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Caffeine Ethanol

Sample mixture. A suitable sample mixture is obtained by weighing out accurately about 0.601 g of aspirin, 0.076 g of phenacetin and 0.092 g of caffeine. Dissolve the mixture in 10 mL absolute ethanol, add 10 mL of 0.5M ammonium formate solution and dilute to lOOmL with de-ionised water. [Pg.233]

Animal studies indicate that trichloroethylene can sensitize the heart to epinephrine-induced arrhythmias. Other chemicals can affect these epinephrine-induced cardiac arrhythmias in animals exposed to trichloroethylene. Phenobarbital treatment, which increases the metabolism of trichloroethylene, has been shown to reduce the trichloroethylene-epinephrine-induced arrhythmias in rabbits (White and Carlson 1979), whereas high concentrations of ethanol, which inhibits trichloroethylene metabolism, have been found to potentiate trichloroethylene-epinephrine-induced arrhythmias in rabbits (White and Carlson 1981). These results indicate that trichloroethylene itself and not a metabolite is responsible for the epinephrine-induced arrhythmias. In addition, caffeine has also been found to increase the incidence of epinephrine-induced arrhythmias in rabbits exposed to trichloroethylene (White and Carlson 1982). [Pg.172]

Figure 5 Separation of pharmaceuticals, including amines, on strong cation exchange. Column 0.46 x 15 cm Merckosorb SI-60-SCX, 5 p. Eluent 50 mM aqueous ammonium formate-10% ethanol, pH 4.8. Flow 1 ml/min. Temperature 50°C. The peaks are (1) aspirin, (2) paracetamol, (3) phenacetin, (4) caffeine, (5) phenylephrine, (6) salbutamol. (Reproduced with permission of Elsevier Science from Cox, G. B., Loscombe, C. R., Slucutt, M. J., Sugden, K., and Upheld, J. A., /. Chromatogr., 117, 269, 1976). Figure 5 Separation of pharmaceuticals, including amines, on strong cation exchange. Column 0.46 x 15 cm Merckosorb SI-60-SCX, 5 p. Eluent 50 mM aqueous ammonium formate-10% ethanol, pH 4.8. Flow 1 ml/min. Temperature 50°C. The peaks are (1) aspirin, (2) paracetamol, (3) phenacetin, (4) caffeine, (5) phenylephrine, (6) salbutamol. (Reproduced with permission of Elsevier Science from Cox, G. B., Loscombe, C. R., Slucutt, M. J., Sugden, K., and Upheld, J. A., /. Chromatogr., 117, 269, 1976).
Liver metabolism is affected by methylxanthines. In high doses, theophylline and caffeine increase the level of cyclic AMP. Very high levels of methylxanthines decrease the level of branched chain and aromatic amino acids in plasma. Coffee appears to have little effect on ethanol metabolism. [Pg.235]

Falk, J. L., Zhang, J., Chen, R., and Lau, C. E., A schedule induction probe technique for evaluating abuse potential Comparison of ethanol, nicotine and caffeine, and caffeine-midazolam interaction. Special Issue Behavioural pharmacology of alcohol. Behavioural Pharmacology 5(4-5), 513-520, 1994. [Pg.301]

Also, hydrates are more soluble in water-miscible solvents than are the corresponding anhydrous forms. For example, the solubility of caffeine hydrate is lower than that of anhydrous caffeine in water but higher in ethanol. The maximum concentration seen may be due to the solubility of the anhydrous crystalline phase or due to a temporary steady state in which the rate of dissolution of the metastable anhydrous form and the rate of crystallization of the stable hydrate are equal. The decreasing concentration represents crystallization of the stable hydrate from a solution supersaturated with respect to it. If the maximum concentration of the solute in the dissolution experiment corresponds to the solubility, then the initial increase in concentration follows the Noyes-Whitney equation [15]. Van t Hoff plots of log solubility versus the reciprocal of temperature give linear relationships (Fig. 16). [Pg.611]

A commercial analgesic tablet is stated on the packet to contain 325 mg of aspirin and 50 mg of caffeine per tablet. Two tablets + 0.0773 g of phenacetin were shaken with 10 cm3 of ethanol for 10 minutes, then 10 cm3 of 0.5 mol dm 3 ammonium formate were added and the mixture made up to 100 cm3. The tablets contain insoluble excipients, so a little of the solution was filtered before chromatography --- ... [Pg.173]

Franks FIM, Flagedorn FI, Flensley VR, Flensley WJ, Starmer GA. (1975). The effect of caffeine on human performance, alone and in combination with ethanol. Psychopharmacologia. 45(2) 177-81. Franks P, Flarp J, Bell B. (1989). Randomized, controlled trial of clonidine for smoking cessation in a primary care setting. JAMA. 262(21) 3011-13. [Pg.451]

Ethanol, nicotine, caffeine, and phencyclidine stimulate both locomotor activity and dopamine turnover (Wise 1987). Sex differences in DA outflow in the NAC has been shown in response to ethanol. Female rats have a greater ethanol-induced DA outflow, as measured by microdialysis in the NAC, than males and this sexually dimorphic response is regionally specific as it is not observed in the striatum additionally, females consume more alcohol (Blanchard et al. 1993). [Pg.268]

Madden PAF, Heath AC, Starmer GA, Whitfield JB, Martin NG (1995) Alcohol sensitivity and smoking history in men and women. Alcohol Clin Exp Res 19 1111-1120 Malin DH, Alvarado CL, Woodhouse KS, Karp H, Urdiales E, Lay D, et al (2002) Passive immunization against nicotine attenuates nicotine discrimination. Life Sci 70 2793-2798 Mitchell SH, deWit H, Zacny JP (1995) Effects of varying ethanol dose on cigarette consumption in healthy normal volunteers, Behav Pharmacol 6 359-365 Mumford GK, Evans SM, Kaminski BJ, Preston KL, Sannerud CA, Silverman K, Griffiths RR (1994) Discriminative stimulus and subjective effects of theobromine and caffeine in humans. Psychopharmacology 115 1-8... [Pg.398]

Examples of solvent-mediated transformation monitoring include the conversion of anhydrous citric acid to the monohydrate form in water [235,236], CBZ with water [237] and ethanol-water mixtures [238,239], and cocrystallization studies of CBZ, caffeine, and theophylline with water [240]. Raman spectroscopy was used to monitor the crystallization rate and solute and solvent concentrations as griseofulvin was removed from an acetone solution using supercritical CO2 as an antisolvent [241]. Progesterone s crystallization profile was monitored as antisolvent was added [242]. [Pg.226]

After terminating the coupling reaction with ascorbic acid, reaction mixture clarified by precipitating protein with ethanol Turbidity decreased by final addition of caffein, sodium benzoate, and Teepol micromethod After the coupling reaction with ascorbic acid is terminated, azo color is extracted and read low blank the extract can be applied directly to a thin-layer plate and be separated rapidly to determine the ratio BMC BDC Micro versions assay artificially activated enzyme... [Pg.246]

Following the development of the test, an in-house validation was conducted to evaluate the performance of FETAX compared to the results in the rat and/or rabbit. Thirteen reference chemicals were tested including eight compounds known to be teratogenic in rats and/or rabbits (caffeine, retinoic acid, hydroxyurea, ethanol, cyclophosphamide, nicotine, acetylsalicylic acid, dexametha-sone) and five non-teratogens (isoniazid, saccharin, paracetamol, penicillin G, sildenafil). The estimation of teratogenicity in rats and rabbits was based on published data (9). [Pg.408]

Certain foreign compounds may cause the retention or excretion of water. Some compounds, such as the drug furosemide, are used therapeutically as diuretics. Other compounds causing diuresis are ethanol, caffeine, and certain mercury compounds such as mersalyl. Diuresis can be the result of a direct effect on the kidney, as with mercury compounds, which inhibit the reabsorption of chloride, whereas other diuretics such as ethanol influence the production of antidiuretic hormone by the pituitary. Changes in electrolyte balance may occur as a result of excessive excretion of an anion or cation. For example, salicylate-induced alkalosis leads to excretion of Na+, and ethylene glycol causes the depletion of calcium, excreted as calcium oxalate. [Pg.236]

Separation selectivity was demonstrated by extraction of salicylic acid from pH 2 solutions in the presence of a 60-fold excess of ethanol and sixfold excesses of barbituric acid and caffeine. No measurable interference was observed. Experiments showed that the principal selectivity is in the extraction rather than the back extraction step. This finding indicated that the polar and/or ionic nature of these interferences prevents retention by polymer. Preconcentration of analyte was examined by means of extraction from a flowing stream and back extraction into a minimum volume. The extractor tube length was 4.3 m, and the sample was 10 mL of 1 mM oxine with an extraction time of 2.0 min. The back extractant was 80 pL of 0.2 M NaOH. A sevenfold increase in concentration was observed. Enhanced preconcentration can be expected with smaller tubing diameter-to-length ratios, larger sample volumes, and repetitive use of back extractant. [Pg.351]

Grant and Higuchi (1990) commented on the solution behavior of solvates in their book on the solubility of organic compounds. The hydrated form will be more stable (less soluble) than the anhydrate in the general case. When the solvate is formed from a nonaqueous solvent that is miscibli in water, the free energy of solution of the solvent into the water reduces the activity of water and increases the apparent solubility of the solvate. An example is cited in which caffeine hydrate is less soluble in water than the anhydrate, but the solubility order reverses in ethanol. [Pg.554]

Drugs that show extensive tissue binding are said to have an apparent volume of distribution many times the total body size. For example, digoxin (see Chapter 35), which binds to plasma protein to the extent of 23%, has an apparent volume of distribution of 8 1/kg. The volume of distribution of drugs that do not bind to plasma or tissue proteins varies between the extracellular fluid volume (16 liters) and the total body water (42 liters). Insulin, sodium, and iodine are confined to the extracellular water, whereas caffeine and ethanol are distributed in the total body water. [Pg.12]

Caffeine-arsenic, butadiene, pylorus ligated Stress, pylorus ligated, Escherichia coll Acetic acid, pylorus ligated Ethanol, indomethacin Psychological stress Stress, HC1... [Pg.596]

Lumley M, Roehrs T, Asker D. Ethanol and caffeine effects on daytime sleepi-ness/alertness. Sleep 1987 10 306-312. [Pg.24]

Noxious substances inhaled when smoking, caffeine absorbed from coffee or other drinks, ethanol-uptake from alcoholic drinks are examples of potentially neurobehavioral teratogens absorbed by pregnant women as part of everyday social life patterns. [Pg.276]


See other pages where Caffeine Ethanol is mentioned: [Pg.1170]    [Pg.109]    [Pg.400]    [Pg.668]    [Pg.1170]    [Pg.1170]    [Pg.109]    [Pg.400]    [Pg.668]    [Pg.1170]    [Pg.65]    [Pg.536]    [Pg.28]    [Pg.33]    [Pg.169]    [Pg.658]    [Pg.261]    [Pg.263]    [Pg.195]    [Pg.101]    [Pg.119]    [Pg.402]    [Pg.373]    [Pg.313]    [Pg.408]    [Pg.55]    [Pg.813]    [Pg.14]    [Pg.71]    [Pg.530]    [Pg.177]    [Pg.441]    [Pg.230]    [Pg.356]   
See also in sourсe #XX -- [ Pg.56 ]




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