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Characterization of the preparation process and the photochemical control of electrical properties of bilayer lipid membranes containing azobenzene chromophores.

We prepared photoresponsive bilayer lipid membranes (BLMs) containing azobenzene derivatives (4'-octylazobenzene-4-oxybutyric acid (AZ)) and observed the rapid and reversible changes in their electrical properties when irradiated with light. The BLMs consist of AZ (8 mol%) and glyceryl monooleate. The changes in capacitance and conductance upon irradiation by light were found to be 10 and 20%, respectively. The changes in the electrical properties of the membrane and in the structure of AZ under light irradiation were analyzed simultaneously by in-situ spectroscopic, electrical and microscopic measurements. These measurements showed that the electrical changes induced by exposure to light resulted from reversible changes in the membrane structure initiated by the photoisomerization reaction of AZ. This structural change in the membrane occurred within 1 s.

Azo Compounds↗

Photoacoustic diagnostics of fast photochemical and photobiological processes. Analysis of inverse problem solution.

Photoacoustic (PA) diagnostics is a time-resolved experimental technique that measures transient photoinduced volume changes on the nano- and microsecond time-scales. The technique has been used to study the energetics and dynamics of chemical and biochemical reactions initiated by absorption of light. The dynamics of the volume changes and associated relaxation processes can be restored from PA-waveforms by solving an ill-posed problem of deconvolution. For the systems with known relaxation kinetics scheme this problem is usually solved by an iterative approximation algorithm. In complex photoactive systems (e.g. photosynthetic samples), where information about kinetics of fast photoinduced volume changes is not available, an algorithm of direct deconvolution must be used. The implementation of one of the linear deconvolution algorithms (Tikhonov's alpha-regularization) for the PA-diagnostics is therefore considered. The problem of the optimal choice of experimental set-up, and restoration algorithm is analyzed by a numerical simulation. It is shown that the quality of PA-diagnostic experiment is mainly determined by a transfer function converting the relaxation spectrum to the spectrum of output electric signal. The analytical expressions to calculate this function (so called PA-filter) are presented. The performance of two widely used schemes of PA-diagnostics are then directly compared. The time-resolution of the PA-diagnostics in analysis of simultaneous bi-exponential decay is evaluated, and the relationship between the resolving power and parameters of the experimental set-up (signal-to-noise ratio, sampling rate, shape of the PA-filter) is found. The advantage of front face irradiation scheme with piezopolymer film detector for time-resolved measurements is demonstrated.

Journal Article↗

Technical development of UV-C- and VUV-photochemically induced oxidative degradation processes.

Technical development work is presented, where the VUV photochemically induced oxidative degradation is used: (i) for analytic purposes, and (ii) for small to medium scale (< 10 m2/d) waste water treatment processes or ultrapure water production. In the first case, small Xe-excimer radiation sources with an integrated reaction space designed for optimal conditions, as far as incident photon flux density, turbulence and concentration of dissolved molecular oxygen are concerned, have been built and tested. Under conditions of exhaustive oxidation and/or mineralization of pollutants in a continuous regime, they may be used for sample pre-treatment modules prior TOC, TOX and electrochemical trace metal analysis. Under conditions of partial oxidation or mineralization, the same lamp/reactor combination may be used for functionalization purposes prior to e.g. GC or HPLC analyses. In the second case, mass transfer limitations between the non-irradiated bulk volume and the irradiated volume are overcome by the electrochemical generation of molecular oxygen within or close to the irradiated volume and by the design of the photochemical part of the reactor.

Chromatography, Gas↗

Removal of hydrophobic dyestuff from dyeing wastewater by photo-sensitization process.

Recently, photochemical reaction became more important in view of using UV in textile dyeing wastewater treatment processes, in which neither chemical sludges nor toxic residues are left in the treated effluent. The photodegradation of hydrophobic dye (Palanil Yellow 5R, PY-5R) in the presence of acetone, which performs as a solvent and/or a photo-sensitizer, was investigated in this study. The results demonstrated that photochemical reaction in the presence of acetone could rapidly and effectively enhance color removal at a wavelength of 253.7 nm. The photodegradation follows pseudo first-order decay. The rate constants and decay quantum yields of dye degradation by UV depend on the solution pH and solvent system, (i.e., acetone to water ratio). The photosensitization of the disperse dye was found to be optimized at pH 9 and in 0.5 (v:v) acetone-water ratio.

Acetone↗

Photochemical inactivation of viruses and bacteria in platelet concentrates by use of a novel psoralen and long-wavelength ultraviolet light.

BACKGROUND: A photochemical treatment process has been developed for the inactivation of viruses and bacteria in platelet concentrates. This process is based on the photochemical reaction of a novel psoralen, S-59, with nucleic acids upon illumination with long-wavelength ultraviolet light (UVA, 320-400 nm). STUDY DESIGN AND METHODS: High levels of pathogens were added to single-donor platelet concentrates containing 3 to 5 x 10(11) platelets in 300 mL of 35-percent autologous plasma and 65-percent platelet additive solution. After treatment with S-59 (150 microM) and UVA (0-3 J/cm2), the infectivity of each pathogen was measured with established biologic assays. In vitro platelet function after photochemical treatment was evaluated during 7 days of storage by using a panel of 14 assays. The in vivo recovery and life span of photochemically treated platelets were evaluated after 24 hours of storage in a primate transfusion model. RESULTS: The following levels of pathogen inactivation were achieved: >10(6.7) plaque-forming units (PFU) per mL of cell-free human immunodeficiency virus (HIV), >10(6.6) PFU per mL of cell-associated HIV, >10(6.8) infectious dose (ID50) per mL of duck hepatitis B virus (a model for hepatitis B virus), >10(6.5) PFU per mL of bovine viral diarrhea virus (a model for hepatitis C virus), >10(6.6) colony-forming units of Staphylococcus epidermidis, and >10(5.6) colony-forming units of Klebsiella pneumoniae. Expression of integrated HIV was inhibited by 0.1 microM S-59 and 1 J per cm2 of UVA. In vitro and in vivo platelet function were adequately maintained after antiviral and antibacterial treatment. CONCLUSION: Photochemical treatment of platelet concentrates offers the potential for reducing transfusion-related viral and bacterial diseases.

Animals↗

Degradation kinetics and mechanisms of phenol in photo-Fenton process.

Phenol degradation in photochemically enhanced Fenton process was investigated in this work. UV-VIS spectra of phenol degradation showed the difference between photo-Fenton process and UV/H(2)O(2), which is a typical hydroxyl radical process. A possible pathway diagram for phenol degradation in photo-Fenton process was proposed, and a mathematical model for chemical oxygen demand (COD) removal was developed. Operating parameters such as dosage of H(2)O(2) and ferrous ions, pH, suitable carrier gas were found to impact the removal of COD significantly. The results and analysis of kinetic parameters calculated from the kinetic model showed that complex degradation of phenol was the main pathway for removal of COD; while hydroxyl radicals acted weakly in the photo-Fenton degradation of phenol.

Computer Simulation↗

Therapeutic efficacy and safety of photochemically treated apheresis platelets processed with an optimized integrated set.

BACKGROUND: This multicenter, randomized, controlled, double-blind Phase III clinical study evaluated the therapeutic efficacy and safety of apheresis platelets (PLTs) photochemically treated (PCT) with amotosalen and ultraviolet A light (INTERCEPT Blood System, Baxter Healthcare Corp.) compared with conventional apheresis PLTs (reference). STUDY DESIGN AND METHODS: Forty-three patients with transfusion-dependent thrombocytopenia were randomly assigned to receive either PCT or reference PLT transfusions for up to 28 days. RESULTS: The mean 1- and 24-hour corrected count increments were lower in response to PCT PLTs (not significant). When analyzed by longitudinal regression analysis, the estimated effect of treatment on 1-hour PLT count was a decrease of 7.2 x 10(9) per L (p = 0.05) and on 24-hour PLT count a decrease of 7.4 x 10(9) per L (p = 0.04). Number, frequency, and dose of PLT transfusions; acute transfusion reactions; and adverse events were similar between the two groups. There was no transfusion-associated bacteremia. Four PCT patients experienced clinical refractoriness; however, only one exhibited lymphocytotoxicity assay seroconversion. Antibodies against potential amotosalen-related neoantigens were not detected. CONCLUSION: PCT PLTs provide effective and safe transfusion support for thrombocytopenic patients.

Adult↗

Chemical and photo-oxidative hair damage studied by dye diffusion and electrophoresis.

Microspectrophotometric and electrophoretic methods were used to characterize and quantify the effects of primary damage to hair from chemical and photochemical oxidative processes. The diffusion of molecules proceeding from the fiber surface to the center of untreated and modified (by chemical and photochemical oxidative processes) hair fibers was mapped by fluorescence microscopy and quantified by calculating diffusion coefficients of a fluorescent molecule. In addition, an electrophoretic separation technique, namely, SDS-PAGE (sodium dodecyl sulfate-polyacrylamide gel electrophoresis), was used not only to substantiate the results obtained in the microfluorometric study, but also to show how the main classes of proteins of unaltered hair are modified by cosmetic chemical treatments, light exposure, and combinations of these two processes. UV microspectrophotometry is an alternate analytical method to evaluate photo-oxidative damage in hair, and supports the results obtained by microfluorometry.

Diffusion↗

Alkyl exchange reactions of organocobalt porphyrins. A bimolecular homolytic substitution reaction.

Reaction of organocobalt(III) porphyrins with a cobalt(II) complex of a distinguishable porphyrin or tetrapyrrole resulted in the reversible exchange of the organic axial ligand. The exchange reaction was facile in such solvents as benzene, toluene, dichloromethane, chloroform, and pyridine; was unaffected by total exclusion of light; was faster than would be expected for a homolytic process given known Co-C bond dissociation energies; and was of broad scope with respect to the organic ligand. Methyl, benzyl, primary alkyl, secondary alkyl, and acyl groups exchanged, but phenyl groups did not. The position of the exchange equilibrium was independent of the direction of approach and was nonstatistical. The relaxation to equilibrium appeared to be consistent with that of a second-order process. The rate of the reaction varied with the identity of the R group in the order Bzl > or = Me > Et approximately n-Pr > i-Pr > i-Bu > acetyl approximately neopentyl approximately 2-adamantyl. However, the total variation in reaction rates was remarkably small. Attempts to find evidence of free-radical intermediates by trapping with TEMPO or CO or by alkyl group interchange with an excess of an alkyl halide of a distinct alkyl group were unsuccessful over a time scale comparable to multiple half-lives of the exchange reaction. In addition, no rearrangement products were detected in exchange reactions of the 5-hexenyl group. Use of cobalt porphyrin reactants that were sterically encumbered on both faces with groups large enough to prevent formation of a bridged, Co-C-Co structure resulted in a 5 or more order of magnitude decrease in the rate of methyl exchange, if not its outright cessation, when run with total exclusion of light. The decrease in the rate of the thermal exchange process revealed the existence a slow photochemical exchange process that was driven by room lights. All evidence was consistent with a bimolecular S(H)2 mechanism for the thermal exchange mechanism.

Cobalt↗

Photochemical reactions in the tropospheric aqueous phase and on particulate matter.

This paper is a tutorial review in the field of atmospheric chemistry. It describes some recent developments in tropospheric photochemistry in the aqueous phase and on particulate matter. The main focus is regarding the transformation processes that photochemical reactions induce on organic compounds. The relevant reactions can take place both on the surface of dispersed particles and within liquid droplets (e.g. cloud, fog, mist, dew). Direct and sensitised photolysis and the photogeneration of radical species are the main processes involved. Direct photolysis can be very important in the transformation of particle-adsorbed compounds. The significance of direct photolysis depends on the substrate under consideration and on the colour of the particle: dark carbonaceous material shields light, therefore protecting the adsorbed molecules from photodegradation, while a much lower protection is afforded for the light-shaded mineral fraction of particulate. Particulate matter is also rich in photosensitisers (e.g. quinones and aromatic carbonyls), partially derived from PAH photodegradation. These compounds can induce degradation of other molecules upon radiation absorption. Interestingly, substrates such as methoxyphenols, major constituents of wood-smoke aerosol, can also enhance the degradation of some sensitisers. Photosensitised processes in the tropospheric aqueous phase have been much less studied: it will be interesting to assess the photochemical properties of Humic-Like Substances (HULIS) that are major components of liquid droplets. The main photochemical sources of reactive radical species in aqueous solution and on particulate matter are hydrogen peroxide, nitrate, nitrite, and Fe(iii) compounds and oxides. The photogeneration of hydroxyl radicals can be important in polluted areas, while their transfer from the gas phase and dark generation are usually prevailing on an average continental scale. The reactions involving hydroxyl radicals can induce very fast transformation of compounds reacting with (*)OH at a diffusion-controlled rate (10(10) M(-1) s(-1)), with time scales of an hour or less. The hydroxyl-induced reactivity in solution can be faster than in the gas phase, influencing the degradation kinetics of water-soluble compounds. Moreover, photochemical processes in fog and cloudwater can be important sources of secondary pollutants such as nitro-, nitroso-, and chloro-derivatives.

Journal Article↗

Leishmania inactivation in human pheresis platelets by a psoralen (amotosalen HCl) and long-wavelength ultraviolet irradiation.

BACKGROUND: Leishmania spp. are protozoans that cause skin and visceral diseases. Leishmania are obligate intracellular parasites of mononuclear phagocytes and have been documented to be transmitted by blood transfusion. STUDY DESIGN AND METHODS: This study examines whether Leishmania can be inactivated in human platelet (PLT) concentrates by a photochemical treatment process that is applicable to blood bank use. Human PLT concentrates were contaminated with Leishmania mexicana metacyclic promastigotes or mouse-derived Leishmania major amastigotes and were exposed to long-wavelength ultraviolet (UV) A light (320-400 nm) plus the psoralen amotosalen HCl. RESULTS: Neither treatment with amotosalen nor UVA alone had an effect on Leishmania viability; however, treatment with 150 micromol per L amotosalen plus 3 J per cm(2) UVA inactivated both metacyclic promastigotes and amastigotes to undetectable levels, more than a 10,000-fold reduction in viability. CONCLUSIONS: This study demonstrates the effectiveness of photochemical treatment to inactivate Leishmania in PLT concentrates intended for transfusion. Both metacylic promastigotes, which represent the infectious form from the sand fly vector, and amastigotes, which represent the form that grows in mononuclear phagocytes, were extremely susceptible to photochemical inactivation by this process. Thus, the photochemical treatment of PLT concentrates inactivates both forms of Leishmania that would be expected to circulate in blood products collected from infected donors.

Animals↗

A photochemical activation scheme of inert dinitrogen by dinuclear Ru(II) and Fe(II) complexes.

A general photochemical activation process of inert dinitrogen coordinated to two metal centers is presented on the basis of high-level DFT and ab initio calculations. The central feature of this activation process is the occupation of an antibonding pi* orbital upon electronic excitation from the singlet ground state S0 to the first excited singlet state S1. Populating the antibonding LUMO weakens the triple bond of dinitrogen. After a vertical excitation, the excited complex may structurally relax in the S1 state and approaches its minimum structure in the S1 state. This excited-state minimum structure features the dinitrogen bound in a diazenoid form, which exhibits a double bond and two lone pairs localized at the two nitrogen atoms, ready to be protonated. Reduction and de-excitation then yield the corresponding diazene complex; its generation represents the essential step in a nitrogen fixation and reduction protocol. The consecutive process of excitation, protonation, and reduction may be rearranged in any experimentally appropriate order. The protons needed for the reaction from dinitrogen to diazene can be provided by the ligand sphere of the complexes, which contains sulfur atoms acting as proton acceptors. These protonated thiolate functionalities bring protons close to the dinitrogen moiety. Because protonation does not change the pi*-antibonding character of the LUMO, the universal and well-directed character of the photochemical activation process makes it possible to protonate the dinitrogen complex before it is irradiated. The pi*-antibonding LUMO plays the central role in the activation process, since the diazenoid structure was obtained by excitation from various occupied orbitals as well as by a direct two-electron reduction (without photochemical activation) of the complex; that is, the important bending of N2 towards a diazenoid conformation can be achieved by populating the pi*-antibonding LUMO.

Iron↗

Novel catalytic photochemical and hydrothermal treatment processes for acid dye wastewater.

The purpose of the present study was to evaluate the catalytic effect of a heteropoly acid, namely H4SiW12O40, on aqueous Acid Orange 7, a well-known, representative textile monoazo dye applied to nylon fabrics, in sub-critical water (T = 160 degrees C-290 degrees C; P = 0.6-3.0 MPa, pH = 2.6) and under near-UV-VIS light irradiation (isopropanol: water ratio = 1:10: pH = 2.8). SiW12O40-catalyzed photochemical Acid Orange 7 bleaching was also explored in the presence of two dye assisting chemicals as well as in simulated acid dye wastewater at its natural, acidic pH under otherwise identical reaction conditions. Though less explored than TiO2-mediated, heterogeneous photocatalytic treatment, heteropolyacid-catalyzed thermal and/or photoatalytic re-mediation could be an attractive alternative for the degradation of refractory, colored compounds using relatively mild wet oxidation operating conditions or even natural solar light.

Azo Compounds↗

Photoelectric response of polarization sensitive bacteriorhodopsin films.

Polarization sensitivity is introduced into oriented bacteriorhodopsin (BR) films through a photochemical bleaching process, which chemically modifies the structure of the purple membrane by breaking the intrinsic symmetry of the membrane-bound BR trimers. The resulting photovoltage generated in an indium-tin oxide (ITO)/BR/ITO detector is found to be anisotropic with respect to cross-polarized probe beams. A model, based on the polarization dependent photoselection of the BR molecules qualitatively explains the photochemical bleaching process and the observed anisotropic response. The effect reported here can be used to construct a polarization sensitive BR-based bio-photoreceiver.

Anisotropy↗

Photochemical and thermal isomerization processes of a chiral auxiliary based donor-acceptor substituted chiroptical molecular switch: convergent synthesis, improved resolution and switching properties.

A new type of chiroptical molecular switch is presented where irradiation employing different wavelengths of light induces a reversible helix inversion of a sterically overcrowded alkene bearing a second chiral entity in the form of a stereogenic center present in a pyrrolidine unit. The additional stereogenic center in the chiral auxiliary group has a distinct influence on the switching selectivity of this system and greatly facilitates the resolution of the different diastereoisomers, which is a considerable improvement compared with previously reported systems. In addition, the pyrrolidine stereogenic center causes small energetic differences between the various states of the switch system resulting in a small but significant directional preference in the helix inversion steps.

Journal Article↗