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Absorption Kinetics (absorption + kinetics)
Selected AbstractsHydrogen Absorption Kinetics and Mechanisms of Rare Earths (La, Ce, Pr, Nd, Tb, Dy) in the H2O Surface Reaction at Room Temperature.CHEMINFORM, Issue 19 2006Hirohisa Uchida Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Absorption kinetics of oxygen scavengersINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 2 2002Gaurav Tewari The oxygen (O2) absorption kinetics of six commercial O2 scavengers were studied. The scavengers were placed in bags which were filled with 240 mL of air, 4.5 L N2 + 15 mL of air, or 3.5 L CO2 + 9 mL of air. The O2 concentration in each bag was measured at hourly intervals for 8 h. The effects of variability among individual scavengers, initial O2 concentrations of 20% or 500 ppm (0.05%), temperatures of 25, 12, 2 or ,1.5 °C, and scavenger capacity on the O2 absorption rate were determined. In addition, the effect of placing scavengers within over-wrapped trays within bags, was examined. Rates of O2 absorption varied by factors of up to 2 between individual O2 scavengers of the same type, but rates of absorption by groups of four scavengers of the same type were similar. Low temperatures gave longer O2 half-life when compared with those at higher temperatures, e.g. O2 half-lives of 7.1 and 1.0 h at ,1.5 and 25 °C, respectively, were obtained for one scavenger type. Shorter O2 half-lives were obtained in air than in N2 atmospheres at the same temperature, e.g. O2 half-lives of 1.0 and 3.3 h in air and N2 at 25 °C, respectively, were obtained for one scavenger type. The O2 absorption reactions were of first order for both high and low initial O2 concentrations. However, O2 concentration was the primary limiting factor for O2 absorption in atmospheres having O2 concentration of 500 ppm because of the dominance of diffusion. Scavengers, when placed within over-wrapped trays within bags had up to 12 times longer O2 half-lives, indicating that the O2 permeable film acts as an O2 barrier when pack atmosphere has low O2 concentrations. To obtain consistent and reproducible results, it is recommended that multiple scavengers be used in a packaging system. The appropriate number should be based on scavenger type, desired O2 absorption rate, storage temperature, and pack atmosphere (air/N2/CO2). [source] Dynamics of 17,-Ethynylestradiol exposure in rainbow trout (Oncorhynchus mykiss): Absorption, tissue distribution, and hepatic gene expression patternENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 11 2006Ann D. Skillman Abstract 17,-Ethynylestradiol (EE2) is a synthetic estrogen identified in sewage effluents. To understand better the absorption kinetics of EE2 and the induction of vitellogenin (VTG) and estrogen receptor , (ER,) mRNA, we subjected male rainbow trout (Onchorynchus mykiss) to continuous water exposures of 125 ng/L of EE2 for up to 61 d. Trout were either repetitively sampled for blood plasma or serially killed at selected time intervals. Vitellogenin, ER, mRNA, and EE2 were measured using enzymelinked immunosorbent assay and using quantitative polymerase chain reaction and gas chromatography,mass spectrometry, respectively. In separate experiments, trout were exposed to EE2 for 7 d, and hepatic gene expression was assessed using a low- and high-density cDNA microarray. The EE2 was rapidly absorbed by the trout, with an apparent equilibrium at 16 h in plasma and liver. The ER, mRNA levels also increased rapidly, reaching near-peak levels by 48 h. In contrast, plasma levels of VTG continuously increased for 19 d. After 61 d, tissues with the highest levels of VTG were the liver, kidney, and testes. Microarray-based gene expression studies provided unexpected results. In some cases, known estrogen-responsive genes (e.g., ER,) were unresponsive, whereas many of the genes that have no apparent link to estrogen function or EE2 toxicity were significantly altered in expression. Of the two microarray approaches tested in the present study, the high-density array appeared to be superior because of the improved quality of the hybridization signal and the robustness of the response in terms of the number of genes identified as being EE2 responsive. [source] Absorption kinetics of oxygen scavengersINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 2 2002Gaurav Tewari The oxygen (O2) absorption kinetics of six commercial O2 scavengers were studied. The scavengers were placed in bags which were filled with 240 mL of air, 4.5 L N2 + 15 mL of air, or 3.5 L CO2 + 9 mL of air. The O2 concentration in each bag was measured at hourly intervals for 8 h. The effects of variability among individual scavengers, initial O2 concentrations of 20% or 500 ppm (0.05%), temperatures of 25, 12, 2 or ,1.5 °C, and scavenger capacity on the O2 absorption rate were determined. In addition, the effect of placing scavengers within over-wrapped trays within bags, was examined. Rates of O2 absorption varied by factors of up to 2 between individual O2 scavengers of the same type, but rates of absorption by groups of four scavengers of the same type were similar. Low temperatures gave longer O2 half-life when compared with those at higher temperatures, e.g. O2 half-lives of 7.1 and 1.0 h at ,1.5 and 25 °C, respectively, were obtained for one scavenger type. Shorter O2 half-lives were obtained in air than in N2 atmospheres at the same temperature, e.g. O2 half-lives of 1.0 and 3.3 h in air and N2 at 25 °C, respectively, were obtained for one scavenger type. The O2 absorption reactions were of first order for both high and low initial O2 concentrations. However, O2 concentration was the primary limiting factor for O2 absorption in atmospheres having O2 concentration of 500 ppm because of the dominance of diffusion. Scavengers, when placed within over-wrapped trays within bags had up to 12 times longer O2 half-lives, indicating that the O2 permeable film acts as an O2 barrier when pack atmosphere has low O2 concentrations. To obtain consistent and reproducible results, it is recommended that multiple scavengers be used in a packaging system. The appropriate number should be based on scavenger type, desired O2 absorption rate, storage temperature, and pack atmosphere (air/N2/CO2). [source] Systematic review: impaired drug absorption related to the co-administration of antisecretory therapyALIMENTARY PHARMACOLOGY & THERAPEUTICS, Issue 12 2009E. LAHNER Summary Background, Due to suppression of gastric acidity during antisecretory therapy, an impaired absorption of co-administered drugs may occur. Aim, To review evidence of impaired drug absorption related to the use of co-administered PPIs or H2RAs. Methods, Systematic search of MEDLINE/EMBASE/SCOPUS databases (1980,September 2008) for English articles with keywords: drug malabsorption and absorption, stomach, anti-secretory/acid inhibitory drugs, histamine H2 antagonists, PPIs, gastric acid, pH, hypochlorhydria, gastric hypoacidity. From 2126 retrieved articles, 16 randomized crossover studies were identified investigating impaired absorption of nine different drugs in association with co-administration of PPIs or H2RAs. Information on investigated drug, study type, features of investigated subjects, study design, type of intervention, and study results were extracted. Results, The identified studies investigated the absorption kinetics of nine drugs. Acid suppression reduced absorption of ketoconazole, itraconazole, atazanavir, cefpodoxime, enoxacin and dipyridamole (median Cmax reduction by 66.5%). An increased absorption of nifedipine and digoxin (median AUC increase by 10%) and a 2-fold-increase in alendronate bioavailability were observed. Conclusions, Gastric pH appears relevant for absorption of some cardiovascular or infectious disease agents. Antisecretory treatment may significantly modify the absorption of co-administered drugs. [source] In situ kinetic modelling of intestinal efflux in rats: functional characterization of segmental differences and correlation with in vitro resultsBIOPHARMACEUTICS AND DRUG DISPOSITION, Issue 5 2007Isabel González-Alvarez Abstract The objective was to devise and apply a novel modelling approach to combine segmental in situ rat perfusion data and in vitro cell culture data, in order to elucidate the contribution of efflux in drug absorption kinetics. The fluoroquinolone CNV97100 was used as a model P-gp substrate. In situ intestinal perfusion was performed in rat duodenum, jejunum, ileum and colon to measure the influence of P-gp expression on efflux. Inhibition studies of CNV97100 were performed in the presence of verapamil, quinidine, cyclosporin A and p -aminohippuric acid. Absorption/efflux parameters were modelled simultaneously, using data from both in situ studies as well as in vitro studies. The maximal efflux velocity was modelled as a baseline value, corrected for each segment based on the expression level. CNV97100 passive diffusional permeability (Pdiff) and its affinity for the efflux carrier (Km) were assumed to be the same in all segments. The results indicate the new approach to combine in situ data and in vitro data succeed in yielding a unified, quantitative model for absorption/efflux. The model incorporated a quantitative relationship between P-gp expression level and the efflux functionality, both across in situ and in vitro systems, as well across different intestinal segments in the in situ studies. Permeability values decreased from duodenum to ileum in accordance with the increasing P-gp expression levels in rat intestine. The developed model reflects a strong correlation between in vitro and in situ results, including intrinsic differences in surface area. The successful application of a model approach to combine absorption data from two different experimental systems holds promise for future efforts to predict absorption results from one system to a second system. Copyright © 2007 John Wiley & Sons, Ltd. [source] Strategies for the Improvement of the Hydrogen Storage Properties of Metal Hydride MaterialsCHEMPHYSCHEM, Issue 15 2008Hui Wu Abstract Metal hydrides are an important family of materials that can potentially be used for safe, efficient and reversible on-board hydrogen storage. Light-weight metal hydrides in particular have attracted intense interest due to their high hydrogen density. However, most of these hydrides have rather slow absorption kinetics, relatively high thermal stability, and/or problems with the reversibility of hydrogen absorption/desorption cycling. This paper discusses a number of different approaches for the improvement of the hydrogen storage properties of these materials, with emphasis on recent research on tuning the ionic mobility in mixed hydrides. This concept opens a promising pathway to accelerate hydrogenation kinetics, reduce the activation energy for hydrogen release, and minimize deleterious possible by-products often associated with complex hydride systems. [source] | |||||||||||||