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Selection product labeling

This enzyme catalyzes the conversion of pyruvate to formate and acetyl CoA and is a key enzyme in the anaerobic degradation of carbohydrates in some Enterobacteriaceae. Using an enzyme selectively C-labeled with glycine, it was shown by EPR that the reaction involves production of a free radical at C-2 of glycine (Wagner et al. 1992). This was confirmed by destruction of the radical with O2, and determination of part of the structure of the small protein that contained an oxalyl residue originating from gly-734. [Pg.289]

Recent data suggest that COX-2 inhibitors, including rofe-coxib, valdecoxib, and celecoxib, may increase the risk for MI and stroke.47 There is also some evidence that the non-selective NSAIDs may increase the risk for cardiovascular events.47,48 Rofecoxib was withdrawn from the market in late 2004 because of safety concerns. The FDA requested the withdrawal of valdecoxib from the market in 2005. The FDA also asked the manufacturers of celecoxib and non-selective NSAIDs (prescription and over-the-counter) to include information about the potential adverse cardiovascular effects of these drugs in their product labeling. The cardiovascular risk with COX-2 inhibitors and NSAIDs may be greatest in patients with a history of, or with risk factors for, cardiovascular disease. The American Heart Association recommends that the use of COX-2 inhibitors be limited to low-dose, short-term therapy in patients for whom there is no appropriate alternative.48 Patients with cardiovascular disease should consult a clinician before using over-the-counter NSAIDs. [Pg.80]

Selectivity for COX-1 versus COX-2 is variable and incomplete for the older NSAIDs, but many selective COX-2 inhibitors have been synthesized. The selective COX-2 inhibitors do not affect platelet function at their usual doses. In testing using human whole blood, aspirin, ibuprofen, indomethacin, piroxicam, and sulindac are somewhat more effective in inhibiting COX-1. The efficacy of -2-selective drugs equals that of the older NSAIDs, while gastrointestinal safety may be improved. On the other hand, selective COX-2 inhibitors may increase the incidence of edema and hypertension. As of December 2008, celecoxib and the less selective meloxicam are the only COX-2 inhibitors marketed in the USA. Rofecoxib and valdecoxib, two previously marketed, selective COX-2 inhibitors, have been withdrawn from the market due to their association with increased cardiovascular thrombotic events. Celecoxib has an FDA-initiated "black box" warning concerning cardiovascular risks. It has been recommended that all NSAID product labels be revised to include cardiovascular risks. [Pg.800]

Possibly the most important, and least understood, aspect of spray-dried flavorings manufacture is the role the wall material plays in this process. The polymers utilized for this product are controlled by FDA constraints, cost, finished product labelling considerations and compatability, functionality and historical usage. Given these considerations, polymers selected for the retention and maintenance of labile flavors and aromas in industrial spray dried, food grade systems include both carbohydrate (hydrolyzed starches, "lipophilic starches, plant exudates) and protein. The importance of these wall materials should not be underestimated. [Pg.13]

R. Bernstein, S.M. Thornberg, R.A. Assink, A.N. Irwin, J.M. Hochrein, J.R. Brown, D.K. Derzon, S.B. Klamo, and R.L. Clough, The origins of volatile oxidation products in the thermal degradation of polypropylene, identified by selective isotopic labeling. Polym. Degrad. Stab., 92, 2076-2094 (2007). [Pg.39]

In the framework of equation 41, it may be observed that the desilylation of the intermediate arenium ion competes with the deprotonation process, so that a H/D kinetic isotope effect (KIE) is expected to arise when the MejSi"1" transfer competes with either H+ or D+ transfer. Indeed, kinetic isotope effects for the formation of silylated products arising from the different rates of H+ vs D+ transfer have been reported from the reaction of selectively D-labelled toluene and 1,2-diphenylethane or from mixtures of unlabelled and labelled substrates (Table l)121 —123. The kinetic isotope effects listed in Table 1 are the ones reported when the base used is Et3N. The use of bases of different strength to effect the H+ or D+ transfer should have an influence on the observed kinetic isotope effect. The role of the base on the values of the KIE was indeed verified in the competitive silylation of CH3C6H5/CD3C6D5 mixtures122. [Pg.1046]

To try to circumvent this limitation, Jestin et al. [68] have designed and tested a selection scheme involving two chemically independent reactions the reaction catalyzed by the enzyme and a chemical reaction leading to phage labeling by the substrate or product of the enzymatic reaction. Selection of labeled phages with a product-specific binder (e.g. a monoclonal antibody) should allow recovery of the product-labeled phages only (Fig. 5.15). [Pg.105]

The most well accepted feature of the mechanism is the formation of an allylic intermediate via a-hydrogen abstraction from propylene in the ratedetermining step. The structure of this intermediate and its subsequent steps involved in its conversion to selective products are much less well understood. It has been suggested from deuterium-labeling studies (77) that this intermediate undergoes a second hydrogen abstraction followed by O (oxidation) or N insertion (ammoxidation) (Scheme 3). The formation of an... [Pg.147]

U.S. laundry detergents are typically Newtonian fluids and the viscosity of six commercial products is summarized in Figure 4.23. Several lots of each product, labeled A to F, were obtained and measurements completed at room temperature, 20 to 25°C, as a function of shear rate from 0 to 500 sec-1. Atypical shear stress-shear rate diagram is shown in Figure 4.24 for a product sampled from a 50 11 oz container. All six products tested are Newtonian with a viscosity less than 0.5 Pa s at room temperature, 21 to 23°C, with the shear rate ramped from 0 to 500 sec-1 at an acceleration rate of 0.83 sec-2. Newtonian behavior was confirmed through additional step shear rate measurements within the selected shear rate range. [Pg.103]

Manufactiirer/Seller In the absence of major constraints the manufacturer approaches labeling from the perspective of sales and market advantage. The label is perceived as a device to facilitate product use and selection, and labeling efforts are devoted toward improvement of the label s effectiveness as a sales support tool, and means of product image differentiation. [Pg.9]

There is a difference between exposure to a product label and perception of that label by the person exposed. Exposure sets up a potential for label perceptions and related behavior, whereas attention processes determine whether and to what extent the potential will become an actual perception. In general, attention deals with the selectivity of perception and cognition in people. People do not perceive or organize every possible stimulus to which they are exposed. They attend or focus on certain aspects of this potential. The process of focusing on a limited portion of the potential information surrounding a person, or, when perception occurs, on a fraction of this information is attention. [Pg.12]

Muir et al. [217,218] also reported a convenient in vitro chemical ligation strategy that allows folded recombinant proteins to be joined together. This strategy permits segmental, selective isotopic labeling of the product [219]. [Pg.409]


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See also in sourсe #XX -- [ Pg.62 ]




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Labeling selective

Product labelling

Product selection

Selection labeling

Selectively labelled

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