Reconstructed mass-spectrometric pattern for characterization of carbon compounds in smoker's lung in situ

BACKGROUND: Cigarette smoke is a major anthropogenic pollutant and contributes to the permanent load of ambient particulate matter in the air, particularly indoors. It is the leading risk factor for premature loss of life due to chronic bronchitis, emphysema and lung cancer. Smoker's lung and graphite pneumoconiosis are pathological states characterized by the deposition of carbonaceous particles. METHODS: Mass spectrometry was used to evaluate unstained lung sections obtained in vivo from a heavy smoker and a patient with occupationally acquired graphite pneumoconiosis. RESULTS AND DISCUSSION: The composition of carbon compounds deposited in lung tissue samples is demonstrated here for the first time. Thirty carbonaceous-containing microareas from ten biopsies (three areas per biopsy) of lung tissues were analyzed mass-spectrometrically. In each case, the samples were taken from a smoker's lung or those demonstrating a graphite pneumoconiosis. The lung-tissue samples were selected by light microscopy before they were evaporated for mass spectrometry. First-order criteria were anionic and cationic mass peaks which occur within the mass patterns in lung tissues of smoker's lung, although not in graphite pneumoconiosis. Second-order criteria were mass peaks from smoker's lung with standard deviations SD < or = 14% of the mean value. First and second-order mass peaks matched the mass peaks of experimental cigarette-smoke condensate in 9 out of 11 peaks. A software program was developed that enabled fast, automated recognition of the typical mass peaks, and thereby confirmed the histological diagnosis of smoker's lung. CONCLUSIONS: The analysis of carbonaceous particles within lung biopsies from a heavy smoker corresponded to the spectra of tobacco condensate and not to the investigated biopsies of graphite peneumoconiosis. RECOMMENDATION AND OUTLOOK: The analyses were performed in order to find out whether mass-spectrometric criteria exist for the differentiation of carbonaceous lung-tissue deposits. Mass spectrometry may be a valuable tool in determining the composition of carbon compounds deposited in human lung tissue. So far, qualitative assessment of the composition of deposits in lung tissue is only possible after the patient is deceased (autopsy).     

Occurrence of organo-arsenicals in jellyfishes and their mucus

Water-soluble arsenic compound fractions were extracted from seven species of jellyfishes and subjected to analysis by high-performance liquid chromatography-inductively coupled plasma mass spectrometry (HPLC-ICP-MS) for arsenicals. A low content of arsenic was found to be the characteristic of jellyfish. Arsenobetaine (AB) was the major arsenic compound without exception in the tissues of the jellyfish species and mucus-blobs collected from some of them. Although the arsenic content in Beroe cucumis, which preys on Bolinopsis mikado, was more than 13 times that in B. mikado, the chromatograms of these two species were similar in the distribution pattern of arsenicals. The nine species of jellyfishes including two species treated in the previous paper can be classified into arsenocholine (AC)-rich and AC-poor species. Jellyfishes belonging to Semaostamae were classified as AC-rich species.     

Determination of arsenic in crude petroleum and liquid hydrocarbons

Total arsenic was determined in crude petroleum and liquid hydrocarbons derived from crude petroleum by extraction with boiling water or boiling aqueous nitric acid (concentration 0.25 to 2.5 M), mineralization of the extracts with concentrated nitric/sulphuric acid, and reduction of the arsenate to arsine in a hydride generator. The arsine was flushed into a helium-DC plasma. The arsenic emission was monitored at 228.8 nm. The total arsenic concentration in 53 crude oil samples ranged from 0.04 to 514 mg L^–1 (median 0.84 mg L^–1). Arsenic was also determined in several refined liquid hydrocarbons and in a commercially available arsenic standard in an organic matrix (triphenylarsine in xylene). The method was checked with NIST 1634b Trace Elements in Residual Fuel Oil. The arsenic concentration found in this standard agreed with the certified value (0.12±0.2 g g^–1) within experimental error. Viscous hydrocarbons such as the fuel oil must be dissolved in xylene for the extraction to be successful. Hydride generation applied to an aqueous not-mineralized extract from an oil containing 1.67 g As mL^–1 revealed, that trimethylated arsenic (520 ng mL^–1) is the predominant arsenic species among the reducible and detectable arsenic compounds. Monomethylated arsenic (104 ng ml^–1), inorganic arsenic (23 ng mL^–1), and dimethylated arsenic (low ng mL^–1) were also detected. The sum of the concentrations of these arsenic species accounts for only 39% of the total arsenic in the sample.On leave from Department of Chemistry, Indian Institute of Technology, New Delhi, India     

Pollution profile of damodar river sediment in Raniganj-Durgapur industrial belt,West Bengal,India

This paper reports on the pollution profile of Damodar river sediment as obtained from analysis of the river sediment at suitable selected sites in the Raniganj-Durgapur industrial belt, West Bengal, India. The parameters measured include (a) silica, mixed oxide, calcium, magnesium, total water-soluble exchangeable cation and anion, chemical oxygen demand, and (b) some toxic and other elements, such as sodium, potassium, arsenic, cadmium, chromium, mercury, manganese, lead, zinc, cobalt, copper, iron nickel, phosphorus, sulphur, and vanadium. The parameters listed under (a) led to the characterization of the sediment, and those under (b) gave an index of metal pollution of the sediment. The elements were estimated by inductively coupled plasma emission spectrometry.     

Quantitative determination of arsenobetaine,the major water-soluble arsenical in three species of crab,using high pressure liquid chromatography and an inductively coupled argon plasma emission spectrometer as the arsenic-specific detector

The major water-soluble arsenic compound in the Alaskan king crab, the Alaskan snow crab, and the Dungeness crab was identified as arsenobetaine by HPLC/ICP analysis. This technique is suitable for the identification and quantitative determination of naturally occurring organic arsenic compounds in purified and partially purified extracts from biota.