Open Talar Body Fracture With Dislocation of the Ankle and Subtalar Joint Accompanying Acute Rupture of the Peroneal Tendons in an Elite Female Gymnast: A Case Report.

Case: A 20-year-old elite female gymnast injured her right ankle on landing during a vaulting attempt. Diagnosis revealed an open fracture of the talar body, prompting referral to our center after wound flushing and closure. Peroneal tendon and lateral ligament ruptures were observed during surgery, necessitating one-stage repair.

Effects of Curing Agents on the Adhesion of Epoxy Resin to Copper: A Density Functional Theory Study.

Epoxy resins are widely used adhesives in industrial fields. To use epoxy resin as an adhesive, it is necessary to mix the epoxy resin with a hardener. Hardeners have various functional groups and skeletons, and the properties of epoxy resins vary depending on the hardener.

Highly-purified rapidly expanding clones, RECs, are superior for functional-mitochondrial transfer.

Background: Mitochondrial dysfunction caused by mutations in mitochondrial DNA (mtDNA) or nuclear DNA, which codes for mitochondrial components, are known to be associated with various genetic and congenital disorders. These mitochondrial disorders not only impair energy production but also affect mitochondrial functions and have no effective treatment. Mesenchymal stem cells (MSCs) are known to migrate to damaged sites and carry out mitochondrial transfer.

Synthesis and Characterization of 1-Hydroxy-4,5-arene-Fused Tropylium Derivatives.

The properties of 1-hydroxy-4,5-arene-fused tropyliums were assessed based on experimental and theoretical investigations. An X-ray crystallographic analysis revealed a decrease of bond alternation in the seven-membered ring of 1-hydroxy-4,5-benzotropylium derivatives compared with that of the parent 4,5-benzotropones, which is indicative of an increase in aromaticity upon protonation. NICS and AICD calculations also supported the increased aromaticity of 1-hydroxy-4,5-arene-fused tropylium.

Synthesis of 4,5-Benzotropone π Complexes of Iron, Rhodium, and Iridium and Their Potential Use in Catalytic Borrowing-Hydrogen Reactions.

The syntheses of rhodium, iridium, and iron π complexes bearing 4,5-benzotropone ligands are reported. X-ray crystallographic analyses revealed that a tropone core coordinates to a metal center in a η manner with a tub-form geometry. Some of the benzotropone π complexes exhibited catalytic activity for -alkylation of aniline by borrowing hydrogen.

Evaluation and improvement of storage stability of astaxanthin isomers in oils and fats.

Astaxanthin Z-isomers potentially have greater bioavailability and biological activity than (all-E)-astaxanthin. However, the stability of the Z-isomers is lower than the all-E-isomer, which is a serious problem affecting its practical use. In this study, we investigated the impacts of different suspension media (oils and fats) and additives on astaxanthin isomer stability and identified suitable ones for astaxanthin stabilization.

-Isomers of Astaxanthin Exhibit Greater Bioavailability and Tissue Accumulation Efficiency than the All--Isomer.

The purpose of the present study was to clarify the differences in the bioavailability and tissue accumulation efficiency between (all-)- and ()-astaxanthin. Astaxanthin with a high proportion of the -isomer (especially rich in the 9- and 13-isomers) was prepared from (all-)-astaxanthin by thermal treatment and solid-liquid separation. The all--isomer- or -isomer-rich diet was fed to male rats for 2 weeks.

Astaxanthin Z-isomer-rich diets enhance egg yolk pigmentation in laying hens compared to that in all-E-isomer-rich diets.

The effects of feeding diets containing astaxanthin with different Z-isomer ratios to laying hens on egg qualities, such as astaxanthin concentration in egg yolk and yolk color, were investigated. As the astaxanthin source, a natural microorganism Paracoccus carotinifaciens was used. Astaxanthin with different Z-isomer ratios was prepared by thermal treatment with different conditions and then added to the basal diet at a final astaxanthin concentration of 8 mg/kg.

Effect of astaxanthin-rich extract derived from on the status of stress and sleep in adults.

This study investigated the effect of a dietary supplement containing astaxanthin-rich extract derived from (astaxanthin supplement) on the status of stress and sleep in individuals aged 20-64 years. Twenty-five subjects orally administered 12 mg astaxanthin/day of astaxanthin supplement for 8 weeks (astaxanthin group) and 29 subjects given a placebo (placebo group) were evaluated with Profile of Mood States 2nd Edition for stress and Oguri-Shirakawa-Azumi Sleep Inventory for Middle-aged and Aged version for sleep. We did not observe any significant intergroup differences in the stress and sleep.

Recurrent Erythema Nodosum in a Child with a Gene Mutation.

We report the case of a 6-year-old male who developed recurrent erythema nodosum (EN) at the age of 3 years. The patient exhibited hypertelorism, low-set ears, micrognathia, moderate intellectual disability, thin long fingers, loose anagen hair, and prominent palmoplantar wrinkles. A heterozygous single nucleotide variant in the gene (c.

Effects of astaxanthin-rich dried cell powder from Paracoccus carotinifaciens on carotenoid composition and lipid peroxidation in skeletal muscle of broiler chickens under thermo-neutral or realistic high temperature conditions.

Thirty-two 15-day old broiler chicks (Chunky strain ROSS 308) were randomly divided into four treatments in a 2 × 2 factorial design. The main factors were diet (basal diet or basal diet supplemented with 0.15% astaxanthin-rich dried cell powder (Panaferd-P [astaxanthin 30 ppm]) and ambient temperature (thermo-neutral [25 ± 1°C] or high [35 ± 1°C for 6 hr]).

Structures of Yellow Xanthophylls and Metabolism of Astaxanthin in the Prawn Penaeus japonicus.

The dried powder of Paracoccus carotinifaciens (PANAFERD-AX) contains (3S,3'S)-astaxanthin as a major carotenoid. Administration of PANAFERD-AX for pigmentation of the prawn Penaeus japonicus was examined. Total carotenoid contents in the carapace, muscle, and head of the prawn were dose-dependently increased depending on the amount of PANAFERD-AX administered.

Total Synthesis of Polycavernosides A and B, Two Lethal Toxins from Red Alga.

Polycavernosides A and B are glycosidic macrolide natural products isolated as the toxins causing fatal human poisoning by the edible red alga Gracilaria edulis (Polycavernosa tsudai). Total synthesis of polycavernosides A and B has been achieved via a convergent approach. The synthesis of the macrolactone core structure is highlighted by the catalytic asymmetric syntheses of the two key fragments using hetero-Diels-Alder reaction and Kiyooka aldol reaction as the key steps, their union through Suzuki-Miyaura coupling, and Keck macrolactonization.

Toward the Total Synthesis of Amphidinolide N: Synthesis of the C8-C29 Fragment.

A synthesis of the C8-C29 fragment of amphidinolide N, a potent cytotoxic macrolide isolated from the marine dinoflagellate Amphidinium sp., has been achieved. The key features of the synthesis involve a convergent union of the C9-C15 and C16-C29 fragments by Steglich esterification and the construction of a pyran unit through a Tebbe methylenation/ring-closing metathesis sequence.

Contrast adaptation to luminance and brightness modulations.

Perceptual brightness and color contrast decrease after seeing a light temporally modulating along a certain direction in a color space, a phenomenon known as contrast adaptation. We investigated whether contrast adaptation along the luminance direction arises from modulation of luminance signals or apparent brightness signals. The stimulus consisted of two circles on a gray background presented on a CRT monitor.

Progress toward the Total Synthesis of Goniodomin A: Stereocontrolled, Convergent Synthesis of the C12-C36 Fragment.

Goniodomin A is a marine polyether macrolide natural product isolated from the dinoflagellate Alexandrium hiranoi. In this paper, we report stereocontrolled, convergent synthesis of a fully functionalized C12-C36 fragment of goniodomin A. The synthesis of the C12-C25 vinylstannane involved a Wittig reaction and a reductive cycloetherification for the construction of the dihydropyran ring.

Modulation of Energy Conversion Processes in Carbonaceous Molecular Bearings.

The energetics and photodynamics of carbonaceous molecular bearings with discrete molecular structures were investigated. A series of supramolecular bearings comprising belt-persistent tubular cycloarylene and fullerene molecules accepted photonic stimuli to afford charge-separated species via a photoinduced electron transfer process. The energy conversion processes associated with the photoexcitation, however, differed depending on the molecular structure.

Graphene oxide-Li(+)@C60 donor-acceptor composites for photoenergy conversion.

An ionic endohedral metallofullerene (Li(+)@C60) with mild hydrophilic nature was combined with graphene oxide (GO) to construct a donor-acceptor composite in neat water. The resulting composite was characterised by UV-Vis and Raman spectroscopy, powder X-ray diffraction, dynamic light scattering measurements and transmission electron microscopy. Theoretical calculations (DFT at the B3LYP/6-31(d) level) were also utilized to gain further insight into the composite formation.

Photoinduced electron transfer in a supramolecular triad produced by porphyrin anion-induced electron transfer from tetrathiafulvalene calix[4]pyrrole to Li(+)@C60.

Binding of a porphyrin carboxylate anion () to tetrathiafulvalene calix[4]pyrrole (TTF-C4P) results in electron transfer from TTF-C4P to Li(+)@C60 to produce the charge-separated state (1/TTF-C4P˙(+)/Li(+)@C60˙(-)) in benzonitrile. Upon photoexcitation of , photoinduced electron transfer from the triplet excited state of to TTF-C4P˙(+) occurs to produce the higher energy charge-separated state (˙(+)/TTF-C4P/Li(+)@C60˙(-)), which decays to the ground state with a lifetime of 4.8 μs.

Near-Infrared Photoelectrochemical Conversion via Photoinduced Charge Separation in Supramolecular Complexes of Anionic Phthalocyanines with Li(+)@C60.

Two phthalocyanines possessing carboxylate groups ((TBA)4H2Pc·1 and (TBA)4H2Pc·2) form 1:2 supramolecular complexes with lithium cation-encapsulated C60 (Li(+)@C60) [H2Pc·1(4-)/(Li(+)@C60)2 and H2Pc·2(4-)/(Li(+)@C60)2] in a polar mixed solvent. From the UV-vis spectral changes, the binding constants (K) were estimated as ca. 10(12) M(-2).

Efficient charge separation in Li(+) @C60 supramolecular complexes with electron donors.

Lithium-ion-encapsulated fullerene (Li(+) @C60 ) exhibits greatly enhanced reactivity in photoinduced electron-transfer reduction with electron donors compared with pristine C60 . The enhanced reactivity of Li(+) @C60 results from the more positive one-electron reduction potential of Li(+) @C60 (+0.14 V versus a standard calomel electrode (SCE)) than that of C60 (-0.

Long-lived charge separation in a rigid pentiptycene bis(crown ether)-Li(+)@C60 host-guest complex.

We report long-lived charge separation in a highly rigid host-guest complex of pentiptycene bis(crown ether) and Li(+)@C60, in which the pentiptycene framework is actively involved as an electron donor in a photoinduced electron-transfer process to the excited states of Li(+)@C60 through a rigid distance in the complex.

Clinical overview of nephrogenic diabetes insipidus based on a nationwide survey in Japan.

Background: Nephrogenic diabetes insipidus (NDI) is a rare disease whose complications include polyuria, renal dysfunction, growth disorder and mental retardation. The details of NDI's clinical course have been unclear. To address this uncertainty, we performed a large investigation of the clinical course of NDI in Japan.