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Yuen CT, Price RG, Richardson AC, Praill PF: The assay of arlesterase in serum using two new colorimetric substrates, omega-nitrostyrylacetate and propionate. Clin Chim Acta. 1981 Apr 27;112(1):99-105.
(1) The synthesis of 4-acetoxy-3-methoxy-omega-nitrostyrene and 4-propionyloxy-3-methoxy-omega-nitrostyrene as substrates for the assay of arylesterase activity is described. These substrates are stable when stored in the dark for at least one year. (2) Serum isolated from normal males and females aged between 25 and 35 years was used as a source of esterase activity. (3) The chromophore (4-hydroxy-3-methoxy-omega-nitrostyrene) absorbs at 505 nm and has a molar extinction coefficient of 26 800 in sodium carbonate/bicarbonate buffer, pH 9.5. (4) Both acetate and propionate substrates are more soluble in aqueous alcohol than in water or buffer alone and the substrates were therefore prepared in 10% methanol. Since some non-enzymic hydrolysis occurs at 37 degrees C, assays were carried out at 30 degrees C. Details of both single point and reaction rate assay procedures are described. (5) The properties of the arylesterases were determined in human serum using the single point and reaction rate assays. The data are similar to those previously described for these esterases using well-established procedures. (6) The assays described using the omega-nitrostyryl acetate and propionate substrates are simple to perform and can be readily adapted for use in the clinical chemistry laboratory. Large numbers of samples can be rapidly assayed with the minimum number of manipulative steps. |
82(1,1,1,2) |