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Nicotinic acid absorption

A lot of features of MALDI are conveyed by its name it is a desorption ionization, produced by a laser beam, and assisted by a matrix (Figure 2.5). The analyte (1 pmol or less) is mixed with a suitable matrix in a 1 1000 or higher molar ratio. The matrix is composed of a compound with a strong absorption at the wavelength of the laser used. These two factors, matrix excess and its strong absorption, ensure that the energy from the laser pulse is absorbed by the matrix and not by the analyte, thus avoiding its decomposition. Nicotinic acid, sinapinic acid (SA), 2,5-dihydroxy benzoic acid (2,5-DHB) and 2-(4-hydroxyphenylazo)benzoic acid (HABA) are some of the most commonly used matrices for MALDI. [Pg.51]

Other potential adverse effects include impaired absorption of fat-soluble vitamins A, D, E, and K hypernatremia and hyperchloremia GI obstruction and reduced bioavailability of acidic drugs such as warfarin, nicotinic acid, thyroxine, acetaminophen, hydrocortisone, hydrochlorothiazide, loperamide, and possibly iron. Drug interactions may be avoided by alternating administration times with an interval of 6 hours or greater between the BAR and other drugs. [Pg.118]

S. A. Hotchkiss, P. Hewitt, J. Caldwell, W. L. Chen, and R. R. Rowe. Percutaneous absorption of nicotinic acid, phenol, benzoic acid and triclopyr butoxyethyl ester through rat and human skin in vitro Further validation of an in vitro model by comparison with in vivo data. Food Chern. Toxicol. 30 891-899 (1992). [Pg.28]

Evered DF, Sadoogh-Abasian F, Patel PD (1980) Absorption of nicotinic acid and nicotinamide across human buccal mucosa in vivo. Life Sci 27 1649-1651... [Pg.105]

Reduced forms of these coenzymes absorb ultraviolet light near 340 nm, whereas the oxidized forms do not. For NAD at neutral pH, the maximal absorbance band (s = 18000 M cm ) occurs at 260 nm another absorbance band (s = 8000 M cm ) occurs at 230 nm. For NADH, the maximal absorbance band (s = 16900 M cm ) occurs at 259 nm a second absorbance band (s = 6220 M cm ) occurs at 339 nm two weaker bands occur at 234 and 290 nm with respective s values of 6600 M cm and 1300 M cm h The same is true for NADP and NADPH at 339 nm. Occasionally, investigators have used thio-NADH which has a much stronger absorbance around 366 nm. See Absorption Spectroscopy (Fig. 4, pg. 5) Nicotinic Acid Analogs and Coenzymes... [Pg.502]

Values of the dissociation constant due to N in the ring of nicotinic acid and the amide were found to be 3.55 x 10-11 and 2.24 x 10 n (from ultraviolet absorption spectra), whereas the value for the dissociation of amide groups is generally much smaller (acetamide, 3.1 x 10"15). It is, therefore, reasonable to assume that Kt and K4 are large compared with K2 and K3. Using these assumptions, the observed rate, v, is given by... [Pg.263]

The physiologically active forms of niacin are nicotinic acid, nicotinamide, and their coenzymes (93,96). Niacytin and the niacynogens appear to have limited bioavailability, although more work is needed in this area. The absorption and metabolism of niacin has been reviewed (20,93). [Pg.429]

The formation of hydrated cobalt(n) complexes of pyridine carboxylic acids and the subsequent thermal decomposition to lower hydrates has been documented.82,83 Cobalt(n) halides react with 6-methylpicolinic acid (6-mpaH), picolinic acid (paH), nicotinic acid (naH), and pyridine-2,6-dicarboxylic acid (2,6-py) to form Co(6-mpa) (6-mpaH)X (X = Cl, Br, or NCS), Co(naH)nX2 (n = 2, X = Cl, Br n = 3, X = NCS), and Co(pa)(paH)X, EtOH (X = Cl, Br, or NCS) which are all probably octahedral.83 6-Methylpicolinic acid also formed Co(6-mpaH)4X2,2HX (X = Cl or Br) which were formulated [(6-mpaH)2H]2[CoX4], since the electronic spectra show absorptions characteristic of tetrahalogenocobaltate(n) ions.83... [Pg.227]

The power of the method is greatly enhanced by using matrix assistance (matrix assisted laser desorption ionization, or MALDI). Two matrix materials, nicotinic acid and sinapinic acid, which have absorption bands coinciding with the laser employed, have found widespread use and sample molecular weights of up to two to three hundred thousand Da have been successfully analyzed. A few picomoles of sample are mixed with the matrix compound fol-... [Pg.6]

Currently available treatments against atherosclerosis include cholesterol-lowering drugs such as statins, fibrates, nicotinic acid (NA) [8-13] and the cholesterol intestinal absorption inhibitor, ezetimibe (Fig. 1) [14]. [Pg.260]

Sadoogh-Abasian, F. and Evered, D.F. (1980) Absorption of nicotinic acid and nicotinamide from rat small intestine in vitro. Biochimica et Biophysica Acta,... [Pg.493]

Niacin (nicotinic acid pyridine-3-carboxylic acid) and nicotinamide are precursors of NAD+ and NADP+ (Figure 38-19). Niacin occurs in meat, eggs, yeast, and whole-grain cereals in conjunction with other members of the vitamin B group. Little is known about absorption, transport, and excretion of niacin and its coenzyme forms. A limited amount of niacin can be synthesized in the body from tryptophan, but it is not adequate to meet metabolic needs. [Pg.924]

Statins Ezitimibe Omega-3 triglycerides Bile acid sequestrants Fibrates Nicotinic acid derivatives Inhibit HMG-CoA reductase Inhibits absorption of cholesterol from the intestine Inhibit VLDL synthesis in the liver Bind bile acids in the intestine Lower levels of circulating VLDLs and LDLs by unknown mechanism Reduce the release of VLDLs from the liver... [Pg.79]

Figure 2. Biosynthesis of tobacco alkaloids. (A) Formation of nicotinic acid, (B) formation of N-methyl-A -pyrroliniumion, and (C) condensation to produce tobacco alkaloids. Constructed from data of Bush LP, Fannin FF, Chelvarajan RL and Burton HR (1993). In Gorrod JW and Wahren J (eds.) Nicotine and Related Alkaloids Absorption, Distribution, Metabolism and Excretion. Chapman Hall, London, UK. Figure 2. Biosynthesis of tobacco alkaloids. (A) Formation of nicotinic acid, (B) formation of N-methyl-A -pyrroliniumion, and (C) condensation to produce tobacco alkaloids. Constructed from data of Bush LP, Fannin FF, Chelvarajan RL and Burton HR (1993). In Gorrod JW and Wahren J (eds.) Nicotine and Related Alkaloids Absorption, Distribution, Metabolism and Excretion. Chapman Hall, London, UK.
Several new isocyanide complexes of chromium(m) have been prepared by the electrochemical reduction of heavy-metal adducts of chromium(iii) aquocyano-complexes, and characterized by their visible spectra. The chromium 2p- and 3s-orbital ionization potentials in K3[Cr(NCS)6] have been reported, and the lattice parameters for this anion in the salt with diaquotris-(nicotinic acid)holmium(iii) determined. " The absorption spectra of the... [Pg.109]

Nicotinic acid Supplement nicotinamide deficiency, impaired absorption, increased requirements Therapy pellagra, vasomotoric headache, migraine, schizophrenia... [Pg.662]

Figure 4 Absorption spectra produced by a series of acidic nicotinic acid solutions, provided as sealed cell certified reference materials. Measured relative to a solvent blank, at the sample position, in a high-performance reference commercial spectrophotometer. Figure 4 Absorption spectra produced by a series of acidic nicotinic acid solutions, provided as sealed cell certified reference materials. Measured relative to a solvent blank, at the sample position, in a high-performance reference commercial spectrophotometer.

See other pages where Nicotinic acid absorption is mentioned: [Pg.9]    [Pg.352]    [Pg.166]    [Pg.255]    [Pg.1164]    [Pg.95]    [Pg.456]    [Pg.275]    [Pg.1164]    [Pg.377]    [Pg.514]    [Pg.352]    [Pg.160]    [Pg.311]    [Pg.347]    [Pg.352]    [Pg.160]    [Pg.13]    [Pg.292]    [Pg.43]    [Pg.193]    [Pg.442]    [Pg.514]    [Pg.524]    [Pg.524]    [Pg.57]    [Pg.577]    [Pg.679]   
See also in sourсe #XX -- [ Pg.559 ]




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