浙江大学学报(理学版)
浙江大學學報(理學版)
절강대학학보(이학판)
JOURNAL OF ZHEJIANG UNIVERSITY
2009年
6期
705-707,713
,共4页
蒋立娣%宣贵达%吴好好%李丽萍
蔣立娣%宣貴達%吳好好%李麗萍
장립제%선귀체%오호호%리려평
槲皮素%山萘酚%高效液相色谱法%桑叶提取物
槲皮素%山萘酚%高效液相色譜法%桑葉提取物
곡피소%산내분%고효액상색보법%상협제취물
quercetin%kaempferol%HPLC%folium mori extract
建立HPLC法测定桑叶提取物中水解槲皮素和山萘酚的含量.先用甲醇-盐酸混合液(甲醇终浓度50%,盐酸终浓度2.0 mol·L~(-1))水解桑叶提取物中的黄酮类成分成槲皮素和山萘酚,以HPLC法测定槲皮素和山萘酚含量.色谱柱为Diamonsil钻石C18柱,流动相为甲醇-0.2%磷酸(63∶37,体积分数),流速为1.0 mL·min~(-1),检测波长为370 nm.结果表明槲皮素在0.84~26.8 mg·L~(-1)之间,山萘酚在0.44~14.2 mg·L~(-1)之间呈良好的线性关系,平均回收率分别为101.3%和99.5%.该测定方法准确、重复性好,可用于桑叶提取物中槲皮素和山萘酚的含量测定.
建立HPLC法測定桑葉提取物中水解槲皮素和山萘酚的含量.先用甲醇-鹽痠混閤液(甲醇終濃度50%,鹽痠終濃度2.0 mol·L~(-1))水解桑葉提取物中的黃酮類成分成槲皮素和山萘酚,以HPLC法測定槲皮素和山萘酚含量.色譜柱為Diamonsil鑽石C18柱,流動相為甲醇-0.2%燐痠(63∶37,體積分數),流速為1.0 mL·min~(-1),檢測波長為370 nm.結果錶明槲皮素在0.84~26.8 mg·L~(-1)之間,山萘酚在0.44~14.2 mg·L~(-1)之間呈良好的線性關繫,平均迴收率分彆為101.3%和99.5%.該測定方法準確、重複性好,可用于桑葉提取物中槲皮素和山萘酚的含量測定.
건립HPLC법측정상협제취물중수해곡피소화산내분적함량.선용갑순-염산혼합액(갑순종농도50%,염산종농도2.0 mol·L~(-1))수해상협제취물중적황동류성분성곡피소화산내분,이HPLC법측정곡피소화산내분함량.색보주위Diamonsil찬석C18주,류동상위갑순-0.2%린산(63∶37,체적분수),류속위1.0 mL·min~(-1),검측파장위370 nm.결과표명곡피소재0.84~26.8 mg·L~(-1)지간,산내분재0.44~14.2 mg·L~(-1)지간정량호적선성관계,평균회수솔분별위101.3%화99.5%.해측정방법준학、중복성호,가용우상협제취물중곡피소화산내분적함량측정.
To establish an method to determine the contents of quercetin and kaempferol in folium mori extract by HPLC,the flavones in folium mori extract were hydrolyted into quercetin and kaempferol with the mixed solution of methanol-hydrochloric acid.The contents of quercetin and kaempferol were determined by HPLC method,performed on Diamonsil C_u column with the mobile phase consisted of methanol -0.20% phosphoric acid solution (63·37).The flow rate was 1.0 mL·min~(-1),the UV wavelength was set at 370 nm.The linear ranges of quercetin and kaempferol were 0.84-26.8 μg·mL~(-1),0.44-14.2 μg · mL~(-1),respectively.The average recoveries of quercetin and kaempferol were 101.3%,99.5%.The method was accurate,reliable and with good reappearance for the determination of quercetin and kaempferol in folium mori extract.