Chemiluminescent Nitrogen Detector Research Articles

A Comparative Evaluation of Nitrogen Compounds in Petroleum Distillates

Although the concentration of nitrogen compounds in crude oil is relatively low, they can become more concentrated in petroleum distillates and poison the catalysts used in refining processes. They cause undesirable deposits, color formation and odor in products; they also contribute to air pollution and some are highly carcinogenic. The poisoned catalyst becomes deactivated for hydrodesulfurization and unable to remove sulfur from middle distillates. In order to understand the effect on catalytic processes, it is desirable to identify the nitrogen compounds in various petroleum distillates. This paper compares the nitrogen species profiles in different petroleum distillates using a nitrogen chemiluminescence detector. In addition, four different petroleum distillate samples from different refineries were analyzed to find the variation in their nitrogen profiles. The nitrogen compounds in petroleum distillate samples were identified as anilines, quinolines, indoles, and carbazoles and their alkyl derivatives. Quantitation was carried out against known reference standards. The quantitative data were compared to the total nitrogen content determined by elemental analysis.

Molecular weight separation of hot-water extractable soil organic matter using high-performance size exclusion chromatography with chemiluminescent nitrogen detection

To characterize soil organic nitrogen (N), we applied high-performance size exclusion chromatography (HPSEC) and chemiluminescent nitrogen detection (CLND) to the molecular weight separation of hot-water extractable organic matter (HWEOM) from soils that had been amended with or without plant residue compost applied at a rate of 2 kg m−2 y−1 for 25 years. The N chromatogram of the HWEOM showed that the HWEOM containing N had molecular weights ranging from 0.1 to 100 kDa. The N chromatograms of HWEOM from soils without compost differed among four soils (Cumulic Andosol, Low-humic Andosol, Gray Lowland soil, and Yellow soil). The N intensities in the HWEOM chromatograms were larger in the soils with compost amended than in those without compost over the whole range of molecular weights. These results demonstrate that HPSEC/CLND is a useful tool to investigate the structure and dynamics of water soluble organic N in soil.

New Sensitive and Quantitative Analysis Method for Organic Nitrogen Compounds in Urban Aerosol Samples

Atmospheric aerosols contain a highly complex mixture of organic and inorganic compounds; however, as a chemical class relatively little is known about organic nitrogen (ON) content, with few satisfactory methods for speciated analysis. In this paper we report a sensitive and quantitative method for the speciation of ON within ambient atmospheric aerosol. Aerosol samples, collected on quartz microfiber filters, were extracted in water followed by solid phase extraction, elution, and concentration before analysis by comprehensive gas chromatography with a nitrogen chemiluminescence detection system (GCxGC-NCD). The NCD detection method was optimized using liquid standards. The GCxGC-NCD method showed high selectivity, sensitivity, and equimolarity in its response to individual organic compounds. Limits of detection (LOD) and limits of quantitation (LOQ) for four ON standards (1-nitropentane, o-toluidine, nonanenitrile, and quinoline) were determined to be in the range 0.16-0.27 pgN and 0.71-1.19 pgN, respectively. Between 21 and 57 different ON compounds were found in urban aerosol, (including 10 nitriles, 9 alkyl nitro compounds, 4 nitro-phenols, 4 amides, 3 nitrosamines, and 2 nitro-PAHs) on different dates from a city center location. Pyrrole (8.26-39.21 ngN m(-3) air) and N-butyl-benzenesulfonamide (6.23-20.87 ngN m(-3) air) were the most abundant ON compounds observed in all samples analyzed. The average mass loading of the total identified ON was 532.51 ngON m(-3) air. The sensitivity, selectivity, and relative ease of quantitation of unknown ON components makes the technique a significant improvement over previous laboratory methods.

Determination of volatile nitrosamines in various meat products using comprehensive gas chromatography–nitrogen chemiluminescence detection

An optimized method was developed for the extraction, pre-concentration and analysis of nitrosamines (NAs) in various meat products. Values of reproducibility, linearity, limit of detection (LOD) and limit of quantitation (LOQ) for six NA standards ( N-nitrosodimethylamine, N-nitrosodiethylamine, N-nitrosodi- n-propylamine, N-nitrosopyrrolidine, N-nitrosopiperidine, N-nitrosodi- n-butylamine) were determined. The LODs using this method were between 1.66–3.86 and LOQs between 6.96–16.71 μg L −1. The screening of four different types of meat samples (sausage, salami, sucuk and doner kebab) showed that all samples contained levels of various NAs, identified with high confidence using comprehensive gas chromatography (GCxGC) and a fast responding element specific nitrogen chemiluminescence detector (NCD). The sum of the six NAs were highest in the doner kebab samples, being between 0.51–16.63 μg kg −1 and were lowest in the sausage samples at 0.45–2.93 μg kg −1. The described method is simple, rapid, selective and sensitive.

Trimethylamine oxide, dimethylamine, trimethylamine and formaldehyde levels in main traded fish species in Hong Kong

Levels of trimethylamine oxide (TMAO), dimethylamine (DMA), trimethylamine (TMA) and formaldehyde (FA) were studied in 266 different fishes, including fresh/frozen raw whole fishes of 89 different species that traded in Hong Kong, China. Determination of TMAO can confirm the source of DMA and FA if present in the sample. These samples were purchased from different commercial outlets between April and August 2007. All samples of raw whole fish were identified for their species by the Agriculture, Fisheries and Conservation Department. The content of TMAO was determined by high-performance liquid chromatography (HPLC) coupled with a chemiluminescent nitrogen detector. The possible decomposition products of TMAO, DMA and TMA were analysed by headspace solid-phase micro-extraction gas chromatography-mass spectrometry (HS-SPME-GC-MS), while FA was conducted by steam distillation then quantified by a HPLC. The range for TMAO of all samples was <5–3800 mg kg−1 with median of 970 mg kg−1, while the endogenous enzymatic cleavage products DMA, TMA and FA were in the range of <2–320, <1–190 and <1–160 mg kg−1, respectively. These cleavage products were mainly found in three fish species, Harpadon nehereus, Saurida elongata and Saurida tumbil, that belong to the family Synodontidae (Lizardfishes) and subfamily Harpadontinae. Besides, freshwater fish species, namely, Micropterus salmoides, Oreochromis niloticus niloticus and Siniperca chuatsi, were found to contain TMAO in the range of 510–760, 85–720 and 400–640 mg kg−1, respectively.

Stability Through the Ages: The GSK Experience

It is common knowledge in the pharmaceutical industry that the quality of a company's compound collection has a major influence on the success of biological screening in drug discovery programs. DMSO is the widely accepted solvent of choice for storage of compounds, despite the hygroscopic nature of the solvent, which can lead to stability issues. Other factors that can affect compound stability (e.g., degradation, precipitation) include concentration of compound, intrinsic compound stability, presence of reactive contaminants, storage format-related factors (vessel, sealing, etc.), storage conditions (temperature, humidity, freeze-thaw technique and cycles, etc.), and storage time. To define the best practice for the storage and handling of solution samples, GlaxoSmithKline has undertaken stability experiments over more than a decade, initially to support the implementation of new automated liquid stores (ALS) and, subsequently, to enhance storage and use of compounds in solution through an understanding of compound degradation under storage and assay conditions. The experiments described used a number of technologies, including hyphenated liquid chromatography, electrospray mass spectrometry, flow chemiluminescence nitrogen detection, nuclear magnetic resonance, and Karl Fischer titration.

Hydrophilic interaction liquid chromatography with alcohol as a weak eluent

There has been a significant increase of interest in polar compound separation by hydrophilic interaction liquid chromatography (HILIC), in which acetonitrile is mostly used as a weak eluent. Although replacing acetonitrile with alcohols as organic modifiers has been previously reported, the separation mechanism was poorly understood. In this paper we explored the separation mechanism through the method development for the analysis of the trace amounts of polar and basic hydrazines, which were genotoxic in nature. Separation parameters such as the type and concentration of alcohol, acid modifier, and buffer in mobile phase as well as the choice of stationary phase and column temperature were studied. The data indicated that both electrostatic and hydrophilic interactions contributed to the retention and separation of the hydrazines. The results presented here provide insight into the adjustment of the retention and separation of analytes in HILIC mode with alcohol as a weak eluent. The optimized HILIC method coupled with chemiluminescent nitrogen detection (CLND) is simple and sensitive (reporting limit at 0.02%) and was applied to simultaneous analysis of hydrazine and 1,1-dimethylhydrazine in a pharmaceutical intermediate.

The practical application of implementing the equimolar response principle of chemiluminescent nitrogen detection in pharmaceutical analysis

Since nearly 90% of all developmental and marketed drugs contain at least one nitrogen atom, the implementation of chemiluminescent nitrogen detection (CLND) in pharmaceutical analysis is intriguing due to its equimolar response for nitrogen. Although the documented accuracy of CLND when using a surrogate nitrogen-containing standard may be inadequate for purity and potency determinations, it is acceptable for the quantitation of low-level impurities. A comparison of the quantitative results obtained using both CLND and UV detection for a developmental drug and its related impurities is presented. The results indicated that the impurities can be accurately quantified using a surrogate standard, based on the equimolar response principle of CLND, when the concentrations of the surrogate standard and the component of interest are similar. When the impurities are present at much lower levels than the surrogate standard however, the common practice of direct conversion of area percent to weight percent can result in significant errors using CLND, due to the limited linear dynamic range for CLND. To increase quantitation accuracy, the authors propose that a secondary dilution of the surrogate reference standard solution should be used for the quantitation of low-level impurities. The practical application of this approach for impurity quantitation or as a means to determine impurity relative response factors for use with a traditional UV based method is discussed.

Nitrogen–phosphorus detection and nitrogen chemiluminescence detection of volatile nitrosamines in water matrices: Optimization and performance comparison

Two nitrogen-specific detection methods, nitrogen–phosphorus detection (NPD) and nitrogen chemiluminescence detection (NCD), were investigated as low cost alternatives to mass spectrometry (MS) with chemical ionization (CI) for analysis of nitrosamines in aqueous samples. NCD showed greater sensitivity to N-nitrosodimethylamine (NDMA) and seven other volatile nitrosamines than did NPD. Instrument detection levels for NDMA were established at 2.6 μg/L and 4.0 μg/L in solvent with 3 μL splitless gas chromatograph (GC) injection for NCD and NPD, respectively. Using a dual-column confirmation method, both NCD and NPD compared favorably with CI-MS results for NDMA analysis in a variety of water sample types. For seven other nitrosamines, both detectors showed excellent accuracy in analyzing high concentrations (greater than 300 ng/L) in complex wastewater matrices, while the accuracy of spike recoveries of very low levels (less than 15 ng/L) in clean matrices varied for each nitrosamine and detection method.

Single-calibrant quantification of drugs in plasma and whole blood by liquid chromatography–chemiluminescence nitrogen detection

Poor availability of drug reference standards may severely complicate clinical and forensic toxicology investigations. To overcome this problem, a new approach is introduced for drug analysis without primary reference standards. Liquid chromatography–chemiluminescence nitrogen detection (LC–CLND) was employed as the analytical technique, based on the detector's equimolar response to nitrogen and using caffeine as single secondary standard. Liquid–liquid extraction recoveries for 33 basic lipophilic drugs were first established by LC–CLND in blood specimens spiked with the respective reference substances. The mean recovery by butyl chloride–isopropyl alcohol extraction for plasma and whole blood was 90 ± 18 and 84 ± 20%, respectively. The validity of the generic extraction recovery-corrected single-calibrant LC–CLND was then verified with proficiency test samples, including 20 different analyses. The mean accuracy was 24 and 17% for the plasma and the whole blood samples, respectively, and the maximum error was 31% for both specimens. All 20 analyses results by LC–CLND fell within the confidence range of the reference concentrations. LC–CLND proved to be an easy-to-use and robust technique, allowing analysis of 1000 injections of biological extracts without a need for major maintenance operations.

Conversion efficiency of the high-temperature combustion technique for dissolved organic carbon and total dissolved nitrogen analysis

The measurements of dissolved organic carbon (DOC) and total dissolved nitrogen (TDN) in seawater are key in global change and coastal eutrophication studies. Nowadays, the high-temperature combustion (HTC) technique is a widely used method for DOC and TDN analysis. However, uncertainties exist about the operation of the catalyst in the conversion process of DOC and TDN in the HTC method. In this study, five different ‘catalyst’ materials were tested for their blanks, calibration slopes, and conversion efficiency of DOC and TDN using the Shimadzu TOC 5000A total organic carbon analyser coupled to a Sievers NCD 255 nitrogen chemiluminescence detector. The materials included four metallic catalysts (Shimadzu and Johnson 0.5% Pt–alumina, 13% Cu(II)O–alumina, 0.5% Pd–alumina) and quartz beads. The results indicated that DOC blank signals for the HTC approach using metallic catalysts with an alumina support are higher compared with quartz beads, as a result of the amphoteric nature of the alumina. However, the slopes of the standard calibration graphs were lowest for DOC and TDN determinations on the quartz beads. The DOC recoveries for the metallic catalysts were close to 100% for all compounds tested, with the exception of ammonium pyrrolidine dithiocarbamate. Using quartz beads, poor recoveries were obtained for a range of organic compounds, including the commonly used calibration compounds potassium hydrogen phthalate and glycine. The TDN recoveries for all compounds were typically >90%, with the exception of NaNO2. Furthermore, analysis using the CuO–alumina and Pd–alumina catalysts and quartz beads showed low recoveries for NH4Cl. This study showed that catalyst performance should be verified on a regular basis using model compounds and blank checks made during every run, and that the Shimadzu 0.5% Pt–alumina material was an efficient catalyst for DOC and TDN analyses using the coupled total organic carbon–nitrogen chemiluminescence detector (TOC-NCD) analyser.

Number of nitrate groups determines reactivity and potency of organic nitrates: a proof of concept study in ALDH‐2−/− mice

Mitochondrial aldehyde dehydrogenase (ALDH-2) has been shown to provide a pathway for bioactivation of organic nitrates and to be prone to desensitization in response to highly potent, but not to less potent, nitrates. We therefore sought to support the hypothesis that bioactivation by ALDH-2 critically depends on the number of nitrate groups within the nitrovasodilator. Nitrates with one (PEMN), two (PEDN; GDN), three (PETriN; glyceryl trinitrate, GTN) and four (pentaerithrityl tetranitrate, PETN) nitrate groups were investigated. Vasodilatory potency was measured in isometric tension studies using isolated aortic segments of wild type (WT) and ALDH-2-/- mice. Activity of the cGMP-dependent kinase-I (reflected by levels of phosphorylated VAsodilator Stimulated Phosphoprotein, P-VASP) was quantified by Western blot analysis, mitochondrial dehydrogenase activity by HPLC. Following incubation of isolated mitochondria with PETN, PETriN-chromophore and PEDN, metabolites were quantified using chemiluminescence nitrogen detection and mass spectrometry. Compared to WT, vasorelaxation in response to PETN, PETriN and GTN was attenuated about 10fold in ALDH-2-/- mice, identical to WT vessels preincubated with inhibitors of ALDH-2. Reduced vasodilator potency correlated with reduced P-VASP formation and diminished biotransformation of the tetranitrate- and trinitrate-compounds. None of these findings were observed for PEDN, GDN and PEMN. Our results support the crucial role of ALDH-2 in bioactivating highly reactive nitrates like GTN, PETN and PETriN. ALDH-2-mediated relaxation by organic nitrates therefore depends mainly on the number of nitrate groups. Less potent nitrates like PEDN, GDN and PEMN are apparently biotransformed by other pathways.

Studies on N-Terminal Glycation of Peptides in Hypoallergenic Infant Formulas: Quantification of α-N-(2-Furoylmethyl) Amino Acids

To obtain information about the extent of the early Maillard reaction between the N-termini of peptides and lactose, alpha-N-(2-furoylmethyl) amino acids (FMAAs) were quantified together with epsilon-N-(2-furoylmethyl)lysine (furosine) in acid hydrolyzates of hypoallergenic infant formulas, conventional infant formulas, and human milk samples using RP-HPLC with UV-detection. FMAAs are formed during acid hydrolysis of peptide-bound N-terminal Amadori products (APs), and furosine is formed from the Amadori products of peptide-bound lysine. Unambiguous identification was achieved by means of LC/MS and UV-spectroscopy using independently prepared reference material. The extent of acid-induced conversion of APs to FMAAs was studied by RP-HPLC with chemiluminescent nitrogen detection (CLND). Depending on the corresponding alpha-N-lactulosyl amino acid, between 6.0% and 18.1% of FMAAs were formed during hydrolysis for 23 h at 110 degrees C in 8 N HCl. From epsilon-N-lactulosyllysine, 50% furosine is formed under these conditions. Whereas furosine was detectable in all assayed samples, five different FMAAs, alpha-FM-Lys, alpha-FM-Ala, alpha-FM-Val, alpha-FM-Ile, and alpha-FM-Leu, were exclusively detected in acid hydrolyzates of hypoallergenic infant formulas in amounts ranging from 35 to 396 mumol/100 g protein. Taking the conversion factors into account, modification of N-terminal amino acids in peptides by reducing carbohydrates was between 0.3% and 8.4%. This has to be considered within the discussion concerning the nutritional quality of peptide-containing foods.

Structure-Dependent Response of a Chemiluminescence Nitrogen Detector for Organic Compounds with Adjacent Nitrogen Atoms Connected by a Single Bond

High-throughput screening (HTS) of chemical libraries is indispensable for drug discovery research. However, the HTS data quality for lead discovery, lead optimization, and quantitative structure activity relationship studies has been severely compromised due to the uncertain compound concentrations in screening plates. In order to address this issue, we compared various high-throughput technologies for quantification of compounds in microtiter plate format without the need for authentic compounds as standards and identified the chemiluminescence nitrogen detector (CLND) as the method of choice at the present time. However, the structure dependence of this detector has not been well studied. A proposed rule suggested that the only exception to equimolar response is for compounds that contain adjacent nitrogen atoms. The response should be zero when the adjacent nitrogen atoms are connected by a double bond and 0.5 when they are connected by a single bond. In this investigation, we studied a broad range of compounds with isolated and adjacent nitrogen atoms. We confirmed that compounds with isolated nitrogen atoms produce an equimolar response with a 15-20% variation depending on structures and compounds with adjacent nitrogen atoms connected by a double bond giving nearly zero response. We discovered that the CLND response for compounds containing adjacent nitrogen atoms that are connected with a single bond is highly structure dependent. Substitutions on the nitrogen atoms or nearby in the molecule can increase the CLND response to approach a value higher than the predicted value 0.5 (maximal value 0.82/nitrogen atom). Without substitution, much lower values than predicted (minimal value 0.0-0.08/nitrogen atom) are obtained. Therefore, the prediction of response of 0.5/nitrogen atom for compounds with adjacent nitrogen atoms connected by a single bond should be abandoned. Compounds with similar structures should be used to generate calibration curves for quantification of this class of compounds.

Prediction of Gas Chromatographic Retention Times of Carbazoles in Light Cycle Oil

Forty-nine individual carbazoles were identified in a fluid-catalytic-cracking light cycle oil (LCO) using gas chromatography (GC) with nitrogen chemiluminescence detection (GC-NCD). Their retention times were correlated with molecular descriptors generated from their molecular structures. The best seven-parameter multilinear-regression models showed good fit with a standard deviation of s = 0.58 min for the retention times. The descriptors involved in the models reflect the geometrical, topological, and electronic properties of the molecules, related to the interactions between the solute and the stationary phase. For forty-five out of the forty-nine carbazoles (carbazole, alkylcarbazoles, and hydrocarbazoles) of most interest in LCO processing, another seven-parameter multilinear-regression model was developed with standard deviation s = 0.37 min. This model further improved the model fit to the database of retention times. QSPR models of this quality can be used as an important source of information in...

Evaluation of the chemiluminescent nitrogen detector for solubility determinations to support drug discovery

Solubility measurements using chemiluminescent nitrogen detection (CLND) has advantages of reduced compound requirement and increased throughput compared to UV-spectrophotometric and HPLC-based measurements. CLND with direct flow injection was evaluated for the measurement of thermodynamic solubility to support drug discovery. The limit of quantitation (LOQ), accuracy, and day-to-day reproducibility of the detector were measured. Measurements made on CLND were compared to those obtained from UV spectrophotometry and HPLC. Based on the results obtained, it was concluded that the CLND performs satisfactorily for discovery stage thermodynamic solubility measurements.

Analytical and Biological Evaluation of High Throughput Screen Actives Using Evaporative Light Scattering, Chemiluminescent Nitrogen Detection, and Accurate Mass LC-MS-MS

In this investigation the utility of evaporative light scattering detection (ELSD) combined with HPLC-MS was demonstrated as a key component of a bioassay-guided fractionation, or "biofractionation" technique, for the evaluation of high throughput screen actives. ELSD provided on-line analyte mass information that was critical for the classification of the samples. Chemiluminescent nitrogen detection (CLND) was also evaluated for sample concentration estimation for nitrogen-containing compounds, and accurate mass LC-MS-MS analysis was employed for rapid structural confirmation and elucidation of components previously identified as active via biofractionation.

Liquid chromatography‐mass spectrometry and related techniques for purity assessment in early drug discovery

The combination of HPLC and MS has become the most valuable analytical tool to determine the identity and purity of a drug substance in the drug discovery arena over the past decade. This article describes different LC/MS configurations and their broad applicability to meet the fundamental analytical requirements involved in discovering new drugs. In addition, the value of chemiluminescence nitrogen detection for absolute purity determination and the convenience of CE as an orthogonal separation technique to HPLC are also discussed. In summary, LC/MS-based methodologies that implicate automation, various levels of throughput and open access systems have proved to be an integral part of the drug discovery process. As a result, the paradigm of high-quality/-quantity information is fulfilled in a timely fashion.

Quantitative Analysis of Conjugated Dienes in Hydrocarbon Feeds and Products

We report a new method for the detailed speciation and quantification of low levels of conjugated dienes (diolefins) in complex hydrocarbon matrixes, such as steam-cracked naphthas, catalytically cracked naphthas, and heavy coker naphthas. Conjugated dienes are responsible for hydrocarbon polymerization (fouling) in various refinery processes. Until now, complete analysis of conjugated dienes, particularly C6+ conjugated dienes, was almost impossible, because of their low concentrations and severe matrix interference. Here, we show that selective derivatization of conjugated dienes with MTAD, in combination with gas chromatography−chemical ionization mass spectrometry (GC/CIMS) and gas chromatography−nitrogen chemiluminescence detection (GC/NCD) can be used to analyze the total conjugated dienes (up to C10) in various hydrocarbon matrixes quantitatively.

Toward Single-Calibrant Quantification in HPLC. A Comparison of Three Detection Strategies: Evaporative Light Scattering, Chemiluminescent Nitrogen, and Proton NMR

There is an urgent need for detection technologies that enable accurate and precise quantification of solutions containing small organic molecules in a manner that is rapid, cheap, non-labor-intensive, readily automated, and without a requirement for specific analyte standards. We provide a theoretical analysis that predicts that the logarithmic nature of the working domain of the evaporative light-scattering detector (ELSD) will normally bias toward underestimation of chromatographically resolved impurities, resulting in an overestimation of analyte purity. This analysis is confirmed by experiments with flow injection analysis (FIA) and gradient reversed-phase high performance liquid chromatography (RP-HPLC). Quantification is further compromised by the dependence of response parameters on the matrix composition and hence on the retention time of the analyte. Attempts were made to ameliorate these problems by using the response surface of a single compound to calibrate throughout the HPLC gradient. A chemiluminescent nitrogen detector (CLND) was also used in a similar manner, and the performance of the two techniques were compared against those of each other and that of a reference standard technique. A protocol for this purpose was developed using proton nuclear magnetic resonance (1H NMR) and the ERETIC method to enable quantification by integrating proton signals. The double-blind comparison exercise confirmed molar nitrogen CLND response to be sufficiently stable and robust across a methanol gradient to be used with a single external nitrogenous calibrant to quantify nitrogen-containing compounds of known molecular formula. The performance of HPLC-CLND was very similar to that of NMR, while that of HPLC-ELSD was seen to be significantly worse, showing it to be unsuitable for the purpose of single-calibrant quantification. We report details and experience of our use of RP-HPLC-CLND-MS to characterize and quantify small amounts of solutions of novel compounds at nominal levels of 10mM in microtiter plate (MTP) format.