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黄芩-黄连药对对药主要活性成分及降糖作用的比较分析。

Comparative analysis of the main active components and hypoglycemic effects after the compatibility of Scutellariae Radix and Coptidis Rhizoma.

机构信息

Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Nanjing University of Chinese Medicine, Nanjing, P. R. China.

出版信息

J Sep Sci. 2019 Apr;42(8):1520-1527. doi: 10.1002/jssc.201801204. Epub 2019 Feb 26.

Abstract

In this study, a rapid and highly sensitive ultra high performance liquid chromatography with triple quadrupole mass spectrometry method with the mobile phase of acetonitrile and 0.1% aqueous formic acid was established and successfully applied to comparatively analyze main active components after their compatibility. Besides, the effects of Scutellariae Radix, Coptidis Rhizoma and combined extracts on type 2 diabetic rats induced by high-fat diet along with low dose of streptozocin were investigated. Under the optimized chromatographic conditions, good separation of seven target components was achieved within 12 min. All calibration curves exhibited good linearity (R  ≥ 0.999). The relative standard deviation of precision, repeatability and stability varied from 0.69 to 2.23, 0.98 to 2.56, and 0.92 to 2.57%, respectively. The recovery ranged from 91.11 to 105.35%. The contents of seven active components were notably reduced after compatibility; however, the hypoglycemic effect of combined extracts was stronger than single drug by decreasing the activities of fructose-1,6-bisphosphatase, glucose 6-phosphatase, phosphoenolpyruvate carboxykinase and increasing the activities of glucokinase, phosphofructokinase, pyruvate kinase. Accordingly, the established analytical method was accurate and sensitive enough for quantitative evaluation of seven investigated compounds. Moreover, the combined extract had definite effects on type 2 diabetes through multiple components against multiple targets.

摘要

在这项研究中,建立了一种快速且高灵敏度的超高效液相色谱-三重四极杆质谱联用方法,以乙腈和 0.1%甲酸水溶液为流动相,成功地应用于比较分析相容性后主要活性成分。此外,还研究了黄芩、黄连和联合提取物对高脂肪饮食加低剂量链脲佐菌素诱导的 2 型糖尿病大鼠的影响。在优化的色谱条件下,7 个目标成分在 12 分钟内得到了良好的分离。所有校准曲线均表现出良好的线性(R≥0.999)。精密度、重复性和稳定性的相对标准偏差分别为 0.69%至 2.23%、0.98%至 2.56%和 0.92%至 2.57%。回收率在 91.11%至 105.35%之间。相容性后,七种活性成分的含量明显降低;然而,联合提取物通过降低果糖-1,6-二磷酸酶、葡萄糖 6-磷酸酶、磷酸烯醇丙酮酸羧激酶的活性和提高葡萄糖激酶、磷酸果糖激酶、丙酮酸激酶的活性,其降血糖作用强于单药。因此,所建立的分析方法足够准确和灵敏,可用于对七种研究化合物进行定量评价。此外,通过多成分针对多靶点,联合提取物对 2 型糖尿病具有明确的作用。

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