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Antioxidant immobile

Acylations of carbohydrate derivatives such as alkyl glucosides and galactosides have also been successfully performed in ionic liquids [63]. Similarly, the flavonoid glycosides naringin and rutin were acylated with vinyl butyrate in ionic liquid media in the presence of a number of lipases, e.g., CaLB (Novozym 435), immobilized TIL, and RmL [119]. The products are of interest for application as strong antioxidants in hydrophobic media. [Pg.238]

Two interesting recent modifications of Anelli s protocol involve the employment of silica-supported TEMPO40 and a kind of polymer-immobilized TEMPO (PIPO)41 PIPO is easily prepared from a cheap polymer called Chimassorb 944 that is used as an antioxidant and light stabilizer for plastics. [Pg.246]

Next, some typical examples will be presented of how a DNA-electrochemical biosensor is appropriate to investigate the DNA damage caused by different types of substances, such as the antioxidant agent quercetin (Scheme 20.1), an anticancer drug adriamycin (Scheme 20.2) and nitric oxide. In all cases, the dsDNA damage is detected by changes in the electrochemical behaviour of the immobilized dsDNA, specifically through modifications of the purinic base oxidation peak current [3,5,40]. [Pg.418]

HYDROPHOBIZED SILICA NANOCOMPOSITES WITH IMMOBILIZED ANTIOXIDANTS (VITAMINS C AND E)... [Pg.307]

Abstract. Adsorption of antioxidants (vitamins C and E) from aqueous and ethanol solutions on unmodified and partially hydrophobized nanosilica A-200 was studied using UV spectroscopy and quantum chemical methods with consideration for the solvent effects. Antioxidant power of silica nanocomposites with immobilized vitamins was evaluated by measuring the total polyphenolic index following the Folin-Ciocalteu method. It has been shown that immobilization of vitamins on silica surface leads to their stabilization. Being released from the carrier molecules of vitamins do not lose their antioxidant properties... [Pg.307]

Oxidative stress or imbalance between formation and deactivation of free radicals is considered to be one of the main causes of many known human diseases.1,2 Vitamins E and C are among the most attractive objects for prophylactic drug development.2,3 Aside from being natural antioxidants of direct action, their combination results in a synergistic effect.4 However, obtaining stable formulations remains a challenge since these vitamins are readily oxidized in a liquid medium. Immobilization of such biomolecules on solid surfaces may result in enhanced stabilization. [Pg.307]

Highly disperse silica is widely used in pharmaceutical formulations as a filler, adsorbent, thickener etc.5 Their high hydrophilicity and the absence of emulsifying ability restrict their application. In contrast to hydroxylated silica, partially or fully hydrophobized silica may exhibit improved properties as a drug carrier. The main goal of this work is to study hydrophobized silica nanocomposites with immobilized vitamins C and E. Investigations of adsorption-desorption processes which involve silica nanoparticles and the antioxidants are described. Factors affecting the antioxidant stability have also been carefully considered. [Pg.308]

Antioxidant activity of silica nanocomposites with immobilized vitamin C was tested using the polyphenolic activity index.8 After adsorption of ascorbic acid on the silica surface and centrifugation, the excess solution was removed to obtain the suspension of a fixed volume (2 ml). Distilled water, sodium carbonate solution, and Folin-Ciocalteu s phenol reagent were subsequently added to suspensions and to the reference Vitamin C solution. The suspensions were then stored for 30 min, and the optical density of supernatant was measured at X = 750 nm. The reference solution of ascorbic acid was used to compare antioxidant activity of vitamin-containing nanocomposites with the activity of dissolved vitamin C. [Pg.309]

To obtain silica nanocomposites with immobilized antioxidants, and to test their antioxidant activity, vitamins C and E were adsorbed onto nanosilica from ethanol solution containing both vitamins. A desorption experiment was then carried out. After the desorption of ascorbic acid from modified silica (0tms -0.40) into aqueous medium, the solvent was changed and the desorption of vitamin E into ethanol was studied. As one can see (Figure 6), both vitamins can be released from the surface for 1-2 hours. It should be noted that no increase in vitamin C concentration was detected in aqueous solution after its contact with A-200 for more than 30 min. Thus, as is the case for vitamins Bj and B6, desorption of vitamin C from the surface of modified silica is slower in... [Pg.312]

Table 1. Antioxidant activity of silica nanocomposites with immobilized vitamin C... Table 1. Antioxidant activity of silica nanocomposites with immobilized vitamin C...
Partial silylation of the highly disperse silica surface enhances the adsorption of vitamin E from ethanol solution, and provides the ability to obtain water-soluble nanocomposites containing vitamin E. Immobilization of vitamin C on the silica surface prevents its oxidation. Its interaction with the adsorbent surface leads to a decrease in proton-donor ability of the OH-groups involved in the oxidation of ascorbic acid. Elydrophobized silica nanocomposites are characterized by a prolonged desorption of immobilized vitamins. It has been shown that vitamin C does not lose its antioxidant properties after desorption. [Pg.313]

Such imbalanced antioxidant systems in schizophrenia could lead to oxidative stress- and ROS-mediated injury as supported by increased lipid peroxidation products and reduced membrane polyunsaturated fatty acids (PUFAs). Decrease in membrane phospholipids in blood cells of psychotic patients (Keshavan et al., 1993 Reddy et al., 2004) and fibroblasts from drug-naive patients (Mahadik et al., 1994) as well as in postmortem brains (Horrobin et al., 1991) have indeed been reported. It has also been suggested that peripheral membrane anomalies correlate with abnormal central phospholipid metabolism in first-episode and chronic schizophrenia patients (Pettegrewet al., 1991 Yao et al., 2002). Recently, a microarray and proteomic study on postmortem brain showed anomalies of mitochondrial function and oxidative stress pathways in schizophrenia (Prabakaran et al., 2004). Mitochondrial dysfunction in schizophrenia has also been observed by Ben-Shachar (2002) and Altar et al. (2005). As main ROS producers, mitochondria are particularly susceptible to oxidative damage. Thus, a deficit in glutathione (GSH) or immobilization stress induce greater increase in lipid peroxidation and protein oxidation in mitochondrial rather than in cytosolic fractions of cerebral cortex (Liu et al., 1996). [Pg.289]

In addition to free fatly acids and their esters as previously described, compounds with antioxidant potency were also used as acyl donors. In order to investigate the synthesis of hybrid antioxidants, the enzymatic acylation of escuhn catalyzed by immobilized CALB in the ionic liquids [bmtm]BF4 and [bmim]PF6 was investigated using several phenolic acids as well as their corresponding vinyl esters. [Pg.131]

The migration principle was suggested as the reason of the enhancement of the antioxidant activity of polyester-polyether elastomer-bound hindered phenol by the addition of 0.25% of an easier migrating AO, 4,4 -bis(a,a-dimethylbenzyl)di-phenylamine (5) [181] this easier migrating amine is regenerated by the immobilized phenolic moiety, by means of the principle of homosynergism [5]. Similarly, a blend of polymeric redox hydroquinone-benzoquinone AO with equal amounts of iV-phenyl-iV -(l,3-dimethylbutyl)-l,4-phenylenediamine exerted a pronounced increase of antioxidant efficiency in SBR [124]. A synergistic combination based... [Pg.158]

All in all, there are at least forty-one elements in most human bodies, of which only twenty-one are known to be essential. We cannot assume that just because an element is found in the human body, it must serve some purpose. Our natural defenses, such as the white blood cells, antibodies, antioxidants, and macrophages, don t attack or immobilize toxic or nonessential chemical elements and remove them from the body as they do with harmful bacteria or viruses.We pick up some of these unneeded or unwanted elements from our food, water, and air, and they simply settle in the body, usually in the fatty tissue, liver, or bones. There are ways of getting them out, which I will mention later. [Pg.57]

Compared to conventional antioxidants, reactive antioxidants that are capable of becoming covalently bound to the polymer backbone are not readily lost from polymers during fabrication and in-service. There is a lot of evidence that demonstrates the performance (in terms of polymer protection) of immobilized antioxidants in practice, especially when polymer products are subjected to harsh environment, e.g., exposure to high temperatures, UV-light and leaching solvents. It is clear from this that high mobility of low molar mass antioxidants is not a necessary prerequisite to achieving stabilization and attachment of antioxidants to polymers can be industrially beneficial. [Pg.97]

Macromolecular stabilizers are immobile in the polymer matrix [284], This is unfavourable for applications where surface concentration of stabilizers in thick-walled products should remain high. It was reported [34] that rubber-bound derivatives of PD provide only very poor antiozonant protection. Their antioxidant efficiency was only comparable with that of conventional HMW PD. This indicates that application of polymer-bound amines in rubbers has the prospect of exclusive long-term use in extracting media. [Pg.171]


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See also in sourсe #XX -- [ Pg.17 ]




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