Alshishani Anas, Salhimi Salizawati Muhamad, Saad Bahruddin
School of Chemical Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia.
School of Pharmaceutical Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia.
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Jan 15;1073:51-59. doi: 10.1016/j.jchromb.2017.12.013. Epub 2017 Dec 9.
A new salting-out assisted liquid-liquid extraction (SALLE) sample preparation method for the determination of the polar anti-diabetic biguanide drugs (metformin, buformin and phenformin) in blood plasma, urine and lake water samples were developed. The SALLE was performed by mixing samples (plasma (0.2mL), urine or lake water (1.0mL)) with acetonitrile (0.4mL for plasma, 0.5mL for urine or lake water), sodium hydroxide powder was then added for the phase separation. The effects of type of salting-out reagent, type of extraction solvent, volumes of acetonitrile and sample, amount of sodium hydroxide, vortexing and centrifugation times on the extraction efficiency were investigated. The upper layer, containing the biguanides, was directly injected into a HPLC unit using ZIC-HILIC column (150mm×2.1mm×3.5μm) and was detected at 236nm. The method was validated and calibration curves were linear with r>0.99 over the range of 20-2000μgL for plasma and 5-2000μgL for urine and lake water samples. The limits of detection were in the range (3.8-5.6)μgL, (0.8-1.5)μgL and (0.3-0.8)μgL for plasma, urine and lake water, respectively. The accuracies in the three matrices were within 87.3-103%, 87.4-109%, 82.2-109% of the nominal concentration for metformin, buformin and phenformin, respectively. The relative standard deviation for inter- and intra -day precision were in the range of 1.0-17% for all analytes in the three matrices.
开发了一种新的盐析辅助液-液萃取(SALLE)样品前处理方法,用于测定血浆、尿液和湖水样品中的极性抗糖尿病双胍类药物(二甲双胍、丁福明和苯乙双胍)。通过将样品(血浆(0.2mL)、尿液或湖水(1.0mL))与乙腈(血浆用0.4mL,尿液或湖水用0.5mL)混合进行SALLE,然后加入氢氧化钠粉末进行相分离。研究了盐析试剂类型、萃取溶剂类型、乙腈和样品体积、氢氧化钠用量、涡旋和离心时间对萃取效率的影响。含有双胍类药物的上层溶液直接注入使用ZIC-HILIC柱(150mm×2.1mm×3.5μm)的高效液相色谱仪中,并在236nm处进行检测。该方法经过验证,校准曲线在血浆20 - 2000μg/L、尿液和湖水5 - 2000μg/L范围内呈线性,r>0.99。血浆、尿液和湖水的检测限分别为(3.8 - 5.6)μg/L、(0.8 - 1.5)μg/L和(0.3 - 0.8)μg/L。三种基质中,二甲双胍、丁福明和苯乙双胍的准确度分别在标称浓度的87.3 - 103%、87.4 - 109%、82.2 - 109%范围内。三种基质中所有分析物的日内和日间精密度的相对标准偏差在1.0 - 17%范围内。