New possibilities of old soft pomeron in DIS

A traditional Regge model with a -independent Pomeron intercept closed (or equal) to one is constructed in order to describe the available data on the proton structure function. A Dipole Pomeron model which does not explicitly violate unitarity is developed and investigated. An excellent agreement with the 1209 data is found () in the whole kinematical domain investigated by experiments. A comparison of the model with already existing ones is made. The x-, slopes and the effective intercept are discussed as and x functions. Received: 9 June 1998 / Revised version: 27 August 1998 / Published online: 14 January 1999     

Effect of linear polymer additives on the electroosmotic characteristics of agarose gels in ultrathin-layer electrophoresis.

Electroosmotic properties of agarose gels with low, medium, high and super high electroendosmosis (EEO) were evaluated based on the apparent electric field mediated mobility of a neutral, fluorescent marker under constant field strength using ultrathin-layer separation configuration. Electroosmotic flow mobility values were measured in different gel concentrations and also in the absence and the presence of various linear polymer additives. Under ultrathin-layer separation conditions, a slight decrease in electroosmotic flow mobility was observed with increasing agarose gel concentration of 1 to 3% for all agarose gels investigated. When linear polymer additives, such as linear polyacrylamide, hydroxyethyl cellulose or polyethylene oxide were added to 1% low electroendosmosis agarose gel, significant reduction of the electroosmotic flow properties were observed with increasing additive concentration. Effect of the intrinsic electroosmotic properties of the various electroendosmosis agaroses on the apparent mobilities and separation performance of double-stranded DNA fragments during automated ultrathin-layer agarose gel electrophoresis was also investigated.     

Synergistic behaviour of crown ethers in the thenoyltrifluoroacetone extraction of technetium

The synergism of the crown ethers /CE/ dibenzene-18-crown-6 /DB18C6/ and 18-crown-6 /18C6/ has been investigated in the thenoyltrifluoroacetone /HTTA/ extraction of technetium from aqueous phase containing NaBH₄ into benzene at room temperature. The extracted synergistic species have the general formula TcO/OH/.TTA.CE. The order of synergism was found to be 18C6>DB18C6.     

On the separation of molybdenum and technetium crown ether as extraction agent

Separation of⁹⁹Mo and^99mTc can be performed with high selectivity using the crown ether 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2,11-diene /DB18C6/ diluted with nitrobenzene. The high efficiency is attributed to the rather low extractability of molybdenum as compared with that of technetium.     

The mass spectra of some α-lactams

The electron-impact induced fragmentation of eight aziridinones has been studied by conventional as well as by high resolution mass spectrometry. All α-lactams exhibit a molecular ion. The major primary step, in the fragmentation, is the ejection of carbon monoxide from the molecular ion. Ions of the general formula R₁? NC and R₂R₃C?O were found in the mass spectra of all α-lactams investigated. A skeletal rearrangement to rationalize these ions is proposed. The fragmentation of the molecular ion is affected by the N-substituent. Exact mass measurement and specific deuterium labeling indicate the absence of McLafferty rearrangement from either the N- or C-substituent.     

Matrix-assisted laser desorption/ionization mass spectrometry for the evaluation of the C-terminal lysine distribution of a recombinant monoclonal antibody

Recombinant monoclonal antibodies produced using mammalian cell lines contain multiple chemical modifications. One specific modification resides on the C-terminus of the heavy chain. Enzymes inside the cell can cleave the C-terminal lysine from the heavy-chain molecules, and variants with and without C-terminal lysine can be produced. In order to fully characterize the protein, there is a need for analytical methods that are able to account for the different product variants. Conventional analytical methods used for the measurement of the distribution of the two different variants are based on chemical or enzymatic degradation of the protein followed by chromatographic separation of the degradation products. Chromatographic separations with gradient elution have long run times, and analyses of multiple samples are time-consuming. This paper reports development of a novel method for the determination of the relative amounts of the two C-terminal heavy-chain variants based on matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) measurements of the cyanogen bromide degraded recombinant monoclonal antibody products. The distribution of the variants is determined from the MALDI-TOF mass spectra by measuring the peak areas of the two C-terminal peptides. The assay was used for the assessment of the C-terminal lysine distribution in different development lots. The method was able to differentiate between the products obtained using the same cell line as well as between products obtained from different cell lines.     

Syntheses and biological evaluation of vinblastine congeners

Sixty-two congeners of vinblastine (VLB), primarily with modifications of the piperidine ring in the carbomethoxycleavamine moiety of the binary alkaloid, were synthesized and evaluated for cytotoxicity against murine L1210 leukemia and RCC-2 rat colon cancer cells, and for their ability to inhibit polymerization of microtubular protein at < 10(-6) M, and for induction of spiralization of microtubular protein, and for microtubular disassembly at 10(-4) M concentrations. An ID50 range of >10(7) M concentrations was found for L1210 inhibition by these compounds, with the most active 1000x as potent as vinblastine.     

Diffusion-induced instability in chemically reacting systems: Steady-state multiplicity,oscillation, and chaos

The dynamical behavior of two coupled cells or reactors is described. The cells are coupled by diffusion, e.g., through a semipermeable membrane, and the chemical reactions and initial or feed concentrations of all species are the same in the two cells. Each cell has only a single stable steady state in the absence of coupling, and the coupled system may exhibit multiple steady states, periodic oscillation, or chaos. The attractors of the coupled system may be either homogeneous (the two cells have equal concentrations) or inhomogeneous. Three two-variable kinetic models are examined: the Brusselator, a model of the chlorine dioxide-iodine-malonic acid reaction, and the Degn-Harrison model. The dynamical behavior of the coupled system is determined by the nonlinearities in the uncoupled subsystems and by two ratios, that of the diffusion constants of the two species and that of the area of the membrane to the product of the membrane thickness and the volume of a cell.     

Investigations on the solvent extraction from molten salts by tracer technique

The distribution of terbium in a three-phase system of an organic extractant, a fused salt and metallic gallium, as well as in the corresponding two-phase subsystems has been studied. Changing the concentrations in the organic and ionic phases the distribution ratios can favourably be varied and so the selectivity of extraction improved.