Spectrofluorimetric flow injection method for the individual and successive determination of L-cysteine and L-cystine in pharmaceutical and urine samples.

A flow injection configuration is proposed for the determination of L-cysteine and L-cystine individually and for mixtures of both analytes. The procedure is based on the rapid oxidation of L-cysteine by thallium(III) with concomitant formation of fluorescent thallium(I). The inclusion of a selecting valve and of a copper-coated cadmium column in the configuration allows the successive determination of two analytes. Linear calibration graphs were obtained between 5 x 10(-6) and 5 x 10(-5) mol dm-3 of L-cysteine and between 2 x 10(-6) and 2 x 10(-5) mol dm-3 of L-cystine. The applicability of the method to the determination of L-cysteine and L-cystine in pharmaceutical preparations was demonstrated by investigating the effect of potential interferents and by the analysis of commercial preparations. The method was successfully applied to the determination of L-cysteine and L-cystine in urine samples.     

Determination of epinephrine, norepinephrine, dopamine and L-dopa in pharmaceuticals by a photokinetic method.

A study of the photochemical reaction of the Rose Bengal (RB)-ethylenediaminetetraacetic acid system in the presence of epinephrine, norepinephrine, dopamine and L-dopa is presented. The rate of photoreduction of RB is dramatically retarded by small amounts of these catecholamines, which have an inhibitory effect on the excited state of RB, which is the activator of the process. Optimum conditions for the determination of catecholamines in the range of concentration between 5 x 10(-6) and 1 x 10(-4) mol dm-3 are described. The proposed method has been applied with excellent results to the determination of catecholamines in pharmaceuticals.     

On the theory of the weighing method for automatic crystal shape control in czochralski growth

We derive the exact analytical expression for the meniscus volume in terms of the crystal radius R, the melt contact angle θ_L, and the meniscus height h for the axisymmetric planar growth interface Czochralski configuration. This relation is applied together with motion and mass balance considerations to find the general rate of change in the force experience by the weighing cell in a standard diameter control arrangement. In contrast to the classical work of Bardsley et al. (1977), which is limited to the close viscinity of stationary right cylinder growth, our results are valid for growth developing any crystal profile. In addition, they also account for the fall of melt level due to finite crucible size. The magnitudes of the capillary contributions to the force, and their implications for diameter servo control, are discussed over a wide range of profile parameters using the Tsivinskii formula for h = h (R, θ_L).     

Using Microfluidic Set-Up to Determine the Adsorption Rate of Sporosarcina pasteurii Bacteria on Sandstone

Transport in Porous Media - Microbial-induced carbonate precipitation (MICP) in porous media is a two-step procedure: First, the suspension of bacteria is injected and some of the bacteria get...     

Spectrofluorometric determination of hesperidin by manual and flow-injection methods

A reliable and highly sensitive method for the determination of hesperidin is described. It involves the formation of a highly fluorescent complex between hesperidin and aluminium (III) in a micellar medium. There is a linear relationship between fluorescence intensity (λ_em = 496 nm, λ_ex = 391 nm) and hesperidin concentration over the range 5 × 10^–7– 2 × 10^–5 mol L^–1. The detection limit is 79 μg L^–1. The method can easily be adapted to a flow system using a three-channel manifold, the peak height being proportional to the hesperidin concentration over the range 1 × 10^–6– 1 × 10^–4 mol L^–1. Manual and flow-injection procedures have been successfully applied to the determination of hesperidin in orange peel and orange juice. Received: 21 October 1998 / Revised: 16 December 1998 / Accepted: 25 December 1998     

A combined density functional theory and molecular mechanics (QM/MM) study of single site ethylene polymerization catalyzed by [Cp{NC(tBu)2}TiR+] in the presence of the counterion,CH3B(C6F5)3−

A density functional study was conducted on the approach and insertion of ethylene monomer into the Ti-C_α bond of the catalyst system, CpNC(^tBu)₂RTi-μ-Me-B(C₆F₅)₃ (R= methyl, propyl). A validated QM/MM model was used to represent the counterion. Solvent effects were incorporated with single point solvent calculations done with cyclohexane (ϵ = 2.023) as the solvent. For R=Me (the initiation step), approach and insertion of the ethylene was found to be endothermic, with the barrier for insertion being 12.7 kcal/mol for the most favourable case. For R=Pr (the propagation step), the insertion barrier was found to decrease slightly (11.5 kcal/mol for the most favorable case), corroborating experimental evidence of decrease in insertion barrier with increase in chain length. Termination by chain transfer to monomer was also considered, and found to be unfavourable, in comparison to insertion, by 8.6 kcal/mol for the propagation step. Solvent effects were found to be significant for the propagation step, changing the rate determining step from insertion to uptake for the most favorable case of insertion.     

The Donor-Dependent and Colon-Region-Dependent Metabolism of (+)-Catechin by Colonic Microbiota in the Simulator of the Human Intestinal Microbial Ecosystem

The intestinal absorption of dietary catechins is quite low, resulting in most of them being metabolized by gut microbiota in the colon. It has been hypothesized that microbiota-derived metabolites may be partly responsible for the association between catechin consumption and beneficial cardiometabolic effects. Given the profound differences in gut microbiota composition and microbial load between individuals and across different colon regions, this study examined how microbial (+)-catechin metabolite profiles differ between colon regions and individuals. Batch exploration of the interindividual variability in (+)-catechin microbial metabolism resulted in a stratification based on metabolic efficiency: from the 12 tested donor microbiota, we identified a fast- and a slow-converting microbiota that was subsequently inoculated to SHIME, a dynamic model of the human gut. Monitoring of microbial (+)-catechin metabolites from proximal and distal colon compartments with UHPLC-MS and UPLC-IMS-Q-TOF-MS revealed profound donor-dependent and colon-region-dependent metabolite profiles with 5-(3′,4′-dihydroxyphenyl)-γ-valerolactone being the largest contributor to differences between the fast- and slow-converting microbiota and the distal colon being a more important region for (+)-catechin metabolism than the proximal colon. Our findings may contribute to further understanding the role of the gut microbiota as a determinant of interindividual variation in pharmacokinetics upon (+)-catechin ingestion.     

Correlated correlation functions in random-bond ferromagnets

The two-dimensional random-bond Q-state Potts model is studied for Q near 2 via the perturbative renormalisation group to one loop. It is shown that weak disorder induces cross-correlations between the quenched-averages of moments of the two-point spin/spin and energy/energy correlation functions, which should be observable numerically in specific linear combinations of various quenched correlation functions. The random-bond Ising model in (2+ε) dimensions is similarly treated. As a byproduct, a simple method for deriving the scaling dimensions of all moments of the local energy operator is presented.