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.

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.

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%.