Ion Source For Mass Spectrometry Research Articles

Low-cost heat assisted ambient ionization source for mass spectrometry in food and pharmaceutical screening.

Ambient Ionization Mass Spectrometry (AI-MS) techniques have revolutionized analytical chemistry by enabling rapid analysis of samples under atmospheric conditions with minimal to no preparation. In this study, the optimization of a cold atmospheric plasma for the analysis of food and pharmaceutical samples, liquid and solid, using a Heat-Assisted Dielectric Barrier Discharge Ionization (HA-DBDI) source is described. A significant enhancement in analyte signals was observed when a heating element was introduced into the design, potentially allowing for greater sensitivity. Furthermore, the synergy between the inlet temperature of the mass spectrometer and the heating element allows for precise control over the analytical process, leading to improved detection sensitivity and selectivity. Incorporating computational fluid dynamic (CFD) simulations into the study elucidated how heating modifications can influence gas transport properties, thereby facilitating enhanced analyte detection and increased signal intensity. These findings advance the understanding of HA-DBDI technology and provide valuable insights for optimizing AI-MS methodologies for a wide range of applications in food and pharmaceutical analysis.

High-Performance, Low-Cost, Additively Manufactured Electrospray Ion Sources for Mass Spectrometry.

We report novel 3D-printed electrospray sources for mass spectrometry (MS) that produce twice the signal strength of their mainstream counterparts. Leveraging 3D printing to fabricate in bulk nano- and microscale-featured electrospray emitters, this work shows a path for scalable integration in clinically relevant diagnostics. This solution improves the device performance by simultaneously tuning the surface hydrophilicity, solvent evaporation, and geometry. The emitters are made of stainless-steel (SS) 316L via binder jetting and coated in a conformal, hydrothermally grown zinc oxide nanowire (ZnONW) forest. The printed emitters are designed as surface mount devices that can be directly soldered to printed circuit boards with built-in digital microfluidics as part of an automated device assembly. The electrospray sources use a novel extractor electrode design that enables operation at ∼24% larger bias voltages compared with conventional MS cylindrical inlets. The 3D-printed electrospray emitters were characterized against their state-of-the-art counterparts (coated blades and paper spray). MS data from the 3D-printed electrospray emitters show detection of therapeutically relevant targets at 1 μg/ml concentrations with a variety of solvents; for nicardipine, such emitters attain 116% higher signal-to-noise ratios and far greater stability than their counterparts.

Direct Online Monitoring of Mouse Exhaled Breath for Diabetes Assessment Using Corona Ionization Mass Spectrometry

Since certain types of diabetes are reversible and curable in the early stages, early detection is crucial for effective treatment. Exhaled breath analysis, a noninvasive technique, is increasingly recognized for its potential in health monitoring, providing insights into an organism’s metabolic state more directly than blood glucose tests. This work developed an in situ method utilizing corona ion source mass spectrometry for real-time direct monitoring of volatile organic compounds (VOCs) in mouse exhaled breath. The method was used to track breath changes in two mouse models with streptozotocin-induced diabetes throughout disease progression. Notably, variations in certain VOCs in exhaled breath correlated with blood glucose levels (BGLs) during diabetes development. For instance, in the type 1 diabetes model, acetone levels remained stable within 8 days after hyperglycemia (not significant, n.s.) compared to those in controls but showed a significant increase after 10 days (p < 0.001). In the type 2 diabetes model, isopropanol levels decreased (p < 0.001) during the prediabetes phase, when BGL changes were not significant (n.s.) compared to those in the healthy state. These results indicate that specific substances in exhaled breath change prior to noticeable BGL alterations. This study thus established the viability of direct online mass spectrometry for breath analysis in early diabetes detection and showed that this technique has potential for identifying clear clinical markers for early diabetes screening.

Quantitative Distributions of Product Ions and Reaction Times with a Binary Mixture of VOCs in Ambient Pressure Chemical Ionization.

A model to quantitatively predict ion abundances from atmospheric pressure chemical ionization (APCI) between hydrated protons and a volatile organic compound (VOC) was extended to binary mixtures of VOCs. The model includes differences in vapor concentrations, rate coefficients, and reaction times and is enhanced with cross reactions between neutral vapors and protonated monomers. In this model, two specific VOCs were considered, a ketone, 6-methyl-5-hepten-2-one (M, and an amine, 2,6-di-tert-butyl-pyridine (N), with measured "conditional rate coefficients" (in cm3·s-1) of kM = 1.11 × 10-9 and kN = 9.17 × 10-10, respectively. The cross reaction of MH+(H2O)x to NH+(H2O)y was measured as kcr = 1.31 × 10-12 at 60 °C. Cross reactions showed an impact on ion abundances at t > 30 ms for equal vapor concentrations of 100 ppb for M and N. In contrast, this impact was negligible for vapor concentrations of 1 ppb and did not exceed 5% change in product ion abundance up to 1000 ms reaction times. The model was validated with laboratory measurements to within ∼10% using an ion mobility spectrometer and effective reaction time obtained from computational fitting of experimental findings. This was necessitated by complex flow patterns in the ion source volume and was determined as ∼10.5 ms. The model has interpretative and predictive value for quantitative analysis of responses with ambient pressure ion sources for mass spectrometry and ion mobility spectrometry.

Accelerated synthesis of energetic precursor cage compounds using confined volume systems

Confined volume systems, such as microdroplets, Leidenfrost droplets, or thin films, can accelerate chemical reactions. Acceleration occurs due to the evaporation of solvent, the increase in reactant concentration, and the higher surface-to-volume ratios amongst other phenomena. Performing reactions in confined volume systems derived from mass spectrometry ionization sources or Leidenfrost droplets allows for reaction conditions to be changed quickly for rapid screening in a time efficient and cost-saving manner. Compared to solution phase reactions, confined volume systems also reduce waste by screening reaction conditions in smaller volumes prior to scaling. Herein, the condensation of glyoxal with benzylamine (BA) to form hexabenzylhexaazaisowurtzitane (HBIW), an intermediate to the highly desired energetic compound 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20), was explored. Five confined volume systems were compared to evaluate which technique was ideal for forming this complex cage structure. Substituted amines were also explored as BA replacements to screen alternative cage structure intermediates and evaluate how these accelerated techniques could apply to novel reactions, discover alternative reagents to form the cage compound, and improve synthetic routes for the preparation of CL-20. Ultimately, reaction acceleration is ideal for predicting the success of novel reactions prior to scaling up and determining if the expected products form, all while saving time and reducing costs. Acceleration factors and conversion ratios for each reaction were assessed by comparing the amount of product formed to the traditional bulk solution phase synthesis.

In-Line Dopant Generation for Atmospheric Pressure Ionization Mass Spectrometry.

A concentric trace gas permeation tube that diffuses chemical reagents to a central carrier gas stream is used to drive chemical reaction pathways and influence gas-phase chemistry for a variety of atmospheric pressure ionization sources for mass spectrometry. Tunable permeation through the reservoir-jacketed polymer membrane is triggered by the heated gas moving through the tube, evaporating the dopant into a sheath dry gas or into a sample stream in room air without diluting the analyte concentration. The permeator is used to add dopants to an electrospray plume for analyte ion charge reduction and to perform hydrogen-deuterium exchange on biomolecules in different spray conditions. Dopants are also added to atmospheric pressure chemical ionization to favor the ionization of select components of diesel fuel. Atmospheric pressure photoionization is performed with the permeation tube in line with tubing transporting sample headspace to an enclosed discharge lamp. Toluene dopant from the permeator increases the proton transfer and charge exchange signal from clove oil and mothballs many times without exposing the laboratory to reagent fumes. Water permeation is also used to humidify the sample gas stream.

Pocket-Size "MasSpec Pointer" for Ambient Ionization Mass Spectrometry.

Current ambient ionization sources for mass spectrometry (MS) are typically connected to gas cylinders, high-voltage supply, injection pump, and other accessory equipment, which hinder the popularization of MS in the field of on-site detection. Here, we developed a wireless pocket-size "MasSpec Pointer" (weights 65 g) based on arc discharge powered by a 3.7 V polymer Li battery for ambient ionization MS. A high voltage of 5600 V and 20 kHz was generated from the boost coil to penetrate air and form a plasma. The relative standard deviation (RSD) of the high-voltage pulses is 3.8%, leading to a stable discharge and a good quantification performance. A mini diaphragm pump was used to cool the plasma from ∼600 to ∼40 °C and to blow the plasma into a jet, which facilitates sampling. MasSpec Pointer can work well at both positive- and negative-ion modes without any modification and can quickly test gaseous, liquid, or solid samples. The limit of detection of this device for atrazine (an agrochemical) is lower than 0.1 ng/mL. MasSpec Pointer has shown its ability to pinpoint the double-bond location of fatty acid isomers without derivatization reagents or light illumination. Agrochemicals from the surface of an apple and daily chemicals from the surface of a finger were detected successfully using MasSpec Pointer coupled with a miniature mass spectrometer. We believe the "point-and-shoot" device coupled with mini-MS brings the hope for an age of detecting chemicals on-site by nonprofessionals.

Effects of solvent composition on ionization and fragmentation within the solution-cathode glow discharge

Recently, solution-electrode glow discharges (SEGDs) have shown great utility as ionization sources for mass spectrometry (MS). The solution composition of SEGD electrodes is pivotal to their performance as it influences analyte-ion formation. The performance of electrospray ionization is heavily dictated by spray-solution composition, which can alter ionization efficiency and pathways. While SEGDs produce Taylor cones similar to electrospray ionization, the influence of solution-electrode composition on molecular-ion formation has not been studied. Here, we examine how additives to an atmospheric-pressure solution-cathode glow discharge (SCGD) influence molecular ionization and fragmentation. The impact of several additives to the acidic solution of an SCGD ionization source was evaluated based on mass-spectrometric performance. Addition of methanol increased molecular- and fragment-ion signals for peptide angiotensin II. This effect is likely due to improved desolvation and a greater interaction of analyte molecules with glow-discharge species. Several high-boiling-point reagents were tested to examine changes in the ion signal, the average charge state, and the degree of fragmentation. Overall, these additives inhibited fragmentation but significantly lowered intact molecular-ion signals. Interestingly, loss of fragment ions trended with the boiling point of the reagent used. We hypothesize that analyte molecules become trapped in droplets produced at the solution-cathode surface. These droplets do not fully desolvate before escaping the discharge region, sparing analyte molecules from fragmentation. For low volatility additives, droplets do not desolvate, even as they enter the heated MS, which yields a loss in molecular ions. The changing composition of the SCGD solution alters analytical performance, but also provides insight into analyte ionization and fragmentation processes.

Optical characterization of miniature flexible micro-tube plasma (FμTP) ionization source: A dielectric guided discharge

Miniature DBD has been obtaining more and more attention. A recently developed miniature flexible micro-tube plasma (FμTP) has proved to be an excellent soft ionization source for mass spectrometry and ion mobility spectrometry. In this paper, the optical characterization of the novel FμTP ionization source was carried out, aiming to cast light on the plasma propagation mechanism in one discharge cycle. To provide a clean environment for investigating the plasma propagation, the plasma was totally sustained in a capillary tube. It was found that in one discharge cycle, three discharge developments, namely two dielectric guided discharges in both positive and negative half cycle, and a negative glow discharge in the negative half cycle. Compared with the conventional dielectric barrier discharge, there is no formation of a dissociative plasma, which improves the soft ionization capacity of the present source. In addition to the whole light emission from 200 nm to 1100 nm, the lines related to the reactive species including He 706 nm, N2+ 391 nm, and O 777 nm were investigated spatially and temporally. Due to the effect of the attached charges, the plasma of the negative half cycle propagates faster than that of the positive half cycle. It was also found that the plasma in the positive half cycle propagates more discretely than that of the negative one, while the negative one has a larger emission intensity due to the overlap of the signal in both temporal and spatial scales. Further on, the electric field distribution was proved to be in Gaussian shape along the diameter of the capillary, while the negative one has a flat shape. By changing the concentration of N2 in He, the electron collision and penning ionization for generating N2+ were experimentally proved and identified. This study identifies the typical discharge process of the FμTP in one discharge cycle, indicating the plasma is indeed a dielectric guided discharge.

Recent Advances of In-Source Electrochemical Mass Spectrometry.

Hyphenation of electrochemistry (EC) and mass spectrometry has become a powerful tool to study redox processes. Approaches that can achieve this hyphenation include integrating chromatography/electrophoresis between electroinduced redox reactions and detection of products, coupling an EC flow cell to a mass spectrometer, and performing electrochemical reactions inside the ion source of a mass spectrometer. The first two approaches have been well reviewed elsewhere. This Minireview highlights the inherent electrochemical properties of many mass spectrometry ion sources and their roles in the coupling of electrochemistry and mass spectrometric analysis. Development of modified ion sources that allow the compatibility of electrochemistry with ionization processes is also surveyed. Applications of different in-source electrochemical devices are provided including intermediate capturing, bioanalytical studies, nanoparticle formation, electrosynthesis, and electrode imaging.

Ionization source for mass spectrometry needs no external power supply

Ionization source for mass spectrometry needs no external power supply

2D-Molybdenum Disulfide-Derived Ion Source for Mass Spectrometry.

Generation of current or potential at nanostructures using appropriate stimuli is one of the futuristic methods of energy generation. We developed an ambient soft ionization method for mass spectrometry using 2D-MoS2, termed streaming ionization, which eliminates the use of traditional energy sources needed for ion formation. The ionic dissociation-induced electrokinetic effect at the liquid-solid interface is the reason for energy generation. We report the highest figure of merit of current generation of 1.3 A/m2 by flowing protic solvents at 22 μL/min over a 1 × 1 mm2 surface coated with 2D-MoS2, which is adequate to produce continuous ionization of an array of analytes, making mass spectrometry possible. Weakly bound ion clusters and uric acid in urine have been detected. Further, the methodology was used as a self-energized breath alcohol sensor capable of detecting 3% alcohol in the breath.

Development of a new atmospheric pressure plasmaspray ionization for ambient mass spectrometry.

A new atmospheric pressure ionization method, plasmaspray ionization, termed as PSI, was developed to be an alternative ambient ion source for mass spectrometry. It comprises a plasma jet device and a sample spray part. While the nonthermal plasma jet strikes the surface of stainless steel tube out of the spray capillary, the sprayed sample will be ionized with the assistant of auxiliary gas. Although PSI is a little bit more complex than electrospray ionization (ESI) in instrument, it shows both better linearity and higher sensitivity for organic compounds. For protein samples, it presents wider distributions of multiply charged ions and higher mass resolution without sacrificing any sensitivity. For the mechanism of PSI, the charge build-up process on the tip of capillary should play a key role for the ion formation, and the stimulated pulsed voltage on the flow tube will promote the ion aggregation speed until the charge density is high enough. PSI source contains the features of plasma ionization and ESI and can be considered as a novel combo bridging these techniques. These results reflect that this method of PSI can be applied and further developed as a versatile new ion source for a wild range of organic and biological samples.

Application of Molecularly Imprinted Polymers (MIP) and Flowing Atmospheric-Pressure Afterglow Mass Spectrometry (FAPA-MS) to Analysis of Nonsteroidal Anti-Inflammatory Drugs (NSAIDs)

In recent years, the rapid development of the pharmaceutical industry and the extensive and illicit use of painkillers have led to increased levels of nonsteroidal anti-inflammatory drugs (NSAIDs) in the environment. In view of the significant impact of NSAIDs on living organisms, including humans, their presence in the environment needs to be continuously monitored at trace levels. For this purpose, a combination of molecularly imprinted solid-phase extraction (MISPE) and HPLC-MS analysis is commonly used. MISPE has been utilized in direct, fast, and ecological analysis of drugs using a flowing atmospheric-pressure afterglow ion source for mass spectrometry (FAPA-MS). The new method was applied herein in the determination of naproxen, diclofenac, and ibuprofen. The linear dependence of the intensity of analytical signals on the amount of drugs is in the range of 0.2 μg to 1 g and the method detection limit (MDL) for all drugs is 0.2 μg in environmental samples. The new method also decreased the number of analytical stages, the time and cost of analysis, and the organic solvent consumption, besides being environmentally friendly.

Optical and spectroscopic study of a supersonic flowing helium plasma: energy transport in the afterglow

Flowing plasma jets are increasingly investigated and used for surface treatments, including biological matter, and as soft ionization sources for mass spectrometry. They have the characteristic capability to transport energy from the plasma excitation region to the flowing afterglow, and therefore to a distant application surface, in a controlled manner. The ability to transport and deposit energy into a specimen is related to the actual energy transport mechanism. In case of a flowing helium plasma, the energy in the flowing afterglow may be carried by metastable helium atoms and long-lived helium dimer ions. In this work a systematic investigation of the optical and spectroscopic characteristics of a supersonic flowing helium plasma in vacuum and its afterglow as function of the helium gas density is presented. The experimental data are compared with numerical modeling of the plasma excitation and helium dimer ion formation supported by a Computational Fluid Dynamic simulation of the helium jet. The results indicate that the plasma afterglow is effectively due to helium dimer ions recombination via a three-body reaction.

UPLC–PDA–ESI–MS analysis and TLC–DPPH· activity of wheat varieties

Wheat is a major crop, an important component of the human diet and important source of animal fodder in the world. Characterization of phenolic profiles of the leading wheat cultivars is important for new opportunities for breeding and eventual commercial production of value-added cultivars rich in beneficial components. A method using ultra-performance liquid chromatography combined with photodiode-array detector–electrospray ion source–mass spectrometry (UPLC–PDA–ESI–MS) has been developed for determination of phenolic compounds contained in twelve winter and thirteen spring wheat varieties. The antioxidant activity was determined by the thin-layer chromatography–2,2-diphenyl-1-picrylhydrazyl (TLC–DPPH•) test with image processing by means of the ImageJ program. Based on retention time, the mass of deprotonated molecule [M−H]− and ultraviolet (UV) spectra, seven phenolic acids, and twelve flavonoids were identified and quantitated in the 80% aqueous methanol extract of the wheat varieties. The average concentrations of total researched compounds were definitely higher in spring wheat cultivars than in winter ones. Varieties Trappe and Kandela showed the most elevated values of total free phenolic acids. Kandela and Ostka Smolicka had the highest content of flavonoids, and isoorientin was detected as the main phenolic in wheat cultivars. Additionally, a correlation between radical scavenging activity and total phenolic acids content was observed. UPLC combined with PDA–ESI–MS could be applied to complete characterization of natural products (e.g., phenolics) in alcoholic extracts from wheat varieties.

Approaching Standardless Quantitative Elemental Analysis of Solids: Microsecond Pulsed Glow Discharge and Buffer-Gas-Assisted Laser Ionization Time-of-Flight Mass Spectrometry.

Among various ionization sources for mass spectrometry, microsecond pulsed glow discharge (MP-GD) and buffer-gas-assisted laser ionization (BGA-LI) sources have the potential for direct quantitative elemental analysis of solids without the requirement of standard reference materials. The analytical potential of these two ionization sources has been evaluated by coupling them to orthogonal time-of-flight mass spectrometry (MS). A straightforward method was proposed to achieve the quantitative result: if a spectrum contains little interference and elemental peak currents are proportional to their concentrations, then the molar concentration of each element is equal to its ion current proportion in the total ion current. Two series of metal standards were applied for the evaluation. Explicit spectra with little interference can be acquired by both techniques. The interferences contribute only a very small portion to the total ion current for MP-GD-MS and BGA-LI-MS; therefore, their influence on the quantitative result can be ignored. All metal elements can be determined quite accurately by the proposed quantitation method, while gaps exist for nonmetal elements due to the high ionization potentials or gas species interference. Between the two techniques, BGA-LI-MS offers a more accurate quantitative result, primarily due to its higher plasma temperature.

Integration of paper spray ionization high-field asymmetric waveform ion mobility spectrometry for forensic applications.

Paper spray ionization (PSI) is an attractive ambient ionization source for mass spectrometry (MS) since it allows the combination of surface sampling and ionization. The minimal sample preparation inherent in this approach greatly reduces the time needed for analysis. However, the ions generated from interfering compounds in the sample and the paper substrate may interfere with the analyte ions. Therefore, the integration of PSI with high-field asymmetric ion mobility spectrometry (FAIMS) is of significant interest since it should reduce the background ions entering the mass analyzer without complicating the analysis or increasing analysis time. Here we demonstrate the integration of PSI with FAIMS/MS and its potential for analysis of samples of forensic interest. In this work, the parameters that can influence the integration, including sampling and ionization by paper spray, the FAIMS separation of analytes from each other and background interferences, and the length of time that a usable signal can be observed for explosives on paper, were evaluated with the integrated system. In the negative ion analysis of 2,4,6-trinitrotoluene (TNT), pentaerythritol tetranitrate (PETN), octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX), and 1,3,5-trinitroperhydro-1,3,5-triazine (RDX), amounts as low as 1ng on paper were readily observed. The successful positive ion separation of a set of illicit drugs including heroin, methamphetamine, and cocaine was also achieved. In addition, the positive ion analysis of the chemical warfare agent simulants dimethyl methylphosphonate (DMMP) and diisopropyl methylphosphonate (DIMP) was evaluated. The integration of PSI-FAIMS/MS was demonstrated for the analyses of explosives in negative ion mode and for illicit drugs and CW simulants in positive mode. Paper background ions that could interfere with these analyses were separated by FAIMS. The compensation voltage of an ion obtained by FAIMS provided an additional identification parameter to be combined with the mass spectrum for each analyte.

A Customizable Flow Injection System for Automated, High Throughput, and Time Sensitive Ion Mobility Spectrometry and Mass Spectrometry Measurements.

To better understand disease conditions and environmental perturbations, multiomic studies combining proteomic, lipidomic, and metabolomic analyses are vastly increasing in popularity. In a multiomic study, a single sample is typically extracted in multiple ways, and various analyses are performed using different instruments, most often based upon mass spectrometry (MS). Thus, one sample becomes many measurements, making high throughput and reproducible evaluations a necessity. One way to address the numerous samples and varying instrumental conditions is to utilize a flow injection analysis (FIA) system for rapid sample injections. While some FIA systems have been created to address these challenges, many have limitations such as costly consumables, low pressure capabilities, limited pressure monitoring, and fixed flow rates. To address these limitations, we created an automated, customizable FIA system capable of operating at a range of flow rates (∼50 nL/min to 500 μL/min) to accommodate both low- and high-flow MS ionization sources. This system also functions at varying analytical throughputs from 24 to 1200 samples per day to enable different MS analysis approaches. Applications ranging from native protein analyses to molecular library construction were performed using the FIA system, and results showed a highly robust and reproducible platform capable of providing consistent performance over many days without carryover, as long as washing buffers specific to each molecular analysis were utilized.

Analysis of hop acids by thin-layer chromatography and the Molecular Ionization Desorption Analysis Source (MIDAS) for mass spectrometry

A thin-layer chromatography ambient mass spectrometry method was developed for the quantitative analysis of hop acids. Hop acids were extracted from three varieties of hop pellets, Apollo, Cluster and Czech Saaz. Reversed-phase thin-layer chromatography provided the optimum stationary phase for separation and ionization. Using standards, a method was developed to separate α-, iso-α- and β-acids by thin-layer chromatography. Each thin-layer chromatography plate was analyzed directly by the Molecular Ionization Desorption Analysis Source (MIDAS). MIDAS is an atmospheric pressure ambient ionization source for mass spectrometry. Quantitative analysis of the hop extracts was made by successive analysis of known amounts of standards and the determination of a response factor. The expected trend of total α-acid content with Apollo>Cluster>Czech Saaz was observed. Variation in the results was attributed to manual TLC plate spotting and not to the ionization source.