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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
完美世界应助ruiruiruiruirui采纳,获得10
1秒前
酷波er应助南挽采纳,获得10
1秒前
jinkk完成签到,获得积分10
1秒前
时运完成签到,获得积分10
2秒前
无望幽月完成签到,获得积分10
2秒前
鳗鱼紫萱完成签到,获得积分10
2秒前
科研通AI6应助略略略采纳,获得10
3秒前
3秒前
wdwyyds完成签到,获得积分10
3秒前
3秒前
4秒前
危险份子发布了新的文献求助10
4秒前
shunli完成签到,获得积分10
4秒前
5秒前
佐佐木淳平完成签到,获得积分10
5秒前
天天快乐应助jignjing采纳,获得10
5秒前
秦尔晗发布了新的文献求助10
5秒前
5秒前
Jasper应助xiaoran采纳,获得10
6秒前
英俊的铭应助turui采纳,获得10
6秒前
常常发布了新的文献求助10
6秒前
科研狗完成签到,获得积分10
6秒前
Angleli完成签到,获得积分10
7秒前
Lynn完成签到,获得积分10
7秒前
asdffgg814完成签到,获得积分10
7秒前
领导范儿应助可靠世平采纳,获得10
8秒前
一站到底完成签到 ,获得积分10
8秒前
LIU完成签到,获得积分10
8秒前
迅速雨琴完成签到,获得积分10
8秒前
tommylike发布了新的文献求助10
8秒前
陶醉书包完成签到 ,获得积分10
9秒前
Pilule完成签到 ,获得积分10
9秒前
9秒前
DZ发布了新的文献求助10
10秒前
芋泥波波完成签到,获得积分10
10秒前
yulj发布了新的文献求助10
10秒前
NexusExplorer应助star采纳,获得10
10秒前
11秒前
snowdrift发布了新的文献求助10
11秒前
Muxi完成签到,获得积分20
11秒前
高分求助中
(应助此贴封号)【重要!!请各位详细阅读】【科研通的精品贴汇总】 10000
Les Mantodea de Guyane: Insecta, Polyneoptera [The Mantids of French Guiana] 3000
F-35B V2.0 How to build Kitty Hawk's F-35B Version 2.0 Model 2500
줄기세포 생물학 1000
The Netter Collection of Medical Illustrations: Digestive System, Volume 9, Part III - Liver, Biliary Tract, and Pancreas (3rd Edition) 600
INQUIRY-BASED PEDAGOGY TO SUPPORT STEM LEARNING AND 21ST CENTURY SKILLS: PREPARING NEW TEACHERS TO IMPLEMENT PROJECT AND PROBLEM-BASED LEARNING 500
2025-2031全球及中国蛋黄lgY抗体行业研究及十五五规划分析报告(2025-2031 Global and China Chicken lgY Antibody Industry Research and 15th Five Year Plan Analysis Report) 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4487138
求助须知:如何正确求助?哪些是违规求助? 3941911
关于积分的说明 12224269
捐赠科研通 3598402
什么是DOI,文献DOI怎么找? 1979094
邀请新用户注册赠送积分活动 1015904
科研通“疑难数据库(出版商)”最低求助积分说明 909123