Photodynamic Therapy with a Diode Laser for Implanted Fibrosarcoma in Mice Employing Mono-L-Aspartyl Chlorin E6

Abstract— The authors performed photodynamic therapy (PDT), avoiding any hyperthermic effects, using a newly developed diode laser and photosensitizer, mono-L-aspar-tyl chlorin e₆ (NPe6), of Meth-A fibrosarcoma implanted in mice and achieved tumor therapeutic benefit. The photodynamic light treatment was performed 5 h following the photosensitizer administration. With 5.0 mg/kg NPe6 and light doses of 50, 100, 150 and 200 J/cm², the tumor cure rates were 20, 50, 70 and 90%, respectively. With 100 J/cm² laser exposure and NPe6 doses of 1.25, 2.5, 5.0, 7.5 and 10.0 mg/kg, the tumor cure rates were 0, 20, 50, 70 and 90%, respectively. A charge-coupled device (CCD) camera system was employed to measure the NPe6 fluorescence intensity correlating with the residual amount of the photosensitizer at deferent depth from the tumor surface. The ratios of the NPe6 fluorescence intensity at 3 mm from the tumor surface following 50, 100, 150 and 200 J/cm² laser exposure to no laser exposure were 0.73, 0.36, 0.22 and 0.16, respectively. With samples sectioned at 1 mm depth, after 50 J/cm² and the same photosensitizer dose (5 mg/kg) this ratio was 0.19. These results suggest that a certain increase in the tumor tissue level of NPe6 and a certain increase of laser light dose reaching deeper layers of tumor caused an increase in percent cure. In addition, the effectiveness of PDT depends on the total laser dose reaching deeper layers of tumors. Furthermore, the effectiveness of PDT tends to correlate with the amount of NPe6 photobleaching by PDT.     

Pilot-plant for NOx, SO2 and HC removal from flue-gas of municipal waste incinerator by electron beam irradiation

According to the basic research performed using a small size reactor at TRCRE of JAERI, the electron beam irradiation process was proved to be very effective for NO_x, SO₂ and HC removals from flue-gas of municipal waste incinerators. Based on this result, a pilot-plant was constructed for the demonstration of NO_x, SO₂ and HC removal performance using electron accelerator of maximum energy 0.95 MeV and maximum power 15kW.The pilot-plant was constructed at Matsudo City waste Disposal Center. The flue-gas of 1,000 Nm³/hr is guided from the waste incinerator flue-gas line of 30,000Nm³/hr to the pilot-plant to be processed by spraying Ca(OH)₂ slurry or powder and irradiation with high-energy electron beam of the accelerator. NO_x, SO₂ and HC are removed simultaneously from the flue-gas by the enhanced reaction with Ca (OH)₂ under irradiation.A brief explanation of the pilot-plant and preliminary results of the experiments are introduced in this paper.     

ESR investigation of a stable trapped hydrogen atom in X-ray-irradiated beta-tricalcium phosphate at room temperature

A stable trapped hydrogen atom in X-ray-irradiated beta-tricalcium phosphate (beta-Ca3(PO4)2, beta-TCP) was successfully detected at room temperature. This hydrogen atom is stable at ambient temperature for several months. Hyperfine structure of the hydrogen atom and superhyperfine structures of the two phosphorus atoms were observed by means of electron spin resonance (ESR) spectroscopy. Electron spin-echo (ESE) of the hydrogen atom was observed in X-ray-irradiated beta-TCP. At room temperature, relaxation times of the hydrogen atom in X-ray-irradiated beta-TCP were very long (phase memory time TM = 19.4 mus, spin-lattice relaxation time T1 = 75.8 mus) compared with those of usual paramagnetic species. The most important facts are the detections of ESE and electron spin-echo envelope modulation (ESEEM) at room temperature. At room temperature, the observations of ESE and ESEEM and the estimations for the relaxation times (TM, T1) of the hydrogen atom were carried out for the first time until now. TM was able to be measured from room temperature to 9 K. The short relaxation time TM below 20 K might be explained by the quantum tunneling effect of the hydrogen atom. Fourier transformation of the electron spin-echo envelope modulation (FT-ESEEM) at room temperature suggests the overlapping of the wave functions between the hydrogen atom and the two phosphorus atoms. The site of the hydrogen atom in the X-ray-irradiated beta-TCP was discussed on the basis of the continuous wave ESR (CW-ESR) and pulse-ESR analyses.     

Asymmetric Synthesis of 2H‐Azirines with a Tetrasubstituted Stereocenter by Enantioselective Ring Contraction of Isoxazoles

Highly strained 2H‐azirines with a tetrasubstituted stereocenter were synthesized by the enantioselective isomerization of isoxazoles with a chiral diene–rhodium catalyst system. The effect of ligands and the coordination behavior support the proposed catalytic cycle in which the coordination site is fixed in favor of efficient enantiodiscrimination by a bulky substituent of the ligand. In silico studies also support the existence of a rhodium–imido complex as a key intermediate for enantiodiscrimination.     

Numerical analysis for finite Fresnel transform

Optical Review - The Fresnel transform is a bounded, linear, additive, and unitary operator in Hilbert space and is applied to many applications. In this study, a sampling theorem for a Fresnel...     

Near-Infrared Circularly Polarized Luminescence through Intramolecular Excimer Formation of Oligo(p-phenyleneethynylene)-Based Double Helicates

Carbon-based double helicates consisting of two anthracene-containing oligo(p-phenyleneethynylene) units and two flexible chiral 1,1′-binaphthyl units or two rigid chiral 9,9′-spirobifluorene units were developed. The curved oligo(p-phenyleneethynylene) fragments in the double helicates were successfully constructed by tin-mediated reductive aromatization. Helical oligo(p-phenyleneethynylene) double strands fixed by two rigid spirobifluorene units showed little structural change under photoirradiation, thereby emitting circularly polarized luminescence (CPL) in the visible region with a high quantum yield (Φ_PL=0.93). In contrast, flexible binaphthyl units induced dynamic structural change of the oligo(p-phenyleneethynylene) luminophores under photoirradiation, leading to strong CPL (|g_lum|=1.1×10⁻²) in the near-infrared (NIR) region. UV/Vis, circular dichroism (CD), CPL and NMR spectroscopic analyses of the binaphthyl-hinged double helicate suggested excimer formation between two π-conjugated strands in the excited state. Theoretical calculations highlight the importance of the tightly interlocked excimer structure of the carbon-based double helicate in controlling the angle between the electric and magnetic transition dipole moments for strong NIR CPL generation.     

α‐Amino acid: an effective ligand for asymmetric catalysis of transfer hydrogenation of ketones

Ruthenium complexes, prepared by mixing the potassium salt of α‐amino acids and [RuCl₂(arene)]₂, acted as catalysts for the asymmetric transfer hydrogenation of ketones from 2‐propanol in the presence of KOH. For example, the transfer hydrogenation of acetophenone from 2‐propanol was catalyzed effectively by the ruthenium complex prepared from potassium L ‐prolinate and [RuCl₂(p‐cymene)]₂ to give (R)‐1‐phenylethanol in 72% yield with 81% ee. The yields and enantioselectivities of the product were influenced strongly by the structure of the α‐amino acidate ligand, arene ligand, and substrate, by the amount of additional base, and by the concentration of the substrates. The best enantiomeric excesses of the products was 92%, when 1‐tetralone was subjected to this reaction using a prolinated ruthenium complex bearing p‐cymene. Furthermore, the potassium salts of dipeptides were tested as a ligand for this transfer hydrogenation. Copyright © 2001 John Wiley & Sons, Ltd.     

X-ray energy dependence of the properties of the focused beams produced by polycapillary X-ray lens

We investigated X-ray energy distribution in an X-ray microbeam produced by a polycapillary X-ray lens in combination with a sealed-type X-ray tube. This polycapillary X-ray lens has an output focal distance (OFD) of approximately 15 mm. The size of the X-ray microbeam and its OFD were estimated by using a wire scanning method. In our case, the sizes of the X-ray microbeams at the output focal distance were 49 microm for Mo L(alpha), 36 microm for W L(alpha), and 28 microm for Mo K(alpha). The spot sizes depend on the energy of the X-ray fluorescence. The reason for the energy dependence is that X-ray capillary optics is based on the principle of propagation through glass capillaries by means of X-ray total external reflection. The evaluated OFD values of Mo L(alpha) and Mo K(alpha) were slightly changed in 17 microm. However, a deviation of 100 microm from the OFD caused only a 3% increase of the focal spot size. Therefore, we concluded that the OFD showed no significant dependence on X-ray energy.     

Electrophilic substitution reactions using an electrogenerated ArS(ArSSAr)+ cation pool as an ArS+ equivalent

Arylbis(arylthio)sulfonium ions (ArS(ArSSAr)⁺), which were generated and accumulated by the low-temperature electrolysis of diaryl disulfide (ArSSAr), were found to serve as ArS⁺ equivalent in electrophilic substitution reactions of aromatic compounds, enolizable ketones, enol acetates, ketene silyl acetals and allylsilanes to give the corresponding arylthiolated products.