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离子液体分散液液微萃取结合高效液相色谱法同时测定苏木中巴西苏木素和原苏木素B的含量

Simultaneous determination of brazilin and protosappanin B in Caesalpinia sappan by ionic-liquid dispersive liquid-phase microextraction method combined with HPLC.

作者信息

Xia Zhaoyang, Li Dongdong, Li Qing, Zhang Yan, Kang Wenyi

机构信息

Institute of Chinese Materia Medica, Henan University, Kaifeng, Henan, 475004, China.

Hebei Food Inspection and Research Institute, Shijiazhuang, 050091, China.

出版信息

Chem Cent J. 2017 Nov 13;11(1):114. doi: 10.1186/s13065-017-0342-9.

Abstract

The conditions of heating, ionic liquid-based ultrasonic-assisted extraction combined with reverse-phase high performance liquid chromatography were optimized to simultaneously isolate and determinate brazilin and protosappanin B in Caesalpinia sappan. Ionic liquids, including [BMIM]Br, [BMIM]BF, [BMIM]PF and [HMIM]PF, were selected as extraction solvents while methanol, acetone, acetonitrile, ethanol and water were selected as dispersants. The chromatographic column was Purospher star RP-C (250 mm × 4.6 mm, 5 μm), a mixture of methanol and 0.2% phosphoric acid-water was used as mobile phase at a flow rate 0.65 mL/min. The result displayed that the extraction yields of brazilin and protosappanin B were highest when the concentration of [BMIM]Br methanol solution as extraction solvent was 0.5 mol/L and the solid-liquid ratio was 1:50 (g/mL). Under the optimal extraction conditions, the contents of brazilin showed a good linearity (r = 1.0000) within the range of 1.25-7.50 μg with the average recovery of 99.33%, the contents of protosappanin B also showed a good linearity (r = 0.9999) within the range of 0.50-3.00 μg with the average recovery of 98.31%. This experiment, which adopted environmentally friendly reagent as extraction solvent, not only improved the extraction efficiency, but also avoided the environmental pollution caused by organic solvent. Moreover, it was simple and reliable, and can be of important significance in the study of Traditional Chinese Medicine active ingredient extraction methods. The antibacterial activities of the ionic liquids and methanol extracts were determined using the paper disc diffusion method. The ionic liquid extract was found to possess antibacterial activity against Staphylococcus aureus and methicillin-resistant S. aureus (MIC value of 37.5 mg crude drug/mL), β-Lactamase producing S. aureus (MIC values of 18.8 mg crude drug/mL), but not against E. coli, Extended spectrum β-Lactamases E. coli and P. aeruginosa. Compared with the ionic liquid extract, the methanol extract was found to have antibacterial activity against S. aureus and methicillin-resistant S. aureus (MIC value of 75.0 mg crude drug/mL), β-Lactamase producing S. aureus (MIC values of 150.0 mg crude drug/mL). However, the same, the methanol extract did not have antibacterial activity against E. coli, Extended spectrum β-Lactamases E. coli and P. aeruginosa.

摘要

对加热条件、离子液体基超声辅助萃取结合反相高效液相色谱法进行优化,以同时分离和测定苏木中的巴西苏木素和原苏木素B。选择离子液体[BMIM]Br、[BMIM]BF、[BMIM]PF和[HMIM]PF作为萃取溶剂,同时选择甲醇、丙酮、乙腈、乙醇和水作为分散剂。色谱柱为Purospher star RP-C(250 mm×4.6 mm,5μm),以甲醇和0.2%磷酸水溶液的混合物作为流动相,流速为0.65 mL/min。结果表明,当以0.5 mol/L的[BMIM]Br甲醇溶液为萃取溶剂且固液比为1:50(g/mL)时,巴西苏木素和原苏木素B的萃取率最高。在最佳萃取条件下,巴西苏木素含量在1.25 - 7.50μg范围内呈良好线性关系(r = 1.0000),平均回收率为99.33%,原苏木素B含量在0.50 - 3.00μg范围内也呈良好线性关系(r = 0.9999),平均回收率为98.31%。本实验采用环境友好型试剂作为萃取溶剂,不仅提高了萃取效率,还避免了有机溶剂造成的环境污染。此外,该方法简单可靠,在中药活性成分提取方法研究中具有重要意义。采用纸片扩散法测定了离子液体提取物和甲醇提取物的抗菌活性。发现离子液体提取物对金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌具有抗菌活性(MIC值为37.5 mg生药/mL),对产β-内酰胺酶金黄色葡萄球菌具有抗菌活性(MIC值为18.8 mg生药/mL),但对大肠杆菌、产超广谱β-内酰胺酶大肠杆菌和铜绿假单胞菌无抗菌活性。与离子液体提取物相比,甲醇提取物对金黄色葡萄球菌和耐甲氧西林金黄色葡萄球菌具有抗菌活性(MIC值为75.0 mg生药/mL),对产β-内酰胺酶金黄色葡萄球菌具有抗菌活性(MIC值为150.0 mg生药/mL)。然而,同样地甲醇提取物对大肠杆菌、产超广谱β-内酰胺酶大肠杆菌和铜绿假单胞菌无抗菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c86e/5684053/8d0afe4874ad/13065_2017_342_Fig1_HTML.jpg

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