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Oxidative aging groups

The 5, 8-cyclonucleosides are now recognized as significant oxidative lesions that are chemically stable and form in mammalian DNA in vivo. In pig liver DNA, the levels of (5 5)-5, 8-cyclo-dA ( 0.7 lesions/10 DNA bases) were approximately four-to seven-fold lower than the levels of 8-oxo-dG, but were approximately three-fold higher than levels of 8-oxo-dA. Elevated levels of (5 S)-5, 8-cyclo-dA have also been observed in the breast connective tissue stroma of women between 33 and 46 years of age, which correlates with the known sharp increase in breast cancer incidence for women of this age group. [Pg.195]

Given the complex biological and chemical interaction between the polymeric implants and the in vivo environment of the host, the physiochemical properties of the polymers must be carefully considered in the selection of polymeric biomaterials that are biochemically appropriate for specific applications in implantable prostheses. Overall, the ideal material should minimize its adverse effects on the host tissues and immune system while resisting hydrolytic and oxidative degradation to achieve successful device integration and the intended long-term functionality. In addition, the choice of materials depends not only on the functions of the prostheses but also on other factors such as the site of implantation, the age group of recipients, and the intended period of use. [Pg.313]

In aged rats, the rates of transient redox responses of cytochrome oxidase (i.e. initial oxidation followed by re-reduction) are slowed by about 50 % in comparison to young rats (Sylvia et al. 1983). Cortical norepinephrine was similar in both age groups. However, while depletion of cortical norepinephrine causes slowing of the rate of rereduction in young rats by about 50 %, such depletion had no effect on the already slow kinetics of the redox shift of aged rats. [Pg.667]

Chao et al. (2002) investigated peroxisomal P-oxidation activity, a major source of H2O2, as well as well as the peroxisomal anti-oxidant enzyme catalase, in male Fischer-344 rats of four age groups (4, 10, 50, and 100 week old). In the senescent group, the level of decline in both peroxisomal enzyme activities of 30% was surprisingly similar to the decline observed in the hepatic expression of the retinoid X receptor-a protein. [Pg.685]

Allyl Glycidyl Ether. This ether is used mainly as a raw material for silane coupling agents and epichlorohydrin mbber. Epichlorohydrin mbber is synthesized by polymerizing the epoxy group of epichlorohydrin, ethylene oxide, propylene oxide, and aHyl glycidyl ether, AGE, with an aluminum alkyl catalyst (36). This mbber has high cold-resistance. [Pg.77]

Sulfur. Low sulfur stocks and EV sulfur-accelerated systems have better aging resistance. Normally, the oxidation rate increases with the amount of sulfur used in the cure. The increased rate may be due to activation of adjacent C—H groups by high levels of combined sulfur. Saturated sulfides are more inert to oxidation than aHyUc sulfides. Polysulfidic cross-links impart excessive hardening of SBR as compared to more stable monosulfidic cross-links. [Pg.246]


See other pages where Oxidative aging groups is mentioned: [Pg.168]    [Pg.349]    [Pg.685]    [Pg.114]    [Pg.683]    [Pg.685]    [Pg.19]    [Pg.27]    [Pg.167]    [Pg.56]    [Pg.36]    [Pg.644]    [Pg.21]    [Pg.924]    [Pg.552]    [Pg.1115]    [Pg.634]    [Pg.87]    [Pg.125]    [Pg.106]    [Pg.117]    [Pg.590]    [Pg.229]    [Pg.343]    [Pg.19]    [Pg.36]    [Pg.662]    [Pg.392]    [Pg.128]    [Pg.252]    [Pg.229]    [Pg.307]    [Pg.645]    [Pg.51]    [Pg.76]    [Pg.202]    [Pg.438]    [Pg.135]    [Pg.347]    [Pg.374]    [Pg.552]    [Pg.32]    [Pg.283]   
See also in sourсe #XX -- [ Pg.29 , Pg.30 ]




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Aging oxides

Group oxides

Oxidation aging

Oxidative aging

Oxidizing group

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