Recent advancements in LC‐MS based analysis of biotoxins: Present and future challenges

化学 探索者 复矩阵 海洋毒素 样品制备 液相色谱-质谱法 串联质谱法 生化工程 质谱法 环境化学 色谱法 毒素 农药残留 工程类 杀虫剂 生物 生物化学 农学
作者
Debabrata Panda,Bisnu Prasad Dash,Sivakumar Manickam,Grzegorz Boczkaj
出处
期刊:Mass Spectrometry Reviews [Wiley]
卷期号:41 (5): 766-803 被引量:44
标识
DOI:10.1002/mas.21689
摘要

Abstract There has been a rising concern regarding the harmful impact of biotoxins, source of origin, and the determination of the specific type of toxin. With numerous reports on their extensive spread, biotoxins pose a critical challenge to figure out their parent groups, metabolites, and concentration. In that aspect, liquid chromatography‐mass spectrometry (LC‐MS) based analysis paves the way for its accurate identification and quantification. The biotoxins are ideally categorized as phytotoxins, mycotoxins, shellfish‐toxins, ciguatoxins, cyanotoxins, and bacterial toxins such as tetrodotoxins. Considering the diverse nature of biotoxins, both low‐resolution mass spectrometry (LRMS) and high‐resolution mass spectrometry (HRMS) methods have been implemented for their detection. The sample preparation strategy for complex matrix usually includes “QuEChERS” extraction or solid‐phase extraction coupled with homogenization and centrifugation. For targeted analysis of biotoxins, the LRMS consisting of a tandem mass spectrometer operating in multiple reaction monitoring mode has been widely implemented. With the help of the reference standard, most of the toxins were accurately quantified. At the same time, the suspect screening and nontarget screening approach are facilitated by the HRMS platforms during the absence of reference standards. Significant progress has also been made in sampling device employment, utilizing novel sample preparation strategies, synthesizing toxin standards, employing hybrid MS platforms, and the associated data interpretation. This critical review attempts to elucidate the progress in LC‐MS based analysis in the determination of biotoxins while pointing out major challenges and suggestions for future development.
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
跳跃小伙发布了新的文献求助10
1秒前
墨月白发布了新的文献求助10
1秒前
勤奋的饼干完成签到 ,获得积分10
2秒前
erin完成签到 ,获得积分10
2秒前
顾矜应助VDC采纳,获得10
7秒前
李文思完成签到,获得积分10
7秒前
konosuba完成签到,获得积分0
8秒前
shuangfeng1853完成签到 ,获得积分10
8秒前
大模型应助跳跃小伙采纳,获得10
9秒前
devil完成签到,获得积分10
9秒前
花开四海完成签到 ,获得积分10
9秒前
彭于晏应助Selenge采纳,获得30
11秒前
loin完成签到,获得积分10
11秒前
滚雪球完成签到,获得积分10
11秒前
S飞完成签到 ,获得积分10
12秒前
yy完成签到,获得积分10
15秒前
fd163c发布了新的文献求助10
16秒前
16秒前
科研通AI5应助zhang采纳,获得10
17秒前
18秒前
善良的剑通应助孔雀翎采纳,获得10
19秒前
伶俐元芹完成签到,获得积分10
19秒前
陈仲完成签到,获得积分10
19秒前
HEIKU应助lawliet采纳,获得10
19秒前
若水完成签到 ,获得积分10
20秒前
20秒前
zehua309完成签到,获得积分10
20秒前
yy发布了新的文献求助10
21秒前
可爱的函函应助清图采纳,获得10
21秒前
zz完成签到,获得积分10
22秒前
滚雪球发布了新的文献求助10
23秒前
斯文败类应助斯文可仁采纳,获得10
24秒前
jyyg发布了新的文献求助10
25秒前
斯文的慕儿完成签到 ,获得积分10
26秒前
九先生吗完成签到,获得积分10
26秒前
思与省发布了新的文献求助10
28秒前
tracer完成签到,获得积分10
28秒前
Cynthia完成签到 ,获得积分10
28秒前
Ava应助yunsww采纳,获得10
29秒前
jyyg完成签到,获得积分10
32秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Technologies supporting mass customization of apparel: A pilot project 450
Mixing the elements of mass customisation 360
Периодизация спортивной тренировки. Общая теория и её практическое применение 310
the MD Anderson Surgical Oncology Manual, Seventh Edition 300
Nucleophilic substitution in azasydnone-modified dinitroanisoles 300
Political Ideologies Their Origins and Impact 13th Edition 260
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 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3780948
求助须知:如何正确求助?哪些是违规求助? 3326414
关于积分的说明 10227154
捐赠科研通 3041649
什么是DOI,文献DOI怎么找? 1669535
邀请新用户注册赠送积分活动 799095
科研通“疑难数据库(出版商)”最低求助积分说明 758734