Surface analysis under ambient conditions using plasma-assisted desorption/ionization mass spectrometry

被引:198
作者
Ratcliffe, Lucy V.
Rutten, Frank J. M.
Barrett, David A.
Whitmore, Terry
Seymour, David
Greenwood, Claire
Aranda-Gonzalvo, Yolanda
Robinson, Steven
McCoustra, Martin
机构
[1] Univ Nottingham, Sch Pharm, Ctr Analyt Biosci, Nottingham NG7 2RD, England
[2] Hiden Analyt Ltd, Warrington WA5 7UN, Cheshire, England
[3] Forens Sci Serv Inc, Birmingham B37 7YN, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1021/ac070109q
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel plasma-assisted desorption/ionization (PADI) method that can be coupled with atmospheric pressure sampling mass spectrometry to yield mass spectral information under ambient conditions of pressure and humidity from a range of surfaces without the requirement for sample preparation or additives is reported. PADI is carried out by generating a nonthermal plasma which interacts directly with the surface of the analyte. Desorption and ionization then occur at the surface, and ions are sampled by the mass spectrometer. The PADI technique is demonstrated and compared with desorption electrospray ionization (DESI) for the detection of active ingredients in a range of over-the-counter and prescription pharmaceutical formulations, including nonsterodial anti-inflammatory drugs (mefenamic acid, Ibugel, and ibuprofen), analgesics (paracetamol, Anadin Extra), and Beecham's "all in one" cold and flu remedy. PADI has also been successfully applied to the analysis of nicotine in tobacco and thiosulfates in garlic. PADI experiments have been performed using a prototype source interfaced with a Waters Platform LCZ single-quadrupole mass spectrometer with limited modifications and a Hiden Analytical HPR-60 molecular beam mass spectrometer (MBMS). The ability of PADI to rapidly detect active ingredients in pharmaceuticals without the need for prior sample preparation, solvents, or exposed high voltages demonstrates the potential of the technique for high-throughput screening in a pharmaceutical or forensic environment.
引用
收藏
页码:6094 / 6101
页数:8
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