A simple rapid immunoassay for S-adenosylhomocysteine in plasma.

The measurement of plasma S-adenosylhomocysteine is a more sensitive indicator of the risk for vascular disease than is plasma homocysteine. Because the level of S-adenosylhomocysteine is normally in the nanomolar range, it has been difficult to measure and necessitated the development of complex fluorometric and mass-spectrophotometric methods. We have now adapted an existing immunoassay used for the measurement of homocysteine to the measurement of S-adenosylhomocysteine in plasma.

Evaluation of novel assays in clinical chemistry: quantification of plasma total homocysteine.

Background: There is a need for systematic evaluation of methods before their release to the market. We addressed this problem in novel homocysteine assays as part of an European Demonstration Project involving six centers in four countries.

Methods: Two immunological methods for measurement of plasma total homocysteine (P-tHcy), the fluorescence polarization immunoassay (FPIA) and the enzyme immunoassay (EIA), were compared with two comparison methods, HPLC and gas chromatography-mass spectrometry (GC-MS).

Enzyme conversion immunoassay for determining total homocysteine in plasma or serum.

A rapid and precise immunoassay for quantification of total homocysteine in blood samples is presented. The method avoids the use of radioisotopes and chromatographic separations and relies on enzymatic conversion of homocysteine to S-adenosyl-L-homocysteine, followed by quantification of S-adenosyl-L-homocysteine by an enzyme-linked immunoassay in microtiter format. The within- and between-assay imprecision is < 6% and 8%, respectively, and results by the method show good correlation with those by HPLC.

Thermal oxidation of polycyclic aromatic hydrocarbons adsorbed on alumina.

The reevaporation of polycyclic aromatic hydrocarbons (PAH) from secondary alumina (alumina used in a fluidized bed for pot gas cleaning) used in the production of aluminum in aluminum reduction plants has been studied. The secondary alumina contains around 100 ppm of PAH when introduced to the pots. The results of this study indicate that only a minor part of the adsorbed PAH is reevaporated at the pot temperature of 300-400 degrees C and that the use of secondary alumina has little effect on the PAH concentration in the workplace atmosphere of the aluminum reduction plants.

A comparison between different high volume sampling systems for collecting ambient airborne particles for mutagenicity testing and for analysis of organic compounds.

Samples of urban air were collected simultaneously using different sampling systems, including electrostatic precipitation (ESP) and high volume filtration (HVF) on various filters for particle sampling and absorption on activated carbon and organic polymers for sampling of volatiles. Acetone extracts of the samples were analyzed for polycyclic aromatic hydrocarbons (PAH) and tested for mutagenicity with the Ames Salmonella/microsome assay. The results show that the concentrations of PAH found in the various particle-samples were in good agreement, whereas the mutagenic activity of these samples showed large variations.