亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Comparison of different approaches for direct coupling of solid-phase microextraction to mass spectrometry for drugs of abuse analysis in plasma

固相微萃取 化学 色谱法 质谱法 分析化学(期刊) 气相色谱-质谱法
作者
Wei Zhou,Martyna N. Wieczorek,Runshan Will Jiang,Janusz Pawliszyn
出处
期刊:Journal of Pharmaceutical Analysis [Elsevier BV]
卷期号:13 (2): 216-222 被引量:43
标识
DOI:10.1016/j.jpha.2022.10.004
摘要

The direct coupling of solid-phase microextraction (SPME) to mass spectrometry (MS) (SPME-MS) has proven to be an effective method for the fast screening and quantitative analysis of compounds in complex matrices such as blood and plasma. In recent years, our lab has developed three novel SPME-MS techniques: SPME-microfluidic open interface-MS (SPME-MOI-MS), coated blade spray-MS (CBS-MS), and SPME-probe electrospray ionization-MS (SPME-PESI-MS). The fast and high-throughput nature of these SPME-MS technologies makes them attractive options for point-of-care analysis and anti-doping testing. However, all these three techniques utilize different SPME geometries and were tested with different MS instruments. Lack of comparative data makes it difficult to determine which of these methodologies is the best option for any given application. This work fills this gap by making a comprehensive comparison of these three technologies with different SPME devices including SPME fibers, CBS blades, and SPME-PESI probes and SPME-liquid chromatography-MS (SPME-LC-MS) for the analysis of drugs of abuse using the same MS instrument. Furthermore, for the first time, we developed different desorption chambers for MOI-MS for coupling with SPME fibers, CBS blades, and SPME-PESI probes, thus illustrating the universality of this approach. In total, eight analytical methods were developed, with the experimental data showing that all the SPME-based methods provided good analytical performance with R2 of linearities larger than 0.9925, accuracies between 81% and 118%, and good precision with an RSD% ≤ 13%.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
2秒前
4秒前
5秒前
7秒前
8秒前
12秒前
15秒前
FashionBoy应助石榴汁的书采纳,获得10
15秒前
emchavezangel发布了新的文献求助10
17秒前
26秒前
Mimi完成签到 ,获得积分10
28秒前
Criminology34举报饮了风求助涉嫌违规
42秒前
emchavezangel完成签到,获得积分10
44秒前
ljq完成签到,获得积分10
49秒前
53秒前
kll完成签到,获得积分10
58秒前
BRUCE完成签到,获得积分10
1分钟前
1分钟前
默默无闻完成签到 ,获得积分10
1分钟前
1分钟前
1分钟前
Criminology34举报ZJJ求助涉嫌违规
1分钟前
1分钟前
2分钟前
君莫笑发布了新的文献求助10
2分钟前
Criminology34举报Ww求助涉嫌违规
2分钟前
2分钟前
Elthrai完成签到 ,获得积分10
2分钟前
2分钟前
丘比特应助君莫笑采纳,获得10
2分钟前
王国发布了新的文献求助10
2分钟前
2分钟前
hitachi完成签到,获得积分10
2分钟前
2分钟前
2分钟前
阿巴完成签到,获得积分10
2分钟前
didididm完成签到,获得积分10
2分钟前
桐桐应助科研通管家采纳,获得10
3分钟前
3分钟前
3分钟前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Matrix Methods in Data Mining and Pattern Recognition 510
Social Skills Improvement System-Rating Scales--Chinese Version 500
Dynamische Polarisation von H-1 und B-11 in (CH-3)-3NBH-3 500
CLSI M07 2024 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7247708
求助须知:如何正确求助?哪些是违规求助? 8870700
关于积分的说明 18712127
捐赠科研通 6925956
什么是DOI,文献DOI怎么找? 3197998
关于科研通互助平台的介绍 2373767
邀请新用户注册赠送积分活动 2172879