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以槐米中芦丁的提取含量为评价指标,以粉碎度、溶剂的用量、提取时间和提取次数为考查因素,采用正交实验优选最佳的提取工艺条件。结果表明:芦丁药材粉碎为粗粉,加入20倍量的溶剂,提取2次,每次提取20min,提取率较高。结论:该提取工艺成本较低,操作简单安全,适用于大规模生产。 相似文献
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超声条件下碱提取酸沉淀法从槐米中提取芦丁的研究 总被引:2,自引:0,他引:2
以新鲜的槐米为原料,65℃下充分干燥,研细后采用超声条件下碱石灰煮沸盐酸酸化沉淀法来提取芦丁。探讨了反应温度、反应液的pH值、溶剂用量及反应时间对产物芦丁提取率的影响。得出提取的最佳条件为:控制反应温度为70~75℃,碱提取时pH=9、酸沉淀时pH=4,溶剂用量以6倍于原料为宜,提取3次,反应时间3.5 h。制得的芦丁为浅黄色针状晶体,提取率17.83%,熔点176~178℃。 相似文献
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依据《中国药典》(2015版)对蜀葵子进行生药学检测,并新建了蜀葵子中芦丁、山奈素和槲皮素的薄层色谱和高效液相色谱检测方法。结果表明,对比10批蜀葵子药材,其横切面有木栓层细胞数列,4~7束维管束排列成环带,外被大量非腺毛;10批蜀葵子中芦丁、山奈素和槲皮素的R_f值均与标准品一致,且斑点清晰。蜀葵子中芦丁、山奈素和槲皮素的平均含量分别为0.617 mg·g~(-1)、0.034 mg·g~(-1)和0.033 mg·g~(-1);线性范围分别为2.55~206.67μg·mL~(-1)(R=0.9993)、2.38~199.33μg·mL~(-1)(R=0.9994)和2.88~233.33μg·mL~(-1)(R=0.9997);精密度RSD(n=6)分别为0.263%、0.290%、0.405%;平均加标回收率分别为99.86%(RSD=1.83%)、100.72%(RSD=2.03%)和105.91%(RSD=1.87%)。为蜀葵子药材质量控制标准提升奠定了基础。 相似文献
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优化芦丁提取纯化工艺。用T型关联度对芦丁提取纯化工艺进行了研究。根据芦丁得率的关联度结果,各因素相关度大小为:X3〉X4〉X6〉X5〉X2〉X1,最佳工艺为95℃下杀酶40min,除胶水温度90℃,除胶水量(V/w),渗漉pH11.0,酸沉pH3~4,收率22.3%,含量94.2%。可将T型关联度分析法用于芦丁提取纯化工艺为工业化生产提供实验依据。 相似文献
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对纸色谱和柱色谱实验的方法进行了改良,改良后的实验具有操作方便、现象明显、实验时间短、经济、环保的优点。 相似文献
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《分离科学与技术》2012,47(3):525-529
In this study, a preparative countercurrent chromatography (CCC) method for isolation and purification of the bioactive component rutin directly from the ethanol extract of Boenninghausenia sessilicarpa was successfully established by using n-butanol-ethyl acetate-water as the two-phase solvent system. The upper phase of n-butanol-ethyl acetate-water (4:1:5, v/v) was used as the stationary phase of CCC. Under the optimum conditions, 112 mg of rutin at 98.6% purity was obtained from 2.0 g of the crude extract in a single CCC separation. The peak fraction of CCC was identified by negative ESI, 1H NMR, and 13C NMR. 相似文献
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采用反相高效液相色谱法测定银杏叶中芦丁的含量。样品经乙醇回流提取、浓缩后,用Eclipse SB-C18(5μm,4.6mm×150mm)色谱柱分离样品,在检测器波长360nm,甲醇∶1.5%醋酸(体积比40∶60)为流动相,流速0.8mL/min,柱温30℃的条件下测定。该方法分离效果好,线性相关系数r=0.99987,平均回收率为98.69%,相对标准偏差为7.8%(n=5)。 相似文献
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Steady-state and time-resolved optical spectroscopy techniques were employed to study the excited-state intramolecular hydrogen transfer (ESIHT) in rutin, a flavonol that contains a disaccharide and is a natural product in plants. The results are compared with those of a similar natural compound, quercetin, which also has a flavonol structure. The fluorescence decay signal of the normal form of these two compounds is composed of three time components. The ESIHT rate in both compounds has a time constant of 70 fs or less. The ESIHT processes of both compounds show a distinctive kinetic isotope effect of 1.5 or more. The intermediate and long-time components are about 300 fs and a few picoseconds, respectively, for both compounds. The amplitude of the intermediate component in rutin is twice that of quercetin. We explain this difference as arising from the hydrogen bonding of the glucose in rutin to the ESIHT active site. 相似文献
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《分离科学与技术》2012,47(4):588-593
Rosmarinic acid and rutin were successfully separated from Glechoma hederaceaL. using high-speed counter-current chromatography for the first time. Eleven milligrams of rosmarinic acid (chromatographic purity 97.2 %) and 10 mg of rutin (chromatographic purity 98.1 %) were obtained from 100 mg ethyl acetate extract and 100 mg n -butanol extract of Glechoma hederacea L., respectively, with the separation procedure less than 2 h. Their structures were characterized by UV, MS, and NMR. The established methods were simple, fast, and convenient, which can be applied to the preparation of reference substances of rosmarinic acid and rutin. 相似文献
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Ivan Kreft Mateja Germ Aleksandra Golob Blanka Vombergar Francesco Bonafaccia Zlata Luthar 《International journal of molecular sciences》2022,23(7)
Tartary buckwheat (Fagopyrum tataricum Gaertn.) is grown in eastern and central Asia (the Himalayan regions of China, Nepal, Bhutan and India) and in central and eastern Europe (Luxemburg, Germany, Slovenia and Bosnia and Herzegovina). It is known for its high concentration of rutin and other phenolic metabolites. Besides the grain, the other aboveground parts of Tartary buckwheat contain rutin as well. After the mixing of the milled buckwheat products with water, the flavonoid quercetin is obtained in the flour–water mixture, a result of rutin degradation by rutinosidase. Heating by hot water or steam inactivates the rutin-degrading enzymes in buckwheat flour and dough. The low buckwheat protein digestibility is due to the high content of phenolic substances. Phenolic compounds have low absorption after food intake, so, after ingestion, they remain for some time in the gastrointestinal tract. They can act in an inhibitory manner on enzymes, degrading proteins and other food constituents. In common and Tartary buckwheat, the rutin and quercetin complexation with protein and starch molecules has an impact on the in vitro digestibility and the appearance of resistant starch and slowly digestible proteins. Slowly digestible starch and proteins are important for the functional and health-promoting properties of buckwheat products. 相似文献