Coulometric determination of NAD+ and NADH in normal and cancer cells using LDH, RVC and a polymer mediator

An electrochemical method for the measurement of NAD(+) and NADH in normal and cancer tissues using flow injection analysis (FIA) is reported. Reticulated vitreous carbon (RVC) electrodes with entrapped l-lactate dehydrogenase (LDH) and a new redox polymer containing covalently bound toluidine blue O (TBO) were employed for this purpose. Both NAD(+) and NADH were estimated coulometrically based on their reaction with LDH. The latter was immobilized on controlled pore glass (CPG) by cross-linking with glutaraldehyde and packed within the RVC. The concentrations of NAD(+) and NADH in the tissues, estimated using different electron mediators such as ferricyanide (FCN), meldola blue (MB) and TBO have also been compared. The effects of flow rate, pH, applied potential (versus Ag/AgCl reference) and adsorption of the mediators have also been investigated. Based on the measurements of NAD(+) and NADH in normal and cancer tissues it has been concluded that the NADH concentration is lower, while the NAD(+) concentration is higher in cancer tissues. Amongst the electron mediators TBO was found to be a more stable mediator for such measurements.     

Gas phase photoisomerization of urocanic acid – a theoretical study

The photochemistry of urocanic acid is investigated theoretically by means of time-dependent density functional theory. The topology of the potential energy surface along the isomerization pathway and close to the Franck–Condon region is investigated and consequences for the photoisomerization reactions are outlined. A recently published supersonic jet spectroscopy study is reinterpreted in the light of these and earlier theoretical results to give a clear picture of the gas phase photochemistry. It is found that the photochemistry of the two isomers is fundamentally different, in contrast to the situation in solution.     

Evaluation of partition measurements in liquid-liquid segmented flow

The different configurations possible for an FIA extraction system for partition measurements have been tested and the corresponding evaluation formulae based on determinations at different phase flow ratios, verified. Increased flexibility results from the possibility of using samples dissolved in either aqueous or organic phase. Choosing the best configuration in every case makes it possible to extend the range of measurable conditional partition constants without excessive losses in precision.     

Double photoionisation spectra of small molecules and a new empirical rule for double ionisation energies

Complete double photoelectron spectra are presented for 18 small molecules where the location of charges in the cations and dications is relatively clearly defined. The data demonstrate the importance of a coulombic repulsion contribution to the double ionisation energies. Examination of data for a wide range of molecules leads to a new empirical rule to calculate double ionisation energies from the molecules’ single ionisation energies and maximum dimensions. Where single and double ionisation energies are known the rule allows the deduction of plausible intercharge distances.     

Evaluation of a dialysis probe for continuous sampling in fermentors and in complex media

A dialysis probe is described for continuous sampling from complex solutions, such as fermentation broth, milk or waste water, to yield samples suitable for liquid chromatography, flow injection analysis, enzyme calorimetry, etc. The analyte is transferred to a flow stream separated from the sample by a dialysis membrane that is protected from fouling by a strong tangential flow of the sample solution. This flow is accomplished by placing a magnetic stirring bar close to the membrane surface. The device is constructed of materials permitting the probe to be steam-sterilized when mounted inside a fermentor.     

Modelling procedures and properties of rubber in rolling contact

Rubber covered cylinders in rolling contact are studied in two cases; rolling over a flat surface and rolling over a groove. In the first case, two different finite element procedures are compared for the purpose of investigating if computational savings can be made when taking amplitude dependent effects into account by using a modified viscoelastic steady state rolling procedure. This procedure is compared with using a more expensive overlay method with an elastoplastic-viscoelastic material model. The two procedures and material models are shown two give equal results in the flat surface case. For the case of rolling over a groove, it is shown how the non-linear dynamic material characteristics of the rubber layer influence the rolling contact. The groove filling capacity of the rubber is shown to be strongly dependent on the material model. It is shown that amplitude dependent rubber materials have better ability to fill out contact surface irregularities such as a groove.     

Studies of two-phase equilibria by liquid-liquid segmented flow extraction of dithiocarbamic acids into various solvents

A method for the study of two-phase equilibria by extraction in liquid-liquid segmented flow is presented. The main advantage of the method is the very rapid equilibration achieved. In many cases a contact time of 5 sec is sufficient. By performing the measurements needed on-line with the extraction the total residence time of a substance studied in the system can be kept below 10 sec. This makes it possible to study two-phase equilibria of moderately unstable compounds. Other advantages are the semi-enclosed design, which minimizes contact with solvent fumes and increases the speed of operation after the system has been set up. The system has been used for a study of the two-phase equilibria of dithiocarbamic acids. The dithiocarbamates are often used for the separation and preconcentration of metals, and co-extraction of the reagent can cause severe interference in the final determination. By means of the extraction constants presented, the extraction of diethyldithiocarbamic acid and pyrrolidine-dithiocarbamic acid into Freon 113, carbon tetrachloride, methyl isobutyl ketone and chloroform can be estimated.     

Extraction of plasmid DNA from Escherichia coli cell lysate in a thermoseparating aqueous two-phase system

The primary purification of a 6.1 kilo base pair (kbp) plasmid from a desalted alkaline lysate has been accomplished by a thermoseparating aqueous two-phase system [(50% ethylene oxide-50% propylene oxide)-Dextran T 500]. The partitioning of the different nucleic acids (plasmid DNA, RNA, genomic DNA) in the thermoseparating aqueous two-phase system was followed both qualitatively by agarose gel electrophoresis and quantitatively by analytical chromatography (size exclusion- and anion-exchange mode) and PicoGreen fluorescence analysis. The experimental results showed a complete recovery of the plasmid DNA to the top phase, while 80% of total RNA and 58% of total protein was discarded to the bottom phase. Moreover, a 3.8-fold volume reduction of the plasmid DNA solution was achieved. By using a final thermoseparating step, the EO50PO50 polymer could be efficiently recycled, resulting in plasmid solution containing less than 1% polymer. The developed thermoseparating aqueous two-phase system shows great potential for the large-scale processing of plasmid DNA.