Mass spectrometry

Mass spectrometry (MS) is an analytical technique that is used to measure the mass-to-charge ratio of ions. The results are presented as a mass spectrum, a plot of intensity as a function of the mass-to-charge ratio. Mass spectrometry is used in many different fields and is applied to pure samples as well as complex mixtures.

A mass spectrum is a type of plot of the ion signal as a function of the mass-to-charge ratio. These spectra are used to determine the elemental or isotopic signature of a sample, the masses of particles and of molecules, and to elucidate the chemical identity or structure of molecules and other chemical compounds.

Discovery of Neon Isotopes

In a typical MS procedure, a sample, which may be solid, liquid, or gaseous, is ionized, for example by bombarding it with a beam of electrons. This may cause some of the sample's molecules to break up into positively charged fragments or simply become positively charged without fragmenting. These ions (fragments) are then separated according to their mass-to-charge ratio, for example by accelerating them and subjecting them to an electric or magnetic field: ions of the same mass-to-charge ratio will undergo the same amount of deflection.^[1] The ions are detected by a mechanism capable of detecting charged particles, such as an electron multiplier. Results are displayed as spectra of the signal intensity of detected ions as a function of the mass-to-charge ratio. The atoms or molecules in the sample can be identified by correlating known masses (e.g. an entire molecule) to the identified masses or through a characteristic fragmentation pattern.

History of the mass spectrometer

Further information: History of mass spectrometry

 

Replica of F.W. Aston's third mass spectrometer

In 1886, Eugen Goldstein observed rays in gas discharges under low pressure that traveled away from the anode and through channels in a perforated cathode, opposite to the direction of negatively charged cathode rays (which travel from cathode to anode). Goldstein called these positively charged anode rays "Kanalstrahlen"; the standard translation of this term into English is "canal rays". Wilhelm Wien found that strong electric or magnetic fields deflected the canal rays and, in 1899, constructed a device with perpendicular electric and magnetic fields that separated the positive rays according to their charge-to-mass ratio (Q/m). Wien found that the charge-to-mass ratio depended on the nature of the gas in the discharge tube. English scientist J. J. Thomson later improved on the work of Wien by reducing the pressure to create the mass spectrograph.

 

Calutron mass spectrometers were used in the Manhattan Project for uranium enrichment.

The word spectrograph had become part of the international scientific vocabulary by 1884.^[2][3] Early spectrometry devices that measured the mass-to-charge ratio of ions were called mass spectrographs which consisted of instruments that recorded a spectrum of mass values on a photographic plate.^[4][5] A mass spectroscope is similar to a mass spectrograph except that the beam of ions is directed onto a phosphor screen.^[6] A mass spectroscope configuration was used in early instruments when it was desired that the effects of adjustments be quickly observed. Once the instrument was properly adjusted, a photographic plate was inserted and exposed. The term mass spectroscope continued to be used even though the direct illumination of a phosphor screen was replaced by indirect measurements with an oscilloscope.^[7] The use of the term mass spectroscopy is now discouraged due to the possibility of confusion with light spectroscopy.^[1][8] Mass spectrometry is often abbreviated as mass-spec or simply as MS.^[1]

Modern techniques of mass spectrometry were devised by Arthur Jeffrey Dempster and F.W. Aston in 1918 and 1919 respectively.

Sector mass spectrometers known as calutrons were developed by Ernest O. Lawrence and used for separating the isotopes of uranium during the Manhattan Project.^[9] Calutron mass spectrometers were used for uranium enrichment at the Oak Ridge, Tennessee Y-12 plant established during World War II.

In 1989, half of the Nobel Prize in Physics was awarded to Hans Dehmelt and Wolfgang Paul for the development of the ion trap technique in the 1950s and 1960s.

In 2002, the Nobel Prize in Chemistry was awarded to John Bennett Fenn for the development of electrospray ionization (ESI) and Koichi Tanaka for the development of soft laser desorption (SLD) and their application to the ionization of biological macromolecules, especially proteins.^[10]

Parts of a mass spectrometer

 

Schematics of a simple mass spectrometer with sector type mass analyzer. This one is for the measurement of carbon dioxide isotope ratios (IRMS) as in the carbon-13 urea breath test.

A mass spectrometer consists of three components: an ion source, a mass analyzer, and a detector. The ionizer converts a portion of the sample into ions. There is a wide variety of ionization techniques, depending on the phase (solid, liquid, gas) of the sample and the efficiency of various ionization mechanisms for the unknown species. An extraction system removes ions from the sample, which are then targeted through the mass analyzer and into the detector. The differences in masses of the fragments allows the mass analyzer to sort the ions by their mass-to-charge ratio. The detector measures the value of an indicator quantity and thus provides data for calculating the abundances of each ion present. Some detectors also give spatial information, e.g., a multichannel plate.

Theoretical example

The following describes the operation of a spectrometer mass analyzer, which is of the sector type. (Other analyzer types are treated below.) Consider a sample of sodium chloride (table salt). In the ion source, the sample is vaporized (turned into gas) and ionized (transformed into electrically charged particles) into sodium (Na⁺) and chloride (Cl⁻) ions. Sodium atoms and ions are monoisotopic, with a mass of about 23 daltons (symbol: Da or older symbol: u). Chloride atoms and ions come in two stable isotopes with masses of approximately 35 u (at a natural abundance of about 75 percent) and approximately 37 u (at a natural abundance of about 25 percent). The analyzer part of the spectrometer contains electric and magnetic fields, which exert forces on ions traveling through these fields. The speed of a charged particle may be increased or decreased while passing through the electric field, and its direction may be altered by the magnetic field. The magnitude of the deflection of the moving ion's trajectory depends on its mass-to-charge ratio. Lighter ions are deflected by the magnetic force to a greater degree than heavier ions (based on Newton's second law of motion, F = ma). The streams of magnetically sorted ions pass from the analyzer to the detector, which records the relative abundance of each ion type. This information is used to determine the chemical element composition of the original sample (i.e. that both sodium and chlorine are present in the sample) and the isotopic composition of its constituents (the ratio of ³⁵Cl to ³⁷Cl).

Creating ions

 

Surface ionization source at the Argonne National Laboratory linear accelerator

The ion source is the part of the mass spectrometer that ionizes the material under analysis (the analyte). The ions are then transported by magnetic or electric fields to the mass analyzer.

Techniques for ionization have been key to determining what types of samples can be analyzed by mass spectrometry. Electron ionization and chemical ionization are used for gases and vapors. In chemical ionization sources, the analyte is ionized by chemical ion-molecule reactions during collisions in the source. Two techniques often used with liquid and solid biological samples include electrospray ionization (invented by John Fenn^[11]) and matrix-assisted laser desorption/ionization (MALDI, initially developed as a similar technique "Soft Laser Desorption (SLD)" by K. Tanaka^[12] for which a Nobel Prize was awarded and as MALDI by M. Karas and F. Hillenkamp^[13]).

Hard ionization and soft ionization

 

Quadrupole mass spectrometer and electrospray ion source used for Fenn's early work

In mass spectrometry, ionization refers to the production of gas phase ions suitable for resolution in the mass analyser or mass filter. Ionization occurs in the ion source. There are several ion sources available; each has advantages and disadvantages for particular applications. For example, electron ionization (EI) gives a high degree of fragmentation, yielding highly detailed mass spectra which when skilfully analysed can provide important information for structural elucidation/characterisation and facilitate identification of unknown compounds by comparison to mass spectral libraries obtained under identical operating conditions. However, EI is not suitable for coupling to HPLC, i.e. LC-MS, since at atmospheric pressure, the filaments used to generate electrons burn out rapidly. Thus EI is coupled predominantly with GC, i.e. GC-MS, where the entire system is under high vacuum.

Hard ionization techniques are processes which impart high quantities of residual energy in the subject molecule invoking large degrees of fragmentation (i.e. the systematic rupturing of bonds acts to remove the excess energy, restoring stability to the resulting ion). Resultant ions tend to have m/z lower than the molecular ion (other than in the case of proton transfer and not including isotope peaks). The most common example of hard ionization is electron ionization (EI).

Soft ionization refers to the processes which impart little residual energy onto the subject molecule and as such result in little fragmentation. Examples include fast atom bombardment (FAB), chemical ionization (CI), atmospheric-pressure chemical ionization (APCI), atmospheric-pressure photoionization (APPI), electrospray ionization (ESI), desorption electrospray ionization (DESI), and matrix-assisted laser desorption/ionization (MALDI).

Inductively coupled plasma

 

Inductively coupled plasma ion source

Inductively coupled plasma (ICP) sources are used primarily for cation analysis of a wide array of sample types. In this source, a plasma that is electrically neutral overall, but that has had a substantial fraction of its atoms ionized by high temperature, is used to atomize introduced sample molecules and to further strip the outer electrons from those atoms. The plasma is usually generated from argon gas, since the first ionization energy of argon atoms is higher than the first of any other elements except He, F and Ne, but lower than the second ionization energy of all except the most electropositive metals. The heating is achieved by a radio-frequency current passed through a coil surrounding the plasma.

Photoionization mass spectrometry

Photoionization can be used in experiments which seek to use mass spectrometry as a means of resolving chemical kinetics mechanisms and isomeric product branching.^[14] In such instances a high energy photon, either X-ray or uv, is used to dissociate stable gaseous molecules in a carrier gas of He or Ar. In instances where a synchrotron light source is utilized, a tuneable photon energy can be utilized to acquire a photoionization efficiency curve which can be used in conjunction with the charge ratio m/z to fingerprint molecular and ionic species. More recently atmospheric pressure photoionization (APPI) has been developed to ionize molecules mostly as effluents of LC-MS systems.

Ambient ionization

Some applications for ambient ionization include environmental applications as well as clinical applications. In these techniques, ions form in an ion source outside the mass spectrometer. Sampling becomes easy as the samples don't need previous separation nor preparation. Some examples of ambient ionization techniques are Direct Analysis in Real Time (DART),DESI, SESI, LAESI, desorption atmospheric-pressure chemical ionization (DAPCI), and desorption atmospheric pressure photoionization DAPPI among others.

Other ionization techniques

Others include glow discharge, field desorption (FD), fast atom bombardment (FAB), thermospray, desorption/ionization on silicon (DIOS), atmospheric pressure chemical ionization (APCI), secondary ion mass spectrometry (SIMS), spark ionization and thermal ionization (TIMS).^[15]

Mass selection

Mass analyzers separate the ions according to their mass-to-charge ratio. The following two laws govern the dynamics of charged particles in electric and magnetic fields in vacuum:

${\displaystyle \mathbf {F} =Q(\mathbf {E} +\mathbf {v} \times \mathbf {B} )}$  (Lorentz force law);

${\displaystyle \mathbf {F} =m\mathbf {a} }$  (Newton's second law of motion in the non-relativistic case, i.e. valid only at ion velocity much lower than the speed of light).

Here F is the force applied to the ion, m is the mass of the ion, a is the acceleration, Q is the ion charge, E is the electric field, and v × B is the vector cross product of the ion velocity and the magnetic field

Equating the above expressions for the force applied to the ion yields:

${\displaystyle (m/Q)\mathbf {a} =\mathbf {E} +\mathbf {v} \times \mathbf {B} .}$ 

This differential equation is the classic equation of motion for charged particles. Together with the particle's initial conditions, it completely determines the particle's motion in space and time in terms of m/Q. Thus mass spectrometers could be thought of as "mass-to-charge spectrometers". When presenting data, it is common to use the (officially) dimensionless m/z, where z is the number of elementary charges (e) on the ion (z=Q/e). This quantity, although it is informally called the mass-to-charge ratio, more accurately speaking represents the ratio of the mass number and the charge number, z.

There are many types of mass analyzers, using either static or dynamic fields, and magnetic or electric fields, but all operate according to the above differential equation. Each analyzer type has its strengths and weaknesses. Many mass spectrometers use two or more mass analyzers for tandem mass spectrometry (MS/MS). In addition to the more common mass analyzers listed below, there are others designed for special situations.

There are several important analyzer characteristics. The mass resolving power is the measure of the ability to distinguish two peaks of slightly different m/z. The mass accuracy is the ratio of the m/z measurement error to the true m/z. Mass accuracy is usually measured in ppm or milli mass units. The mass range is the range of m/z amenable to analysis by a given analyzer. The linear dynamic range is the range over which ion signal is linear with analyte concentration. Speed refers to the time frame of the experiment and ultimately is used to determine the number of spectra per unit time that can be generated.

Sector instruments

 

ThermoQuest AvantGarde sector mass spectrometer

Further information: Sector mass spectrometer

A sector field mass analyzer uses a static electric and/or magnetic field to affect the path and/or velocity of the charged particles in some way. As shown above, sector instruments bend the trajectories of the ions as they pass through the mass analyzer, according to their mass-to-charge ratios, deflecting the more charged and faster-moving, lighter ions more. The analyzer can be used to select a narrow range of m/z or to scan through a range of m/z to catalog the ions present.^[16]

Time-of-flight

Further information: time-of-flight mass spectrometry

The time-of-flight (TOF) analyzer uses an electric field to accelerate the ions through the same potential, and then measures the time they take to reach the detector. If the particles all have the same charge, their kinetic energies will be identical, and their velocities will depend only on their masses. Ions with a lower mass will reach the detector first.^[17] However, in reality, even particles with the same m/z can arrive at different times at the detector, because they have different initial velocities. The initial velocity is often not dependent on the mass of the ion, and will turn into a difference in the final velocity. Because of this, ions with the same m/z ratio will reach the detector at a variety of times, which broadens the peaks shown on the count vs m/z plot, but will generally not change the central location of the peaks, since the starting velocity of ions is generally centered at zero. To fix this problem, time-lag focusing/delayed extraction has been coupled with TOF-MS.^[18]

Quadrupole mass filter

Further information: Quadrupole mass analyzer

Quadrupole mass analyzers use oscillating electrical fields to selectively stabilize or destabilize the paths of ions passing through a radio frequency (RF) quadrupole field created between four parallel rods. Only the ions in a certain range of mass/charge ratio are passed through the system at any time, but changes to the potentials on the rods allow a wide range of m/z values to be swept rapidly, either continuously or in a succession of discrete hops. A quadrupole mass analyzer acts as a mass-selective filter and is closely related to the quadrupole ion trap, particularly the linear quadrupole ion trap except that it is designed to pass the untrapped ions rather than collect the trapped ones, and is for that reason referred to as a transmission quadrupole. A magnetically enhanced quadrupole mass analyzer includes the addition of a magnetic field, either applied axially or transversely. This novel type of instrument leads to an additional performance enhancement in terms of resolution and/or sensitivity depending upon the magnitude and orientation of the applied magnetic field.^[19][20] A common variation of the transmission quadrupole is the triple quadrupole mass spectrometer. The "triple quad" has three consecutive quadrupole stages, the first acting as a mass filter to transmit a particular incoming ion to the second quadrupole, a collision chamber, wherein that ion can be broken into fragments. The third quadrupole also acts as a mass filter, to transmit a particular fragment ion to the detector. If a quadrupole is made to rapidly and repetitively cycle through a range of mass filter settings, full spectra can be reported. Likewise, a triple quad can be made to perform various scan types characteristic of tandem mass spectrometry.

Ion traps

Three-dimensional quadrupole ion trap

Further information: quadrupole ion trap

The quadrupole ion trap works on the same physical principles as the quadrupole mass analyzer, but the ions are trapped and sequentially ejected. Ions are trapped in a mainly quadrupole RF field, in a space defined by a ring electrode (usually connected to the main RF potential) between two endcap electrodes (typically connected to DC or auxiliary AC potentials). The sample is ionized either internally (e.g. with an electron or laser beam), or externally, in which case the ions are often introduced through an aperture in an endcap electrode.

There are many mass/charge separation and isolation methods but the most commonly used is the mass instability mode in which the RF potential is ramped so that the orbit of ions with a mass a > b are stable while ions with mass b become unstable and are ejected on the z-axis onto a detector. There are also non-destructive analysis methods.

Ions may also be ejected by the resonance excitation method, whereby a supplemental oscillatory excitation voltage is applied to the endcap electrodes, and the trapping voltage amplitude and/or excitation voltage frequency is varied to bring ions into a resonance condition in order of their mass/charge ratio.^[21][22]

Cylindrical ion trap

The cylindrical ion trap mass spectrometer (CIT) is a derivative of the quadrupole ion trap where the electrodes are formed from flat rings rather than hyperbolic shaped electrodes. The architecture lends itself well to miniaturization because as the size of a trap is reduced, the shape of the electric field near the center of the trap, the region where the ions are trapped, forms a shape similar to that of a hyperbolic trap.

Linear quadrupole ion trap

A linear quadrupole ion trap is similar to a quadrupole ion trap, but it traps ions in a two dimensional quadrupole field, instead of a three-dimensional quadrupole field as in a 3D quadrupole ion trap. Thermo Fisher's LTQ ("linear trap quadrupole") is an example of the linear ion trap.^[23]

A toroidal ion trap can be visualized as a linear quadrupole curved around and connected at the ends or as a cross-section of a 3D ion trap rotated on edge to form the toroid, donut-shaped trap. The trap can store large volumes of ions by distributing them throughout the ring-like trap structure. This toroidal shaped trap is a configuration that allows the increased miniaturization of an ion trap mass analyzer. Additionally, all ions are stored in the same trapping field and ejected together simplifying detection that can be complicated with array configurations due to variations in detector alignment and machining of the arrays.^[24]

As with the toroidal trap, linear traps and 3D quadrupole ion traps are the most commonly miniaturized mass analyzers due to their high sensitivity, tolerance for mTorr pressure, and capabilities for single analyzer tandem mass spectrometry (e.g. product ion scans).^[25]

Orbitrap

 

Orbitrap mass analyzer

Further information: Orbitrap

Orbitrap instruments are similar to Fourier-transform ion cyclotron resonance mass spectrometers (see text below). Ions are electrostatically trapped in an orbit around a central, spindle shaped electrode. The electrode confines the ions so that they both orbit around the central electrode and oscillate back and forth along the central electrode's long axis. This oscillation generates an image current in the detector plates which is recorded by the instrument. The frequencies of these image currents depend on the mass-to-charge ratios of the ions. Mass spectra are obtained by Fourier transformation of the recorded image currents.

Orbitraps have a high mass accuracy, high sensitivity and a good dynamic range.^[26]

Fourier-transform ion cyclotron resonance

 

Fourier-transform ion cyclotron resonance mass spectrometer

Further information: Fourier-transform ion cyclotron resonance

Fourier-transform mass spectrometry (FTMS), or more precisely Fourier-transform ion cyclotron resonance MS, measures mass by detecting the image current produced by ions cyclotroning in the presence of a magnetic field. Instead of measuring the deflection of ions with a detector such as an electron multiplier, the ions are injected into a Penning trap (a static electric/magnetic ion trap) where they effectively form part of a circuit. Detectors at fixed positions in space measure the electrical signal of ions which pass near them over time, producing a periodic signal. Since the frequency of an ion's cycling is determined by its mass-to-charge ratio, this can be deconvoluted by performing a Fourier transform on the signal. FTMS has the advantage of high sensitivity (since each ion is "counted" more than once) and much higher resolution and thus precision.^[27][28]

Ion cyclotron resonance (ICR) is an older mass analysis technique similar to FTMS except that ions are detected with a traditional detector. Ions trapped in a Penning trap are excited by an RF electric field until they impact the wall of the trap, where the detector is located. Ions of different mass are resolved according to impact time.

Detectors

 

A continuous dynode particle multiplier detector

The final element of the mass spectrometer is the detector. The detector records either the charge induced or the current produced when an ion passes by or hits a surface. In a scanning instrument, the signal produced in the detector during the course of the scan versus where the instrument is in the scan (at what m/Q) will produce a mass spectrum, a record of ions as a function of m/Q.

Typically, some type of electron multiplier is used, though other detectors including Faraday cups and ion-to-photon detectors are also used. Because the number of ions leaving the mass analyzer at a particular instant is typically quite small, considerable amplification is often necessary to get a signal. Microchannel plate detectors are commonly used in modern commercial instruments.^[29] In FTMS and Orbitraps, the detector consists of a pair of metal surfaces within the mass analyzer/ion trap region which the ions only pass near as they oscillate. No direct current is produced, only a weak AC image current is produced in a circuit between the electrodes. Other inductive detectors have also been used.^[30]

Tandem mass spectrometry

 

Tandem mass spectrometry for biological molecules using ESI or MALDI

A tandem mass spectrometer is one capable of multiple rounds of mass spectrometry, usually separated by some form of molecule fragmentation. For example, one mass analyzer can isolate one peptide from many entering a mass spectrometer. A second mass analyzer then stabilizes the peptide ions while they collide with a gas, causing them to fragment by collision-induced dissociation (CID). A third mass analyzer then sorts the fragments produced from the peptides. Tandem MS can also be done in a single mass analyzer over time, as in a quadrupole ion trap. There are various methods for fragmenting molecules for tandem MS, including collision-induced dissociation (CID), electron capture dissociation (ECD), electron transfer dissociation (ETD), infrared multiphoton dissociation (IRMPD), blackbody infrared radiative dissociation (BIRD), electron-detachment dissociation (EDD) and surface-induced dissociation (SID). An important application using tandem mass spectrometry is in protein identification.^[31]

Tandem mass spectrometry enables a variety of experimental sequences. Many commercial mass spectrometers are designed to expedite the execution of such routine sequences as selected reaction monitoring (SRM) and precursor ion scanning. In SRM, the first analyzer allows only a single mass through and the second analyzer monitors for multiple user-defined fragment ions. SRM is most often used with scanning instruments where the second mass analysis event is duty cycle limited. These experiments are used to increase specificity of detection of known molecules, notably in pharmacokinetic studies. Precursor ion scanning refers to monitoring for a specific loss from the precursor ion. The first and second mass analyzers scan across the spectrum as partitioned by a user-defined m/z value. This experiment is used to detect specific motifs within unknown molecules.

Another type of tandem mass spectrometry used for radiocarbon dating is accelerator mass spectrometry (AMS), which uses very high voltages, usually in the mega-volt range, to accelerate negative ions into a type of tandem mass spectrometer.

The METLIN Metabolite and Chemical Entity Database^[32][33][34] is the largest repository of experimental tandem mass spectrometry data acquired from standards. The tandem mass spectrometry data on over 850,000 molecular standards (as of 24 August 2020)^[32] is provided to facilitate the identification of chemical entities from tandem mass spectrometry experiments. In addition to the identification of known molecules it is also useful for identifying unknowns using its similarity searching/analysis.^[35] All tandem mass spectrometry data comes from the experimental analysis of standards at multiple collision energies and in both positive and negative ionization modes.^[32]

Common mass spectrometer configurations and techniques

When a specific combination of source, analyzer, and detector becomes conventional in practice, a compound acronym may arise to designate it succinctly. One example is MALDI-TOF, which refers to a combination of a matrix-assisted laser desorption/ionization source with a time-of-flight mass analyzer. Other examples include inductively coupled plasma-mass spectrometry (ICP-MS), accelerator mass spectrometry (AMS), thermal ionization-mass spectrometry (TIMS) and spark source mass spectrometry (SSMS).

Certain applications of mass spectrometry have developed monikers that although strictly speaking would seem to refer to a broad application, in practice have come instead to connote a specific or a limited number of instrument configurations. An example of this is isotope-ratio mass spectrometry (IRMS), which refers in practice to the use of a limited number of sector based mass analyzers; this name is used to refer to both the application and the instrument used for the application.

Separation techniques combined with mass spectrometry

An important enhancement to the mass resolving and mass determining capabilities of mass spectrometry is using it in tandem with chromatographic and other separation techniques.

Gas chromatography

 

A gas chromatograph (right) directly coupled to a mass spectrometer (left)

Main article: Gas chromatography–mass spectrometry

A common combination is gas chromatography-mass spectrometry (GC/MS or GC-MS). In this technique, a gas chromatograph is used to separate different compounds. This stream of separated compounds is fed online into the ion source, a metallic filament to which voltage is applied. This filament emits electrons which ionize the compounds. The ions can then further fragment, yielding predictable patterns. Intact ions and fragments pass into the mass spectrometer's analyzer and are eventually detected.^[36] However, the high temperatures (300°C) used in the GC-MS injection port (and oven) can result in thermal degradation of injected molecules, thus resulting in the measurement of degradation products instead of the actual molecule(s) of interest.^[37]

Liquid chromatography

Main article: Liquid chromatography–mass spectrometry

 

Indianapolis Museum of Art conservation scientist performing liquid chromatography–mass spectrometry

Similarly to gas chromatography MS (GC-MS), liquid chromatography-mass spectrometry (LC/MS or LC-MS) separates compounds chromatographically before they are introduced to the ion source and mass spectrometer. It differs from GC-MS in that the mobile phase is liquid, usually a mixture of water and organic solvents, instead of gas. Most commonly, an electrospray ionization source is used in LC-MS. Other popular and commercially available LC-MS ion sources are atmospheric pressure chemical ionization and atmospheric pressure photoionization. There are also some newly developed ionization techniques like laser spray.

Capillary electrophoresis–mass spectrometry

Main article: Capillary electrophoresis–mass spectrometry

Capillary electrophoresis–mass spectrometry (CE-MS) is a technique that combines the liquid separation process of capillary electrophoresis with mass spectrometry.^[38] CE-MS is typically coupled to electrospray ionization.^[39]

Ion mobility

Main article: Ion-mobility spectrometry–mass spectrometry

Ion mobility spectrometry-mass spectrometry (IMS/MS or IMMS) is a technique where ions are first separated by drift time through some neutral gas under an applied electrical potential gradient before being introduced into a mass spectrometer.^[40] Drift time is a measure of the radius relative to the charge of the ion. The duty cycle of IMS (the time over which the experiment takes place) is longer than most mass spectrometric techniques, such that the mass spectrometer can sample along the course of the IMS separation. This produces data about the IMS separation and the mass-to-charge ratio of the ions in a manner similar to LC-MS.^[41]

The duty cycle of IMS is short relative to liquid chromatography or gas chromatography separations and can thus be coupled to such techniques, producing triple modalities such as LC/IMS/MS.^[42]

Data and analysis

 

Mass spectrum of a peptide showing the isotopic distribution

Data representations

See also: Mass spectrometry data format

Mass spectrometry produces various types of data. The most common data representation is the mass spectrum.

Certain types of mass spectrometry data are best represented as a mass chromatogram. Types of chromatograms include selected ion monitoring (SIM), total ion current (TIC), and selected reaction monitoring (SRM), among many others.

Other types of mass spectrometry data are well represented as a three-dimensional contour map. In this form, the mass-to-charge, m/z is on the x-axis, intensity the y-axis, and an additional experimental parameter, such as time, is recorded on the z-axis.

Data analysis

Mass spectrometry data analysis is specific to the type of experiment producing the data. General subdivisions of data are fundamental to understanding any data.

Many mass spectrometers work in either negative ion mode or positive ion mode. It is very important to know whether the observed ions are negatively or positively charged. This is often important in determining the neutral mass but it also indicates something about the nature of the molecules.

Different types of ion source result in different arrays of fragments produced from the original molecules. An electron ionization source produces many fragments and mostly single-charged (1-) radicals (odd number of electrons), whereas an electrospray source usually produces non-radical quasimolecular ions that are frequently multiply charged. Tandem mass spectrometry purposely produces fragment ions post-source and can drastically change the sort of data achieved by an experiment.

Knowledge of the origin of a sample can provide insight into the component molecules of the sample and their fragmentations. A sample from a synthesis/manufacturing process will probably contain impurities chemically related to the target component. A crudely prepared biological sample will probably contain a certain amount of salt, which may form adducts with the analyte molecules in certain analyses.

Results can also depend heavily on sample preparation and how it was run/introduced. An important example is the issue of which matrix is used for MALDI spotting, since much of the energetics of the desorption/ionization event is controlled by the matrix rather than the laser power. Sometimes samples are spiked with sodium or another ion-carrying species to produce adducts rather than a protonated species.

Mass spectrometry can measure molar mass, molecular structure, and sample purity. Each of these questions requires a different experimental procedure; therefore, adequate definition of the experimental goal is a prerequisite for collecting the proper data and successfully interpreting it.

Interpretation of mass spectra

 

Toluene electron ionization mass spectrum

Main article: Mass spectrum analysis

Since the precise structure or peptide sequence of a molecule is deciphered through the set of fragment masses, the interpretation of mass spectra requires combined use of various techniques. Usually the first strategy for identifying an unknown compound is to compare its experimental mass spectrum against a library of mass spectra. If no matches result from the search, then manual interpretation^[43] or software assisted interpretation of mass spectra must be performed. Computer simulation of ionization and fragmentation processes occurring in mass spectrometer is the primary tool for assigning structure or peptide sequence to a molecule. An a priori structural information is fragmented in silico and the resulting pattern is compared with observed spectrum. Such simulation is often supported by a fragmentation library^[44] that contains published patterns of known decomposition reactions. Software taking advantage of this idea has been developed for both small molecules and proteins.

Analysis of mass spectra can also be spectra with accurate mass. A mass-to-charge ratio value (m/z) with only integer precision can represent an immense number of theoretically possible ion structures; however, more precise mass figures significantly reduce the number of candidate molecular formulas. A computer algorithm called formula generator calculates all molecular formulas that theoretically fit a given mass with specified tolerance.

A recent technique for structure elucidation in mass spectrometry, called precursor ion fingerprinting, identifies individual pieces of structural information by conducting a search of the tandem spectra of the molecule under investigation against a library of the product-ion spectra of structurally characterized precursor ions.^[45]

Applications

 

NOAA Particle Analysis by Laser Mass Spectrometry aerosol mass spectrometer aboard a NASA WB-57 high-altitude research aircraft

Mass spectrometry has both qualitative and quantitative uses. These include identifying unknown compounds, determining the isotopic composition of elements in a molecule, and determining the structure of a compound by observing its fragmentation. Other uses include quantifying the amount of a compound in a sample or studying the fundamentals of gas phase ion chemistry (the chemistry of ions and neutrals in a vacuum). MS is now commonly used in analytical laboratories that study physical, chemical, or biological properties of a great variety of compounds. Quantitation can be relative (analyzed relative to a reference sample) or absolute (analyzed using a standard curve method).^[46][47]

As an analytical technique it possesses distinct advantages such as: Increased sensitivity over most other analytical techniques because the analyzer, as a mass-charge filter, reduces background interference, Excellent specificity from characteristic fragmentation patterns to identify unknowns or confirm the presence of suspected compounds, Information about molecular weight, Information about the isotopic abundance of elements, Temporally resolved chemical data.

A few of the disadvantages of the method is that it often fails to distinguish between optical and geometrical isomers and the positions of substituent in o-, m- and p- positions in an aromatic ring. Also, its scope is limited in identifying hydrocarbons that produce similar fragmented ions.

Isotope ratio MS: isotope dating and tracing

 

Mass spectrometer to determine the ¹⁶O/¹⁸O and ¹²C/¹³C isotope ratio on biogenous carbonate

Main article: Isotope-ratio mass spectrometry

Mass spectrometry is also used to determine the isotopic composition of elements within a sample. Differences in mass among isotopes of an element are very small, and the less abundant isotopes of an element are typically very rare, so a very sensitive instrument is required. These instruments, sometimes referred to as isotope ratio mass spectrometers (IR-MS), usually use a single magnet to bend a beam of ionized particles towards a series of Faraday cups which convert particle impacts to electric current. A fast on-line analysis of deuterium content of water can be done using flowing afterglow mass spectrometry, FA-MS. Probably the most sensitive and accurate mass spectrometer for this purpose is the accelerator mass spectrometer (AMS). This is because it provides ultimate sensitivity, capable of measuring individual atoms and measuring nuclides with a dynamic range of ~10¹⁵ relative to the major stable isotope.^[48] Isotope ratios are important markers of a variety of processes. Some isotope ratios are used to determine the age of materials for example as in carbon dating. Labeling with stable isotopes is also used for protein quantification. (see protein characterization below)

Membrane-introduction mass spectrometry: measuring gases in solution

Membrane-introduction mass spectrometry combines the isotope ratio MS with a reaction chamber/cell separated by a gas-permeable membrane. This method allows the study of gases as they evolve in solution. This method has been extensively used for the study of the production of oxygen by Photosystem II.^[49]

Trace gas analysis

Several techniques use ions created in a dedicated ion source injected into a flow tube or a drift tube: selected ion flow tube (SIFT-MS), and proton transfer reaction (PTR-MS), are variants of chemical ionization dedicated for trace gas analysis of air, breath or liquid headspace using well defined reaction time allowing calculations of analyte concentrations from the known reaction kinetics without the need for internal standard or calibration.

Another technique with applications in trace gas analysis field is secondary electrospray ionization (SESI-MS), which is a variant of electrospray ionization. SESI consist of an electrospray plume of pure acidified solvent that interacts with neutral vapors.  Vapor molecules get ionized at atmospheric pressure when charge is transferred from the ions formed in the electrospray to the molecules. One advantage of this approach is that it is compatible with most ESI-MS systems.^[50][51]

Residual gas analysis

This section is an excerpt from Residual gas analyzer.[edit]

 

Residual gas analyzer installed on a laboratory-scale freeze dryer

A residual gas analyzer (RGA) is a small and usually rugged mass spectrometer, typically designed for process control and contamination monitoring in vacuum systems. When constructed as a quadrupole mass analyzer, there exist two implementations, utilizing either an open ion source (OIS) or a closed ion source (CIS). RGAs may be found in high vacuum applications such as research chambers, surface science setups, accelerators, scanning microscopes, etc. RGAs are used in most cases to monitor the quality of the vacuum and easily detect minute traces of impurities in the low-pressure gas environment. These impurities can be measured down to ${\displaystyle 10^{-14}}$  Torr levels, possessing sub-ppm detectability in the absence of background interferences.

RGAs would also be used as sensitive in-situ leak detectors commonly using helium, isopropyl alcohol or other tracer molecules. With vacuum systems pumped down to lower than ${\displaystyle 10^{-5}}$  Torr—checking of the integrity of the vacuum seals and the quality of the vacuum—air leaks, virtual leaks and other contaminants at low levels may be detected before a process is initiated.

Atom probe

An atom probe is an instrument that combines time-of-flight mass spectrometry and field-evaporation microscopy to map the location of individual atoms.

Pharmacokinetics

Main article: Pharmacokinetics

Pharmacokinetics is often studied using mass spectrometry because of the complex nature of the matrix (often blood or urine) and the need for high sensitivity to observe low dose and long time point data. The most common instrumentation used in this application is LC-MS with a triple quadrupole mass spectrometer. Tandem mass spectrometry is usually employed for added specificity. Standard curves and internal standards are used for quantitation of usually a single pharmaceutical in the samples. The samples represent different time points as a pharmaceutical is administered and then metabolized or cleared from the body. Blank or t=0 samples taken before administration are important in determining background and ensuring data integrity with such complex sample matrices. Much attention is paid to the linearity of the standard curve; however it is not uncommon to use curve fitting with more complex functions such as quadratics since the response of most mass spectrometers is less than linear across large concentration ranges.^[52][53][54]

There is currently considerable interest in the use of very high sensitivity mass spectrometry for microdosing studies, which are seen as a promising alternative to animal experimentation.

Recent studies show that secondary electrospray ionization (SESI) is a powerful technique to monitor drug kinetics via breath analysis.^[55][56] Because breath is naturally produced, several datapoints can be readily collected. This allows for the number of collected data-points to be greatly increased.^[57] In animal studies, this approach SESI can reduce animal sacrifice.^[56] In humans, SESI-MS non-invasive analysis of breath can help study the kinetics of drugs at a personalized level.^[55][58][59]

Protein characterization

Main article: Protein mass spectrometry

Mass spectrometry is an important method for the characterization and sequencing of proteins. The two primary methods for ionization of whole proteins are electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI). In keeping with the performance and mass range of available mass spectrometers, two approaches are used for characterizing proteins. In the first, intact proteins are ionized by either of the two techniques described above, and then introduced to a mass analyzer. This approach is referred to as "top-down" strategy of protein analysis. The top-down approach however is largely limited to low-throughput single-protein studies. In the second, proteins are enzymatically digested into smaller peptides using proteases such as trypsin or pepsin, either in solution or in gel after electrophoretic separation. Other proteolytic agents are also used. The collection of peptide products are often separated by chromatography prior to introduction to the mass analyzer. When the characteristic pattern of peptides is used for the identification of the protein the method is called peptide mass fingerprinting (PMF), if the identification is performed using the sequence data determined in tandem MS analysis it is called de novo peptide sequencing. These procedures of protein analysis are also referred to as the "bottom-up" approach, and have also been used to analyse the distribution and position of post-translational modifications such as phosphorylation on proteins.^[60] A third approach is also beginning to be used, this intermediate "middle-down" approach involves analyzing proteolytic peptides that are larger than the typical tryptic peptide.^[61]

Space exploration

 

NASA's Phoenix Mars Lander analyzing a soil sample from the "Rosy Red" trench with the TEGA mass spectrometer

As a standard method for analysis, mass spectrometers have reached other planets and moons. Two were taken to Mars by the Viking program. In early 2005 the Cassini–Huygens mission delivered a specialized GC-MS instrument aboard the Huygens probe through the atmosphere of Titan, the largest moon of the planet Saturn. This instrument analyzed atmospheric samples along its descent trajectory and was able to vaporize and analyze samples of Titan's frozen, hydrocarbon covered surface once the probe had landed. These measurements compare the abundance of isotope(s) of each particle comparatively to earth's natural abundance.^[62] Also on board the Cassini–Huygens spacecraft was an ion and neutral mass spectrometer which had been taking measurements of Titan's atmospheric composition as well as the composition of Enceladus' plumes. A Thermal and Evolved Gas Analyzer mass spectrometer was carried by the Mars Phoenix Lander launched in 2007.^[63]

Mass spectrometers are also widely used in space missions to measure the composition of plasmas. For example, the Cassini spacecraft carried the Cassini Plasma Spectrometer (CAPS),^[64] which measured the mass of ions in Saturn's magnetosphere.

Respired gas monitor

Mass spectrometers were used in hospitals for respiratory gas analysis beginning around 1975 through the end of the century. Some are probably still in use but none are currently being manufactured.^[65]

Found mostly in the operating room, they were a part of a complex system, in which respired gas samples from patients undergoing anesthesia were drawn into the instrument through a valve mechanism designed to sequentially connect up to 32 rooms to the mass spectrometer. A computer directed all operations of the system. The data collected from the mass spectrometer was delivered to the individual rooms for the anesthesiologist to use.

The uniqueness of this magnetic sector mass spectrometer may have been the fact that a plane of detectors, each purposely positioned to collect all of the ion species expected to be in the samples, allowed the instrument to simultaneously report all of the gases respired by the patient. Although the mass range was limited to slightly over 120 u, fragmentation of some of the heavier molecules negated the need for a higher detection limit.^[66]

Preparative mass spectrometry

The primary function of mass spectrometry is as a tool for chemical analyses based on detection and quantification of ions according to their mass-to-charge ratio. However, mass spectrometry also shows promise for material synthesis.^[48] Ion soft landing is characterized by deposition of intact species on surfaces at low kinetic energies which precludes the fragmentation of the incident species.^[67] The soft landing technique was first reported in 1977 for the reaction of low energy sulfur containing ions on a lead surface.^[68]

See also

• Dumas method of molecular weight determination
• Evolved gas analysis
• Helium mass spectrometer
• Isotope dilution
• MassBank (database), a Japanese spectral database
• Mass spectrometry imaging
• Mass spectrometry software
• MasSpec Pen
• Micro-arrays for mass spectrometry
• Nanoscale secondary ion mass spectrometry
• Reflectron

References

1. Sparkman, O. David (2000). Mass spectrometry desk reference. Pittsburgh: Global View Pub. ISBN 978-0-9660813-2-9.
2. "Definition of spectrograph^{[permanent dead link]}." Merriam Webster. Accessed 13 June 2008.
3. Downard K (2004). Mass Spectrometry - A Foundation Course. Royal Society of Chemistry. doi:10.1039/9781847551306. ISBN 978-0-85404-609-6.
4. Squires G (1998). "Francis Aston and the mass spectrograph". Dalton Transactions (23): 3893–3900. doi:10.1039/a804629h.
5. Downard KM (2007). "Historical account: Francis William Aston: the man behind the mass spectrograph". European Journal of Mass Spectrometry. 13 (3): 177–90. doi:10.1255/ejms.878. PMID 17881785. S2CID 25747367.
6. Thomson JJ (1913). Rays Of Positive Electricity and Their Application to Chemical Analysis. London: Longman's Green and Company.
7. Siri W (1947). "Mass spectroscope for analysis in the low-mass range". Review of Scientific Instruments. 18 (8): 540–545. Bibcode:1947RScI...18..540S. doi:10.1063/1.1740998.
8. Price P (August 1991). "Standard definitions of terms relating to mass spectrometry : A report from the committee on measurements and standards of the American society for mass spectrometry". Journal of the American Society for Mass Spectrometry. 2 (4): 336–48. doi:10.1016/1044-0305(91)80025-3. PMID 24242353. S2CID 20236081.
9. Parkins WE (2005). "The uranium bomb, the calutron, and the space-charge problem". Physics Today. 58 (5): 45–51. Bibcode:2005PhT....58e..45P. CiteSeerX 10.1.1.579.4119. doi:10.1063/1.1995747. ISSN 0031-9228.
10. "The Nobel Prize in Chemistry 2002: Information for the Public". The Nobel Foundation. 9 October 2002. Retrieved 2007-08-29.
11. Fenn JB, Mann M, Meng CK, Wong SF, Whitehouse CM (October 1989). "Electrospray ionization for mass spectrometry of large biomolecules". Science. 246 (4926): 64–71. Bibcode:1989Sci...246...64F. CiteSeerX 10.1.1.522.9458. doi:10.1126/science.2675315. PMID 2675315.
12. Tanaka K, Waki H, Ido Y, Akita S, Yoshida Y, Yoshida T (1988). "Protein and Polymer Analyses up to m/z 100 000 by Laser Ionization Time-of flight Mass Spectrometry". Rapid Commun Mass Spectrom. 2 (20): 151–3. Bibcode:1988RCMS....2..151T. doi:10.1002/rcm.1290020802.
13. Karas M, Bachman D, Bahr U, Hillenkamp F (1987). "Matrix-Assisted Ultraviolet Laser Desorption of Non-Volatile Compounds". Int J Mass Spectrom Ion Proc. 78: 53–68. Bibcode:1987IJMSI..78...53K. doi:10.1016/0168-1176(87)87041-6.
14. Osborn DL, Zou P, Johnsen H, Hayden CC, Taatjes CA, Knyazev VD, et al. (October 2008). "The multiplexed chemical kinetic photoionization mass spectrometer: a new approach to isomer-resolved chemical kinetics". The Review of Scientific Instruments (Submitted manuscript). 79 (10): 104103–104103–10. Bibcode:2008RScI...79j4103O. doi:10.1063/1.3000004. PMID 19044733. S2CID 25452748.
15. Bruins, A. P. (1991). "Mass spectrometry with ion sources operating at atmospheric pressure". Mass Spectrometry Reviews. 10 (1): 53–77. Bibcode:1991MSRv...10...53B. doi:10.1002/mas.1280100104.
16. Cottrell JS, Greathead RJ (1986). "Extending the Mass Range of a Sector Mass Spectrometer". Mass Spectrometry Reviews. 5 (3): 215–247. Bibcode:1986MSRv....5..215C. doi:10.1002/mas.1280050302.
17. If the ions do not start at identical kinetic energies, then some ions may lag behind higher kinetic energy ions decreasing resolution. Reflectron geometries are commonly employed to correct this problem. Wollnik, H. (1993). "Time-of-flight mass analyzers". Mass Spectrometry Reviews. 12 (2): 89–114. Bibcode:1993MSRv...12...89W. doi:10.1002/mas.1280120202.
18. Guilhaus M (1998). (PDF). Journal of Mass Spectrometry. 30 (11): 1519–1532. doi:10.1002/jms.1190301102. S2CID 9444467. Archived from the original (PDF) on 2018-02-06 – via Google Scholar.
19. Syed SU, Maher S, Taylor S (December 2013). "Quadrupole mass filter operation under the influence of magnetic field". Journal of Mass Spectrometry. 48 (12): 1325–39. Bibcode:2013JMSp...48.1325S. doi:10.1002/jms.3293. PMID 24338888.
20. Maher S, Syed SU, Hughes DM, Gibson JR, Taylor S (August 2013). "Mapping the stability diagram of a quadrupole mass spectrometer with a static transverse magnetic field applied". Journal of the American Society for Mass Spectrometry. 24 (8): 1307–14. Bibcode:2013JASMS..24.1307M. doi:10.1007/s13361-013-0654-5. PMID 23720050. S2CID 45734248.
21. Paul W, Steinwedel H (1953). "Ein neues Massenspektrometer ohne Magnetfeld". Zeitschrift für Naturforschung A. 8 (7): 448–450. Bibcode:1953ZNatA...8..448P. doi:10.1515/zna-1953-0710. S2CID 96549388.
22. March RE (2000). "Quadrupole ion trap mass spectrometry: a view at the turn of the century". International Journal of Mass Spectrometry. 200 (1–3): 285–312. Bibcode:2000IJMSp.200..285M. doi:10.1016/S1387-3806(00)00345-6.
23. Schwartz JC, Senko MW, Syka JE (June 2002). "A two-dimensional quadrupole ion trap mass spectrometer". Journal of the American Society for Mass Spectrometry. 13 (6): 659–69. doi:10.1016/S1044-0305(02)00384-7. PMID 12056566. S2CID 26965687.
24. Lammert SA, Rockwood AA, Wang M, Lee ML, Lee ED, Tolley SE, et al. (July 2006). "Miniature toroidal radio frequency ion trap mass analyzer". Journal of the American Society for Mass Spectrometry. 17 (7): 916–922. doi:10.1016/j.jasms.2006.02.009. PMID 16697659. S2CID 45444397.
25. Snyder DT, Pulliam CJ, Ouyang Z, Cooks RG (January 2016). "Miniature and Fieldable Mass Spectrometers: Recent Advances". Analytical Chemistry. 88 (1): 2–29. doi:10.1021/acs.analchem.5b03070. PMC 5364034. PMID 26422665.
26. Hu Q, Noll RJ, Li H, Makarov A, Hardman M, Graham Cooks R (April 2005). "The Orbitrap: a new mass spectrometer". Journal of Mass Spectrometry. 40 (4): 430–43. Bibcode:2005JMSp...40..430H. doi:10.1002/jms.856. PMID 15838939.
27. Comisarow MB, Marshall AG (1974). "Fourier-transform ion cyclotron resonance spectroscopy". Chemical Physics Letters. 25 (2): 282–283. Bibcode:1974CPL....25..282C. doi:10.1016/0009-2614(74)89137-2.
28. Marshall AG, Hendrickson CL, Jackson GS (1998). "Fourier-transform ion cyclotron resonance mass spectrometry: a primer". Mass Spectrometry Reviews. 17 (1): 1–35. Bibcode:1998MSRv...17....1M. doi:10.1002/(SICI)1098-2787(1998)17:1<1::AID-MAS1>3.0.CO;2-K. PMID 9768511.
29. Dubois F, Knochenmuss R, Zenobi R, Brunelle A, Deprun C, Le Beyec Y (1999). "A comparison between ion-to-photon and microchannel plate detectors". Rapid Communications in Mass Spectrometry. 13 (9): 786–791. Bibcode:1999RCMS...13..786D. doi:10.1002/(SICI)1097-0231(19990515)13:9<786::AID-RCM566>3.0.CO;2-3.
30. Park MA, Callahan JH, Vertes A (1994). "An inductive detector for time-of-flight mass spectrometry". Rapid Communications in Mass Spectrometry. 8 (4): 317–322. Bibcode:1994RCMS....8..317P. doi:10.1002/rcm.1290080407.
31. Boyd, Robert K. (1994). "Linked-scan techniques for MS/MS using tandem-in-space instruments". Mass Spectrometry Reviews. 13 (5–6): 359–410. Bibcode:1994MSRv...13..359B. doi:10.1002/mas.1280130502.
32. Xue J, Guijas C, Benton HP, Warth B, Siuzdak G (October 2020). "METLIN MS² molecular standards database: a broad chemical and biological resource". Nature Methods. 17 (10): 953–954. doi:10.1038/s41592-020-0942-5. PMC 8802982. PMID 32839599. S2CID 221285246.
33. Smith CA, O'Maille G, Want EJ, Qin C, Trauger SA, Brandon TR, et al. (December 2005). "METLIN: a metabolite mass spectral database". Therapeutic Drug Monitoring. 27 (6): 747–51. doi:10.1097/01.ftd.0000179845.53213.39. PMID 16404815. S2CID 14774455.
34. Guijas C, Montenegro-Burke JR, Domingo-Almenara X, Palermo A, Warth B, Hermann G, et al. (March 2018). "METLIN: A Technology Platform for Identifying Knowns and Unknowns". Analytical Chemistry. 90 (5): 3156–3164. doi:10.1021/acs.analchem.7b04424. PMC 5933435. PMID 29381867.
35. Benton HP, Wong DM, Trauger SA, Siuzdak G (August 2008). "XCMS2: processing tandem mass spectrometry data for metabolite identification and structural characterization". Analytical Chemistry. 80 (16): 6382–9. doi:10.1021/ac800795f. PMC 2728033. PMID 18627180.
36. Eiceman, G.A. (2000). Gas Chromatography. In R.A. Meyers (Ed.), Encyclopedia of Analytical Chemistry: Applications, Theory, and Instrumentation, pp. 10627. Chichester: Wiley. ISBN 0-471-97670-9
37. Fang M, Ivanisevic J, Benton HP, Johnson CH, Patti GJ, Hoang LT, et al. (November 2015). "Thermal Degradation of Small Molecules: A Global Metabolomic Investigation". Analytical Chemistry. 87 (21): 10935–41. doi:10.1021/acs.analchem.5b03003. PMC 4633772. PMID 26434689.
38. Loo JA, Udseth HR, Smith RD (June 1989). "Peptide and protein analysis by electrospray ionization-mass spectrometry and capillary electrophoresis-mass spectrometry". Analytical Biochemistry. 179 (2): 404–12. doi:10.1016/0003-2697(89)90153-X. PMID 2774189.
39. Maxwell EJ, Chen DD (October 2008). "Twenty years of interface development for capillary electrophoresis-electrospray ionization-mass spectrometry". Analytica Chimica Acta. 627 (1): 25–33. Bibcode:2008AcAC..627...25M. doi:10.1016/j.aca.2008.06.034. PMID 18790125.
40. Verbeck GF, Ruotolo BT, Sawyer HA, Gillig KJ, Russell DH (June 2002). "A fundamental introduction to ion mobility mass spectrometry applied to the analysis of biomolecules". Journal of Biomolecular Techniques. 13 (2): 56–61. PMC 2279851. PMID 19498967.
41. Matz LM, Asbury GR, Hill HH (2002). "Two-dimensional separations with electrospray ionization ambient pressure high-resolution ion mobility spectrometry/quadrupole mass spectrometry". Rapid Communications in Mass Spectrometry. 16 (7): 670–5. Bibcode:2002RCMS...16..670M. doi:10.1002/rcm.623. PMID 11921245.
42. Sowell RA, Koeniger SL, Valentine SJ, Moon MH, Clemmer DE (September 2004). "Nanoflow LC/IMS-MS and LC/IMS-CID/MS of protein mixtures". Journal of the American Society for Mass Spectrometry. 15 (9): 1341–53. doi:10.1016/j.jasms.2004.06.014. PMID 15337515. S2CID 11531292.
43. Tureček F, McLafferty FW (1993). Interpretation of mass spectra. Sausalito: University Science Books. ISBN 978-0-935702-25-5.
44. Mistrik R. . Highchem.com. Archived from the original on 11 January 2012.
45. Sheldon MT, Mistrik R, Croley TR (March 2009). "Determination of ion structures in structurally related compounds using precursor ion fingerprinting". Journal of the American Society for Mass Spectrometry. 20 (3): 370–6. doi:10.1016/j.jasms.2008.10.017. PMID 19041260.
46. Metabolon (2022-01-06). "Solutions to Overcome Limitations of Mass Spectrometry". Metabolon. Retrieved 2022-10-27.
47. Zhou B, Xiao JF, Tuli L, Ressom HW (2012). "LC-MS-based metabolomics". Mol. BioSyst. 8 (2): 470–481. doi:10.1039/c1mb05350g. ISSN 1742-206X. PMC 3699692. PMID 22041788.
48. Maher S, Jjunju FP, Taylor S (2015). "100 years of mass spectrometry: Perspectives and future trends". Rev. Mod. Phys. 87 (1): 113–135. Bibcode:2015RvMP...87..113M. doi:10.1103/RevModPhys.87.113.
49. Shevela D, Messinger J (November 2013). "Studying the oxidation of water to molecular oxygen in photosynthetic and artificial systems by time-resolved membrane-inlet mass spectrometry". Frontiers in Plant Science. 4: 473. doi:10.3389/fpls.2013.00473. PMC 3840314. PMID 24324477.
50. Li X, Huang L, Zhu H, Zhou Z (February 2017). "Direct human breath analysis by secondary nano-electrospray ionization ultrahigh-resolution mass spectrometry: Importance of high mass resolution and mass accuracy". Rapid Communications in Mass Spectrometry. 31 (3): 301–308. Bibcode:2017RCMS...31..301L. doi:10.1002/rcm.7794. PMID 27859758.
51. Barrios-Collado C, Vidal-de-Miguel G, Martinez-Lozano Sinues P (February 2016). "Numerical modeling and experimental validation of a universal secondary electrospray ionization source for mass spectrometric gas analysis in real-time". Sensors and Actuators B: Chemical. 223: 217–225. doi:10.1016/j.snb.2015.09.073. hdl:20.500.11850/105470.
52. Hsieh Y, Korfmacher WA (June 2006). "Increasing speed and throughput when using HPLC-MS/MS systems for drug metabolism and pharmacokinetic screening". Current Drug Metabolism. 7 (5): 479–89. doi:10.2174/138920006777697963. PMID 16787157. S2CID 13612670.
53. Covey TR, Lee ED, Henion JD (October 1986). "High-speed liquid chromatography/tandem mass spectrometry for the determination of drugs in biological samples". Analytical Chemistry. 58 (12): 2453–60. doi:10.1021/ac00125a022. PMID 3789400.
54. Covey TR, Crowther JB, Dewey EA, Henion JD (February 1985). "Thermospray liquid chromatography/mass spectrometry determination of drugs and their metabolites in biological fluids". Analytical Chemistry. 57 (2): 474–81. doi:10.1021/ac50001a036. PMID 3977076.
55. Gamez G, Zhu L, Disko A, Chen H, Azov V, Chingin K, et al. (May 2011). "Real-time, in vivo monitoring and pharmacokinetics of valproic acid via a novel biomarker in exhaled breath". Chemical Communications. 47 (17): 4884–6. doi:10.1039/c1cc10343a. PMID 21373707.
56. Li X, Martinez-Lozano Sinues P, Dallmann R, Bregy L, Hollmén M, Proulx S, et al. (June 2015). "Drug Pharmacokinetics Determined by Real-Time Analysis of Mouse Breath". Angewandte Chemie. 54 (27): 7815–8. doi:10.1002/anie.201503312. hdl:20.500.11850/102558. PMID 26015026.
57. Gaugg MT, Engler A, Nussbaumer-Ochsner Y, Bregy L, Stöberl AS, Gaisl T, et al. (September 2017). "Metabolic effects of inhaled salbutamol determined by exhaled breath analysis". Journal of Breath Research. 11 (4): 046004. Bibcode:2017JBR....11d6004G. doi:10.1088/1752-7163/aa7caa. hdl:20.500.11850/220016. PMID 28901297.
58. Martinez-Lozano Sinues P, Kohler M, Brown SA, Zenobi R, Dallmann R (February 2017). "Gauging circadian variation in ketamine metabolism by real-time breath analysis". Chemical Communications. 53 (14): 2264–2267. doi:10.1039/C6CC09061C. PMID 28150005.
59. Tejero Rioseras A, Singh KD, Nowak N, Gaugg MT, Bruderer T, Zenobi R, Sinues PM (June 2018). "Real-Time Monitoring of Tricarboxylic Acid Metabolites in Exhaled Breath". Analytical Chemistry. 90 (11): 6453–6460. doi:10.1021/acs.analchem.7b04600. PMID 29767961.
60. Ferries S, Perkins S, Brownridge PJ, Campbell A, Eyers PA, Jones AR, Eyers CE (September 2017). "Evaluation of Parameters for Confident Phosphorylation Site Localization Using an Orbitrap Fusion Tribrid Mass Spectrometer". Journal of Proteome Research. 16 (9): 3448–3459. doi:10.1021/acs.jproteome.7b00337. PMID 28741359.
61. Chait BT (2011). "Mass spectrometry in the postgenomic era". Annual Review of Biochemistry. 80: 239–46. doi:10.1146/annurev-biochem-110810-095744. PMID 21675917. S2CID 2676180. – via Annual Reviews (subscription required)
62. Petrie S, Bohme DK (2007). "Ions in space". Mass Spectrometry Reviews. 26 (2): 258–80. Bibcode:2007MSRv...26..258P. doi:10.1002/mas.20114. PMID 17111346.
63. Hoffman JH, Chaney RC, Hammack H (October 2008). "Phoenix Mars Mission--the thermal evolved gas analyzer". Journal of the American Society for Mass Spectrometry. 19 (10): 1377–83. doi:10.1016/j.jasms.2008.07.015. PMID 18715800.
64. . Southwest Research Institute. Archived from the original on 2018-10-08. Retrieved 2008-01-04.
65. Riker JB, Haberman B (1976). "Expired gas monitoring by mass spectrometry in a respiratory intensive care unit". Critical Care Medicine. 4 (5): 223–9. doi:10.1097/00003246-197609000-00002. PMID 975846. S2CID 6334599.
66. Gothard JW, Busst CM, Branthwaite MA, Davies NJ, Denison DM (September 1980). "Applications of respiratory mass spectrometry to intensive care". Anaesthesia. 35 (9): 890–5. doi:10.1111/j.1365-2044.1980.tb03950.x. PMID 6778243. S2CID 41696370.
67. Verbeck G, Hoffmann W, Walton B (October 2012). "Soft-landing preparative mass spectrometry". The Analyst. 137 (19): 4393–407. Bibcode:2012Ana...137.4393V. doi:10.1039/C2AN35550G. PMID 22900257.
68. Franchetti V, Solka BH, Baitinger WE, Amy JW, Cooks RG (1977). "Soft landing of ions as a means of surface modification". Mass Spectrom. Ion Phys. 23 (1): 29–35. Bibcode:1977IJMSI..23...29F. doi:10.1016/0020-7381(77)80004-1.

Bibliography

• Tureček F, McLafferty FW (1993). Interpretation of mass spectra. Sausalito, Calif: University Science Books. ISBN 978-0-935702-25-5.{{cite book}}: CS1 maint: overridden setting (link)
• de Hoffman E, Stroobant V (2001). Mass Spectrometry: Principles and Applications (2nd ed.). John Wiley and Sons. ISBN 978-0-471-48566-7.{{cite book}}: CS1 maint: overridden setting (link)
• Downard K (2004). Mass Spectrometry – A Foundation Course. Cambridge UK: Royal Society of Chemistry. ISBN 978-0-85404-609-6.{{cite book}}: CS1 maint: overridden setting (link)
• Siuzdak G (1996). Mass spectrometry for biotechnology. Boston: Academic Press. ISBN 978-0-12-647471-8.{{cite book}}: CS1 maint: overridden setting (link)
• Dass C (2001). Principles and practice of biological mass spectrometry. New York: John Wiley. ISBN 978-0-471-33053-0.{{cite book}}: CS1 maint: overridden setting (link)
• Muzikar P, et al. (2003). "Accelerator Mass Spectrometry in Geologic Research". Geological Society of America Bulletin. 115: 643–654. Bibcode:2003GSAB..115..643M. doi:10.1130/0016-7606(2003)115<0643:AMSIGR>2.0.CO;2. ISSN 0016-7606. S2CID 55076131.
• Maher S, Jjunju FP, Taylor S (2015). "100 years of mass spectrometry: Perspectives and future trends". Rev. Mod. Phys. 87 (1): 113–135. Bibcode:2015RvMP...87..113M. doi:10.1103/RevModPhys.87.113.
• Sobott F (2014). Biological Mass Spectrometry. Boca Raton: Crc Pr I Llc. ISBN 978-1439895276.{{cite book}}: CS1 maint: overridden setting (link)
• Sparkman OD (2006). Mass Spectrometry Desk Reference. Pittsburgh: Global View Pub. ISBN 978-0-9660813-9-8.{{cite book}}: CS1 maint: overridden setting (link)
• Watson JT, Sparkman OD (2007). Introduction to Mass Spectrometry: Instrumentatio, Applications, and Strategies for Data Interpretation (4th ed.). Chichester: Jonh Wiley & Sons. ISBN 978-0-470-51634-8.{{cite book}}: CS1 maint: overridden setting (link)
• Tuniz C (1998). Accelerator mass spectrometry: ultrasensitive analysis for global science. Boca Raton: CRC Press. ISBN 978-0-8493-4538-8.
• Kandiah M, Urban PL (June 2013). "Advances in ultrasensitive mass spectrometry of organic molecules". Chemical Society Reviews. 42 (12): 5299–322. doi:10.1039/c3cs35389c. PMID 23471277.
• Calmes J (2011). Mass spec : the biography of a scientific instrument (MS). Massachusetts Instite of Technology. hdl:1721.1/68473.

External links

 

Wikibooks has more on the topic of: Mass spectrometry

 

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Look up mass spectrometry in Wiktionary, the free dictionary.

• Mass Spectrometry at Curlie
• National High Magnetic Field Laboratory
• Mass spectrometer simulation An interactive application simulating the console of a mass spectrometer
• Realtime Mass Spectra simulation Tool to simulate mass spectra in the browser