1995
DOI: 10.1016/0891-5849(94)00105-s
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A practical method for preparing peroxynitrite solutions of low ionic strength and free of hydrogen peroxide

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Cited by 218 publications
(161 citation statements)
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“…Aqueous stock solutions of NO, ONOO − and HbO # were prepared as described [28,38]. The O # − d -generating system consisted of 250 µM hypoxanthine and up to 100 m-units\ml xanthine oxidase resulting in, for example, an O # − d flux at 0.75 munits\ml xanthine oxidase of 0.5 µM\min.…”
Section: No Onoo − Hbo 2 H 2 O 2 and O 2 − D -Generating System mentioning
confidence: 99%
“…Aqueous stock solutions of NO, ONOO − and HbO # were prepared as described [28,38]. The O # − d -generating system consisted of 250 µM hypoxanthine and up to 100 m-units\ml xanthine oxidase resulting in, for example, an O # − d flux at 0.75 munits\ml xanthine oxidase of 0.5 µM\min.…”
Section: No Onoo − Hbo 2 H 2 O 2 and O 2 − D -Generating System mentioning
confidence: 99%
“…SSDI 0014-5793(95)01530-2 complex sodium salt (DEA/NO; Research Biochemicals International), essentially as described by Maragos et al [18]. Peroxynitrite was synthesized by ozonization of ice-cooled aqueous sodium azide at pH 12, essentially as described [19] (precautions for the procedure are described in ref. [19]).…”
Section: Chemicalsmentioning
confidence: 99%
“…Peroxynitrite was synthesized by ozonization of ice-cooled aqueous sodium azide at pH 12, essentially as described [19] (precautions for the procedure are described in ref. [19]). The actual peroxynitrite concentrations were determined before each experiment at "~max = 302 nm taking es02 = 1,670 M -I "cm -1 [20].…”
Section: Chemicalsmentioning
confidence: 99%
“…PMSF was from Nacalai Tesque (Kyoto, Japan). 3-Morpholinosydnonimine (SIN-1) was from Dojindo (Kumamoto, Japan 23,25) The solution was stored at Ϫ80°C until use. The concentration of the peroxynitrite solution was determined spectrophotometrically by measuring the absorbance at 302 nm (eϭ1670 M Ϫ1 cm…”
Section: Methodsmentioning
confidence: 99%