Synthesis and in vitro evaluation of iodinated derivatives of piperazine as a new ligand for sigma receptor imaging by single photon emission computed tomography

A new series of radioiodinated analogues of 1-[2-(3,4-dimethoxyphenyl)ethyl]-4-(3-phenylpropyl)piperazine (SA4503) was synthesized and evaluated as a potential brain sigma-1 receptor imaging ligands by single photon emission computed tomography (SPECT). Iodinated analogues of SA4503 (4a-c) were prepared from piperazine in a high yield. The in vitro competition binding studies using [3H] DTG (sigma-1, 2), [3H] (+)-pentazocine (sigma-1), and [3H] DTG in the presence of carbetapentane (sigma-2) as sigma receptor selective radioligands were revealed that iodinated analogues 4a-c possess high affinities to sigma receptors (IC50: 4a=7.1, 4b=31.0, and 4c=77.3 nM). In particular, the affinity of 4a, bearing iodine at ortho position on the phenyl ring, was 4.4 times greater than SA4503, and 3 times greater than that of haloperidol. The meta-iodo analogue 4b was the same to SA4503, the lead compound. The radioiodinated derivatives, [125I] 4a, 4b were synthesized no-carrier-added from the corresponding tributyltin precursors by the iododestannylation reaction with high yields. The binding of [125I] 4a, 4b have been characterized in the rat brain membranes. These compounds were indicated single population binding to sigma receptor with high affinity (4a: Kd=1.86+/-0.34 nM, Bmax=205+/-28.9 fmol/mg protein, 4b: Kd=3.30+/-0.51 nM, Bmax=231.5+/-13.8 fmol/mg protein). In vitro blocking studies were confirmed that the high specificity of 4a, 4b. These results suggest that radioiodinated 4a and 4b are promising sigma receptors imaging ligand for pursuing further in vivo studies.     

Carboxyfluorescein leakage from poly(ethylene glycol)-grafted liposomes induced by the interaction with serum

The effects of fetal bovine serum (FBS) on carboxyfluorescein (CF) leakage from poly(ethylene glycol)-grafted liposomes (PEG-liposomes) were investigated. PEG-liposomes were prepared from dipalmitoylphosphatidylcholine (DPPC) and distearoyl-N-monomethoxy poly(ethylene glycol)-succinyl-phosphatidylethanolamines (DSPE-PEG) having PEG molecular weights of 1000, 2000, 3000 and 5000. The presence of FBS dramatically increased CF leakage from liposomes near the gel-liquid crystalline phase transition temperature, but had little effect at lower and higher temperatures. The CF leakage from PEG-liposomes whose molecular weight in PEG units was above 2000 was suppressed compared with that of liposomes without PEG. And, there was hardly any difference in the effect of the PEG molecular weight of the PEG-lipids on CF leakage from PEG-liposomes with FBS when PEG-lipids with a molecular weight in PEG units above 2000 were used. On the other hand, the leakage of CF from liposomes containing 0.145 mol fractions of DSPE-PEG1000 was larger than that of liposomes without PEG. Furthermore, the effects of FBS on the cooperative units of lipid molecules during the gel-liquid crystalline phase transition of liposomes were examined. However, the cooperative units of liposomes with FBS had little change compared with that of liposomes without FBS.     

A unified treatment of dividend payment problems under fixed cost and implementation delays

In this paper we study the dividend optimization problem for a corporation or a financial institution when the management faces (regulatory) implementation delays. We consider several cash reservoir models for the firm including two mean-reverting processes, Ornstein–Uhlenbeck and square-root processes. Since the cash flow structure of different companies have different qualitative behaviors, it makes sense to use different diffusions to model them. The delay causes significant difficulties to the optimization problem since the cash reservoir fluctuates during the delay period. We provide a uniform mathematical framework to analyze all the models and provide optimal threshold strategies at which the management initiates actions, i.e., declaration and payment of dividends. Our solution depends on a new characterization of the value function for one-dimensional diffusions and provide easily implementable algorithms to find the optimal control and the value function.     

Pattern-effect-free all-optical wavelength conversion using a hydrogenated amorphous silicon waveguide with ultra-fast carrier decay

Ultra-fast carrier decay, recently discovered in a hydrogenated amorphous silicon waveguide, can be exploited for pattern-effect-free all-optical signal processing based on optical Kerr nonlinearity. In this study, we utilized a 10 Gbit/s RZ-OOK data stream as a pump for degenerate four-wave mixing in a low-loss hydrogenated amorphous silicon waveguide. The propagation loss of the waveguide used was 1.0±0.2 dB/cm at 1550 nm. Unlike crystalline silicon waveguides, no noticeable difference was observed in the BER characteristics between the cases of PRBS 2(7)-1 and 2(31)-1.     

Comparative investigation of elastic properties in a trabecula using micro-Brillouin scattering and scanning acoustic microscopy

Micro-Brillouin scattering (μ-BR) and a 200 MHz scanning acoustic microscope (SAM) with similar spatial resolutions were applied to evaluate tissue elastic properties in two directions in a trabecula. Acoustic impedance measured by SAM was in the range of 5-9 Mrayl. Wave velocities determined by μ-BR were in the range of (4.75-5.11) × 10(3) m/s. Both exhibited a similar trend of variation across the trabecula and were significantly correlated (R(2) = 0.63-0.67, p < 0.01). μ-BR is useful for the evaluation of tissue stiffness within a trabecula. Combined with SAM or nanoindentation, it can provide additional information to assess elastic anisotropy at the micro-scale.     

Visible light-induced water oxidation catalyzed by molybdenum-based polyoxometalates with mono- and dicobalt(III) cores as oxygen-evolving centers

The Mo-based polyoxometalates containing mono- and dicobalt(III) catalyst cores, [CoMo(6)O(24)H(6)](3-) and [Co(2)Mo(10)O(38)H(4)](6-), were found to serve as O(2)-evolving catalysts in a system consisting of tris(2,2'-bipyridine)ruthenium(II) (Ru(bpy)(3)(2+)) and sodium persulfate (S(2)O) in an aqueous borate buffer solution at pH 8.0. Kinetics of O(2) evolution reveals that the higher cobalt nuclearity is not necessary to attain the highly active nature of the catalyst.     

Aerobic oxidation of alcohols in the liquid phase with nanoporous gold catalysts

Aerobic oxidation of alcohols in the liquid phase proceeded smoothly in the presence of nanoporous gold catalyst. The catalyst is reusable multiple times without leaching and loss of the catalytic activity. The reaction was applied successfully to a flow system. Adsorptions of O(2) and 1-phenylethanol into the AuNPore were confirmed by TDS analysis.     

Metal-free α-CH amination of ethers with hypervalent sulfonylimino-λ3-bromane that acts as an active nitrenoid

Hypervalent N-triflylimino-λ(3)-bromane undergoes direct and regioselective α-C-H amination of ethers at room temperature under transition metal-free conditions. Kinetic results, substituent and deuterium isotope effects suggest an asynchronous concerted organonitrenoid transition state with some hydride transfer character, analogous to that for alkane C-H insertions.     

Probing the onset of strong localization and electron–electron interactions with the presence of a direct insulator–quantum Hall transition

We have performed low-temperature transport measurements on a disordered two-dimensional electron system (2DES). Features of the strong localization leading to the quantum Hall effect are observed after the 2DES undergoes a direct insulator–quantum Hall transition on increasing the perpendicular magnetic field. However, such a transition does not correspond to the onset of strong localization. The temperature dependences of the Hall resistivity and Hall conductivity reveal the importance of the electron–electron interaction effects for the observed transition in our study.     

Synthesis and ring size effect of macrocyclic ethynylhelicene oligomers

[reaction: see text] The cyclization of acyclic ethynylhelicene oligomers with decyl 3,5-diiodobenzoate under optimized conditions gave the corresponding optically active [n+n]cycloalkynes (n = 4-8) in high yields. Their structures were compared in terms of ring size by using (1)H NMR, UV-vis, and CD spectroscopies and vapor pressure osmometry (VPO). The UV-vis spectra exhibited an increase in absorbance in proportion to n. In contrast, the CD spectra of the macrocycles exhibited a large ring size effect, comparable Deltaepsilon values despite the increase in n and temperature-dependent properties of the [8+8]cycloalkyne. It was concluded that [4+4]cycloalkyne, [5+5]cycloalkyne, [6+6]cycloalkyne, and [7+7]cycloalkyne have rigid structures, while [8+8]cycloalkyne has a flexible structure.