1.河北师范大学 化学与材料科学学院,河北 石家庄 050024
2.西北师范大学 化学化工学院, 甘肃 兰州 730070
刘德龙,博士,教授,研究方向:中药分析,E-mail:delongliu9012@sina.com
纸质出版日期:2024-03-15,
收稿日期:2023-10-25,
修回日期:2023-11-30,
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唐芃,刘铁,刘德龙.分散固相萃取/荧光检测法选择性富集和定量人体血浆中的α-细辛醚[J].分析测试学报,2024,43(03):432-439.
TANG Peng,LIU Tie,LIU De-long.Selective Enrichment and Quantification of α-Asarone in Human Plasma by Dispersive Solid-phase Extraction with Fluorescence Detection[J].Journal of Instrumental Analysis,2024,43(03):432-439.
唐芃,刘铁,刘德龙.分散固相萃取/荧光检测法选择性富集和定量人体血浆中的α-细辛醚[J].分析测试学报,2024,43(03):432-439. DOI: 10.12452/j.fxcsxb.23102501.
TANG Peng,LIU Tie,LIU De-long.Selective Enrichment and Quantification of α-Asarone in Human Plasma by Dispersive Solid-phase Extraction with Fluorescence Detection[J].Journal of Instrumental Analysis,2024,43(03):432-439. DOI: 10.12452/j.fxcsxb.23102501.
该研究采用基于共价有机框架TpBD-Me
2
(COF-TpBD-Me
2
)的分散固相萃取/荧光检测法对人体血浆中的α-细辛醚进行选择性富集和定量检测。优化了COF-TpBD-Me
2
对α-细辛醚的最佳吸附条件,包括吸附剂质量浓度、吸附时间、pH值、解吸试剂和解吸时间。此外,还通过吸附等温线和吸附动力学实验阐明了吸附行为和机理。
α
-细辛醚在0.1~10 μg/mL范围内呈良好的线性关系,相关系数(
r
2
)大于0.999,检出限(LOD)为0.002 5 μg/mL。该方法对人体血浆中
α
-细辛醚的加标回收率为92.2%~98.0%,相对标准偏差为1.9%~3.8%。实验结果证明所建方法可选择性富集人体血浆中的
α
-细辛醚并实现准确定量。该方法为选择性富集和快速定量复杂生物基质中的药物活性成分提供了参考。
This work used a covalent organic framework TpBD-Me
2
(COF-TpBD-Me
2
) based dispersive solid-phase extraction fluorescence detection method to enrich and quantify
α
-asarone in human plasma. The optimal adsorption conditions of COF-TpBD-Me
2
on α-asarone were also investigated,including the mass concentration of adsorbent,adsorption time,pH,desorption solvent and desorption time. Furthermore,the adsorption behaviour and mechanism were elucidated by static adsorption and adsorption kinetics studies. α-asarone exhibited a good linear range of 0.1-10 μg/mL,with correlation coefficients(
r
2
) greater than 0.999,and the limit of detection(LOD) was 0.002 5 μg/mL. The proposed method applied for the α-asarone in actual human plasma samples for detection recoveries of spiked samples in the range of 92.2%-98.0% with relative standard deviations of 1.9%-3.8%. The results demonstrated that the method can effectively selectively enrich α-asarone in human plasma and accurate quantification. The methodology strategy provided a reference for the selective enrichment and rapid quantification of drug active ingredients in complex biological matrices.
共价有机框架分散固相萃取吸附α-细辛醚荧光检测
covalent organic frameworkdispersive solid-phase extractionadsorptionα-asaronefluorescence detection
Williams K M,Arthur S J,Burrell G,Kelly F,Phillips D W,Marshall T. J. Biochem. Biophys. Methods,2003,57(1):45-55.
Sun Y,Xu J,Xie X,Song H. Anal. Methods,2023,15(9):1116-1122.
Xi J,Yan L G. Sep. Purif. Technol.,2017,175:170-176.
Zgoła-Grześkowiak A,Grześkowiak T. Trends Anal. Chem.,2011,30(9):1382-1399.
Zan Y N,Zhang X Y,Shang S H,Chen N,Ding Y M. J. Instrum. Anal.(昝艳楠,张晓芸,商少华,陈宁,丁逸梅. 分析测试学报),2023,42(3):357-362.
Ghorbani M,Aghamohammadhassan M,Chamsaz M,Akhlaghi H,Pedramrad T. Trends Anal. Chem.,2019,118:793-809.
González-Sálamo J,Jiménez-Skrzypek G,Ortega-Zamora C,Ángel González-Curbelo M,Hernández-Borges J. Molecules,2020,25(14):3288.
Geng K Y,He T,Liu R Y,Dalapati S,Tan K T,Li Z P,Tao S S,Gong Y F,Jiang Q H,Jiang D L. Chem. Rev.,2020,120(16):8814-8933.
Cui X,Lei S,Wang C A,Gao L K,Zhang Q,Yang Y K,Lin Z Q. Nano Energy,2020,70:104525.
Chandra S,Kandambeth S,Biswal B P,Lukose B,Kunjir S M,Chaudhary M,Babarao R,Heine T,Banerjee R. J. Am. Chem. Soc.,2013,135(47):17853-17861.
Płotka-Wasylka J,Szczepańska N,Guardia M,Namieśnik J. Trends Anal. Chem.,2016,77:23-43.
Romero V,Lavilla I,Álvarez A,Bendicho C,Espiña B,Salonen L M. Anal. Chim. Acta,2022,1191:339293.
Fernandes S P S,Fonseca V F,Romero V,Duarte I A,Freitas A,Barbosa J,Reis-Santos P,Salonen L M,Espiña B. Chemosphere,2021,278:130364.
Wang J X,Li J,Gao M X,Zhang X M. Trends Anal. Chem.,2018,108:98-109.
Shang X L,Ji X,Dang J,Wang L Z,Sun C,Liu K C,Attila S,Jin M. Toxicol. Lett.,2020,324:1-11.
Huang C,Li W G,Zhang X B,Wang L,Xu T L,Wu D,Li Y. Neuropharmacology,2013,65:1-11.
Pérez-Pastén R,García R V,Garduño L,Reyes E,Labarrios F,Tamariz J,Chamorro G. J. Pharm. Pharmacol.,2006,58(10):1343-1349.
Yu X,Zhe Z,Tang B Q,Li S B,Tang L,Wu Y G,Chen X R,Fang H. Acta Biochim. Biophys. Sin.(Shanghai),2017,49(7):598-608.
Chen Y L,Chen Z L. Talanta,2017,165:188-193.
Guo M X,Fan W T,Wu X,Shen Y,Hu Z Q. China Pharm. (郭明鑫,范文韬,吴霞,沈颖,胡志强. 中国药房),2022,33(24):2990-2994.
Wei W,Han Q,Tian S,Wang Y P,Zhang H Y,Wang H B,Liang Q L. Microchem. J.,2022,175:107015.
Sun F R,Wang L S,Yu C Q,Liu H Y,Yan H Y,Bai L G. Microchem. J.,2021,169:106591.
Liu H X,Yang C L,Rao H H,Liu F,Zhang L,Zhao G H. J. Instrum. Anal.(刘海霞,杨彩玲,饶红红,刘芳,张丽,赵国虎. 分析测试学报),2023,42(12):1573-1579.
Ma Y F ,Wang L J ,Zhou Y L ,Zhang X X. Nanoscale,2019,11(12):5526-5534.
Yang X M,Zhang S H,Wang J M,Wang W J,Li J Q,Chen J W,Zhao Y J,Wang C,Wang Z. Anal. Chim. Acta,2020,1134:50-57.
Gao M J,Wang D D,Deng L L,Liu S C,Zhang K L,Quan T,Yang L J,Kang X,Xia Z N,Gao D. Chem. Mater.,2021,33:8036-8051.
Guo W J,Shi Z S,Zhang J,Zeng T,He Y,Cai Z W. Talanta,2021,235:122774.
Zhao N N,Liu S,Xing J P,Pi Z F,Song F R,Liu Z Q. J. Pharm. Anal.,2020,10(1):86-95.
Liu W,Zhu X S. Spectrochim. Acta A,2018,196:141-147.
Hu L Q,Yin C L. Anal. Methods,2015,7:5913-5923.
Karak S,Kandambeth S,Biswal B P,Sekhar S H,Kumar S,Pachfule P,Banerjee R. J. Am. Chem. Soc.,2017,139(5):1856-1862.
Cui X Y,Gu Z Y,Jiang D Q,Li Y,Wang H F,Yan X P. Anal. Chem.,2009,81(23):9771-9777.
Zhang L,Lv J N,Xu T C,Yang L J,Jiang X Q,Li Q. Sep. Purif. Technol.,2013,116:145-153.
Chen L L,Zhao D L,Chen S H,Wang X B,Chen C L. J. Colloid Interface Sci.,2016,472:99-107.
Li L Y,Xu D H,Pei Z G. RSC Adv.,2016,6:60145-60151.
Ofomaja A E,Naidoo E B,Modise S J. J. Environ. Manage.,2010,91(8):1674-1685.
Yang F,Zhang Y,Liang H. Int. J. Mol. Sci.,2014,15:3580-3595.
Zhu X,An X H,Liu Y,Hu J,Liu H L,Tian C C,Dai S,Yang X J,Wang H L,Abney C,Dai S. AIChE J.,2017,63:3470-3478.
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