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Biological systems hydrogen peroxide determination

Two methods were examined for digestion of biological samples prior to trace element analysis. In the first one a nitric acid-hydrogen peroxide-hydrofluoric acid mixture was used in an open system, and in the second one nitric acid in a closed Teflon bomb. The latter method was superior for Ge determination, however, germanium was lost whenever hydrogen fluoride had to be added for disolving sihcious material. End analysis by ICP-AES was used for Ge concentrations in the Xg/g range13. [Pg.344]

In an early application, an enzyme electrode system was reported for the determination of creatinine and creatine, using a combination of creatinine amidohy-drolase, creatine amidinohydrolase and sarcosine oxidase, co-immobilized on an asymmetric cellulose acetate membrane. Thus, the hydrogen peroxide produced was detected to give a quantitative measure of creatine and creatinine in biological fluids [70]. [Pg.57]


See other pages where Biological systems hydrogen peroxide determination is mentioned: [Pg.574]    [Pg.1442]    [Pg.1468]    [Pg.574]    [Pg.84]    [Pg.827]    [Pg.186]    [Pg.153]    [Pg.828]    [Pg.154]    [Pg.825]    [Pg.35]    [Pg.133]    [Pg.100]    [Pg.115]    [Pg.350]    [Pg.31]    [Pg.290]    [Pg.142]    [Pg.340]    [Pg.793]    [Pg.92]    [Pg.32]    [Pg.1367]    [Pg.139]    [Pg.20]    [Pg.438]    [Pg.268]    [Pg.480]    [Pg.239]    [Pg.171]    [Pg.387]    [Pg.549]    [Pg.201]   
See also in sourсe #XX -- [ Pg.626 ]




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