Electron Capture Negative Ionization Mass Research Articles

Simultaneous detection of multiple hydroxylated polychlorinated biphenyls from a complex tissue matrix using gas chromatography/isotope dilution mass spectrometry

In this study, we developed a comprehensive, highly sensitive, and robust method for determining 53 congeners of three to eight chlorinated OH-PCBs in liver and brain samples by using isotope dilution gas chromatography (GC) coupled with electron capture negative ionization mass spectrometry (ECNI-MS). These results were compared with those from GC coupled with electron ionization high-resolution mass spectrometry (EI-HRMS). Clean-up procedures for analysis of OH-PCBs homologs in liver and brain samples involve a pretreatment step consisting of acetonitrile partition and 5% hydrated silica-gel chromatography before derivatization. Recovery rates of tri- and tetra-chlorinated OH-PCBs in the acetonitrile partition method followed by the 5% hydrated silica-gel column (82% and 91%) were higher than conventional sulfuric acid treatment (2.0% and 3.5%). The method detection limits of OH-PCBs for each matrix obtained by GC/ECNI-MS and GC/EI-HRMS were 0.58-2.6 pg g(-1) and 0.36-1.6 pg g(-1) wet wt, respectively. Recovery rates of OH-PCB congeners in spike tests using sample matrices (10 and 50 pg) were 64.7-117% (CV: 4.7-14%) and 70.4-120% (CV: 2.3-12%), respectively. This analytical method may enable the simultaneous detection of various OH-PCBs from complex tissue matrices. Furthermore, this method allows more comprehensive assessment of the biological effects of OH-PCB exposure on critical organs.

Improved GC/ECNI-MS sensitivity of decabromodiphenyl ether determination on 30 m columns by increasing the carrier gas flow after a modified gel permeation chromatographic cleanup protocol employing cyclohexane/ethyl acetate as eluent

BDE-209 is the predominant constituent of the commercial mixture decabromodiphenyl ether which is used as brominated flame retardant (BFR). Owing to difficulties associated with the high mass (thermal instability and low vapour pressure), short GC columns (≤15 m) have been suggested for its analysis while longer columns (30–50 m) are suggested for other polybrominated diphenyl ether (PBDE) congeners. To overcome this considerable expenditure in the analysis of PBDEs, we aimed at increasing the sensitivity of BDE-209 analysis by gas chromatography coupled with electron-capture negative ion mass spectrometry (GC/ECNI-MS) on a 30 m column. The chromatographic performance of BDE-209 on the 30 m GC column was improved by increasing the carrier gas flow from initially 1.2 mL min−1 to 5 or 10 mL min−1 after the last octabromo diphenyl ether (Br8DE) congener was eluted. With this high carrier gas flow, the column residence time of BDE-209 was shortened by ∼25%, the peak height was increased and, consequently, the limit of detection by GC/ECNI-MS in selected ion monitoring (SIM) mode was improved. When this high-flow GC/ECNI-MS-SIM method was applied to a sediment sample, we realized that gel permeation chromatography (GPC) – used for the removal of lipids and/or sulphur – provided low recovery rates for BDE-209. The large molecule BDE-209 eluted late and only 50% was recovered by our previous standard protocol for polyhalogenated compounds. Application of a modified GPC procedure with a longer collection time increased the recovery of BDE-209 in the GPC step to ∼90%.

Electron impact, electron capture negative ionization and positive chemical ionization mass spectra of organophosphorus flame retardants and plasticizers

Phosphate esters are important commercial products that have been used both as flame retardants and as plasticizers. To analyze these compounds by gas chromatographic mass spectrometry, it is important to understand the mass spectra of these compounds using various ionization modes. This paper is a systematic overview of the electron impact (EI), electron capture negative ionization (ECNI) and positive chemical ionization (PCI) mass spectra of 13 organophosphate esters. These data are useful for developing and optimizing analytical measurements. The EI spectra of these 13 compounds are dominated by ions such as H4 PO4 (+) , (M - Cl)(+) , (M - CH2 Cl)(+) or (M)(+) depending on specific chemical structures. The ECNI spectra are generally dominated by (M - R)(-) . The PCI spectra are mainly dominated by the protonated molecular ion (M + H)(+) . The branching of the alkyl substituents, the halogenation of the substituents and, for aromatic phosphate esters, ortho alkylation of the ring are all significant factors controlling the details of the fragmentation processes. EI provides the best sensitivity for the quantitative measurement of these compounds, but PCI and ECNI both have considerable qualitative selectivity.

Occurrence of chlorinated paraffins in house dust samples from Bavaria, Germany

Levels and distribution of chlorinated paraffins were studied in randomly taken house dust samples (<63 μm) from the greater area of Munich, Germany. Quantification of short- (SCCPs, C10–C13) and medium-chain chlorinated paraffins (MCCPs, C14–C16) were performed using gas chromatography electron capture negative ion mass spectrometry (GC–ECNI–MS). Concentrations of MCCPs in private household samples varied between 9 μg/g and 892 μg/g, and exceeded levels of SCCPs, which were in the range of 4–27 μg/g. Two dust samples from a public building contained up to 2050 μg/g SCCPs but no MCCPs. Among MCCPs, chlorinated tetradecanes were major components with a proportion of almost 50%. Among SCCPs, chlorinated dodecanes were usually present at higher concentrations than the congeners of any C10, C11, and C13 chains. The results indicate that particularly MCCPs may be present in relatively high concentrations in house dusts.

Sample pretreatment optimization for the analysis of short chain chlorinated paraffins in soil with gas chromatography–electron capture negative ion-mass spectrometry

Accurately quantifying short chain chlorinated paraffins (SCCPs) in soil samples with gas chromatograph coupled with electron capture negative ionization mass spectrometry (GC–ECNI-MS) is difficult because many other polychlorinated pollutants are present in the sample matrices. These pollutants (e.g., polychlorinated biphenyls (PCBs), organochlorine pesticides (OCPs) and toxaphene) can cause serious interferences during SCCPs analysis with GC–MS. Four main columns packed with different adsorbents, including silica gel, Florisil and alumina, were investigated in this study to determine their performance for separating interfering pollutants from SCCPs. These experimental results suggest that the optimum cleanup procedure uses a silica gel column and a multilayer silica gel–Florisil composite column. This procedure completely separated 22 PCB congeners, 23 OCPs and three toxaphene congeners from SCCPs. However, p,p′-DDD, cis-nonachlor and o,p′-DDD were not completely removed and only 53% of the total toxaphene was removed. This optimized method was successfully and effectively applied for removing interfering pollutants from real soil samples. SCCPs in 17 soil samples from different land use areas within a suburban region were analyzed with the established method. The concentrations of SCCPs in these samples were between 7 and 541ngg−1 (mean: 84ngg−1). Similar homologue SCCPs patterns were observed between the soil samples collected from different land use areas. In addition, lower chlorinated (Cl6/7) C10- and C11- SCCPs were the dominant congeners.

Retracted: β-Carotene in Golden Rice is as good as β-carotene in oil at providing vitamin A to children

Golden Rice (GR) has been genetically engineered to be rich in β-carotene for use as a source of vitamin A. The objective was to compare the vitamin A value of β-carotene in GR and in spinach with that of pure β-carotene in oil when consumed by children. Children (n = 68; age 6-8 y) were randomly assigned to consume GR or spinach (both grown in a nutrient solution containing 23 atom% ²H₂O) or [²H₈]β-carotene in an oil capsule. The GR and spinach β-carotene were enriched with deuterium (²H) with the highest abundance molecular mass (M) at M(β-C)+²H₁₀. [¹³C₁₀]Retinyl acetate in an oil capsule was administered as a reference dose. Serum samples collected from subjects were analyzed by using gas chromatography electron-capture negative chemical ionization mass spectrometry for the enrichments of labeled retinol: M(retinol)+4 (from [²H₈]β-carotene in oil), M(retinol)+5 (from GR or spinach [²H₁₀]β-carotene), and M(retinol)+10 (from [¹³C₁₀]retinyl acetate). Using the response to the dose of [¹³C₁₀]retinyl acetate (0.5 mg) as a reference, our results (with the use of AUC of molar enrichment at days 1, 3, 7, 14, and 21 after the labeled doses) showed that the conversions of pure β-carotene (0.5 mg), GR β-carotene (0.6 mg), and spinach β-carotene (1.4 mg) to retinol were 2.0, 2.3, and 7.5 to 1 by weight, respectively. The β-carotene in GR is as effective as pure β-carotene in oil and better than that in spinach at providing vitamin A to children. A bowl of ~100 to 150 g cooked GR (50 g dry weight) can provide ~60% of the Chinese Recommended Nutrient Intake of vitamin A for 6-8-y-old children.

Enhanced pressurized liquid extraction technique capable of analyzing polychlorodibenzo-p-dioxins, polychlorodibenzofurans, and polychlorobiphenyls in fish tissue

A high-throughput enhanced pressurized liquid extraction technique was developed by incorporating pressurized liquid extraction and multiple cleanup techniques. USEPA methods of polychlorodibenzo-p-dioxins, polychlorodibenzofurans (PCDD/Fs) and dioxin-like polychlorobiphenyls (dl-PCBs) analysis in fish tissue include independent silica gel, florisil, alumina, and carbopack/celite column cleanup techniques following extraction. Under the improved method, fish composites (∼10g) were extracted and cleaned simultaneously using alumina (∼10g), florisil (∼10g), silica gel (∼5g), celite (∼5g), and carbopack (∼0.5g). Clean extracts were concentrated and then analyzed by high resolution gas chromatography coupled with electron capture negative ionization mass spectrometry. Carbopack/celite within the extraction cell provided the analytical separation of dl-PCBs from PCDD/Fs, reducing potential molecular interferences. The average recoveries (n=3) of dl-PCBs in dichloromethane:hexane (1:1, v/v) extracts were 93±2.4% and PCDD/Fs in toluene extracts were 85±3.0%. The developed method was applied to measure the PCDD/Fs and dl-PCBs in catfish from San Jacinto River Waste Pits, a Superfund site in Houston, TX. The dl-PCBs were measured at 5.0–17,000pgg−1 ww. Sample preparation time and solvents were reduced as much as 95% and 65%, respectively, as compared to USEPA method 1613.

Determination of chlorinated paraffins in sediments from the Firth of Clyde by gas chromatography with electron capture negative ionisation mass spectrometry and carbon skeleton analysis by gas chromatography with flame ionisation detection

Short chain chlorinated paraffins (SCCPs) are a group of persistent organic pollutants (POPs) of increasing concern, but are to date not widely investigated in the environment, largely due to the challenges involved in their quantification. Here, SCCPs were quantified in marine sediments from the Firth of Clyde, Scotland, by gas chromatography with electron capture negative ionisation mass spectrometry (GC–ECNIMS) and through carbon skeleton analysis by gas chromatography with flame ionisation detection (GC–FID), and the analytical challenges encountered are discussed. Concentrations in the sediments ranged from 0.4 to 69μgkg−1 when determined by GC–ECNIMS, and from 5.6 to 379μgkg−1 when determined by GC–FID. For 8 out of 11 samples, analysis by GC–FID gave higher results than analysis by GC–ECNIMS. Unexpected aspects of the analysis, such as the presence of high concentrations of longer chain chlorinated paraffins in the samples, are also presented.

Comment on “Novel Methoxylated Polybrominated Diphenoxybenzene Congeners and Possible Sources in Herring Gull Eggs from the Laurentian Great Lakes of North America”

An increasing number of brominated flame retardants and other brominated substances are being reported in herring gull eggs from the Laurentian Great Lakes basin. Yet, in extracts from gulls’ eggs, numerous bromide anion response peaks in electron capture negative ion (ECNI) mass chromatograms remain unidentified. Using archived herring gull egg homogenates, we characterize the structures of three major and three minor, new and unique brominated substances. After extensive cleanup and separation to isolate these substances from the extracts, high-quality ECNI and electron impact (EI) mass spectra revealed fragmentation patterns consistent with congeners of methoxylated polybrominated diphenoxybenzene (MeO-PBDPB), where four congeners contained five bromines and the other two contain four and six bromines, respectively. Optimized, semiquantitative analysis revealed sum concentrations of the MeO-PBDBP congeners ranged from <0.2 to 36.8 ng/g ww in pooled egg homogenates (collected in 2009) from fourteen herr...

Multi-residue method for the determination of brominated and organophosphate flame retardants in indoor dust

A new method was optimized for the simultaneous determination of several flame retardants (FRs) in indoor dust, namely polybrominated diphenyl ethers (PBDEs), hexabromocyclododecanes (HBCDs), novel brominated flame retardants (NBFRs) and organophosphate ester flame retardants (OPFRs). The method was based on two previously validated analytical methods for NBFRs and OPFRs, which were combined in order to include even a large number of FRs. An ultrasonic extraction method and two-stage clean-up by adsorption chromatography was optimized using an indoor dust standard reference material (SRM 2584). The 1st cleanup step was essential for fractionation of analytes in the dust extracts, while the 2nd step was important for the further removal of interferences. Analysis of cleaned dust extracts was performed with gas chromatography electron impact ionization mass spectrometry for OPFRs, gas chromatography electron capture negative ionization mass spectrometry for PBDEs and NBFRs and liquid chromatography electrospray ionization tandem mass spectrometry for HBCDs. Method validation by matrix spiking demonstrated good accuracy ranging from 81 to 130%. Matrix effects were investigated by spiking sodium sulfate and dust with analyte standards. Typical recoveries ranged between 80 and 110% at both spiking levels, though occasional deviations were observed at low spiking concentrations. Precision between different days was generally below 24% relative standard deviation (RSD) at low concentrations and below 11% RSD at high concentrations. Method limits of quantification for BFRs ranged between 0.04 (BDE 28) and 17ng/g (BDE 209), 6ng/g for sum HBCDs, and for OPFRs between 10 (triphenyl phosphate) and 370ng/g (tri-isobutyl phosphate). The method was applied to SRM 2585 and to a set of indoor dust samples from various countries. The newly developed method will be employed for the monitoring of human exposure via dust ingestion to phased-out and alternate FRs.

Novel Methoxylated Polybrominated Diphenoxybenzene Congeners and Possible Sources in Herring Gull Eggs from the Laurentian Great Lakes of North America

An increasing number of brominated flame retardants and other brominated substances are being reported in herring gull eggs from the Laurentian Great Lakes basin. Yet, in extracts from gulls' eggs, numerous bromide anion response peaks in electron capture negative ion (ECNI) mass chromatograms remain unidentified. Using archived herring gull egg homogenates, we characterize the structures of three major and three minor, new and unique brominated substances. After extensive cleanup and separation to isolate these substances from the extracts, high-quality ECNI and electron impact (EI) mass spectra revealed fragmentation patterns consistent with congeners of methoxylated polybrominated diphenoxybenzene (MeO-PBDPB), where four congeners contained five bromines and the other two contain four and six bromines, respectively. Optimized, semiquantitative analysis revealed sum concentrations of the MeO-PBDBP congeners ranged from <0.2 to 36.8 ng/g ww in pooled egg homogenates (collected in 2009) from fourteen herring gull colony sites across the Great Lakes, with the highest concentration being for Channel-Shelter Island in Saginaw Bay (Lake Huron). To our knowledge, there are no published reports on the environmental presence and sources of MeO-PBDPBs. We hypothesize that these MeO-PBDPBs are degradation products of the polybrominated diphenoxybenzenes, for example, tetradecabromodiphenoxybenzene (currently marketed as SAYTEX 120) or polybromo 3P2E. MeO-PBDPBs in Great Lakes herring gull eggs indicates their bioaccumulation potential, and raises concerns about their origin, environmental behavior and influences on wildlife and environmental health.

Determination of ultra-trace levels of priority PBDEs in water samples by isotope dilution GC(ECNI)MS using 81Br-labelled standards

A gas chromatography electron capture negative ionization mass spectrometry (GC(ECNI)MS) procedure for the determination of priority polybrominated diphenyl ethers (PBDEs; congeners 28, 47, 99, 100, 153 and 154) in water samples at regulatory EU levels has been developed. The method is based on the use of (81)Br-labelled PBDEs for isotope dilution analysis and the measurement of (79)Br/(81)Br isotope ratios in gas chromatography peaks with the electron capture negative ionization technique. The suitability of this ion source for the precise and accurate measurement of bromine isotope ratios has been demonstrated. The general ECNI-IDMS procedure was evaluated by the analysis of NIST SRM 1947 (Lake Michigan fish tissue) with satisfactory results. For the analysis of water samples, 500 mL of the samples were spiked with the labelled PBDEs and extracted with 10 mL isooctane for 30 min. The extract was evaporated down to ca. 100 μL and injected in the GC(ECNI)MS. Detection limits ranged from 0.014 (-1) to 0.089 pg mL(-1) depending on the congener. Recoveries from real water samples, spiked at a level of 0.5 pg mL(-1), ranged from 77% to 102%.

Optimisation of the analytical method for octa-, nona- and deca-brominated diphenyl ethers using gas chromatography–quadrupole mass spectrometry and isotope dilution

An analytical method for higher brominated congeners of polybrominated diphenyl ethers (PBDEs) was optimised using a gas chromatograph equipped with an electron impact ionisation-quadrupole mass spectrometer (GC-EI-qMS) and five native PBDEs and three 13C12-labelled congeners in biological and environmental samples (mussels, sediment, dust). In the optimised instrumental conditions, abundance and repeatability improved with increase in temperature of the ion source. The instrumental detection limits (IDLs) for BDE-196, BDE-197, BDE-206, BDE-207 and BDE-209 were 0.1, 0.1, 0.2, 0.3 and 0.6 pg, respectively. When compared to the previous reports, the IDLs were the same as for electron capture negative ionisation (ECNI) or EI-double focusing magnetic sector (EI-Sector) mass spectrometer, indicating that sensitive determination could be achieved using a conventional GC-EI-qMS. Validation of the method was carried out by the analysis of reference materials and mussel samples. We confirmed that the concentrations quantified using this method was in the range of reported values for reference materials. Similar concentrations were found in mussels, which were analysed previously by our group. Thus, we conclude that a conventional GC-EI-qMS can be applied for analysis of higher brominated PBDEs in various environmental and biota matrices.

On the delay mechanism of Cl 2 − diatomic anion dissociation up to the microsecond timescale

The dissociative capture of slow electrons by tetrachlorethylene (C2Cl4) has been investigated by resonant electron capture negative ion mass spectrometry. Metastable ions with fractional mass numbers 7.5, 17.5, and 19 corresponding to the C2Cl4− → Cl− + C2Cl3 and Cl2− → Cl− + Cl decays occurring at the microsecond timescale have been detected. It has been revealed that Cl2− anions, which are fragment ions, can dissociate at the microsecond timescale, which is very surprising for a system with one internal degree of freedom. This process is assumingly attributed to the rotational excitation of Cl2− anions. Thus, the experimental estimate of the time of rovibronic relaxation in the Cl2− anion has been obtained.

Levels of Chlorinated Paraffins in Water

AbstractWastewater treatment plant influents, effluents, and river water samples were analyzed for chlorinated paraffins (CPs). CPs were not detected in river water samples, in effluents, and in filtered influents by using gas chromatography electron capture negative ion mass spectrometry (GC‐ECNI‐MS) (LOQ = 100 ng/L). However, middle chain chlorinated paraffins (MCCPs) were frequently present in suspended solid matter from influents while short chain chlorinated paraffins (SCCPs) were detected only in 2 of 15 samples. Concentrations of SCCPs and MCCPs measured by GC‐ECNI‐MS varied between n.d. and 4600 ng/L adsorbed on suspended solid matter.

Flame-Retardants and Other Organohalogens Detected in Sewage Sludge by Electron Capture Negative Ion Mass Spectrometry

Numerous halogenated organic compounds have been identified as pollutants of concern. Those with high persistence and hydrophobicity may concentrate in biota, sediments, and wastewater sludge. Nonetheless, the release to the environment of many remains largely unrecognized. Stabilized sewage sludge (biosolids) is increasingly being land-applied as a soil amendment. However, understanding the risks of land application has been hampered by the compositional complexity of biosolids. Compound specific analytical approaches may also underestimate environmental impact of land application by overlooking additional contaminants. However, utilizing an alternative analytical approach based on compound functional group (i.e., alkyl halides) enhanced the information content of the analysis. To illustrate, 49 organohalogens were observed by gas chromatography with electron capture negative ionization mass spectrometry in sewage sludge; 23 identified as flame-retardants: that is, PBDEs, hexabromocyclododecane, 2-ethylhexyl 2,3,4,5-tetrabromobenzoate (TBB), 2-ethylhexyl tetrabromophthalate, decabromodiphenyl ethane, 1,2-bis (2,4,6-tribromophenoxy) ethane and Dechlorane Plus. Concentrations ranged from 25 to 1,600,000 ng g(-1) total organic carbon. An additional 16 compounds were tentatively identified as triclosan, chlorinated-methoxy triclosan, chlorinated pesticides, hexachlorobiphenyl, TBB degradation products, brominated furans and nonabromochlorodiphenyl ethers. Such an analytical approach may enhance evaluations of the risks associated with biosolids land-application and assist in prioritizing specific chemicals for future environmental fate and toxicology studies.

Trace Analytical Methods for Semifluorinated n-Alkanes in Snow, Soil, and Air

Semifluorinated n-alkanes (SFAs) are anthropogenic chemicals that are used in ski waxes and, thus, are released directly into the environment, but their subsequent fate and distribution are as yet unknown. Therefore, simple, selective, and sensitive methods were developed for analyzing trace amounts of SFAs in snow/water, soil, and air samples by gas chromatography coupled to electron capture negative ionization mass spectrometry (GC/ECNI-MS). Recoveries were generally in the range of 70-120%, depending on the compound and matrix. The analytical sensitivity was higher for SFAs with longer fluorinated chains, and the instrumental limits of detection ranged from 0.3 to 260 pg injected, providing method detection limits of 0.54-311 ng L(-1), 0.004-9.86 ng g(-1), and 0.4-531 ng m(-3) for snow (analyzed as its meltwater), soil, and air samples, respectively. Using the developed procedures, SFAs were found in snow (meltwater) and soil samples from a small cross-country ski area in Sweden at concentrations up to 1.3 microg L(-1) and 47 pg g(-1), respectively.

Application of the novel 5-chloro-2,2,3,3,4,4,5,5-octafluoro-1-pentyl chloroformate derivatizing agent for the direct determination of highly polar water disinfection byproducts

A novel derivatizing agent, 5-chloro-2,2,3,3,4,4,5,5-octafluoropentyl chloroformate (ClOFPCF), was synthesized and tested as a reagent for direct water derivatization of highly polar and hydrophilic analytes. Its analytical performance satisfactorily compared to a perfluorinated chloroformate previously described, namely 2,2,3,3,4,4,5,5-octafluoropentyl chloroformate (OFPCF). The chemical properties (reactivity, selectivity, derivatization products, and their chromatographic and spectral features) for ClOFPCF were investigated using a set of 39 highly polar standard analytes, including, among others, hydroxylamine, malic and succinic acids, resorcinol, hydroxybenzaldehyde, and dihydroxybenzoic acid. Upon derivatization, the analytes were extracted from the aqueous solvent and analyzed by gas chromatography (GC)-mass spectrometry (MS) in the electron-capture negative ionization (ECNI) mode. Positive chemical ionization (PCI)-MS was used for confirming the molecular ions, which were virtually absent in the ECNI mass spectra. ClOFPCF showed good reaction efficiency, good chromatographic and spectroscopic properties (better than with OFPCF), good linearity in calibration curves, and low detection limits (0.3-1 microg/L). A unique feature of the derivatizations with ClOFPCF, and, in general, highly fluorinated chloroformates, is their effectiveness in reacting with carboxylic, hydroxylic, and aminic groups at once, forming multiply-substituted non-polar derivatives that can be easily extracted from the aqueous phase and determined by GC-ECNI-MS. The entire procedure from raw aqueous sample to ready-to-inject hexane solution of the derivatives requires less than 10 min. Another benefit of this procedure is that it produced stable derivatives, with optimal volatility for GC separation, and high electron affinity, which allows their detection as negative ions at trace level. In addition, their mass spectra exhibits chlorine isotopic patterns that clearly indicate how many polar hydrogens of the analyte undergo derivatization. Finally, derivatization with ClOFPCF was used successfully to identify 13 unknown highly polar disinfection byproducts (DBPs) in ozonated fulvic and humic acid aqueous solutions and in real ozonated drinking water.

Detection Limits of Electron and Electron Capture Negative Ionization-Mass Spectrometry for Aldehydes Derivatized with o-(2,3,4,5,6-Pentafluorobenzyl)-Hydroxylamine Hydrochloride

In contrast to common expectations, the differences in limits of detection (LODs) between electron capture negative ionization (ECNI) and electron ionization (EI) mass spectrometry (MS) were found to be insignificant for a wide range of aldehydes derivatized with o-(2,3,4,5,6-pentafluorobenzyl)-hydroxylamine hydrochloride. Comparison of the two ionization methods based on LOD confidence intervals revealed that a traditional presentation of the LOD or limit of quantitation (LOQ) as a single value may over/underestimate the significance of obtained results. LODs were between 20 and 150 pg injected for the majority of tested derivatized carbonyls using both ionization methods. ECNI-MS improved LODs by approximately 10- to 20-fold only for two derivatized aldehydes, 4-hydroxybenzaldehyde and 5-(hydroxymethyl)furfural. Selectivity of ECNI did not appear to be beneficial when analyzing a wood smoke particulate matter (WS-PM) extract, possibly because the majority of interferences were removed during sample preparation (i.e., liquid-liquid extraction). The impact of four different data acquisition modes of transmission quadrupole (TQ)-MS on LODs and their precisions was also investigated. As expected, LODs in the selected ion monitoring (SIM) were approximately two to four times lower than those obtained using total ion current (TIC) mode. More importantly, TQ-MS in the selected ion-total ion (SITI) mode (i.e., acquiring SIM and TIC data in a single analysis) provided signal-to-noise ratios and precisions, which were comparable to SIM alone.

Developments in bile acid kinetic measurements using 13C and 2H: 105 times improved sensitivity during the last 40 years†

Bile acid kinetics involve the measurement of pool sizes and turnover rates of individual bile acids. The technique is based on isotope dilution and was first described in the 1950s using radioactive 14C-labelled cholic acid (CA). It took until the 1970s before stable isotopes were introduced for this purpose (13C, 2H) and isotope analysis methods were developed for CA and chenodeoxycholic acid (CDCA) applying gas chromatography/electron impact mass spectrometry. Until the 1980s, the isotope enrichment measurements were performed in bile samples aspirated from the duodenum. Thereafter, methodology became available allowing measurements to be performed in blood requiring at least 2 ml serum samples. Simultaneous measurement of kinetics of metabolically dependent CA and deoxycholic acid using 13C and 2H labels was introduced. Until the 1990s, this technique was only possible in adult humans due to the large sample sizes. Introduction of pentafluorobenzyl bromide derivatisation and electron capture negative ion mass spectrometry (GC/ECN-MS) reduced the sample volume to 50 μ l serum. This allowed isotope abundance measurement of CA in rats and in mice. However, repetitive collection of 100 μl blood samples in mice is too invasive (collection via the orbita) and exhaustive. Therefore, the method development is now focussing on enhanced sensitivity and reduction of blank effects originating from the sample preparation. The final goal is to determine CA isotope enrichments in 20 μl mouse blood obtained from the tail vein. This paper shows the feasibility of reaching this goal.