Reusable, Ultrasensitive, Patterned Conjugated Polyelectrolyte-Surfactant Complex Film with a Wide Detection Range for Copper Ion Detection.

Conjugated polyelectrolytes (CPEs) are emerging as promising materials in the sensor field because they enable high-sensitivity detection of various substances in aqueous media. However, most CPE-based sensors have serious problems in real-world application because the sensor system is operated only when the CPE is dissolved in aqueous media. Here, the fabrication and performance of a water-swellable (WS) CPE-based sensor driven in the solid state are demonstrated. The WS CPE films are prepared by immersing a water-soluble CPE film in cationic surfactants of different alkyl chain lengths in a chloroform solution. The prepared film exhibits rapid, limited water swellability despite the absence of chemical crosslinking. The water swellability of the film enables the highly sensitive and selective detection of Cu2+ in water. The fluorescence quenching constant and the detection limit of the film are 7.24 × 106 L mol-1 and 4.38 nM (0.278 ppb), respectively. Moreover, the film is reusable via a facile treatment. Furthermore, various fluorescent patterns introduced by different surfactants are successfully fabricated by a simple stamping method. By integrating the patterns, Cu2+ detection in a wide concentration range (nM-mM) can be achieved.

Simple and rapid electrochemical monitoring for depolymerization of polyamic acid.

Excellent thermal and mechanical properties of aromatic polyimides (PIs) make them attractive materials in various fields. PIs is performed using polyamic acid (PAA) precursors due to their limited solubility. However, PAAs can be easily depolymerized by moisture and heat, which can degrade the properties of PIs. Therefore, quality control of PAAs is an important task in researches and industrial applications. Here, we propose a simple, rapid, and novel method to observe the depolymerization of PAAs. The method is based on the principle that, as the molecular weight of the polymer decreases, the solution viscosity decreases, and the viscosity of the solution can be easily and rapidly measured using electrochemistry. We accelerated depolymerization by applying heat to a PAA solution and measured the change in viscosity of the solution through cyclic voltammetry. The proposed method, which also makes it possible to determine the dynamic viscosity of a polymer solution, is presented as a model system to observe state changes in various polymers.

Comparison of the Diagnostic Accuracies of 1.5T and 3T Stress Myocardial Perfusion Cardiovascular Magnetic Resonance for Detecting Significant Coronary Artery Disease.

Objective: To compare the diagnostic performance of cardiovascular magnetic resonance (CMR) myocardial perfusion at 1.5- and 3-tesla (T) for detecting significant coronary artery disease (CAD), with invasive coronary angiography (ICA) as the reference method. Materials and Methods: We prospectively enrolled 281 patients (age 62.4 ± 8.3 years, 193 men) with suspected or known CAD who had undergone 1.5T or 3T CMR and ICA. Two independent radiologists interpreted perfusion defects. With ICA as the reference standard, the diagnostic performance of 1.5T and 3T CMR for identifying significant CAD (≥ 50% diameter reduction of the left main and ≥ 70% diameter reduction of other epicardial arteries) was determined. Results: No differences were observed in baseline characteristics or prevalence of CAD and old myocardial infarction (MI) using 1.5T (n = 135) or 3T (n = 146) systems. Sensitivity, specificity, positive and negative predictive values, and area under the receiver operating characteristic curve (AUC) for detecting significant CAD were similar between the 1.5T (84%, 64%, 74%, 76%, and 0.75 per patient and 68%, 83%, 66%, 84%, and 0.76 per vessel) and 3T (80%, 71%, 71%, 80%, and 0.76 per patient and 75%, 86%, 64%, 91%, and 0.81 per vessel) systems. In patients with multi-vessel CAD without old MI, the sensitivity, specificity, and AUC with 3T were greater than those with 1.5T on a per-vessel basis (71% vs. 36%, 92% vs. 69%, and 0.82 vs. 0.53, respectively). Conclusion: 3T CMR has similar diagnostic performance to 1.5T CMR in detecting significant CAD, except for higher diagnostic performance in patients with multi-vessel CAD without old MI.

Effect of ion-chelating chain lengths in thiophene-based monomers on in situ photoelectrochemical polymerization and photovoltaic performances.

We synthesized thiophene-based monomers (bis-EDOTs) with different ethylene glycol oligomer (EGO) lengths (TBO3, TBO4, and TBO5) and investigated their polymerization characteristics during photoelectrochemical polymerization (PEP) at the surfaces of dye (D205)-sensitized TiO2 nanocrystalline particles. During the PEP reaction, monomers were expected to diffuse toward neighboring dyes through the growing polymer layers to enable continuous chain growth. We found that the less bulky monomer (TBO3) formed a more compact polymer layer with a high molecular weight. Its diffusion to the active sites through the resulting growing polymer layer was, therefore, limited. We deployed layers of the polymers (PTBO3, PTBO4, and PTBO5) in iodine-free solid-state hybrid solar cells to investigate the lithium ion chelating properties of the polymers as a function of the number of oxygen atoms present in the EGOs. PTBO4 and PTBO5 were capable of chelating lithium ions, yielding a photovoltaic performance that was 142% of the performance obtained without the polymer layers (3.0→5.2%).

Well-defined all-conducting block copolymer bilayer hybrid nanostructure: selective positioning of lithium ions and efficient charge collection.

A block copolymerization of nonfunctionalized conducting monomers was developed to enable the successful synthesis of a highly insoluble 3,4-(ethylenedioxy)thienyl-based all-conducting block copolymer (PEDOT-b-PEDOT-TB) that could encapsulate nanocrystalline dyed TiO2 particles, resulting in the formation of an all-conducting block copolymer bilayer hybrid nanostructure (TiO2/Dye/PEDOT-b-PEDOT-TB). Lithium ions were selectively positioned on the outer PEDOT-TB surface. The distances through which the positively charged dye and PEDOT-TB(Li(+)) interacted physically or through which the TiO2 electrode and the Li(+) centers on PEDOT-TB(Li(+)) interacted ionically were precisely tuned and optimized within ca. 1 nm by controlling the thickness of the PEDOT blocking layer (the block length). The optimized structure provided efficient charge collection in an iodine-free dye-sensitized solar cell (DSC) due to negligible recombination of photoinduced electrons with cationic species and rapid charge transport, which improved the photovoltaic performance (η = 2.1 → 6.5%).

Detection of cardiac myxomas with non-contrast chest CT.

BACKGROUND: Cardiac myxomas are sources of systemic embolism. Currently a large volume of chest CT and calcium-scoring CT scans are performed without contrast injection. PURPOSE: To evaluate the diagnostic capability of non-contrast CT covering heart in detecting cardiac myxomas. MATERIAL AND METHODS: This retrospective study included 36 non-contrast CT scans of 36 consecutive patients (16 men, 20 women) who underwent CT scan before surgery for left atrial myxomas and 20 patients without myxoma as a control group. Two independent readers who were blinded to medical information reviewed non-contrast CT scans of 36 patients with cardiac myxomas and 20 scans in the control group patients. They determined the presence of lesions suspicious of myxomas using a five-point scale. The other reader measured attenuation number in the non-calcific areas of the tumors and sizes of the masses on the non-contrast CT images. RESULTS: The average attenuation of cardiac myxoma (22.5 Hounsfield units [HU]; range, 8.9-32.9 HU) and adjacent unopacified blood (44.6 HU; range, 31.5-57 HU) were significantly different (P < 0.001). Twelve cardiac myxomas (31.6%) had internal calcification and all of them were detected by both of readers. Cardiac myxomas were measured smaller on non-contrast CT (mean, 3.5 cm; range, 1.1-9.7 cm) than on pathologic specimens (mean, 4.1 cm, 1.4-10.0 cm) (P < 0.001). Considering grade 3-5 on a five-grade scale as the detectability, the sensitivity, specificity, positive predictive value, negative predictive value, and diagnostic accuracy of non-contrast CT in detecting cardiac myxomas were 88.8%/86.1%, 95.0%/100%, 96.9%/100%, 82.6%/80.0%, and 91.1%/91.1%, by reader 1 and reader 2, respectively and there was good inter-observer reliability (kappa value = 0.92, P = 0.157). CONCLUSION: Non-contrast CT scan is useful for detecting cardiac myxomas. Therefore, radiologists should be familiar with imaging findings of cardiac myxomas on non-contrast CT.

Digital tomosynthesis of the thorax: the influence of respiratory motion artifacts on lung nodule detection.

BACKGROUND: Digital tomosynthesis considerably reduces problems created by overlapping anatomy compared with chest X-ray (CXR). However, digital tomosynthesis requires a longer scan time compared with CXR, and thus may be vulnerable to motion artifacts. PURPOSE: To compare the diagnostic performance of digital tomosynthesis in subjects with and without respiratory motion artifacts. MATERIAL AND METHODS: The institutional review board approved this retrospective study, and the requirement for written informed consent was waived. A total of 46 subjects with imaging containing respiratory motion artifacts were enrolled in this study, 18 of whom were positive and 28 of whom were negative for lung nodules on computed tomography (CT). The control group was comprised of 92 age-matched subjects with imaging devoid of motion artifacts. Of these, 36 were positive and 56 were negative for lung nodules on subsequent CT scan. The size criteria of nodules were 4-10 mm. Three chest radiologists independently evaluated the radiographs and digital tomosynthesis images for the presence of pulmonary nodules. Multireader multicase receiver-operating characteristic (ROC) analyses was used for statistical comparisons. RESULTS: Within the control group, the areas under curve (AUC) for observer performances in detecting lung nodules on digital tomosynthesis was higher than that on CXR (P = 0.017). Within the study group, there were no significant differences in AUCs for observer performances (P = 0.576). CONCLUSION: When no motion artifacts are present, the detection performance of nodules (4-10 mm) on digital tomosynthesis is significantly better than that on CXR, whereas there is not a significant difference in cases with motion artifacts.

Facile fabrication of aligned doubly open-ended TiO2 nanotubes, via a selective etching process, for use in front-illuminated dye sensitized solar cells.

A simple selective etching process easily removed a 2nd anodized TiO(2) nanotubes (TNTs) layer from a physically stable 1st anodized TNTs layer to produce noncurling, freestanding, large-area aligned doubly open-ended TNTs. These TNTs were easily transferred to a conducting glass for use in fabricating front-illuminated dye sensitized solar cells.

Exploring the heterogeneous interfaces in organic or ruthenium dye-sensitized liquid- and solid-state solar cells.

The interfacial properties were systematically investigated using an organic sensitizer (3-(5'-{4-[(4-tert-butyl-phenyl)-p-tolyl-amino]-phenyl}-[2,2']bithiophenyl-5-yl)-2-cyano-acrylic acid (D)) and inorganic sensitizer (bis(tetrabutylammonium) cis-bis(thiocyanato)bis(2,2'-bipyridine-4,4'-dicarboxylato) ruthenium(II) (N719)) in a liquid-state and a solid-state dye-sensitized solar cell (DSC). For liquid-DSCs, the faster charge recombination for the surface of D-sensitized TiO2 resulted in shorter diffusion length (LD) of ∼3.9 µm than that of N719 (∼7.5 µm), limiting the solar cell performance at thicker films used in liquid-DSCs. On the other hand, for solid-DSCs using thin TiO2 films (∼ 2 µm), D-sensitized device outperforms the N719-sensitized device in an identical fabrication condition, mainly due to less perfect wetting ability of solid hole conductor into the porous TiO2 network, inducing the dye monolayer act as an insulation layer, while liquid electrolyte is able to fully wet the surface of TiO2. Such insulation effect was attributed to the fact that the significant increase in recombination resistance (from 865 to 4,400 Ω/cm(2)) but shorter electron lifetime (from 10.8 to 0.8 ms) when compared to liquid-DSCs. Higher recombination resistance for solid-DSCs induced the electron transport-limited situation, showing poor performance of N719-sensitized device which has shorter electron transport time and similar LD (2.9 µm) with D-sensitized device (3.0 µm).

Thermodynamic control over the competitive anchoring of N719 dye on nanocrystalline TiO2 for improving photoinduced electron generation.

TiO(2) electrodes, sensitized with the N719 dye at high immersion temperatures during the sensitization process, were found to have large fractions of weakly bound N719 on the electrode surface, which resulted in dye aggregation and decreased device longevity. These disadvantages were ameliorated using a low-temperature stearic acid (SA)-assisted anchoring method described here. The activation energy (ΔE(NS)(++)) and relative fraction of strongly bound N719 were twice as large as the respective values obtained without the use of SA. Slowing of adsorption, both by thermal means and through SA-mediated processes, effectively controlled the binding mode of N719 on the surface of TiO(2). The resulting sensitized electrodes displayed enhanced device longevity and improved generation of photoinduced electrons.

A novel hole transport material for iodine-free solid state dye-sensitized solar cells.

A novel bis-EDOT-based monomer with ethylene glycol oligomers was synthesized and shown to exhibit strong ion solvation, good transport properties, and effective charge screening. These properties greatly improved J(SC) (4.2 to 7.0 mA cm(-2)) and η (1.6 to 2.9%) in an iodine-free solid state dye-sensitized solar cell (DSSC) employing a Z-907 sensitizer, compared with the corresponding values of DSSCs fabricated using the standard bis-EDOT.

Polymeric vesicles with a hydrophobic interior formed by a thiophene-based all-conjugated amphiphilic diblock copolymer.

The diblock copolymer, BP26, assembled into polymeric vesicles with double layers that formed a hydrophobic crystalline interior and a hydrophilic amorphous exterior in methanol, a selective solvent for the PEGT block. The vesicles were demonstrated to encapsulate a hydrophobic guest polyfluorene (PF).

Kidney-specific activity of the bovine uromodulin promoter.

A 10-kilobase (kb) lambda bacteriophage bovine genomic clone containing 5.4 kb of the 5'-flanking region, exons, and introns of bovine uromodulin gene was isolated. Transgenic mice containing 3.9 kb of the bovine uromodulin promoter and a lacZ reporter gene were generated by pronuclear microinjection. RT-PCR and northern blot analyses of transgene expression in various tissues of founder and F1 mice showed that the transgene was expressed exclusively in the kidney. In situ hybridization and histochemistry for lacZ demonstrated that transgene expression was restricted to tubule epithelial cells of the loop of Henle in the kidney. Stepwise 5' deletion analysis revealed that transfection of luciferase reporter constructs fused to various proximal 5'-flanking regions of the bovine uromodulin gene markedly increased luciferase activity in mouse renal epithelial cells but not in mesenchymal cells and that the most critical cis elements of the uromodulin gene are located within the 600 bp upstream region.