高效液相色谱法同时测定竹叶中13种黄酮类化合物(英文)  被引量:10

Simultaneous Determination of 13 Flavonoids in Bamboo Leaves by HPLC

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作  者:魏琦[1,2] 王淑英 汤锋 张华新[2] 喻谨 岳永德 

机构地区:[1]国际竹藤中心竹藤科学与技术重点实验室,北京100102 [2]国家林业局盐碱地研究中心,北京100091

出  处:《林业科学》2015年第8期81-87,共7页Scientia Silvae Sinicae

基  金:National Science and Technology Infrastructure Program(2012BAD23B03)

摘  要:【目的】建立一种同时测定竹叶中13种黄酮类化合物(异荭草苷、荭草苷、异牡荆苷、牡荆苷、芹菜素、木犀草素、苜蓿素、7-甲氧基-苜蓿素、苜蓿素-7- O -葡萄糖苷、芹菜素-7- O -葡萄糖苷、Demethyltorosaflavone、芹菜素-7-O-葡萄糖-6″-O-鼠李糖苷、6-反式-(2″-O -α-鼠李糖基)乙烯基-5,7,3′,4′-四羟基黄酮)含量的高效液相色谱法,并用此方法对牡竹属10种竹种(麻竹、龙竹、牡竹、黄竹、梁山慈竹、花吊丝竹、云南龙竹、福贡龙竹、勃氏甜龙竹、版纳甜龙竹)竹叶黄酮类化合物进行分析比较,以期为黄酮类化合物的定性定量检测、牡竹属竹叶的开发利用及提取竹叶黄酮时的竹种选择提供参考。【方法】采用 HPLC梯度洗脱分离黄酮类化合物,通过仪器精密度、LOD值、LOQ值、日内稳定性、日间稳定性及添加回收率对方法进行验证。竹叶样品用70%乙醇超声提取,经石油醚萃取后采用 HPLC 进行检测。【结果】各黄酮类化合物标准品分离效果良好,保留时间在13.23~54.67 min之间。13种黄酮类化合物标准品在0.01~500 mg·L -1的线性范围内呈良好的线性关系,相关系数 R2在0.9996~1.0000之间。仪器精密度 RSD 在1.06%~2.55%之间, LOD 值在0.01~0.10 mg·kg -1之间,LOQ值在0.03~0.34 mg·kg -1之间。方法准确性、日间与日内精密度良好,日内稳定性 RSD在0.15%~0.67%之间,日间稳定性在0.44%~5.61%之间,13种黄酮类化合较稳定。7种黄酮类化合物的添加回收率高于70%,其余6种黄酮类化合物的添加回收率在39.76%~68.75%之间。采用此方法对牡竹属10种竹种竹叶黄酮类化合物进行分析,结果显示各竹种竹叶黄酮类化合物含量存在差异,除木犀草素、6-反式-(2″-O-α-鼠李糖基)乙烯基-5,7,3′,4′-四羟基黄酮和 DemethyltorosaflavoObjective]Most flavonoids possess a variety of medical and biological activities such as anti-free radical, antioxidant,antiaging,anti-inflammatory,etc. They are widely used in pharmaceutical,health products and cosmetic fields. The objective of this paper was to establish a HPLC method for simultaneously qualitative-quantitative analysis of 13 flavonoids ( isoorientin, orientin, vitexin, isovitexin, apigenin, luteolin, tricin, 7-methoxy-tricin, tricin-7-O-glucopyranoside, apigenin-7-O-glucopyranoside, demethyltorosaflavone, apigenin-7-O-glucopyranoside-6″-O-rhamnoside and 6-trans-(2″-O-α-rhamnopyranosyl)ethenyl-5,7,3′,4′-tetrahydroxyflavone ) in bamboo leaves,and leaf flavonoids in 10 species of Dendrocalamus ( D. latiflorus,D. giganteus,D. strictus,D. membranceus,D. farinosus,D. minor var. amoenus,D. yunnanicus, D. fugongensis, D. brandisii and D. hamiltonii ) were comparatively analyzed by the established method with the aims to provide a guidance for qualitative and quantitative analysis of flavonoids, the development and utilization of Dendrocalamus bamboo leaves and the selection of bamboo species for flavonoids extraction.[Method]The flavonoids were separated by HPLC gradient elution method,and the validation was guaranteed by accuracy of equipment,LOD,LOQ,intraday/interday precision and recovery rate. Bamboo leaves were extracted with 70% ( v/v) ethanol-water by ultrasonic extraction,and then tested by HPLC after petroleum ether extraction. [Result]A good separation was found for each flavonoid,the retention times were ranged from 13. 23 to 54. 67 min. The standard curves showed a good linearity in the corresponding ranges between 0. 01 and 500 mg·L -1 ( R2≥0. 999 6). The equipment accuracy RSD were 1. 06% -2. 55%,LOD and LOQ ranged from 0. 01 to 0. 10 mg·kg -1 ,and from 0. 03 to 0. 34 mg· kg -1 ,respectively. The RSD values of instrument accuracy, and intraday/interday precision indicated that it was reasonable to analyze the samples within 5 days. The RSD of intraday an

关 键 词:黄酮类化合物 竹叶 牡竹属 

分 类 号:S781.41[农业科学—木材科学与技术]

 

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