6 mm),以甲醇-0.4%磷酸溶液(50∶50)为流动相,流速为1 mL/min ,检测波长为360 nm ,柱温为25℃。结果在薄层色谱中能检测到槲皮素和山萘酚,槲皮素、山萘素、异鼠李素分别在0.01~0.1、0.0025~0.025、0.0025~0.025 mg/mL范围内线性良好,其平均回收率分别为100.7%、100.4%、101.7%。RSD分别为1.3%、1.4%和1.9%。样品黄酮类化合物的平均含量为1.25%。结论该方法简便、快速、准确、重复性好,可用于测定金雀花中黄酮类化合物的含量。
目的研究金雀花的薄層色譜鑒彆特徵,建立HPLC法測定黃酮類化閤物的方法。方法採用薄層色譜法對金雀花中槲皮素和山萘酚進行定性鑒彆,槲皮素以甲苯-乙痠乙酯-甲痠=5∶2∶1為展開劑,山萘素以甲苯-乙痠乙酯-甲痠=5∶4∶1為展開劑;採用色譜柱:Shim-pack VP-ODS(150 mm ×4.6 mm),以甲醇-0.4%燐痠溶液(50∶50)為流動相,流速為1 mL/min ,檢測波長為360 nm ,柱溫為25℃。結果在薄層色譜中能檢測到槲皮素和山萘酚,槲皮素、山萘素、異鼠李素分彆在0.01~0.1、0.0025~0.025、0.0025~0.025 mg/mL範圍內線性良好,其平均迴收率分彆為100.7%、100.4%、101.7%。RSD分彆為1.3%、1.4%和1.9%。樣品黃酮類化閤物的平均含量為1.25%。結論該方法簡便、快速、準確、重複性好,可用于測定金雀花中黃酮類化閤物的含量。
목적연구금작화적박층색보감별특정,건립HPLC법측정황동류화합물적방법。방법채용박층색보법대금작화중곡피소화산내분진행정성감별,곡피소이갑분-을산을지-갑산=5∶2∶1위전개제,산내소이갑분-을산을지-갑산=5∶4∶1위전개제;채용색보주:Shim-pack VP-ODS(150 mm ×4.6 mm),이갑순-0.4%린산용액(50∶50)위류동상,류속위1 mL/min ,검측파장위360 nm ,주온위25℃。결과재박층색보중능검측도곡피소화산내분,곡피소、산내소、이서리소분별재0.01~0.1、0.0025~0.025、0.0025~0.025 mg/mL범위내선성량호,기평균회수솔분별위100.7%、100.4%、101.7%。RSD분별위1.3%、1.4%화1.9%。양품황동류화합물적평균함량위1.25%。결론해방법간편、쾌속、준학、중복성호,가용우측정금작화중황동류화합물적함량。
Objective To establish a HPLC method for the determination of flavonoids content in caragana altaica Kom .Pojark by the studies on TLC identification characteristics of Caragana flowers in Aletai . Methods Quercetin and kaempferol were identified by TLC ,The HPLC analysis was performed on a Sun-fire C18 (150 mm × 4 .6 mm ,5 μm)column .a mixture of acetonitrile -0 .4% phosphoric acid aqueous solu-tion (50∶50) was used as the mobile phase with the flow rate at 1 mL/min .The detection wavelength was set at 360 nm .The column temperature was set at 25℃ .Results Quercetin and kaempferol could be de-tected by TLC quercetin ,kaempferol and isorhamnetin showed good linearity in the ranges of 0 .01 -0 .10 mg/mL ,0 .0025-0 .025 mg/mL and 0 .0025-0 .025 mg/mL .The average recoveries were 100 .7% , 100 .4% ,101 .7% .RSD1 .3% ,1 .4% and 1 .9% .Samples of flavonoid content averaged 1 .3% .Conclu-sion T he method is simple ,rapid ,accurate and reproducible and it can be used for the determination of the caragana altaica Kom .Pojark in the flavonoids content .