Desorption electrospray ionization developments

DESI Desorption electrospray ionization (DESI) is a recently developed technique that permits formation of gas-phase ions at atmospheric pressure without requiring prior sample extraction or preparation. A solvent is electrosprayed at the surface of a condensed-phase target substance. Volatilized ions containing the electrosprayed droplets and the surface composition of the target are formed from the surface and subjected to mass analysis (Takats et al., 2005 Wiseman et al., 2005 Kauppila et al., 2006). 

Ifa D, Wiseman J, Song Q, Cooks G (2007) Development of capabilities for imaging mass spectrometry under ambient conditions with desorption electrospray ionization (DESI). Int J Mass Spectrom 259 8-15. doi 10.106/j.ijms.2006.08.003... 

Analyses of tropane alkaloids are mainly carried out by GC and HPLC and to a lesser extent by CE. This review describes recent applications developed for the analysis of this class of compounds in plant materials and biological matrices. Of course, mass spectrometry is generally used as the detection technique because of its high sensitivity and selectivity, but other techniques such as UV, fluorescence, flame ionization detection, nuclear magnetic resonance, among others have also been investigated. Finally, desorption electrospray ionization mass spectrometry is reported as a new interesting detection technique for the rapid analysis of samples without any sample preparation. 

Recently, a new family of ionization techniques that are distinguished by their ability to ionize analytes from surfaces under ambient conditions have been developed.61 These methods are also characterized by the fact that no prior separation or extraction of the sample is required. Of these methods two have so far been well characterized, desorption electrospray ionization (DESI)62 and direct analysis in real time (DART).63... 

Techniques for the Ionization of Molecules The measurability of molecules by MSI is enabled through the local desorption and ionization of the molecules from a surface. In theory, all types of molecules that can undergo these two chemical processes can be measured. Many techniques have been developed or adapted to achieve desorption and ionization of molecules from surfaces, but three different desorption/ioniza-tion techniques made their way to commercially available products. The acronyms of these technologies are desorption electrospray ionization (DESI), MALDI, and secondary ion mass spectrometry (SIMS). The principles of these three methods and a comparison of their possibilities and limitations are outlined throughout this section and summarized in Figure 1 and Table 2, respectively. 

The development of ambient MS was initiated with the introduction of desorption electrospray ionization (DESI) by Cooks in 2004 (35). Since then, a variety of possibilities combining different desorption and ionization... 

One of the most significant developments in mass spectrometry in the recent years is the introduction of a new class of ionization methods where samples in either solid or liquid state can be directly ionized in their native environment under ambient conditions (rather than inside a mass spectrometer) without any sample preparation. This new class of ionization methods is often referred to as ambient ionization methods [1,2], Because these methods generally ionize analytes on the surface or near the surface of the samples at atmospheric pressure, they have also been called atmospheric pressure surface sampling/ionization methods or direct/open air ionization methods [3], Since the first reports on ambient ionization with desorption electrospray ionization (DESI) [4] and direct analysis in real time (DART) [5], numerous reports have been published on the applications of these new ionization methods as well as the introduction of many related ambient ionization methods such as desorption atmospheric pressure chemical ionization (DAPCI) [6], atmospheric solid analysis probe (ASAP) [7], and electrospray-assisted laser desorption/ionization (ELDI) [8], Recently, two reviews of the various established and emerging ambient ionization methods have been published [2,3],... 

Several innovative ion sources that are based on ESI were developed, including secondary electrospray ionization (SESI), desorption electrospray ionization (DESl) (Figure 4.4), and nanoelectrospray ionization (nESI). These were described in some detail in Chapter 3 in the context of sample introduction techniques and are only briefly discussed here. 

Atmospheric pressure ionization (API). The need to analyze polar componnds and the necessity to interface LC with MS led to the development of techniqnes where the ionization occurs at atmospheric pressure outside the vacuum chamber, and the resulting ions are transferred directly into the mass analyzer. Electrospray ionization (ESI) is the most successful of the API methods because of the range of molecular masses to which it can be applied, from small molecules to proteins. Other API methods include atmospheric pressure chemical ionization (APCI) and atmospheric pressure photo-ionization (APPI), and also the recently developed surface ionization methods such as desorption electrospray ionization (DESI) and direct analysis in real time (DART) (see below and Sections 2.2.2 and 2.2.3). 

A series of technologies has been developed during the last 5 years (with an alphabet soup of acronyms) for the identification of compounds adsorbed on surfaces. The most common methods are desorption electrospray ionization (DESI) (and related techniques) and direct analysis in real time (DART). Applications range from the identification of explosives and drugs in forensics to biological arenas, such as the characterization of tissue sections. 

Examples of reports demonstrating development or applications of various TRMS approaches are listed in Table 4.1. The most common interfaces used in TRMS incorporate the following ion sources electrospray ionization (ESI), desorption electrospray ionization... 

More than a decade ago, the group of Graham Cooks introduced a modified version of ESI, which they called desorption electrospray ionization (DESI) [107] (see also Chapter 2). In this technique, the ESI plume is directed onto the sample surface. A very rapid chemical analysis of the sample surface is possible [5]. While the technique was originally presented as a way to analyze samples supported on solids, it has been modified to enable analysis of liquid samples [108]. This development facilitated implementations of DESI in TRMS. For example, in the work mentioned earlier in this chapter, Miao et al. [2] demonstrated the possibility to monitor reactions with sub-millisecond time resolution. Here, two reactant solutions mix rapidly to form a free liquid jet which is then ionized by... 

Miao, Z., Chen, H., Liu, P Liu, Y. (2011) Development of Submillisecond Ume-resolved Mass Spectrometry Using Desorption Electrospray Ionization. Anal. Chem. 83 3994-3997. 

In terms of the hardware, TRMS methods described in this book use most common types of ion sources and analyzers. Electrospray ionization (ESI), electron ionization (El), atmospheric pressure chemical ionization (APCI), or photoionization systems, and their modified versions, are all widely used in TRMS measurements. The newly developed atmospheric pressure ionization schemes such as desorption electrospray ionization (DESI) and Venturi easy ambient sonic-spray ionization (V-EASI) have already found applications in this area. Mass analyzers constitute the biggest and the most costly part of MS hardware. Few laboratories can afford purchasing different types of mass spectrometers for use in diverse applications. Therefore, the choice of mass spectrometer for TRMS is not always dictated by the optimum specifications of the instrument but its availability. Fortunately, many real-time measurements can be conducted using different mass analyzers equipped with atmospheric pressure inlets - with better or worse results. For example, triple quadrupole mass spectrometers excel at quantitative capabilities however, in many cases, popular ion trap (IT)-MS instruments can be used instead. On the other hand, applications of TRMS in fundamental studies often require a particular type of instrument (e.g., Fourier transform ion cyclotron resonance mass spectrometer for photodissociation studies on trapped ions). 

Another interesting development in the field of synthetic polymer charaeteriza-tion is the emergence of ambient-pressure desorption ionization techrriques such as desorption electrospray ionization mass spectrometry (DESI-MS) and many... 

Desorption electrospray ionization (DESI) [1] was introduced at the end of 2004, and direct analysis in real time (DART) [2] soon after in 2005. The apparent potential of both DESI and DART in high-throughput applications soon led to the development of some derivatives with the intention to broaden the field of applications or to adapt the underlying methodology to specific analytical needs. Now, the repertoire of methods includes variations of the DESI theme such as desorption sonic spray ionization (DeSSI) [3], later renamed easy sonic spray ionization (EASI) [4] or extractive electrospray ionization (EESI) [5,6]. Then, there are the DESI analogs of APCI and APPI, i.e., desorption atmospheric-pressure chemical ionization (DAPCI) [7,8] and desorption atmospheric pressure photoionization (DAPPI) [9]. 

A connnon feature of all mass spectrometers is the need to generate ions. Over the years a variety of ion sources have been developed. The physical chemistry and chemical physics communities have generally worked on gaseous and/or relatively volatile samples and thus have relied extensively on the two traditional ionization methods, electron ionization (El) and photoionization (PI). Other ionization sources, developed principally for analytical work, have recently started to be used in physical chemistry research. These include fast-atom bombardment (FAB), matrix-assisted laser desorption ionization (MALDI) and electrospray ionization (ES). 

The growing interest for the identification and characterization of polar and large compounds caused the development and the introduction of new ionization techniques, such as electrospray ionization (ESI)[4], and matrix assisted laser desorption ionization (MALDI),[5] and their more recent improvements, thus establishing new MS based approaches for studying large molecules, polymers and biopolymers, such as proteins, carbohydrates, nucleic acids. 

Mass spectrometry requires that the material being studied be converted into a vapor. Great strides have been taken in recent years to address this problem, especially in enticing large, thermally fragile (bio)molecules into the vapor state. Matrix assisted laser ionization-desorption (MALDI) and electrospray ionization (ESI) are two current forefront methods that accomplish this task. Even components of bacteria and intact viruses are being examined with these approaches. John B. Fenn and Koichi Tanaka shared in the award of a Nobel Prize in 2002 for their respective contributions to development of electrospray ionization and soft laser desorption. 

The development of soft ionization methods (electrospray ionization and matrix-assisted laser desorption ionization, and others not discussed here) has contributed to the remarkable progress seen in mass spectrometry applied to biochemistry and molecular biology research progress, and is beginning to find applications in archaeology. 

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