Dissociative ionization and post-ionization alignment of aligned O in an intense femtosecond laser field.

We examined dissociative ionization of O in an intense femtosecond laser field (782 nm, 120 fs, 4 × 10 W cm) by recording the kinetic energy distribution of O emitted along the laser polarization direction as a function of the delay time between the pump pulse (9 × 10 W cm) for the molecular alignment and the probe pulse for the dissociative ionization. We found the two distinct rotational revival patterns which are out-of-phase by π with each other in the kinetic energy distribution of O. One of the patterns shows the dissociative ionization is enhanced when the O axis is parallel to the laser polarization direction, suggesting that the ionization is induced by the electron emission from the 3σ orbital.

Estrogen, via ESR2 receptor, prevents oxidative stress-induced Müller cell death and stimulates FGF2 production independently of NRF2, attenuating retinal degeneration.

In this study, we aimed to investigate the effects of the deficient antioxidative gene, nuclear factor-erythroid 2-related factor 2 (Nrf2), on 17β-estradiol (E)-mediated oxidative stress response, with a specific focus on growth factor production and cell death in Müller cells and retinal tissue. Administration of hydrogen peroxide (HO) reduced the viability of Müller cells derived from Nrf2 wild-type (WT) and knockout (KO) mice. However, this effect was more significant in the KO cells than in the WT cells.

Glutathione trisulfide prevents lipopolysaccharide-induced retinal inflammation via inhibition of proinflammatory cytokine production in glial cells.

We aimed to investigate the impact of glutathione trisulfide (GSSSG) on lipopolysaccharide (LPS)-induced inflammation in retinal glia. Inflammatory responses in mouse-derived glial cells and Wistar rat retinas were stimulated with administration of LPS. Cell survival and proinflammatory cytokine production were examined using the Calcein-AM assay, and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and enzyme-linked immunosorbent assay (ELISA), respectively.

Single and sequential double ionization of NO radical in intense laser fields.

We examine the dependences of the single and double ionization probabilities of NO radical on the angle between the NO axis and the laser polarization direction in an intense laser field (790 nm, 100 fs, 1-10 × 10 W/cm) and show that the double ionization is enhanced when the NO axis is parallel to the laser polarization direction. We reveal that the angular dependence of the sequential double ionization probability is determined by the shape of the 5σ orbital of NO from which the second photoelectron is emitted in the ionization from NO to NO. We also reveal that the fast oscillation in the probability of the tunnel ionization of NO originating from a coherent superposition of the two spin-orbit components in the electronic ground XΠ state is described well based on the molecular Ammosov-Delone-Krainov (MO-ADK) theory in which the time evolution of the electron density distribution of the 2π orbital is taken into account.

Rotational dynamics and transitions between Λ-type doubling of NO induced by an intense two-color laser field.

We numerically investigate the rotational dynamics of NO in the electronic ground XΠ state induced by an intense two-color laser field (10 TW/cm) as a function of pulse duration (0.3-25 ps). In the short pulse duration of less than 12 ps, rotational Raman excitation is effectively induced and results in molecular orientation.

3D-TEM study on the novel bicontinuous microdomain structure.

An ordered bicontinuous double-diamond (OBDD) morphology was found in polystyrene-block-(poly-4-vinylphenyldimethylvinylsilane-graft-polyisoprene), PS-b-(PVS-g-PI), block-graft copolymer. We obtained a 3D image of the microdomain structure formed in PS-b-(PVS-g-PI) using 3D-TEM. The 3D image shows that the polystyrene (PS) phase consists of two independent and interwoven networks.

Comparison of lesion enhancement between BB Cube and 3D-SPGR images for brain tumors with 1.5-T magnetic resonance imaging.

Purpose: This study aimed to compare the detectability of neoplastic lesion enhancement after gadolinium-based contrast media injection in three-dimensional T1-weighted black blood Cube (3D-T1W BB Cube) and three-dimensional T1-weighted fast spoiled gradient-echo (3D-T1W fast SPGR) images obtained with 1.5-T magnetic resonance imaging (MRI).

Materials And Methods: Phantom and clinical studies were performed to compare the lesion detectability and contrast ratio (CR) between 3D-T1W BB Cube and 3D-T1W fast SPGR pulse sequences.

Spectroscopic study on deuterated benzenes. II. High-resolution laser spectroscopy and rotational structure in the S(1) state.

High-resolution spectra of the S1←S0 transition in jet-cooled deuterated benzenes were observed using pulse dye amplification of single-mode laser light and mass-selective resonance enhanced multiphoton ionization (REMPI) detection. The vibrational and rotational structures were accurately analyzed for the vibronic levels in the S1 state. The degenerate 6(1) levels of C6H6 or C6D6 are split into 6a(1) and 6b(1) in many of deuterated benzenes.

Quantum unidirectional rotation directly imaged with molecules.

A gas-phase molecular ensemble coherently excited to have an oriented rotational angular momentum has recently emerged as an appropriate microscopic system to illustrate quantum mechanical behavior directly linked to classical rotational motion, which has a definite direction. To realize an intuitive visualization of such a unidirectional molecular rotation, we report high-resolution direct imaging of direction-controlled rotational wave packets in nitrogen molecules. The rotational direction was regulated by a pair of time-delayed, polarization-skewed laser pulses, introducing the dynamic chirality to the system.

Multiple primary malignancies in patients with prostate cancer: increased risk of secondary malignancies after radiotherapy.

Background: New treatment strategies for prostate cancer have recently been developed, but multiple malignancies remain a major concern. The aim of this study was to evaluate the characteristics of multiple malignancies and to analyze the risk of secondary malignancies after radiotherapy for prostate cancer.

Methods: From 2000 to 2011, 150 patients with prostate cancer were treated with curative radiotherapy in our department.

Transfer of chirality from molecule to phase in self-assembled chiral block copolymers.

Here, we report the mechanisms of chiral transfer at various length scales in the self-assembly of enantiomeric chiral block copolymers (BCPs*). We show the evolution of homochirality from molecular chirality into phase chirality in the self-assembly of the BCPs*. The chirality of the molecule in the BCP* is identified from circular dichroism (CD) spectra, while the handedness of the helical conformation in the BCP* is determined from a split-type Cotton effect in vibrational circular dichroism spectra.

Defining the nanostructured morphology of triblock copolymers using resonant soft X-ray scattering.

The morphologies of a poly(1,4-isoprene)-block-polystyrene-block-poly(2-vinyl pyridine) (IS2VP) copolymer were investigated using resonant soft X-ray scattering (RSoXS) together with scanning force microscopy, small-angle X-ray scattering, and electron microscopy. Differences in the nanoscopic morphologies in the bulk and thin film samples were observed arising from the competition between segmental interactions between the blocks and the substrate and the surface energies of each block. Using soft X-rays at selected photon energies to isolate the scattering contribution from different polymer blocks, RSoXS unambiguously defined the complex morphology of the triblock copolymer.

Unveiling the nonadiabatic rotational excitation process in a symmetric-top molecule induced by two intense laser pulses.

We experimentally investigate the nonadiabatic rotational excitation process of a symmetric-top molecule, benzene, in the electronic ground state irradiated by intense nonresonant ultrafast laser fields. The initial rotational-state distribution was restricted mostly to the five lowest levels with different nuclear spin modifications by an extensive adiabatic cooling with the rotational temperature well below 1 K, and distributions after the interaction with a femtosecond double-pulse pair (3-5 TW/cm(2) each with 160 fs duration) with time delays were probed in a quantum-state resolved manner by employing resonant enhanced multiphoton ionization via the S(1) ← S(0) 6(0) (1) vibronic transition. Populations of 10 rotational levels with J ranging from 0 to 4 and K from 0 to 3 were examined to show an oscillatory dependence on the time delay between the two pulses.

Coherent correlation between nonadiabatic rotational excitation and angle-dependent ionization of NO in intense laser fields.

We investigate coherent correlation between nonadiabatic rotational excitation and angle-dependent ionization of NO in intense laser fields in the state-resolved manner. When neutral NO molecules are partly ionized in intense laser fields (I(0) > 35 TW/cm(2)), a hole in the rotational wave packet of the remaining neutral NO is created because of the ionization rate depending on the alignment angle of the molecular axis with respect to the laser polarization direction. Rotational state distributions of NO are experimentally observed, and then the characteristic feature that the population at higher J levels is increased by the ionization can be identified.

Ultrafast angular momentum orientation by linearly polarized laser fields.

We theoretically show and experimentally verify that a pair of linearly polarized intense femtosecond pulses can create molecular ensembles with oriented rotational angular momentum on an ultrafast (approximately ps) time scale, when the delay and the mutual polarization between them are appropriately arranged. An asymmetric distribution for +M and -M sublevels relies on quantum interference between rotational wave packets created in stimulated Raman excitation by the first and second pulses. The present approach provides spatiotemporally propagating ensembles, of which the classical perspective is molecules rotating in a clockwise or counterclockwise direction.

Block copolymers with a twist.

Chiral block copolymers (BCPs*) comprising chiral entities were designed to fabricate helical architectures (i.e., twisted morphologies) from self-assembly.

High therapeutic effectiveness of postoperative irinotecan chemotherapy in a typical case of radiographically and pathologically diagnosed pleuropulmonary blastoma.

A 2-year 9-month-old girl with a large mass in the right chest underwent middle and inferior lobectomy, after which the mass was pathologically diagnosed as a pleuropulmonary blastoma (PPB). The clinical, radiographic, and pathologic findings were typical. Three courses of postoperative chemotherapy with 2 different regimens were ineffective in preventing multiple metastases of the lung.

Helical nanocomposites from chiral block copolymer templates.

Three-dimensional hexagonally packed PLLA nanohelices in the PS matrix were formed in the self-assembly of PS-PLLA chiral block copolymer. After hydrolysis of the PLLA blocks, PS with hexagonally packed helical nanochannels can be fabricated and treated as the template for the following sol-gel process. Subsequently, silica precursor mixture was introduced into the PS template by a pore-filling process.

Nonlinear optical properties of gold nanoparticles selectively introduced into the periodic microdomains of block copolymers.

Nonlinear-optical nanocomposite materials with a photonic crystal structure were fabricated using block copolymers and gold nanoparticles. By dispersing the gold nanoparticles into the selective microdomains of the block copolymers, we could achieve the enhancement of nonlinear optical properties as revealed by the Z-scan technique. The optical nonlinearities were enhanced by the local field effect and the effect of the periodic distribution of the microdomains filled with gold nanoparticles.

Control of the microdomain orientation in block copolymer thin films with homopolymers for lithographic application.

Block copolymer lithography is a promising method for fabricating periodical nanopatterns of less than 20 nm by self-assembly and can be applicable for fabricating patterned magnetic media with a recording density over 1 Tb/in.2. We found a simple technique to control the orientation of cylindrical microdomains in thin films.

Quantitative comparison between dynamic structure factors obtained experimentally and those calculated with Doi-Onuki theory.

This paper reports results of quantitative comparison between dynamic structure factors obtained experimentally and those calculated by using the Doi and Onuki (DO) theory for semidilute polymer solutions. The authors obtained the dynamic structure factors with dynamic light scattering (DLS) experiment while the dynamic structure factors were calculated by using DO theory with osmotic compressibility, viscoelastic relaxation function, and friction coefficient which are obtained independently of DLS experiment. Calculated dynamic structure factors agree with experimental ones well and can express the q-dependent fast modes and the q-insensitive slow mode which experimental ones show.