Increased Photosensitivity in HL60 Cells Expressing Wild-Type p53

Loss of p53 function has been correlated with decreased sensitivity to chemotherapy and radiation therapy in a variety of human tumors. Comparable analysis of p53 status with sensitivity to oxidative stress induced by pho-todynamic therapy has not been reported. In the current study we examined photosensitivity in human promye-locytic leukemia HL60 cells exhibiting either wild-type p53, mutated p53 or deleted p53 expression. Experiments were performed using a purpurin, tin ethyl etiopurpurin (SnET2)-, or a porphyrin, Photofrin (PH)-based photo-sensitizer. Total SnET2 accumulation was comparable in all three cell lines. Uptake of PH was highest in cells expressing wild-type p53 but incubation conditions could be adjusted to achieve equivalent cellular PH levels during experiments that analyzed photosensitivity. Survival measurements demonstrated that HL60 cells expressing wild-type p53 were more sensitive to PH- and SnET2-mediated photosensitization, as well as to UVC irradiation, when compared to HL60 cells exhibiting deleted or mutated p53 phenotypes. A rapid apoptotic response was observed following purpurin- and porphyrin-induced photosensitization in all cell lines. Results of this study indicate that photosensitivity is increased in HL60 cells expressing wild-type p53 and that photosensitizer-medi-ated oxidative stress can induce apoptosis through a p53-independent mechanism in HL60 cells .     

The influence of activated carbon on the thermal decomposition of sodium ethyl xanthate

The thermal decomposition of SEX in a nitrogen atmosphere was studied by coupled thermogravimetry-Fourier transform infrared spectroscopy (TG-FTIR), and by pyrolysis-gas chromatography-mass spectrometry (py-GC-MS). The TG curve exhibited two discrete mass losses of 45.8% and 17.8% respectively, at 200 and 257–364°C. The evolved gases identified as a result of the first mass loss were carbonyl sulfide (COS), ethanol (C₂H₅OH), ethanethiol (C₂H₅SH), carbon disulfide (CS₂), diethyl sulfide ((C₂H₅)₂S), diethyl carbonate ((C₂H₅O)₂CO), diethyl disulfide ((C₂H₅)₂S₂), and carbonothioic acid, O, S, diethyl ester ((C₂H₅S)(C₂H₅O)CO). The gases identified as a result of the second mass loss were carbonyl sulfide, ethanethiol, and carbon disulfide. Hydrogen sulfide was detected in both mass losses by py-GC-MS, but not detected by FTIR. The solid residue was sodium hydrogen sulfide (NaSH).SEX was adsorbed onto activated carbon, and heated in nitrogen. Two discrete mass losses were still observed, but in the temperature ranges 100–186°C (7.8%) and 186–279°C (11.8%). Carbonyl sulfide and carbon disulfide were now the dominant gases evolved in each of the mass losses, and the other gaseous products were relatively minor. It was demonstrated that water adsorbed on the carbon hydrolysed the xanthate to cause the first mass loss, and any unhydrolysed material decomposed to give the second mass loss.Mr. N. G. Fisher would like to thank the A. J. Parker CRC for Hydrometallurgy for the provision of a PhD scholarship.     

Quinol-containing ligands enable high superoxide dismutase activity by modulating coordination number,charge, oxidation states and stability of manganese complexes throughout redox cycling

Reactivity assays previously suggested that two quinol-containing MRI contrast agent sensors for H₂O₂, [Mn(H2qp1)(MeCN)]²⁺ and [Mn(H4qp2)Br₂], could also catalytically degrade superoxide. Subsequently, [Zn(H2qp1)(OTf)]⁺ was found to use the redox activity of the H2qp1 ligand to catalyze the conversion of O₂˙⁻ to O₂ and H₂O₂, raising the possibility that the organic ligand, rather than the metal, could serve as the redox partner for O₂˙⁻ in the manganese chemistry. Here, we use stopped-flow kinetics and cryospray-ionization mass spectrometry (CSI-MS) analysis of the direct reactions between the manganese-containing contrast agents and O₂˙⁻ to confirm the activity and elucidate the catalytic mechanism. The obtained data are consistent with the operation of multiple parallel catalytic cycles, with both the quinol groups and manganese cycling through different oxidation states during the reactions with superoxide. The choice of ligand impacts the overall charges of the intermediates and allows us to visualize complementary sets of intermediates within the catalytic cycles using CSI-MS. With the diquinolic H4qp2, we detect Mn(iii)-superoxo intermediates with both reduced and oxidized forms of the ligand, a Mn(iii)-hydroperoxo compound, and what is formally a Mn(iv)-oxo species with the monoquinolate/mono-para-quinone form of H4qp2. With the monoquinolic H2qp1, we observe a Mn(ii)-superoxo ↔ Mn(iii)-peroxo intermediate with the oxidized para-quinone form of the ligand. The observation of these species suggests inner-sphere mechanisms for O₂˙⁻ oxidation and reduction that include both the ligand and manganese as redox partners. The higher positive charges of the complexes with the reduced and oxidized forms of H2qp1 compared to those with related forms of H4qp2 result in higher catalytic activity (k_cat ∼ 10⁸ M⁻¹ s⁻¹ at pH 7.4) that rivals those of the most active superoxide dismutase (SOD) mimics. The manganese complex with H2qp1 is markedly more stable in water than other highly active non-porphyrin-based and even some Mn(ii) porphyrin-based SOD mimics.

Manganese complexes with polydentate quinol-containing ligands are found to catalyze the degradation of superoxide through inner-sphere mechanisms. The redox activity of the ligand stabilizes higher-valent manganese species.     

Generalizations of Non-Commutative Neutrix Convolution Products of Functions

The non-commutative neutrix convolution product of the functions x ^r cos_–(x) and x ^s cos₊(x) is evaluated. Further similar non-commutative neutrix convolution products are evaluated and deduced.     

Resolving Extensions of Finitely Presented Systems

In this paper we extend certain central results of zero dimensional systems to higher dimensions. The first main result shows that if (Y,f) is a finitely presented system, then there exists a Smale space (X,F) and a u-resolving factor map π ₊:X→Y. If the finitely presented system is transitive, then we show there is a canonical minimal u-resolving Smale space extension. Additionally, we show that any finite-to-one factor map between transitive finitely presented systems lifts through u-resolving maps to an s-resolving map.     

Interactive optimization

Optimization algorithms or heuristics in which the user interacts significantly either during the solution process or as part of post-optimality analysis are becoming increasingly popular. An important underlying premise of such man/machine systems is that there are some steps in solving a problem in which the computer has an advantage and other steps in which a human has an advantage. This paper first discusses how man/machine systems can be useful in facilitating model specification and revision, coping with aspects of a problem that are difficult to quantify and assisting in the solution process. We then survey successful systems that have been developed in the areas of vehicle scheduling, location problems, job shop scheduling, course scheduling, and planning language-based optimization.     

Surface-enhanced emission from single semiconductor nanocrystals

The fluorescence behavior of single CdSe(ZnS) core-shell nanocrystal (NC) quantum dots is dramatically affected by electromagnetic interactions with a rough metal film. Observed changes include a fivefold increase in the observed fluorescence intensity of single NCs, a striking reduction in their fluorescence blinking behavior, complete conversion of the emission polarization to linear, and single NC exciton lifetimes that are >10(3) times faster. The enhanced excited state decay process for NCs coupled to rough metal substrates effectively competes with the Auger relaxation process, allowing us to observe both charged and neutral exciton emission from these NC quantum dots.     

Sterling stirling play

In this paper we analyze a recently proposed impartial combinatorial ruleset that is played on a permutation of the set \(\left[ n\right] \). We call this ruleset Stirling Shave. A procedure utilizing the ordinal sum operation is given to determine the nim value of a given normal play position. Additionally, we enumerate the number of permutations of \(\left[ n\right] \) which are \(\mathcal {P}\)-positions. The formula given involves the Stirling numbers of the first-kind. We also give a complete analysis of the Misère version of Stirling Shave using Conway’s genus theory. An interesting by-product of this analysis is insight into how the ordinal sum operation behaves in Misère Play.     

Geometric lattice actions, entropy and fundamental groups

Let be a lattice in a noncompact simple Lie Group G, where . Suppose acts analytically and ergodically on a compact manifold M preserving a unimodular rigid geometric structure (e.g. a connection and a volume). We show that either the action is isometric or there exists a "large image" linear representation of . Under an additional assumption on the dynamics of the action, we associate to a virtual arithmetic quotient of full entropy. Received: December 14, 2000     

Modeling the acoustic radiation force in microfluidic chambers

A procedure is demonstrated to quantitatively evaluate the acoustic radiation forces in microfluidic particle manipulation chambers. Typical estimates of the acoustic pressure and the acoustic radiation force are based on an analytical solution for a simple one-dimensional standing wave pattern. The complexities of a typical microfluidic channel limit the usefulness of this approach. By leveraging finite elements, and a generalized equation for the acoustic radiation force, channel designs can be investigated in two and three dimensions. Calculations and experimental observations in this report and the literature, confirm these claims.