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Introduction: 3-[18F]fluoro-α-methyl-L-tyrosine ([18F]FAMT) is a promising amino acid tracer targeting L-type amino acid transporter 1 (LAT1). One concern regarding the diagnosis using [18F]FAMT is the possibility of false-negative findings because of its relatively low accumulation level even in malignant tumors. Moreover, preloading probenecid, an organic anion transporter inhibitor, markedly increased the tumor accumulation level of radioiodine-labeled α-methyltyrosine. In this study, we evaluated the usefulness of preloading probenecid in improving the tumor-imaging capability of [18F]FAMT. Methods: Three biodistribution studies of [18F]FAMT were conducted in normal mice to elucidate the usefulness of probenecid preloading. Then, a biodistribution study and positron emission tomography (PET) imaging of [18F]FAMT were conducted with or without probenecid injection in tumor-bearing mice. Results: Probenecid preloading significantly delayed blood clearance and consequently enhanced the accumulation of [18F]FAMT in the pancreas, a LAT1-positive organ. The effects of probenecid preloading were independent of the administration route. Tumor accumulation level in the biodistribution study and the maximum standardized uptake value in tumors on PET imaging of the probenecid preloading group were significantly higher than those of the control (without probenecid injection) group in tumor-bearing mice. Conclusions: Preloading probenecid significantly delayed blood clearance and consequently enhanced the accumulation of [18F]FAMT in tumors. These results indicate that preloading probenecid could improve the diagnostic accuracy of [18F]FAMT.

Excess lipid accumulation is associated with obesity-related chronic kidney disease, but the mechanisms of fatty acid (FA) uptake have been poorly understood. To this end, we investigated how FAs are taken up by tubular epithelial cells (TECs) in mice by using in vivo FA tracing and histological methods. Immunohistochemistry showed that CD36, which is a well-known FA transporter, was abundantly expressed on the basolateral side of proximal TECs (PTECs). The uptake of 125I-BMIPP (a radiolabeled FA tracer) was significantly reduced in CD36-knockout kidneys at 1 min after injection. In vivo imaging with multiphoton microscopy revealed that BODIPY-C12 (a fluorescence-labeled FA tracer) accumulated on both the basolateral and apical sides of PTECs. Numerous lipid droplets accumulated in PTECs after accelerated lipolysis. Furthermore, PTEC-specific injury via diphtheria toxin (DT) injection in transgenic mice expressing the DT receptor resulted in a compensatory increase in lipid accumulation in downstream TECs. Importantly, urinary FAs were undetectable, even in mice and humans with remarkable albuminuria. Our data demonstrate that renal TECs take up FAs from blood (CD36-dependent) and primary urine (CD36-independent) and can store excess FAs as neutral lipids. The results further show that renal tubules have hitherto largely unappreciated mechanisms by which the excretion of FAs into the urine is avoided.

This study investigates the photoluminescence (PL) spectra of Cu2Sn1−x Ge x S3 (CTGS) thin films, which are currently the most suitable composition ratio for high-efficiency absorbers through low temperature-PL measurements to reveal the effects of the x ratio on defect properties of CTGS thin films. The PL spectrum of Cu2SnS3 (CTS) thin films with x= 0.00 exhibits five peaks at 0.782, 0.832, 0.862, 0.885, and 0.933 eV. Moreover, all PL peak positions in the CTGS thin films shift to higher energies with increasing x ratios because the defect levels in the films changed with an increase in the x ratio. Moreover, we obtain the estimated activation energy (E a) values of the CTS thin films with x = 0.00 ranging from 6 to 20 meV. The E a values of CTGS are similar to those of the CTGS thin films, even at x ratios of up to 0.19 in CTGS thin films. The increasing x ratio in CTGS thin films does not influence the acceptor in CTGS. Therefore, the CTGS is advantageous as an absorption layer in solar cells rather than a CTS because E g can be large while maintaining a shallow acceptor. Hence, CTGS can be expected to be increasingly used like CuIn1−x Ga x Se2 and Cu2ZnSnS4 as next-generation absorption materials.

In this work, a comprehensive study on the influences of the various synthesizing parameters of monoclinic Cu2SnS3 using the RF sputtering method, followed by the sulfurization process, is investigated. In particular, the impact of sputtering power and pressure on multi-material target Cu–Sn (compositional ratio Cu:Sn of 52:48%) was examined. All samples exhibited a monoclinic structure with similar split bandgaps around 0.9 eV. Increasing sputtering power showed direct effects on the sputtered Cu/Sn atoms ratio and the secondary phases obtained. The increase of sputtering pressure causes gas droplets and blistering on the film surfaces. The effects of changing the sulfurization temperature and the sulfur powder amount were also studied. The increase in the sulfurization temperature reduces the surface roughness, increases film crystallinity, and minimizes Cu-based secondary phases. The sulfur amount used during the sulfurization process showed a vital impact on film formation. Using a small amount of sulfur produced a partially sulfurized film that exhibited a poor performance solar cell. A power conversion efficiency of 1.94% is achieved with the optimized condition for the bare Cu2SnS3 without doping or heat treatment for the fabricated cell.

Introduction: The kidney combusts a large amount of fatty acid (FA) for body fluid homeostasis. Despite the high demand for FA, however, little is known about the mechanisms of FA uptake. We aimed to determine how FAs are taken up by tubular epithelial cells. Methods and Results: Immunohistochemistry showed that CD36, known as an important FA transporter in the heart, was also expressed in the basolateral side of proximal tubule epithelial cells (PTECs). The uptake of 125 I-BMIPP, radio-labeled FA tracer, was significantly reduced in the kidney in CD36 knockout mice 1 min after its injection compared with wild-type mice, while the significant difference disappeared 30 min after the injection. In vivo imaging with two-photon microscopy revealed that BODIPY-C 12 , fluorescence-labeled FA tracer, was accumulated in the basolateral side (blood side) of PTECs shortly after its injection, which was followed by accumulation in the apical side (primary urine side), suggesting bidirectional FA uptake by PTECs. A large amount of neutral lipid was accumulated in the kidney when serum FA concentration was increased by accelerated lipolysis by administration of a β3 adrenergic receptor agonist. Immunofluorescence with cell-specific antibodies revealed that the cells with the most abundant lipid accumulation were PTECs, followed by tubular epithelial cells of the distal nephron. In addition, neutral lipid accumulation was enhanced even in the distal nephron when PTECs were injured with administrations of diphtheria toxin (DT) in mice overexpressing DT-receptor in a PTEC-specific manner. Importantly, the PTEC-injured mice exhibited marked albuminuria, suggesting disturbance of protein reabsorption. Despite marked albuminuria, however, urinary FA was not detected at all, suggesting complete FA reabsorption independently of albumin reabsorption in the kidney. Conclusions: Our results revealed the unique and prominent capability of proximal and distal tubular epithelial cells to take up FA from both blood (CD36-dependent) and primary urine (CD36-independent) and to store them as neutral lipids. We further suggest that the kidney acts not only as FA consuming tissue but also as FA keeping tissue to completely reabsorb FA from primary urine for unwasted energy use.

The fundamental defects around the p–n interface were analyzed based on low temperature photoluminescence measurements to determine the origin of the various defects around the n-CdS/p-SnS structure in tin sulfide (SnS) solar cells. Particularly, the effects of Cd, S, and Na atoms on PL at the interface of a CdS layer and various treated SnS layers were examined. The PL peaks at 1.08 and 1.23 eV in the CdS/SnS structure, which were observed using the Cd partial electrolyte-treated SnS film, were associated with the formation of Cd-related defects. Furthermore, the PL peak at 1.27 eV in the CdS/SnS structure, which was observed using the sulfurized-SnS film and the excess Na-diffused SnS film, was associated with the formation of S-related defects such as OS defects. These findings present considerable potential for improving the efficiency of SnS solar cells.

3-[Three biodistribution studies of [Probenecid preloading significantly delayed blood clearance and consequently enhanced the accumulation of [Preloading probenecid significantly delayed blood clearance and consequently enhanced the accumulation of [

Backgrounds Overexpression of epidermal growth factor receptor (EGFR) has been established as a valid therapeutic target of non-small cell lung cancer (NSCLC). However, the clinical benefit of cetuximab as an EGFR-targeting drug is still controversial, partially due to the lack of effective means to identify suitable patients. This study aimed to investigate the potential of radiolabeled cetuximab as a non-invasive tool to predict cetuximab accumulation in NSCLC tumor xenografts with varying EGFR expression levels. Methods The NSCLC tumors in model mice were subjected to in vivo biodistribution study and positron emission tomography (PET) imaging 48 h after injection of either 111In- or 64Cu-labeled cetuximab. The EGFR expression levels of NSCLC tumors were determined by ex vivo immunoblotting. Results We found that tumors with high EGFR expression had significantly higher [111In]In-DOTA-cetuximab accumulation than tumors with moderate to low EGFR expression (P 111In]In-DOTA-cetuximab tumor uptake and EGFR expression level (r = 0.893), and between [64Cu]Cu-DOTA-cetuximab tumor uptake with EGFR expression level (r = 0.915). PET imaging with [64Cu]Cu-DOTA-cetuximab allowed clear visualization of tumors. Conclusion Our findings suggest that this immuno-PET imaging can be clinically translated as a tool to predict cetuximab accumulation in NSCLC cancer patients prior to cetuximab therapy.

The fundamental electrical properties of undoped and Sb-induced Cu2SnS3 (CTS) thin films were evaluated. Furthermore, the relationship between defect properties during intentional degradation and thin film/solar cell properties was investigated. The carrier concentration decreased after Sb induction in the CTS film, and the resistivity increased by one order of magnitude. These values were independent of the Sb volume. These results imply that a small quantity of Sb atoms passivates the defects, such as Sb atoms at Sn or Cu sites that compensate for the intrinsic acceptors at Cu vacancies. In addition, the number of defects around the grain boundary tended to decrease with Sb induction because of passivation. The carrier concentration of the CTS layer remained unchanged following proton irradiation at 1 × 1014 cm−2. Furthermore, the number of defects increased, independent of the Sb induction.

Progesterone receptor membrane associated component 1 (PGRMC1) exhibits haem-dependent dimerization on cell membrane and binds to EGF receptor and cytochromes P450 to regulate cancer proliferation and chemoresistance. However, its physiological functions remain unknown. Herein, we demonstrate that PGRMC1 is required for adipogenesis, and its expression is significantly enhanced by insulin or thiazolidine, an agonist for PPARγ. The haem-dimerized PGRMC1 interacts with low-density lipoprotein receptors (VLDL-R and LDL-R) or GLUT4 to regulate their translocation to the plasma membrane, facilitating lipid uptake and accumulation, and de-novo fatty acid synthesis in adipocytes. These events are cancelled by CO through interfering with PGRMC1 dimerization. PGRMC1 expression in mouse adipose tissues is enhanced during obesity induced by a high fat diet. Furthermore, adipose tissue-specific PGRMC1 knockout in mice dramatically suppressed high-fat-diet induced adipocyte hypertrophy. Our results indicate a pivotal role of PGRMC1 in developing obesity through its metabolic regulation of lipids and carbohydrates in adipocytes., Ryogo Furuhata, Yasuaki Kabe et al. discover that PGRMC1 is required for adipogenesis in mice and its expression is increased by insulin or PPARγ agonists. They find that knocking out PGRMC1 protects against diet-induced obesity by regulating lipid uptake and accumulation.

Sesamin [(7α,7′α,8α,8′α)-3,4:3′,4′-bis(methylenedioxy)-7,9′:7′,9-diepoxylignane] is a major lignan in sesame seeds. Sesamin is converted to the catechol metabolite, SC1 [(7α,7′α,8α,8′α)-3′,4′-methylenedioxy-7,9′:7′,9-diepoxylignane-3,4-diol] with anti-inflammatory effects after oral administration. However, its molecular target remains unknown. Analysis using high-performance affinity nanobeads led to the identification of annexin A1 (ANX A1) as an SC1-binding protein. SC1 was found to bind to the annexin repeat 3 region of ANX A1 with a high-affinity constant (Kd = 2.77 μmol L−1). In U937 cells, SC1 exhibited an anti-inflammatory effect dependent on ANX A1. Furthermore, administration of sesamin or SC1 attenuated carbon tetrachloride-induced liver damage in mice and concurrently suppressed inflammatory responses dependent on ANX A1. The mechanism involved SC1-induced ANX A1 phosphorylation at serine 27 that facilitates extracellular ANX A1 release. Consequently, the ANX A1 released into the extracellular space suppressed the production of tumor necrosis factor α. This study demonstrates that ANX A1 acts as a pivotal target of sesamin metabolites to attenuate inflammatory responses.

Simple Summary Carbon ion radiotherapy is an emerging cancer treatment modality that has a greater therapeutic window than conventional photon radiotherapy. To maximize the efficacy of this extremely scarce medical resource, it is important to identify predictive biomarkers of higher carbon ion relative biological effectiveness (RBE) over photons. Here we show that the carbon ion RBE in human cancer cells correlates with the cellular uptake of 64Cu(II)-diacetyl-bis(N4-methylthiosemicarbazone) (64Cu-ATSM), a potential radioligand that reflects an over-reduced intracellular environment. High RBE/64Cu-ATSM cells show greater steady-state levels of antioxidant proteins and increased capacity to scavenge reactive oxygen species in response to X-rays than low RBE/64Cu-ATSM counterparts. These data suggest that the cellular antioxidant activity is a possible determinant of carbon ion RBE predictable by 64Cu-ATSM uptake. Abstract Carbon ion radiotherapy is an emerging cancer treatment modality that has a greater therapeutic window than conventional photon radiotherapy. To maximize the efficacy of this extremely scarce medical resource, it is important to identify predictive biomarkers of higher carbon ion relative biological effectiveness (RBE) over photons. We addressed this issue by focusing on cellular antioxidant capacity and investigated 64Cu(II)-diacetyl-bis(N4-methylthiosemicarbazone) (64Cu-ATSM), a potential radioligand that reflects an over-reduced intracellular environment. We found that the carbon ion RBE correlated with 64Cu-ATSM uptake both in vitro and in vivo. High RBE/64Cu-ATSM cells showed greater steady-state levels of antioxidant proteins and increased capacity to scavenge reactive oxygen species in response to X-rays than low RBE/64Cu-ATSM counterparts; this upregulation of antioxidant systems was associated with downregulation of TCA cycle intermediates. Furthermore, inhibition of nuclear factor erythroid 2-related factor 2 (Nrf2) sensitized high RBE/64Cu-ATSM cells to X-rays, thereby reducing RBE values to levels comparable to those in low RBE/64Cu-ATSM cells. These data suggest that the cellular activity of Nrf2-driven antioxidant systems is a possible determinant of carbon ion RBE predictable by 64Cu-ATSM uptake. These new findings highlight the potential clinical utility of 64Cu-ATSM imaging to identify high RBE tumors that will benefit from carbon ion radiotherapy.

The effects of Na on Cu2SnS3 (CTS) solar cells were investigated by focusing on the electrical properties obtained using electrochemical impedance spectroscopy and Hall measurements to clarify which factors and regions are strongly affected by sulfurization with a NaF layer. The increase in the depletion layer width (xdep) suggested that the number of non-radiative recombination centers decreased at the p–n interface of the CTS solar cell owing to the sulfurization process with the NaF layer. Thus, the increase in Jsc indicated that the carrier collection width widened as xdep increased. Furthermore, Voc increased because the CTS lifetime was lengthened. The performance of the CTS solar cells was improved by these factors. Moreover, as a result of an investigation of the dark and light J–V properties, suppression of the crossover behavior was accomplished by sulfurization with the NaF layer. This technique improved the CTS/Mo and CdS/CTS interfaces owing to the Na content, leading to increases in all desirable solar cell properties. Therefore, the induction of Na from a soda-lime glass substrate as well as sulfurization with a NaF layer is required to obtain highly efficient CTS solar cells. As a result of this study, a CTS solar cell with an efficiency higher than 5.24% was achieved.

Cu2SnS3 (CTS) thin films were synthesized onto soda lime glass substrate coated molybdenum by sulfurization the Cu-Sn stacks prepared using RF sputtering. The influence of Na-doped CTS, Sb-doped CTS, and Sb+Na co-doped CTS films on their physical properties has been investigated. The undoped and doped films have been illustrated a monoclinic structure with no shift in peaks position. A larger grain size has been obtained with Sb doping compared to undoped CTS. Enhancement in photoluminescence sharpening and yield spectra were indicated in the existence of Na and/or Sb. The power conversion efficiency was enhanced by addition of Na and/or Sb to the CTS absorber layer, from 0.32% for undoped CTS to 1.54, 1.89 and 0.76 % for Na, Sb, and co-doping CTS, respectively. As a result, the influence of doping has improved all cell efficiency with an increasing ratio of 381, 490, 137 % with Na, Sb, and co-doping, respectively.

Simple Summary Progesterone receptor membrane component 1 (PGRMC1) is highly expressed in cancer cells and enhances cancer proliferation and chemoresistance. It is therefore considered a potential target for cancer treatment. However, a chemical compound that directly regulates PGRMC1 has not been identified. Here, we showed that the natural active compound in licorice, glycyrrhizin (GL), directly binds to heme-dimerized PGRMC1 to inhibit PGRMC1-mediated EGF receptor (EGFR) activation in cancer cells. Chemical screening using GL derivatives revealed that the glucoside derivative glucoglycyrrhizin (GlucoGL) binds more potently to PGRMC1 and contributes to the suppression of PGRMC1-mediated cancer chemoresistance. This study provides the first evidence of chemical compounds that directly bind to PGRMC1 to inhibit its function, and the findings provide new insights for cancer treatments that target PGRMC1. Abstract Progesterone receptor membrane component 1 (PGRMC1) is highly expressed in various cancer cells and contributes to tumor progression. We have previously shown that PGRMC1 forms a unique heme-stacking functional dimer to enhance EGF receptor (EGFR) activity required for cancer proliferation and chemoresistance, and the dimer dissociates by carbon monoxide to attenuate its biological actions. Here, we determined that glycyrrhizin (GL), which is conventionally used to ameliorate inflammation, specifically binds to heme-dimerized PGRMC1. Binding analyses using isothermal titration calorimetry revealed that some GL derivatives, including its glucoside-derivative (GlucoGL), bind to PGRMC1 potently, whereas its aglycone, glycyrrhetinic acid (GA), does not bind. GL and GlucoGL inhibit the interaction between PGRMC1 and EGFR, thereby suppressing EGFR-mediated signaling required for cancer progression. GL and GlucoGL significantly enhanced EGFR inhibitor erlotinib- or cisplatin (CDDP)-induced cell death in human colon cancer HCT116 cells. In addition, GL derivatives suppressed the intracellular uptake of low-density lipoprotein (LDL) by inhibiting the interaction between PGRMC1 and the LDL receptor (LDLR). Effects on other pathways cannot be excluded. Treatment with GlucoGL and CDDP significantly suppressed tumor growth following xenograft transplantation in mice. Collectively, this study indicates that GL derivatives are novel inhibitors of PGRMC1 that suppress cancer progression, and our findings provide new insights for cancer treatment.

Intrinsic and extrinsic defects around the p–n interface in Cu2SnS3 (CTS) solar cells were evaluated using low-temperature photoluminescence (LT-PL) measurements. The intrinsic defects were investigated based on the PL-dependence of CTS films on the excitation power and temperature. Donor–acceptor pair recombination was observed with shallow acceptors (copper vacancies, V Cu) located approximately 18 meV above the valence band maximum and typical donors located 72 and 112 meV below the conduction band minimum (CBM). The PL spectra of various CTS solar cell structures were measured to identify the Cd-related defects formed by Cd diffusion from the CdS layer. A new LT-PL peak was observed at 0.87 eV for the CdS/CTS solar cells, corresponding to D–A pair recombination with Cd on Cu site donors located 62 meV below the CBM. A p–n homojunction may form in CTS by V Cu passivation by Cd diffusion and suppressed interface recombination.

Ternary compound Cu2SnS3 (CTS) thin films were synthesized using two simple and non-vacuum processes: chemical spray pyrolysis and rapid thermal annealing (RTA). The crystal quality of CTS films improved and the band tailing, shown in Tauc's plot, tended to vanish after annealing in a nitrogen atmosphere using RTA. Although ethanol was used as a solvent in the spray pyrolysis, the CTS film was not contaminated by carbon and oxygen. The bandgap of CTS was changed via sulfurization. The optimization of the RTA process affected the composition of the CTS thin films, modifying material defects and improving the crystal quality. These results represent the initial step toward the practical application of CTS solar cells using an inexpensive fabrication process.

Authors report an effect of F substitution on layered SnSe2 through the successful synthesis of polycrystalline SnSe2−δF x (0.000 ≤ x ≤ 0.010) by solid-state reaction. Accompanied with density functional theory calculations, the blue shift of A1g peak in Raman spectra reveal that F− ions are substituted at Se vacancy sites as decreasing the reduced mass of vibrational mode associated with Sn–Se bonding. From the measurements of electrical parameters, conductivity as well as carrier concentration are governed by thermally activated behavior, while such behavior is suppressed in Hall mobility, which occurs as F ratio increases. Based on Arrhenius relation, it is found that the potential barrier height at the grain boundary is suppressed with increasing F amount, suggesting that the F− ion is a promising candidate for the grain boundary passivation in the two-dimensional dichalcogenide system.

The ternary compound Cu2SnS3 (CTS) is composed of elements that are low in cost, non-toxic, and abundant in the Earth's crust. In addition, CTS is a p-type semiconductor with a high reported absorption coefficient of more than 104 cm−1 and a band gap energy of 0.92–1.77 eV. It is, therefore, considered to be a suitable candidate for the absorber layer in thin film solar cells. In the present study, CTS thin films were produced by first depositing precursor films by co-evaporation of Cu, Sn, and S, and then annealing them. Solar cells were then fabricated using the CTS films as absorber layers, and the dependence of their photovoltaic properties on the annealing temperature was investigated. The solar cell using the CTS thin film annealed at 570 °C exhibited an open-circuit voltage of 248 mV, a short-circuit current density of 33.5 mA/cm2, a fill factor of 0.439, and a conversion efficiency of 3.66%.

Authors report an effect of F substitution on layered SnSe2 through the successful synthesis of polycrystalline SnSe2−δFx (0.000 ≤ x ≤ 0.010) by solid-state reaction. Accompanied with density functional theory calculations, the blue shift of A1g peak in Raman spectra reveal that F− ions are substituted at Se vacancy sites as decreasing the reduced mass of vibrational mode associated with Sn–Se bonding. From the measurements of electrical parameters, conductivity as well as carrier concentration are governed by thermally activated behavior, while such behavior is suppressed in Hall mobility, which occurs as F ratio increases. Based on Arrhenius relation, it is found that the potential barrier height at the grain boundary is suppressed with increasing F amount, suggesting that the F− ion is a promising candidate for the grain boundary passivation in the two-dimensional dichalcogenide system.

The sulfurization effect of Cu2(Sn1−x ,Ge x )S3 (CTGS) thin films deposited by low-temperature co-evaporation was investigated. As-deposited CTGS films with large Cu2GeS3 molar fractions show poor crystal quality and contamination with extra phases. After sulfurization using sulfur powder, the full width at half-maximum of X-ray diffraction peaks for CTGS films was smaller than that of the as-deposited CTGS films. Moreover, contamination of the extra phases was not observed in the sulfurized CTGS film. These results imply that single-phase thin-film CTGS is difficult to obtain by only low-temperature co-evaporation. Therefore, sulfurization is necessary to suppress extra phases and obtain single-phase CTGS films.

A 12-membered polyazamacrocycle, 1-oxa-4,7,10-triazacyclododecane-N,N',N″-triacetic acid (ODTA), has been reported to provide an indium chelate of net neutral charge with thermodynamic stability higher than 1,4,7,10-tetraazacyclododecane-N,N',N″,N‴-tetraacetic acid (DOTA). However, neither synthetic procedure for a C-functionalized ODTA (C-ODTA) nor its chelating ability with a trace amount of radioactive indium-111 ((111)In) has been elucidated. We herein present a facile synthetic procedure for C-ODTA, and estimated its ability as a chelating agent for radiolabeling peptides and proteins with (111)In. The synthetic procedure involves the synthesis of a linear precursor using a para-substituted phenylalanine derivative as a starting material. The following intramolecular cyclization reaction was best performed (>73% yield) when Boc-protected linear compound and the condensation reagent, HATU, were simultaneously added to the reaction vessel at the same flow rate. The cyclic compound was then reduced with BH(3) and alkylated with tert-butyl bromoacetate. The synthetic procedure was straightforward and some optimization would be required. However, most of the intermediate compounds were obtained easily in good yields, suggesting that the present synthetic procedure would be useful to synthesize C-ODTA derivatives. The intramolecular cyclization reaction might also be applicable to synthesize polyazamacrocycles of different ring sizes and cyclic peptides. In (111)In radiolabeling reactions, C-ODTA provided (111)In chelates in higher radiochemical yields at low ligand concentrations when compared with C-DOTA. The (111)In-labeled C-ODTA remained unchanged in the presence of apo-transferrin. The biodistribution studies also showed that the (111)In-labeled compound was mainly excreted into urine as intact. These findings indicate that C-ODTA would be useful to prepare (111)In-labeled peptides of high specific activities in high radiochemical yields.

Cu2Sn1−xGexS3 (CTGS) thin films were prepared by co-evaporation of Cu, Sn, and S to form Cu2SnS3 (CTS) precursors, which were then annealed at 570 °C in an atmosphere composed of N2, GeS2, and S vapor. The films were then used to fabricate photovoltaic cells with the structure glass/Mo/CTGS/CdS/ZnO:Al/Al. A cell with a film composition of Cu2(Sn0.86Ge0.14)S3 fabricated from slightly Cu-rich CTS (Cu/Sn = 2.07) exhibited a conversion efficiency of 3.4% and an open-circuit voltage of 0.29 V. The band gap based on the external quantum efficiency was estimated to be approximately 1.0 eV. The open-circuit voltage was found to be larger than that for a CTS thin film solar cell and increased with band gap energy.

A 12-membered polyazamacrocycle, 1-oxa-4,7,10-triazacyclododecane-N,N',N″-triacetic acid (ODTA), has been reported to provide an indium chelate of net neutral charge with thermodynamic stability higher than 1,4,7,10-tetraazacyclododecane-N,N',N″,N‴-tetraacetic acid (DOTA). However, neither synthetic procedure for a C-functionalized ODTA (C-ODTA) nor its chelating ability with a trace amount of radioactive indium-111 ((111)In) has been elucidated. We herein present a facile synthetic procedure for C-ODTA, and estimated its ability as a chelating agent for radiolabeling peptides and proteins with (111)In. The synthetic procedure involves the synthesis of a linear precursor using a para-substituted phenylalanine derivative as a starting material. The following intramolecular cyclization reaction was best performed (73% yield) when Boc-protected linear compound and the condensation reagent, HATU, were simultaneously added to the reaction vessel at the same flow rate. The cyclic compound was then reduced with BH(3) and alkylated with tert-butyl bromoacetate. The synthetic procedure was straightforward and some optimization would be required. However, most of the intermediate compounds were obtained easily in good yields, suggesting that the present synthetic procedure would be useful to synthesize C-ODTA derivatives. The intramolecular cyclization reaction might also be applicable to synthesize polyazamacrocycles of different ring sizes and cyclic peptides. In (111)In radiolabeling reactions, C-ODTA provided (111)In chelates in higher radiochemical yields at low ligand concentrations when compared with C-DOTA. The (111)In-labeled C-ODTA remained unchanged in the presence of apo-transferrin. The biodistribution studies also showed that the (111)In-labeled compound was mainly excreted into urine as intact. These findings indicate that C-ODTA would be useful to prepare (111)In-labeled peptides of high specific activities in high radiochemical yields.

The defect levels in Cu2SnS3 (CTS) were investigated using photoluminescence (PL) spectroscopy. A CTS thin film was prepared on a soda-lime glass/molybdenum substrate by thermal co-evaporation and sulfurization. The crystal structure was determined to be monoclinic, and the compositional ratios of Cu/Sn and S/Metal were determined to be 1.8 and 1.2, respectively. The photon energy of the PL spectra observed from the CTS thin film was lower than that previously reported. All fitted PL peaks were associated with defect related luminescence. The PL peaks observed at 0.843 and 0.867 eV were assigned to donor-acceptor pair recombination luminescence, the thermal activation energies of which were determined to be 22.9 and 24.8 meV, respectively.

Cu2SnS3 (CTS) thin films were produced by the co-evaporation of Cu, Sn, and cracked sulfur, followed by annealing. The as-deposited films were then annealed at 570 °C for 5 min in the presence of 100 mg of sulfur lumps in a rapid thermal processing furnace filled with N2 gas at atmospheric pressure. Solar cells were then fabricated using the CTS films as absorber layers, and their efficiency was evaluated for different Cu/Sn compositional ratios. The largest grain size was found for films with a slightly Sn-rich composition. The highest performance was obtained for solar cells containing a CTS thin film with a Cu/Sn ratio of about 1.9. A cell with a Cu/Sn ratio of 1.87 exhibited an open-circuit voltage of 258 mV, a short-circuit current density of 35.6 mA/cm2, a fill factor of 0.467, and a power conversion efficiency of 4.29%.

We report on the sulfurization of metal-alloyed precursors in Cu2SnS3 (CTS)-based thin-film solar cells. CTS thin films were prepared through the sulfurization of Cu?Sn alloy precursors at sulfurization temperatures of 500?580 ?C for 2 h in a N2 atmosphere with sulfur vapor. The Cu/Sn composition ratios of the sulfurized films were determined by X-ray fluorescence analysis to be in the range of 1.77?1.89. The photovoltaic properties of CTS-based solar cells improved with increasing sulfurization temperature owing to the higher external quantum efficiency at long wavelengths. The solar cell comprising a CTS thin film with a sulfurization temperature of 580 ?C exhibited the optimum performance among the cells examined: an open-circuit voltage of 244 mV, a short-circuit current density of 29 mA/cm2, a fill factor of 0.385, and a conversion efficiency of 2.7% were obtained.

2021