1.西南政法大学 司法鉴定中心,重庆 401120
2.长江师范学院 现代农业与生物工程学院,重庆 408100
3.重庆医科大学 药学院,重庆 400016
4.重庆海关技术中心,重庆 401147
5.西南政法大学 刑事侦查学院,重庆 401120
曹淑瑞,博士,教授级高级工程师,研究方向:纳米材料与物证技术,E-mail:caoshurui@yeah.net
扫 描 看 全 文
刘正宏,刘诗敏,朱蓉等.磁性纳米碳复合材料快速检测毛发中甲基苯丙胺的应用[J].分析测试学报,2023,42(07):856-862.
LIU Zheng-hong,LIU Shi-min,ZHU Rong,et al.Application of a Magnetic Nanocarbon Composite Material in Rapid Detection of Methamphetamine in Hair[J].Journal of Instrumental Analysis,2023,42(07):856-862.
刘正宏,刘诗敏,朱蓉等.磁性纳米碳复合材料快速检测毛发中甲基苯丙胺的应用[J].分析测试学报,2023,42(07):856-862. DOI: 10.19969/j.fxcsxb.23030302.
LIU Zheng-hong,LIU Shi-min,ZHU Rong,et al.Application of a Magnetic Nanocarbon Composite Material in Rapid Detection of Methamphetamine in Hair[J].Journal of Instrumental Analysis,2023,42(07):856-862. DOI: 10.19969/j.fxcsxb.23030302.
合成了一种磁性还原氧化石墨烯/金属有机框架物(MrGO/ZIF-67)新型纳米碳复合材料,并将其用于甲基苯丙胺(MAMP)的吸附,建立了磁固相萃取/超高效液相色谱-串联质谱法快速测定毛发中MAMP的新方法。分别利用透射电镜、振动样品磁强计(VSM)和傅里叶变换红外光谱对MrGO/ZIF-67进行综合表征,采用单因素实验重点优化溶液pH值,采用Box-Behnken Design考察萃取时间、吸附剂用量、MAMP初始浓度对MAMP吸附性能的影响。得到的最优条件为:溶液pH值11.0、吸附剂用量4 mg,萃取时间20 min,MAMP的初始浓度为110 μg/L。MAMP在1 ~ 200 μg/L范围内线性关系良好,相关系数(,r,2,)为0.999 9,检出限(LOD)和定量下限(LOQ)分别为0.188 μg/L和0.572 μg/L。在1.0、5.0、9.6 μg/L加标水平下的回收率为80.2% ~ 94.4%,日内和日间相对标准偏差(RSD,,n, = 3)分别为1.6% ~ 2.7%和6.0% ~ 8.2%,表明该材料能用于实际毛发中MAMP的检测。
A novel type of nano-carbon composite,magnetic reduced graphene oxide/metal-organic frameworks(MrGO/ZIF-67) was synthesized by combining Fe,3,O,4, nanoparticles with metal-organic framework(ZIF-67) and reduced graphene oxide(rGO),which was employed for the efficient adsorption of methamphetamine(MAMP).Based on this,a novel ultra-high performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) with magnetic solid phase extraction(MSPE) was established for the rapid determination of MAMP in hair.Scanning electronic microscopy(SEM),transmission electronic microscopy(TEM),Fourier transform infrared spectroscopy(FT-IR) and vibrating sample magnetometer(VSM) were adopted for the comprehensive characterization of MrGO/ZIF-67.The results showed that Fe,3,O,4, magnetic nanoparticles were successfully attached to the surface of carbon composite.MrGO/ZIF-67 possessed a three-dimensional porous structure,multifunctional groups,and sufficient magnetic force for rapid separation by external magnets.A variety of experimental parameters affecting the sample pretreatment effects were evaluated and optimized.The effect of the solution pH value(2.0 to 12.0) was firstly screened by the one-variable-at-a-time(OVAT) analysis,and single factor experiment showed that the solution pH of 11.0 was the most favorable for the adsorption of MAMP.The influences of magnetic nanomaterials amount(1-5 mg),extraction time(10-90 min) and initial concentration of MAMP(100-500 μg/L) on the adsorption performance of MAMP were further investigated via a three level Box-Behnken design and response surface methodology(RSM).According to the model recommendations,the optimal extraction conditions were as follows:MrGO/ZIF dosage:4 mg,extraction time:20 min,initial concentration of MAMP:110 μg/L.The results showed that there was a good linear relationship for MAMP in the range of 1-200 μg/L,with a correlation coefficient(,r,2,) of 0.999 9,a limit of detection(LOD) of 0.188 μg/L,and a limit of quantitation(LOQ) of 0.572 μg/L.It was found that MrGO/ZIF-67 material had good adsorption capacity,fast adsorption kinetics and easy separation.The spiked recoveries for the actual hair samples at three levels of 1.0,5.0 and 9.6 μg/L ranged from 80.2% to 94.4%,with intra-day and inter-day relative standard deviations(RSDs,,n ,= 3) of 1.6%-2.7% and 6.0%-8.2%,respectively,indicating that the method had good linearity,high sensitivity,good accuracy and precision.The synthesized magnetic nano-carbon composite MrGO/ZIF-67 and the developed UPLC-MS/MS method could be used to adsorb and detect the content of MAMP in actual hair samples.
MrGO/ZIF-67复合材料磁性纳米碳材料甲基苯丙胺毛发
MrGO/ZIF-67 compositemagnetic nano carbon materialsmethamphetaminehair
Wu G P,Xiang B R.J. Instrum. Anal. (吴国萍,相秉仁.分析测试学报),2007,26(5):698-701.
Meredith C W,Jaffe C,Ang-Lee K,Saxon A J.Harv. Rev. Psychiatry,2005,13(3):141-154.
Zhang S J,Liu X Y,Zhuo X Y.Chin. J. Drug Depend. (张素静,刘晓云,卓先义.中国药物依赖性杂志),2017,26(4):267-269.
Madry M M,Kraemer T,Baumgartner M R.Forensic Sci. Int.,2018,282:137-143.
Kwon N H,Lee Y R,Kim H S,Cheong J C,Kim J Y.Molecules,2019,24(13):2501-2513.
Tabernero M J,Felli M L,Bermejo A M,Chiarotti M.Anal. Bioanal. Chem.,2009,395(8):2547-2557.
Netto J D,Musk G C,Maker G L,TrengoveR D.Biomed. Chromatogr.,2011,25(12):1374-1380.
Castro A L,Tarelho S,Silvestre A,Teixeira H M.J. Forensic Legal Med.,2012,19(2):77-82.
Xiong J,Chen J,He M,Hu B.Talanta,2010,(82):969-975.
Sergi M,Compagnone D,Curini R,D’Ascenzo G,Del Carlo M,Napoletano S,Risoluti R.Anal. Chim. Acta,2010,675(2):132-137.
Chen M,Suo L,Gao Q,Feng Y Q.Electrophoresis,2011,32(16):2099-2106.
Baprtista F R,Belhout S A,Giordani S,Quinn S J.Chem. Soc. Rev.,2015,44(13):4433-4453.
Baker S N.Baker G A.Angew. Chem. Int. Ed.,2010,49(38):6726-6744.
Song F J,Cao S R,Liu Z H,Su H T,Chen Z Q.J. Mol. Liquids,2022,364:119950-119963.
Ma S,You J D,Wu D H,Jiang M L,Zhou Q,Cao S R.J. Instrum. Anal. (马双,游嘉德,巫端浩,江茉莉,周琴,曹淑瑞.分析测试学报),2022,41(11):1671-1677.
Taghvimi A,Tabrizi A B,Dastmalchi S,Yousef J.J. Chromatogr. B,2019,1109:149-154.
Zhang T,Li Y L,Yang H,Xiao J C,Jin H W,Liu Y C.Phys. Test. Chem. Anal. (张婷,李跃龙,杨豪,肖久长,靳翰文,刘禹诚.理化检验),2019,55(9):1085-1090.
0
浏览量
5
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构