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首页> 外文期刊>Journal of liquid chromatography and related technologies >HPLC determination and MS identification of dehydroabietic acid and abietic acid in propolis
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HPLC determination and MS identification of dehydroabietic acid and abietic acid in propolis

机译:蜂胶中脱氢松香酸和松香酸的HPLC测定和MS鉴定

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摘要

In the present study, the HPLC method on a C-18 column with on-line spectrophotometric and fluorimetric detection was used for separation and determination of dehydroabietic acid and abietic acid in propolis. The samples of propolis tincture were prepared prior to the HPLC analysis. The mobile phase for isocratic elution was methanol-water 87:13 containing 0.05% formic acid. Abietic acid was detected with spectrophotometric detection at 238 nm, and dehydroabietic acid was detected with fluorimetric detection (excitation 225 urn, emission 285 nm). The limits of determination (signaloise ratio 10) were 100 ng/mL for dehydroabietic acid and 200 ng/mL abietic acid. The calibration graphs were linear over a wide interval from the limit of determination to 1 mg/mL. Analytical recovery and reproducibility exceeded more than 89%. The developed method was used for analysis of propolis from Slovakia. Mass spectrometry was used for identification of the studied acids. The results demonstrated that dehydroabietic acid was present in all tested samples of propolis. Its content was different (3.7 mu g/g-44.7 mu g/g of propolis) depending on the source of propolis.
机译:在本研究中,采用在线分光光度法和荧光检测法在C-18柱上的HPLC方法分离和测定蜂胶中的脱氢松香酸和松香酸。在HPLC分析之前制备蜂胶tin样品。等度洗脱的流动相是含有0.05%甲酸的甲醇-水87:13。通过在238 nm处的分光光度检测法检测到松果酸,并通过荧光检测法(激发225 n,发射285 nm)来检测脱氢松香酸。脱氢松香酸和200 ng / mL松香酸的测定极限(信号/噪声比10)为100 ng / mL。从测定限到1 mg / mL,校准曲线在很宽的间隔内呈线性。分析回收率和重现性超过89%。所开发的方法用于分析来自斯洛伐克的蜂胶。质谱用于鉴定所研究的酸。结果表明,在所有测试的蜂胶样品中都存在脱氢松香酸。根据蜂胶的来源,其含量是不同的(3.7克/克-44.7克/克蜂胶)。

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