Multielement Detection of Nonmetals by Barium-Based Post-ICP Chemical Ionization Coupled to Orbitrap-MS.

Prevalence of F, Cl, S, P, Br, and I in pharmaceuticals and environmental contaminants has promoted standard-free quantitation using analyte-independent heteroatom responses in inductively coupled plasma (ICP)-MS. However, in-plasma ionization challenges and element-dependent isobaric interference removal methods have hampered the multielement nonmetal detection in ICP-MS. Here, we examine an alternative approach to enhance multielement detection capabilities. Analytes are introduced into an ICP leading to post-plasma formation of HF, HCl, H3PO3, H2SO4, HBr, and HI, which are then chemically ionized to BaF+, BaCl+, BaH2PO3+, BaHSO4+, BaBr+, and BaI+ via reactions with barium-containing ions supplied by a nanospray. Subsequent ion detection by high-resolution MS provides an element-independent approach for resolving isobaric interferences. We show that elemental response factors using these ions are linear within 2 orders of magnitude and independent of analytes' chemical structures. Using a single set of operating parameters, detection limits <1 ng/mL are obtained for Cl, Br, I, and P, while those for F and S are 1.8 and 6.2 ng/mL, respectively, offering improved multielement quantitation of nonmetals. Further, insights into ionization mechanisms indicate that the reactivities of reagent ions follow the order BaNO2+ > BaHCO2+ > Ba(H2O)n2+ ∼ BaCH3CO2+. Notably, the least reactive ions are generated directly by nanospray, suggesting that modification of these ions via interaction with plasma afterglow is critical for achieving good sensitivities. Moreover, our experiments indicate that the element-specific plasma products follow the order HF < H2SO4 ∼ HCl < H3PO3 ∼ HBr ∼ HI for their propensity to react with reagent ions. These insights provide guidelines to manage matrix effects and offer pathways to further improve the technique.

Solution Cathode Glow Discharge Coupled to Atmospheric Pressure Chemical Ionization for Elemental Detection of S and P in Organic Compounds.

We report a post-plasma chemical ionization approach to evaluate solution cathode glow discharge (SCGD) for S and P elemental analysis. Here, the SCGD serves as a reactor to produce chemical vapors for S and P from organic compounds containing these elements, while a corona discharge operated in negative mode is used to ionize the products. The approach creates long-lived ions in atmospheric pressure, enabling direct investigation of chemical vapor products via mass spectrometric and ion mobility separations. The investigations indicate that SCGD converts S and P to H2SO4 and H3PO4, respectively. These species are then ionized as HSO4HNO3 - and H3PO4NO3HNO3- via reactions with NO3HNO3- produced by corona discharge. The response factors for P among several small molecules varies within 10% of the average response from the compounds, suggesting a reasonable species-independent characteristic. The response factors for S show larger variations among compounds, indicating a higher dependence of chemical vapor generation efficiency on analytes' chemical structures. Detection limits of 15 and 29 ng/mL are achieved for P and S detection, respectively. These figures are limited by background equivalent concentrations and low ion flux in the utilized ion mobility-time of flight mass spectrometer, indicating potential for significant improvements. In particular, the specificity of clustering for S and P-containing ions produced in this approach suggest facile analysis of S and P using quadrupole-based mass spectrometers for improved analytical performance.

Synthesis and Characterization of Cerium-Oxo Clusters Capped by Acetylacetonate.

Cerium-oxo clusters have applications in fields ranging from catalysis to electronics and also hold the potential to inform on aspects of actinide chemistry. Toward this end, a cerium-acetylacetonate (acac1-) monomeric molecule, Ce(acac)4 (Ce-1), and two acac1--decorated cerium-oxo clusters, [Ce10O8(acac)14(CH3O)6(CH3OH)2]·10.5MeOH (Ce-10) and [Ce12O12(OH)4(acac)16(CH3COO)2]·6(CH3CN) (Ce-12), were prepared and structurally characterized. The Ce(acac)4 monomer contains CeIV. Crystallographic data and bond valence summation values for the Ce-10 and Ce-12 clusters are consistent with both clusters having a mixture of CeIII and CeIV cations. Ce L3-edge X-ray absorption spectroscopy, performed on Ce-10, showed contributions from both CeIII and CeIV. The Ce-10 cluster is built from a hexameric cluster, with six CeIV sites, that is capped by two dimeric CeIII units. By comparison, Ce-12, which formed upon dissolution of Ce-10 in acetonitrile, consists of a central decamer built from edge sharing CeIV hexameric units, and two monomeric CeIII sites that are bound on the outer corners of the inner Ce10 core. Electrospray ionization mass spectrometry data for solutions prepared by dissolving Ce-10 in acetonitrile showed that the major ions could be attributed to Ce10 clusters that differed primarily in the number of acac1-, OH1-, MeO1-, and O2- ligands. Small angle X-ray scattering measurements for Ce-10 dissolved in acetonitrile showed structural units slightly larger than either Ce10 or Ce12 in solution, likely due to aggregation. Taken together, these results suggest that the acetylacetonate supported clusters can support diverse solution-phase speciation in organic solutions that could lead to stabilization of higher order cerium containing clusters, such as cluster sizes that are greater than the Ce10 and Ce12 reported herein.

High-Resolution Elemental Mass Spectrometry Using LC-ICP-Nanospray-Orbitrap for Simultaneous and Species-Independent Quantitation of Fluorinated and Chlorinated Compounds.

Simultaneous elemental detection of F and Cl offers quantitation of fluorinated and chlorinated compounds and their transformation products without compound-specific standards. Despite wide-ranging applications, this capability has been hindered by fundamental and technical shortcomings of current inductively coupled plasma (ICP)-MS methods in ion formation and isobaric interference elimination. These hurdles are alleviated here via a chemical ionization method. Fluorine and chlorine in analytes are first converted to HF and HCl by an ICP with post-plasma recombination and subsequently react with barium-containing ions supplied by a nanospray, yielding BaF+ and BaCl+ as elemental reporter ions. Notably, the method is readily interfaced to an Orbitrap MS which eliminates isobaric interferences at resolving powers as low as 35,000, far greater than that of current ICP-MS instruments. Moreover, the instrument is easily reverted to the ESI-MS mode for complementary molecular characterization. To demonstrate analytical capabilities, a workflow for rapid quantitation of compounds separated by reversed-phase liquid chromatography is developed using a species-independent calibration. The independent F and Cl measurements agree with each other, providing recoveries of >90% and LODs of 8-12 pmol Cl and 5-12 pmol F on the column. The workflow along with LC-ESI-MS on the same instrument is then applied to identify and quantify in-vitro drug metabolites, yielding total drug-related material recoveries of >80% and quantitation of minor metabolites summing to 8% of the total drug-related compounds. These results highlight the strengths of simultaneous F and Cl speciation for rapid quantitation with applications in early drug development.

Effects of outdoor weathering and laundering on the detection and classification of fluorinated oil-and-water-repellent fabric coatings.

Fluorinated polymer coatings are used to impart durable oil-and-water-repellent properties on fabrics, potentially offering a persistent fiber characteristic for forensic fiber comparisons. To evaluate the persistence of these coatings, we investigate effects of outdoor weathering and laundering on detection and classification of the fluorinated oil-and-water-repellent coatings on 9 garments and 2 spray-coated fabric samples. Single fibers from the samples are pyrolyzed and subjected to gas chromatography coupled to a fluorine-selective detector. The positive detection of coatings is indicated by a signal-to-noise ratio (S/N) >50 for the tallest peak in the pyrograms. Moreover, a multinomial logistic regression model trained using fibers prior to weathering and laundering is utilized to determine the class of the weathered and laundered fibers, providing a metric to evaluate the effect of these processes on fiber classification. Notably, fluorinated coatings are detected on all of the fibers exposed to outdoor elements in Arlington, VA, up to 12 weeks from August to October 2020, while a detection rate of 95.5% is achieved for samples laundered up to 10 wash cycles. The detection rate prior to weathering and laundering was 98%, indicating negligible effect of these processes on detection of coatings. The classification accuracy is determined to be 99% and 100% for weathered and laundered samples, respectively, illustrating that these processes do not significantly affect the major pyrolysis products of the coatings responsible for classification. These results highlight the persistence of the fluorinated oil-and-water-repellent fabric coatings and their potential for forensic fiber discrimination at single-fiber level.

Detection and diversity of fluorinated oil- and water-repellent coatings on apparel fibers.

Fluorinated coatings, often used for oil and water repellency and stain resistance in fabrics, are potentially persistent forensic fiber markers. However, they have received limited attention because of challenges in their detection caused by the small size of a single fiber and thin nature of stain-resistant coatings. Here, we utilize a sensitive fluorine-selective analytical technique to detect and evaluate diversity of fluorinated coatings in apparel. Twelve clothing items marketed as stain-resistant were tested with nine showing oil- and water-repellent properties. Fluorinated pyrolysis products of single fibers from all of the nine items were detected by gas chromatography coupled to plasma-assisted reaction chemical ionization mass spectrometry (GC-PARCI-MS), indicating the prevalence of fluoropolymer coatings in stain-resistant clothing articles. Furthermore, three major classes of fluorinated coatings were identified via principal component analysis of pyrogram patterns. The classes were coating-specific and did not correlate with fiber core and color, highlighting a robust detection methodology. To evaluate the effect of fiber lifting in crime scenes, fibers from the 9 clothing items were used to develop a multinomial logistic regression model based on pyrogram principal components. The model was then tested using fibers subjected to contact with Post-it® notes. The test set fibers were sampled from the clothing items of the training set and from three additional garments of differing color but the same brands as the training set. The coating classes were predicted with 98.4% accuracy, confirming robust classification of fiber coatings using py-GC-PARCI-MS regardless of fiber color, core, and fiber lifting.

Perturbation-induced high-frequency pulsing of nano-ESI with facile ion selection at atmospheric pressure.

Nano-ESI is a commonly used ionization technique with continually expanding analytical advantages. Here, we report a facile way for high-frequency (500-3800 Hz) pulsing of nano-ESI, providing a high flux of mobility-selected ions. The pulsing is accomplished using a relatively low-voltage modulation (80 V peak-to-peak) of an electrode placed <1 cm downstream of a nano-ESI emitter biased to a constant potential. Configuring the electrode as an ion gate enables mobility-based ion selection by scanning the modulation frequency. Our investigations indicate that the electrode modulation perturbs continuous nano-ESI, resulting in solution accumulation at the emitter tip between spray pulses. Selective transmission of ions occurs at frequencies corresponding to harmonics of a fundamental frequency determined by the travel time of each ion from the emitter to the ion gate (pulsing electrode). Remarkably, the intensities of ions selected in this fashion are similar across the harmonics, suggesting that the ionization efficiencies of analytes have minimal dependence on the accumulated volume at the emitter tip. Moreover, intensities of ion-mobility-selected analytes using this technique reach >50% of those in continuous nano-ESI without ion selection, underscoring efficient ion generation via high-frequency pulsing. These findings indicate the potential of the pulsed nano-ESI for enhanced analytical utility, such as a high-flux selected-reagent-ion supplier at atmospheric pressure, and chart new avenues to further enhance the analytical performance of nano-ESI.

Elemental Fluorine Detection by Dielectric Barrier Discharge Coupled to Nanoelectrospray Ionization Mass Spectrometry for Nontargeted Analysis of Fluorinated Compounds.

The growing use of fluorochemicals has elevated the need for nontargeted detection of unknown fluorinated compounds and transformation products. Elemental mass spectrometry (MS) coupled to chromatography offers a facile approach for such analyses by using fluorine as an elemental tag. However, efficient ionization of fluorine has been an ongoing challenge. Here, we demonstrate a novel atmospheric-pressure elemental ionization method where fluorinated compounds separated by gas chromatography (GC) are converted to Na2F+ for nontargeted detection. The compounds are first introduced into a helium dielectric barrier discharge (DBD) for breakdown. The plasma products are subsequently ionized by interaction with a nanoelectrospray ionization (nano-ESI) plume of sodium-containing aqueous electrolytes. Our studies point to HF as the main plasma product contributing to Na2F+ formation. Moreover, the results reveal that Na2F+ is largely formed by the ion-neutral reaction between HF and Na2A(NaA)n+, gas-phase reagent ions produced by nano-ESI where A represents the anion of the electrolyte. Near-uniform fluorine response factors are obtained for a wide range of compounds, highlighting good efficiency of HF formation by DBD regardless of the chemical structure of the compounds. Detection limits of 3.5-19.4 pg of fluorine on-column are obtained using the reported GC-DBD-nano-ESI-MS. As an example of nontargeted screening, extractions from oil-and-water-repellent fabrics are analyzed via monitoring Na2F+, resulting in detection of a fluorinated compound on a clothing item. Notably, facile switching of the ion source to atmospheric-pressure chemical ionization with the exact same chromatographic method allows identification of the detected compound at the flagged retention time.

Pulsed Nano-ESI: Application in Ion Mobility-MS and Insights into Spray Dynamics.

We have previously shown that pulsed nano-ESI offers direct ion introduction into an AP-IM cell in the absence of conventional gates and desolvation. Here, we further characterize this ion injection method and utilize it to gain insights into nano-ESI pulsed spray dynamics. We demonstrate that a pulsed nano-ESI operated at 20 Hz with ion generation pulses of 170-510 µs offers reproducible ion arrival times (0.09-0.21% RSD). Arrival times are then translated to effective collision cross sections (CCSs) using tetraalkylammonium ions as CCS internal standards. For ions with low solvent affinity, effective CCS values match those reported for fully desolvated ions. For amino acids and a series of alkylamine homologues, the effective CCS values are higher than those for fully desolvated ions and correlate with solvent affinity, suggesting that ions with high hydration affinities traverse the mobility cell as hydrated ions. Notably, hydrates are not observed in the MS spectra due to ion activation during the transport into vacuum. Using these observations as a framework to interpret effective CCS values, we investigate the impact of nano-ESI pulse duration on ion properties. We observe that longer pulse durations lead to the enhancement of ion abundance for low-ionization-efficiency analytes and a reduction in clustering. However, effective CCSs are not significantly altered by spray pulse duration, implying that similar ion structures emerge rapidly at all investigated pulse durations. Ion abundance results suggest a temporal evolution of droplets in pulsed nano-ESI where droplets emitted later in the spray formation appear to be smaller, providing enhanced ionization.

Classifying single fibers based on fluorinated surface treatments.

Fibers are an important form of forensic evidence, but their evidential value can be severely limited when the identified characteristics of the fibers are common, such as blue cotton. Detecting chemical fiber treatments offers an avenue to further classify fibers and to improve their evidential value. In this report, we investigate the potential of fluoropolymer fiber coatings, used to impart oil and water-repellent properties in fabrics, for differentiating between fibers. The thin nature of these fiber surface modifications creates an analytical challenge for their detection on a single fiber, a typical sample size for forensic evidence. Specifically, pyrolysis-gas chromatography-mass spectrometry (py-GC-MS) has shown promising selectivity but the sensitivity of the method is not adequate for single-fiber analysis of fluorinated coatings. To overcome this challenge, we utilize a newly developed elemental ionization source, plasma-assisted reaction chemical ionization (PARCI). The high sensitivity of py-GC-PARCI-MS for elemental fluorine analysis offers selective and sensitive detection of fluorinated pyrolysates among the non-fluorinated pyrolysates of the fiber core. As a result, fluoropolymer coatings are detected from 10-mm single-fiber samples. The technique is applied for classification of 22 fiber types, resulting in 4 distinct groups via hierarchical cluster analysis based on similarity of fluorine pyrograms. These results present the first study to classify fibers based on fluorinated coatings, and highlight the potential of py-GC-PARCI-MS for forensic analyses. Graphical Abstract ᅟ.

High-Sensitivity Elemental Mass Spectrometry of Fluorine by Ionization in Plasma Afterglow.

Fluorine elemental analysis using inductively coupled plasma mass spectrometry (ICPMS) is challenging because of low F ionization efficiency in the plasma and severe isobaric interferences. Notably, there is an increasing demand for ppb level fluorine measurements due to the rising importance of fluorinated compounds in pharmaceutical, environmental, and food analyses. Here, we report a new elemental ionization method where fluorinated analytes are introduced into an ICP to produce NaF followed by Na2F+ formation in the atmospheric-pressure plasma afterglow. The new method offers over 2 orders of magnitude improved sensitivities (180-500 cps/ppb versus 1.6-3.2 cps/ppb) for F detection. This approach also yields compound-independent F response for quantitation without compound-specific standards. Detection limits of ∼50 ppb F are attained using a single-quadrupole instrument without discrimination against isobaric interferences. Similar LODs are achievable only by isobaric interference reduction in ICPMS/MS. Importantly, the new approach offers facile interfacing to molecular MS instruments where LODs can be further improved via MS/MS and high-resolution MS techniques. The tolerance to matrix is demonstrated by quantitation of fluoride in infant formula, yielding recoveries of 86%-98% with repeatabilities of 3.5-6.3 RSD%.

Atmospheric-Pressure Dielectric Barrier Discharge as an Elemental Ion Source for Gas Chromatographic Analysis of Organochlorines.

Atmospheric-pressure dielectric barrier discharge (AP-DBD) plasma has emerged in recent years as a versatile plasma for molecular ionization and elemental spectroscopy. However, its capabilities as an elemental ion source have been less explored, partly because of difficulties in the detection of positive elemental ions from this low-gas-temperature plasma. In this work, we investigate the detection of negative elemental ions to enable elemental mass spectrometry (MS) using AP-DBD. A gas chromatograph is coupled to a helium AP-DBD apparatus and positioned in front of an atmospheric-pressure-sampling mass spectrometer with no modifications to the ion sampling interface. We demonstrate that Cl- ions are detected with a compound-independent efficiency, enabling elemental quantification of organochlorines. Further, addition of oxygen at low concentration (11 ppm, v/v) to the helium plasma improves the analytical performance by reducing postcolumn peak broadening, whereas high oxygen concentrations (>110 ppm, v/v) lead to loss of the compound-independent response. The optimized GC-AP-DBD-MS setup shows close to 2 orders of magnitude of linearity for its compound-independent Cl response and offers detection limits of 0.5-1 pg of Cl on column (0.6 pg/s), suitable for analysis of organochlorines in food samples. We demonstrate this capability by analyzing orange juice spiked with pesticides at 9 µg/L and a single internal standard. Importantly, we demonstrate that a quick, easy, cheap, effective, rugged, and safe (QuEChERS) extraction followed by GC-AP-DBD-MS quantification using the single standard provides acceptable recoveries (80-120%). These results highlight uniform QuEChERS extraction of a range of compounds and the compound-independent response of AP-DBD for Cl, making the combination of the two methods desirable for the rapid quantification of organochlorines. Furthermore, we discuss ionization matrix effects in AP-DBD for chlorine detection and offer strategies to flag matrix-impacted analytes. These results suggest that AP-DBD has the potential to become a unified ion source for both elemental quantification and molecular identification of GC eluents on a single MS platform.

Elemental quantitation of carbon via production of polyatomic anions in gas chromatography-plasma assisted reaction chemical ionization mass spectrometry.

Elemental mass spectrometry offers quantitation and isotopic analysis without the need for compound-specific standards. We have recently introduced plasma assisted reaction chemical ionization (PARCI) as an efficient elemental ionization method for halogens. Here, we report a new ionization chemistry in PARCI for facile quantitation of elemental carbon in gas chromatography eluates. We demonstrate that in-plasma reactions of organic compounds followed by afterglow ionization lead to formation of polyatomic anions (CN-, OCN-, and CO3-), among which CN- offers the best analytical sensitivity with a detection limit of ~25 pg (21 pg/s) carbon on column. Using a mixture of pesticides with wide variations in structures and heteroatom content, we demonstrate that CN- ion response is quantitatively correlated with the carbon concentration over two orders of magnitude (r 2 = 0.985). We show that the novel GC-PARCI-MS method provides recoveries within 80-120% using a single standard for all analytes, highlighting the strength of elemental quantitation. Further, the ability of GC-PARCI-MS to identify 13C-tagged molecules without a priori knowledge of chemical formulas of analytes is demonstrated. Graphical abstract ᅟ.

Pulsed Nano-ESI Atmospheric-Pressure Ion Mobility Mass Spectrometry with Enhanced Ion Sampling.

Ion mobility-mass spectrometry (IM-MS) has gained considerable attention for detection of clusters and weakly bound species created by electrospray ionization (ESI). Atmospheric-pressure (AP) IM-MS offers an advantage in these studies compared to its low-pressure counterpart, owing to soft introduction of ions into the mobility cell with minimal ion activation. Here, we report new approaches to improve the sensitivity and soft ion introduction in AP-IM-MS. For the former, we demonstrate enhanced aerodynamic sampling of ions from the mobility cell into the MS using pulsed-field sampling. In this approach, ions are driven toward the MS, and the field is shut down once the ions reach the vicinity of the MS inlet orifice. The pulsed-field operation provides arrival times without the need for an exit ion gate in the mobility cell and leads to improvements in sensitivity of up to 1 order of magnitude. For soft ion generation, we report a pulsed nano-ESI source to introduce a packet of ions into the room-temperature mobility cell without induced desolvation. Further, we demonstrate the application of the pulsed nano-ESI AP-IM-MS with enhanced ion sampling for detection of solvent clusters of amines and peptide aggregates.

High-sensitivity elemental ionization for quantitative detection of halogenated compounds.

The rising importance of organohalogens in environmental, pharmaceutical, and biological applications has drawn attention to analysis of these compounds in recent years. Elemental mass spectrometry (MS) is particularly advantageous in this regard because of its ability to quantify without compound-specific standards. However, low sensitivity of conventional elemental MS for halogens has hampered applications of this powerful method in organohalogen analyses. To this end, we have developed a high-sensitivity elemental ion source compatible with widely available atmospheric-sampling mass spectrometers. We utilize a helium-oxygen plasma for atomization followed by negative ion formation in plasma afterglow, a configuration termed as plasma-assisted reaction chemical ionization (PARCI). The effect of oxygen on in-plasma and afterglow reactions is investigated, leading to fundamental understanding of ion generation processes as well as optimized operating conditions. Coupled to a gas chromatograph, PARCI shows constant ionization efficiency for F, Cl, and Br regardless of the chemical structure of the compounds. Negative ionization in the afterglow improves halide ion formation efficiency and eliminates isobaric interferences, offering sub-picogram elemental detection for F, Cl, and Br using low-resolution MS. Notably, the detection limit for F is about one order of magnitude better than other elemental MS techniques. The high sensitivity and facile adoptability of PARCI pave the way for combined elemental-molecular characterization, a comprehensive analytical scheme for rapid identification and quantification of organohalogens.

Gas chromatography plasma-assisted reaction chemical ionization mass spectrometry for quantitative detection of bromine in organic compounds.

We have recently introduced plasma-assisted reaction chemical ionization mass spectrometry (PARCI-MS) for elemental analysis of halogens in organic compounds. Here, we utilize gas chromatography (GC) coupled to PARCI-MS to investigate the mechanism of Br(-) ion generation from organobromines and to evaluate analytical performance of PARCI for organobromine analysis. Bromine atoms in compounds eluting from GC are converted to HBr in a low-pressure microwave induced helium plasma with trace amounts of hydrogen added as a reaction gas. Ionization is achieved by introducing nitrogen into the afterglow region of the plasma, liberating electrons via penning ionization and leading to formation of negative ions. We demonstrate that N2 largely affects the ionization process, whereas H2 affects both the ionization process and in-plasma reactions. Our investigations also suggest that dissociative electron capture is the main ionization route for formation of Br(-) ions. Importantly, GC-PARCI-MS shows a uniform response factor for bromine across brominated compounds of drastically different chemical structures, confirming PARCI's ability to quantify organobromines in the absence of compound-specific standards. Over 3 orders of magnitude linear dynamic range is demonstrated for bromine quantification. We report a detection limit of 29 fg of bromine on-column, ~4-fold better than inductively coupled plasma-MS.

Plasma-assisted reaction chemical ionization for elemental mass spectrometry of organohalogens.

We present plasma-assisted reaction chemical ionization (PARCI) for elemental analysis of halogens in organic compounds. Organohalogens are broken down to simple halogen-containing molecules (e.g., HBr) in a helium microwave-induced plasma followed by negative mode chemical ionization (CI) in the afterglow region. The reagent ions for CI originate from penning ionization of gases (e.g., N2) introduced into the afterglow region. The performance of PARCI-mass spectrometry (MS) is evaluated using flow injection analyses of organobromines, demonstrating 5-8 times better sensitivities compared with inductively coupled plasma MS. We show that compound-dependent sensitivities in PARCI-MS mainly arise from sample introduction biases.

Reagent delivery by partial coalescence and noncoalescence of aqueous microdroplets in oil.

Reagent delivery constitutes a key step for reaction initiation in droplet-in-oil microfluidic platforms. Currently, this function is performed by complete fusion of a reagent droplet with the reactor droplet. The full coalescence, however, constrains the lower limit of volume delivery because reproducible droplet generation becomes exceedingly difficult as the reagent droplet volume is decreased. Here, we demonstrate fractional volume delivery based on partially coalescent and noncoalescent droplet collisions as a new reagent delivery mechanism. A charged reagent droplet is generated by pulsing a flow carrying needle to high voltage. The charged droplet is directed toward a grounded reactor droplet. Upon collision, the reagent droplet inverts its charge and is pulled away from the reactor droplet prior to full fusion, injecting only a fraction of its volume. The undelivered portion of the reagent drop is then merged with a collector droplet. We demonstrate that a wide range of fractional injections (0.003%-56%) can be reproducibly achieved, providing a means for minute volume delivery without small drop generation.

Ambient analysis by thermal desorption atmospheric pressure photoionization.

Ambient mass spectrometry has attracted substantial attention in recent years. Among ambient ionization methods, thermal desorption ionization stands out because of two attributes: (1) simplicity, rendering the technique suitable for in-field applications, and (2) ability to couple with a variety of gas-phase ionization methods thereby broadening the range of molecules that can be analyzed with this method. Here, we report on improving the performance of a direct analysis in real time (DART) source by implementing atmospheric pressure photoionization (APPI) downstream of the desorption region. At identical desorption and ion sampling conditions, APPI leads to detection of radical molecular ions from non-polar compounds that are absent from the spectra generated by DART alone. Moreover, a factor of 3-5 improvement in sensitivity is observed using APPI for positive ions commonly detected by DART and DART-APPI. Using helium and nitrogen as desorption gases, APPI shows identical performance regardless of desorption gas type. In contrast, a dramatic decrease in sensitivity is observed for DART operated with nitrogen compared to DART with helium. Comparable performance for DART and DART-APPI are observed in negative ion mode, although both show a drastic improvement in the absence of the Vapur interface. This interface creates a differentially pumped chamber prior to inlet of the mass spectrometer and reduces the mass spectrometer gas load when helium is used as desorption gas.

Integrated microfluidic device for automated single cell analysis using electrophoretic separation and electrospray ionization mass spectrometry.

A microfabricated fluidic device was developed for the automated real-time analysis of individual cells using capillary electrophoresis (CE) and electrospray ionization-mass spectrometry (ESI-MS). The microfluidic structure incorporates a means for rapid lysis of single cells within a free solution electrophoresis channel, where cellular constituents were separated, and an integrated electrospray emitter for ionization of separated components. The eluent was characterized using mass spectrometry. Human erythrocytes were used as a model system for this study. In this monolithically integrated device, cell lysis occurs at a channel intersection using a combination of rapid buffer exchange and an increase in electric field strength. An electroosmotic pump is incorporated at the end of the electrophoretic separation channel to direct eluent to the integrated electrospray emitter. The dissociated heme group and the alpha and beta subunits of hemoglobin from individual erythrocytes were detected as cells continuously flowed through the device. The average analysis throughput was approximately 12 cells per minute, demonstrating the potential of this method for high-throughput single cell analysis.