Predictive value of maternal serum placental growth factor levels for discordant fetal growth in twins: a retrospective cohort study.

BACKGROUND: Accurate prenatal recognition of discordant fetal growth in twins is critical for deciding suitable management strategies. We explored the predictive value of the level of maternal second-trimester placental growth factor (PLGF) as a novel indicator of discordant fetal growth. METHODS: A total of 860 women pregnant with twins were enrolled, including 168 women with monochorionic twins (31 cases of discordant fetal growth and 137 without) and 692 with dichorionic twins (79 cases of discordant fetal growth and 613 without). Maternal second-trimester PLGF concentrations were measured via immunofluorescence. RESULTS: Maternal second-trimester PLGF levels were significantly lower in women pregnant with twins who subsequently developed discordant fetal growth than in those who did not (monochorionic twin pregnancy: P < 0.001; dichorionic twin pregnancy: P < 0.001). A 3-4 fold difference in median PLGF concentrations was detected between the two groups with both monochorionic and dichorionic twin pregnancies. Maternal second-trimester PLGF levels were significantly correlated with birth weight differences (monochorionic twin pregnancy: r = - 0.331, P < 0.001; dichorionic twin pregnancy: r = - 0.234, P < 0.001). A receiver operating characteristic curve was used to evaluate the predictive efficiency. In monochorionic twin pregnancies, the area under the curve (AUC) was 0.751 (95% confidence interval [CI]: 0.649-0.852), and the cutoff value was 187.5 pg/mL with a sensitivity of 77.4% and specificity of 71.0%. In dichorionic twin pregnancies, the AUC was 0.716 (95% CI; 0.655-0.777), and the cutoff value was 252.5 pg/mL with a sensitivity of 65.1% and specificity of 69.6%. Based on the above cutoff values, univariate and multivariate logistic regression analyses were performed to calculate the odds ratios (OR) for the PLGF levels. After adjustment for potential confounding factors, low PLGF concentrations still significantly increased the risk of discordant fetal growth (monochorionic twin pregnancy: adjusted OR: 7.039, 95% CI: 2.798-17.710, P < 0.001; dichorionic twin pregnancy: adjusted OR: 4.279, 95% CI: 2.572-7.120, P < 0.001). CONCLUSIONS: A low maternal second-trimester PLGF level is considered a remarkable risk factor and potential predictor of discordant fetal growth. This finding provides a complementary screening strategy for the prediction of discordant fetal growth and offers a unique perspective for the subsequent research in this field.

Periodic Surface-Enhanced Raman Scattering-Encoded Magnetic Beads for Reliable Quantitative Surface-Enhanced Raman Scattering-Based Multiplex Bioassay.

Surface-enhanced Raman scattering (SERS)-based immunoassay on encoded beads is highly attractive with the advantages of ultrasensitivity, multiplex and high throughput. However, it was a great challenge to screen out in-focus signals of the immunoconjugated SERS nanoprobes on spherical bead conveniently. Here, periodic SERS-encoded magnetic beads (PSE-MBs) were developed through droplet optofluidic technique by using monodisperse SERS-encoded magnetic nanospheres as building blocks. The designed PSE-MBs not only exhibit huge coding capacity, but also provide the strongest and reproducible SERS coding signals as "in-focus beacons". When PSE-MBs are used as capture carriers in SERS-based immunoassay, both multiple target analytes and in-focus signals of SERS nanoprobes could be easily identified according to the collected SERS coding signals. Thus, reliable quantitative analysis of multiple target analytes could be conveniently achieved by such detection protocol. Additionally, the magnetic ingredient in PSE-MBs made the operation easily during the bioassay. The multiple advantages of PSE-MBs including large coding capacity, in-focus beacons and magnetic operation endorse them to be robust capture carriers in reliable quantitative SERS-based multiplex immunoassay.

Highly Sensitive and Reproducible SERS Performance from Uniform Film Assembled by Magnetic Noble Metal Composite Microspheres.

To realize highly sensitive and reproducible SERS performance, a new route was put forward to construct uniform SERS film by using magnetic composite microspheres. In the experiment, monodisperse Fe3O4@SiO2@Ag microspheres with hierarchical surface were developed and used as building block of SERS substrate, which not only realized fast capturing analyte through dispersion and collection under external magnet but also could be built into uniform film through magnetically induced self-assembly. By using R6G as probe molecule, the as-obtained uniform film exhibited great improvement on SERS performance in both sensitivity and reproducibility when compared with nonuniform film, demonstrating the perfect integration of high sensitivity of hierarchal noble metal microspheres and high reproducibility of ordered microspheres array. Furthermore, the as-obtained product was used to detect pesticide thiram and also exhibited excellent SERS performance for trace detection.

Ultrahigh power factor and enhanced thermoelectric performance of individual Te/TiS2 nanocables.

Here, we present the successful fabrication of Te/TiS2 heterostructure nanocables with enhanced thermoelectric (TE) performance by a two-step route (a facile solvothermal approach for Te nanowires and then the Te nanowires are used as templates for the controllable growth of the Te/TiS2 nanocables), which is scalable for practical nanodevice applications. The heterostructure nanocables of different sizes can be prepared by varying the synthetic composition. Measurements of the Seebeck coefficient (S), electrical conductivity (σ), and thermal conductivity (κ) are carried out on the same nanowires over a temperature range of 2-350 K. The heterostructure nanocables show an ultrahigh power factor (S(2) σ) with a maximum value of 0.58 Wm(-1) K(-2), which comes from a high electrical conductivity and a strongly enhanced Seebeck coefficient. The figure of merit (ZT) can reach 1.91 at room temperature from a single nanocable with a diameter of 60 nm, which is thought to contribute to the formation of the hetero-phase core/shell structure. These results are expected to open up new application possibilities in nanoscale TE devices based on individual Te/TiS2 heterostructure nanocables.

Ultraviolet electroluminescence of light-emitting diodes based on single n-ZnO/p-AlGaN heterojunction nanowires.

We present successful fabrication of single n-ZnO/p-AlGaN heterojunction nanowires with excellent optoelectronic properties. Because of the formation of high-quality interfacial structure, heterojunction nanowire showed a diodelike rectification behavior and an electroluminescence (EL) ultraviolet (UV) emission centered at 394 nm from a single nanowire was observed when the injection current is 4 µA due to high exciton efficiency in the interfacial layer between ZnO and AlGaN. With the increase of the applied current, the EL peak at 5 µA becomes weaker revealing an optimal injection current of less than 5 µA. These results are expected to open up new application possibilities in nanoscale UV light-emitting devices based on single ZnO heterostructure.

Simultaneous speciation analysis of arsenic and iodine in human urine by high performance liquid chromatography-inductively coupled plasma mass spectrometry.

A high-performance liquid chromatography-inductively coupled plasma mass spectrometry-based method was developed for the simultaneous determination of four iodine species (i.e. iodate, 3-iodo-tyrosine, 3,5-diiodo-tyrosine, and iodide) and six arsenic species (i.e. arsenobetaine, arsenite, dimethylarsinic acid, arsenocholine, methylarsonic acid, and arsenate) in human urine. The chromatographic separation was performed on a Dionex IonPac As7 anion exchange column. The mobile phase was initiated with 0.5 mmol/L ammonium carbonate solution, followed by 50 mmol/L ammonium carbonate/100 mmol/L ammonium nitrate solution (with 4% methanol). The limits of quantification of the analytes ranged from 0.045 to 2.26 µg/L. At three spiked levels (10.0, 20.0, 50.0 µg/L), the average recoveries (%) ranged from 87.4 to 113.1%, and the relative standard deviations (RSD, %) ranged from 0.4 to 17.2%. The ratio of the sum of six arsenic species to the total arsenic measured by ICPMS ranged from 77.4 to 121.2%, and the ratio of the sum of the four iodine species to the total iodine ranged from 70.7 to 114.7%, indicating a good agreement between these two methods for both arsenic and iodine.

Design of Raman reporter-embedded magnetic/plasmonic hybrid nanostirrers for reliable microfluidic SERS biosensors.

Magnetic-based microfluidic SERS biosensors hold great potential in various biological analyses due to their integrated advantages including easy manipulation, miniaturization and ultrasensitivity. However, it remains challenging to collect reliable SERS nanoprobe signals for quantitative analysis due to the irregular aggregation of magnetic carriers in a microfluidic chamber. Here, magnetic/plasmonic hybrid nanostirrers embedded with a Raman reporter are developed as capture carriers to improve the reliability of microfluidic SERS biosensors. Experimental results revealed that SERS signals from magnetic hybrid nanostirrers could serve as microenvironment beacons of their irregular aggregation, and a signal filtering method was proposed through exploring the relationship between the intensity range of beacons and the signal reproducibility of SERS nanoprobes using interleukin 6 as a model target analyte. Using the signal filtering method, reliable SERS nanoprobe signals with high reproducibility could be picked out from similar microenvironments according to their beacon intensity, and then the influence of irregular aggregation of magnetic carriers on the SERS nanoprobe could be eliminated. The filtered SERS nanoprobe signals also exhibited excellent repeatability from independent tests, which lay a solid foundation for a reliable working curve and subsequent accurate bioassay. This study provides a simple but promising route for reliable microfluidic SERS biosensors, which will further promote their practical application in biological analysis.

Metabolic changes in bile acids with pregnancy progression and their correlation with perinatal complications in intrahepatic cholestasis of pregnant patients.

Intrahepatic cholestasis of pregnancy (ICP) is a rare liver disease occurring during pregnancy that is characterized by disordered bile acid (BA) metabolism. It is related to adverse clinical outcomes in both the mother and fetus. Our aim was to evaluate the BA metabolism profiles in different types of ICP and investigate the association between specific BAs and perinatal complications in ICP patients. We consecutively evaluated 95 patients with ICP, in which 53 patients were diagnosed with early-onset ICP (EICP) and 42 patients were diagnosed with late-onset ICP (LICP). Concentrations of 15 BA components were detected using high-performance liquid chromatography tandem mass spectrometry. Clinical information was abstracted from the medical records. The percentage of conjugated bile acids increased in ICP patients. Specifically, taurocholic acid (TCA) accumulated in LICP patients, and glycocholic acid (GCA) predominated in EICP patients. A higher preterm birth incidence was observed among ICP patients. Albumin, total bile acids, total bilirubin and GCA percentage values at ICP diagnosis predicts 83.5% of preterm birth in EICP, and the percentage of TCA in total bile acids at ICP diagnosis predicts 93.2% of preterm birth in LICP. This analysis showed that the BA metabolism profiles of EICP and LICP were distinct. Increased hepatic load was positively correlated with preterm birth in EICP. An elevated TCA percentage in total bile acids provides a biomarker to predict preterm birth in LICP.

Template-assisted synthesis of Ag/AgCl hollow microcubes and their composition-dependent photocatalytic activity for the degradation of phenol.

Plasmonic photocatalysts with hollow structures and tunable composition exhibit significant advantages due to their high efficiency in light collection and effective charge transfer across the tight contact heterojunction interface. Herein, hollow Ag/AgCl microcubes were developed by treating nanosheet-assembled hollow Ag microcubes with FeCl3, where a part of Ag at the interface could be in situ transformed and oxidized into AgCl. Equally, by adjusting the concentration of Fe3+ ions, Ag/AgCl hollow microcubes with different compositions could be easily achieved. Electron transfer was favored by a lot of tiny Ag/AgCl heterojunctions induced by the in situ oxidation of the multicrystalline Ag hollow microcube template containing a number of grain boundaries. The designed hollow Ag/AgCl microcubes exhibited strong visible-light adsorption owing to the surface plasmon resonance effect of Ag nanoparticles, in addition to the multiple light-reflections inside the hollow structure. The as-obtained products were then used as visible-light photocatalysts, where the results indicated that 91.6% of phenol was degraded within 150 min under visible light by the as-obtained sample with a Ag to AgCl ratio of 1 : 3. The superior visible-light photocatalytic activity resulted from the enhancement of the visible light-harvesting and the efficient charge separation at the Ag and AgCl contact interfaces.

Cu-Embedded SnSe2 with a High Figure of Merit at Ecofriendly Temperature.

There are many studies concentrated on high-temperature performance of SnSe2, but few studies were conducted on low-temperature properties of embedded SnSe2. In this work, a series of SnCu x Se2 (x = 0, 0.01, 0.02, and 0.05) layered structures have been successfully synthesized by a melt quenching, mechanical milling process, and spark plasma sintering (SPS) method. Meanwhile, the thermal and electrical transport properties of all synthesized samples are measured. These results suggest that the embedding of Cu into SnSe2 results in a high carrier concentration (1019/cm3). In addition, the enhancement of defect and interfacial phonon scattering caused by Cu embedding as well as the weak van der Waals force between layers makes a low thermal conductivity (0.81 W/mK) for the SnCu0.01Se2 at 300 K. Moreover, the maximum ZT is acquired up to 0.75 for the SnCu0.01Se2 sample at 300 K, which is about 2 orders of magnitude higher than the pristine sample (0.009). These features indicate that Cu-embedded SnSe2 can be a promising thermoelectric material at gentle temperature.

Eukaryal composition and diversity in anaerobic soils influenced by the novel chiral insecticide Paichongding.

Paichongding (IPP) is a neonicotinoid chiral insecticide with independent intellectual property in China. IPP application can increase crop yield, and also lead to insecticide residue and pollution in soils, which will affect microbial population and community composition in soils. In this study, four different types of soils were employed to inquire into the impact of IPP on eukaryal community and species-group through pyrosequencing of 18S rRNA gene amplicons. Fungal population differed in different soils at different days after IPP treatment (DAT). Eukaryal community species in CK (control check) groups were more rich than that with Paichongding sprayed at 5 DAT, while eukaryal species in CK soils at 60 DAT was relatively slight. Shannon's H' analysis indicated fungal species in CK soils were also higher at 5 DAT and relative lower at 60 DAT, except in soil C. There are also differences in the phyla and genus levels of the eukaryotic communities in the soil. After IPP application, the relative abundance of Nectriaceae increased 3-4 times in soil C. In soil F, Phaeosphaeriaceae increased to 57.3% at 5 DAT. The genus of Guehomyces, Aspergillus and Alternaria increased from 3.1 to 9.7, 1.1 to 4.6, 1.5 to 6.7% in soil H, respectively.

Transmission electron microscopy investigation of Sb-doped ZnO nanoribbons and Zn7Sb2O12 branched ZnO nanoribbon structure.

Sb-doped ZnO nanoribbons have been synthesized by simple thermal evaporation of powder mixtures of Zn and Sb2O3. The Sb-doped ZnO nanoribbons with hexagonal wurtzite structure have a growth direction of [0110], widths of 100-300 nm, and lengths up to several hundreds of micrometers. The atomic ratio of Sb and Zn is about 1:40 by energy dispersive X-ray spectroscopy measurement. A stripe contrast is found in the center of the Sb-doped ZnO nanoribbon, which is speculated to be due to the enrichment of Sb in the center of the Sb-doped ZnO nanoribbon by energy dispersive X-ray spectroscopy line scanning element mapping. Furthermore, a novel Zn7Sb2O12 branched ZnO nanoribbon structure is investigated. The growth direction of the branch and the backbone are [211] and [0110], respectively. The mechanisms of formation of such nanomaterials are also discussed.

Large-scale fabrication and characterization of Cd-doped ZnO nanocantilever arrays.

We demonstrate bulk synthesis of highly crystalline Cd-doped ZnO nanocantilever arrays (CZNAs) using Cd and Zn powders at 600 degrees C, which is characterized via scanning electron microscopy, powder X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy, selected area electron diffraction, and high resolution TEM. The results show that the as-prepared CZNAs have diameters of about 15-50 nm, and lengths up to 400 nm and the corresponding process of growth is suggested for conventional vapor solid mechanism.

The template-assisted synthesis of polypyrrole hollow microspheres with a double-shelled structure.

Double-shelled polypyrrole hollow microspheres were synthesized via a novel template-assisted concept, using iron oxide hollow microspheres as both the sacrificial template and initiator in acidic solution.

Gel-limited synthesis of dumbbell-like Fe3O4-Ag composite microspheres and their SERS applications.

A novel gel-limited strategy was developed to synthesize dumbbell-like Fe3O4-Ag composite microspheres through a simple one-pot solvothermal method. In such a reaction system, a special precursor solution containing oleic, water, ethanol and silver ions was used and transformed into a bulk gel under heating at the very beginning of the reaction, thus all the subsequent reactions proceeded in the interior of the gel. The gel-limited reactions had two advantages, on the one hand, the magnetic Fe3O4 microspheres were fixed in the gel which avoided them aggregating together, whereas on the other hand, the silver ions stored in the gel could be gradually released and tended to diffuse towards the nearest Fe3O4 microsphere, which favored the generation of a dumbbell-like Fe3O4-Ag structure. From the time-dependent experiments under optimal conditions, the typical growth process of dumbbell-like structures clearly demonstrated that a silver seed first appeared on the surface of a single Fe3O4 microsphere, which then grew bigger slowly and finally formed a dumbbell-like Fe3O4-Ag structure. Moreover, the formation of the gel was found to be strongly affected by the ratio of water and ethanol in the precursor solution, which further influenced the morphologies of the Fe3O4-Ag microspheres. Furthermore, the effect of lattice match between Fe3O4 and Ag on the final products was also proven from the control experiments by using a template with a different surface crystalline structure. When used as SERS substrates, the final dumbbell-like Fe3O4-Ag microspheres show fast magnetic separation and the selective detection of thiram for the surface capped oleic chain during the growth process.

Facile and economical synthesis of large hollow ferrites and their applications in adsorption for As(V) and Cr(VI).

Unlike the previous ferrites (MFe2O4; M=Fe, Co, Zn, and Mn) solid nanospheres/nanoparticles, which were prepared by polluted solvothermal (glycol) approaches, here controllable monodisperse porous ferrites hollow nanospheres are promptly synthesized by a nontemplate hydrothermal method which has introduced an addition agent, polyacrylamide. The hollow nanospheres with different size can be prepared by varying the synthetic compositions. Scanning/transmission micros-graphs show the outside diameters of ferrite nanospheres are 180-380 nm and the shell thicknesses of that are only 20-45 nm, which could be adjusted by controlling CH3COONa concentration. X-ray diffraction (XRD) and X-ray photoelectron (XPS) spectroscopy, scanning electron (SEM) and transmission electron (TEM) microscopy, energy-dispersive spectrometer (EDS), the measurement of N2 adsorption-desorption isotherms and Brunauer-Emmett-Teller (BET) surface area, and superconducting quantum interference device (SQID) magnetometer were adopted to analyze their phase composition, morphology, porosity, and magnetic properties, respectively. The results of controlled experiments show that citrate and polyacrylamide are vital for the phase purities and morphology of ferrites. In particular, the as-obtained samples exhibit a large adsorption capacity for the toxic solution containing As(V) and Cr(VI) ions, and the calculated result of the maximum adsorption capacity is 340 mg/g based on Langmuir model, which shows excellent As(V) and Cr(VI) ions uptake capacity in contrast to other solid nanosphere materials.

Morphological evolution, growth mechanism, and magneto-transport properties of silver telluride one-dimensional nanostructures.

Single crystalline one-dimensional (1D) nanostructures of silver telluride (Ag2Te) with well-controlled shapes and sizes were synthesized via the hydrothermal reduction of sodium tellurite (Na2TeO3) in a mixed solution. The morphological evolution of various 1D nanostructures was mainly determined by properly controlling the nucleation and growth process of Ag2Te in different reaction times. Based on the transmission electron microscopy and scanning electron microscopy studies, the formation mechanism for these 1D nanostructures was rationally interpreted. In addition, the current-voltage (I-V) characteristics as a function of magnetic field of the highly single crystal Ag2Te nanowires were systematically measured. From the investigation of I-V characteristics, we have observed a rapid change of the current in low magnetic field, which can be used as the magnetic field sensor. The magneto-resistance behavior of the Ag2Te nanowires with monoclinic structure was also investigated. Comparing to the bulk and thin film materials, we found that there is generally a larger change in R (T) as the sample size is reduced, which indicates that the size of the sample has a certain impact on magneto-transport properties. Simultaneously, some possible reasons resulting in the observed large positive magneto-resistance behavior are discussed.

Controlled synthesis of homogeneous Ag nanosheet-assembled film for effective SERS substrate.

Homogeneous Ag nanosheet-assembled film was successfully fabricated by using Cu plate through a simple modified solution method, where weak reductive Cu2O layer and complexing agent citrate ions were both introduced into the reaction system to control the reaction process. Meanwhile, citrate ions were used as morphology-controlled reagent to lead Ag units to grow in the form of nanosheet. The growth process exhibited that Ag nanosheet-assembled film formed slowly with reaction proceeding. Additionally, the pack density of nanosheets in the final product was found to be adjusted by the concentrations of Ag(+) ions in precursor solution. Using Rhodamine 6G (R6G) as probing molecules, the surface-enhanced Raman scattering (SERS) experiments showed that the Ag film assembled by nanosheets with high pack density exhibited excellent detecting performance, which could be used as effective SERS substrate for ultrasensitive detecting. Besides, a novel quintuplet SERS substrate could be synthesized in one batch by our method, which showed good reproducibility and a linear dependence between analyte concentrations and intensities, revealing the advantage of this method for easily scale-up production.

Structural, optical, and magnetic studies of manganese-doped zinc oxide hierarchical microspheres by self-assembly of nanoparticles.

In this study, a series of manganese [Mn]-doped zinc oxide [ZnO] hierarchical microspheres [HMSs] are prepared by hydrothermal method only using zinc acetate and manganese acetate as precursors and ethylene glycol as solvent. X-ray diffraction indicates that all of the as-obtained samples including the highest Mn (7 mol%) in the crystal lattice of ZnO have a pure phase (hexagonal wurtzite structure). A broad Raman spectrum from as-synthesized doping samples ranges from 500 to 600 cm-1, revealing the successful doping of paramagnetic Mn2+ ions in the host ZnO. Optical absorption analysis of the samples exhibits a blueshift in the absorption band edge with increasing dopant concentration, and corresponding photoluminescence spectra show that Mn doping suppresses both near-band edge UV emission and defect-related blue emission. In particular, magnetic measurements confirm robust room-temperature ferromagnetic behavior with a high Curie temperature exceeding 400 K, signifying that the as-formed Mn-doped ZnO HMSs will have immense potential in spintronic devices and spin-based electronic technologies.