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DETERMINATION OF SELECTED FLAVONOIDS IN HOP EXTRACT BY HPLC

机译:高效液相色谱法测定蛇麻草提取物中的精选黄酮

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An HPLC method with DAD was developed to quantify some flavonoids (rutin, quercetin, and kaempferol) in hop extracts. Quercetin and kaempferol were determined in the free forms and they can also be found in the form of glycosides (rutin and others). The glycosides were hydrolyzed during the extraction step with 0.1 mol/L HCl or 1.5 mol/L HCl. If 1.5 mol/L HCl was used for extraction, the lower results of flavonoid determination were achieved due to decomposition of hydrolysis products. Free forms of quercetin and kaempferol were quantified in the water extract because the hydrolysis of glycosides in water was negligible. Pre-column in off-line mode was used for purification of extracts. The limits of detection were 0.25mug/mL for rutin, 0.3 mug/mLfor quercetin, 0.25mug/mL for kaempferol, 0.2mug/mL for hesperidin, 0.34 ug/mL for hesperetin, 0.23 fig/ mL for naringenin, 0.42 mug/mL rhamnetin, 0.16mug/mL for patuletin, 0.25 fmug/mL for patuli-trin, and 0.32 fmug/ mL for isorhamnetin-3-O-glc. The limits of quantification were 0.5 mug/mL for rutin, 0.6mug/mL for quercetin, 0.38mug/mL for hesperidin, 0.7mug/mL for hesperetin, 0.4mug/mL for naringenin, 0.8mug/mL rhamnetin, 0.38mug/mL for patuletin, 0.5mug/mL for patulitrin, and 0.4 mug/mL for isorhamnelin-3-O-glc 0.5 mug/mL for kaempferol. The concentration of quercetin was 165.3+- 5.0 mug/'g of dry sample; the concentration of kaempferol was 125.9+- 4.3 mug/g of dry sample after 2hr of extraction using 0.1 mol/L HCl in methanol solutions. The concentrations of the other flavonoids were under the limit of quantification. If pure water and methanol were used for extraction, the lower concentrations were determined, which indicated that higher amounts of flavonoids under study existed in glycoside forms.
机译:开发了一种使用DAD的HPLC方法来定量蛇麻草提取物中的某些类黄酮(芦丁,槲皮素和山emp酚)。槲皮素和山emp酚以游离形式测定,它们也可以以糖苷形式(芦丁和其他)发现。在提取步骤中,糖苷用0.1 mol / L HCl或1.5 mol / L HCl水解。如果使用1.5 mol / L HCl进行萃取,则由于水解产物的分解,导致类黄酮测定的结果较低。由于水中糖苷的水解作用可忽略不计,因此对水提取物中的槲皮素和山奈酚的游离形式进行了定量。离线模式的预柱用于提取物的纯化。检出限为芦丁为0.25马克/毫升,槲皮素为0.3马克/毫升,山ol酚为0.25马克/毫升,橙皮苷为0.2马克/毫升,橙皮素为0.34 ug /毫升,柚皮苷为0.23图/毫升,柚皮素为0.42马克/毫升鼠李素,patuletin的0.16ug / mL,patuli-trin的0.25 fmug / mL,异鼠李素-3-O-glc的0.32 fmug / mL。定量限为芦丁0.5杯/毫升,槲皮素0.6杯/毫升,橙皮苷0.38杯/毫升,橙皮素0.7杯/毫升,柚皮素0.4杯/毫升,鼠李素,0.8杯/毫升鼠李素,0.38杯/毫升对于patuletin而言,对于0.5杯/毫升对于patulitrin,对于0.4杯/ mL对于异鼠李素-3-O-glc对于0.5杯/ mL对于山ka酚。槲皮素的浓度为165.3±5.0杯/克干样品;使用0.1 mol / L HCl的甲醇溶液萃取2小时后,山ka酚的浓度为125.9±4.3杯/克干样品。其他类黄酮的浓度在定量限内。如果使用纯水和甲醇萃取,则测定的浓度较低,这表明所研究的黄酮类化合物以糖苷形式存在。

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