To explore the pathogenesis of anterior resection syndrome by magnetic resonance imaging rectal defecography.

BACKGROUND: Over 90% of rectal cancer patients develop low anterior resection syndrome (LARS) after sphincter-preserving resection. The current globally recognized evaluation method has many drawbacks and its subjectivity is too strong, which hinders the research and treatment of LARS. AIM: To evaluate the anorectal function after colorectal cancer surgery by quantifying the index of magnetic resonance imaging (MRI) defecography, and pathogenesis of LARS. METHODS: We evaluated 34 patients using the standard LARS score, and a new LARS evaluation index was established using the dynamic images of MRI defecography to verify the LARS score. RESULTS: In the LARS score model, there were 10 (29.41%) mild and 24 (70.58%) severe cases of LARS. The comparison of defecation rate between the two groups was 29.36 ± 14.17% versus 46.83 ± 18.62% (P = 0.004); and MRI-rectal compliance (MRI-RC) score was 3.63 ± 1.96 versus 7.0 ± 3.21 (P = 0.001). Severe and mild LARS had significant differences using the two evaluation methods. There was a significant negative correlation between LARS and MRI-RC score (P < 0.001), and they had a negative correlation with defecation rate (P = 0.028). CONCLUSION: MRI defecography and standard LARS score can both be used as an evaluation index to study the pathogenesis of LARS.

Recent advances in graphene nanoribbons for biosensing and biomedicine.

In recent years, a new type of quasi-one-dimensional graphene-based material, graphene nanoribbons (GNRs), has attracted increasing attention. The limited domain width and rich edge configurations of GNRs endow them with unique properties and wide applications in comparison to two-dimensional graphene. This review article mainly focuses on the electrical, chemical and other properties of GNRs, and further introduces the typical preparation methods of GNRs, including top-down and bottom-up strategies. Then, their biosensing and biomedical applications are highlighted in detail, such as biosensors, photothermal therapy, drug delivery, etc. Finally, the challenges and future prospects in the synthesis and application of functionalized GNRs are discussed. It is expected that GNRs will have significant practical use in biomedical applications in the future.

A disposable paper-based hydrophobic substrate for highly sensitive surface-enhanced Raman scattering detection.

Detection of target analytes with high sensitivity and reproducibility remains a challenge for surface-enhanced Raman scattering (SERS) due to the lack of cost-effective and highly sensitive substrates. In this study, a hydrophobic SERS substrate capable of concentrating nanoparticles and analytes was prepared by spin-coating lubricating liquid onto commercial paper. The condensation effect of the paper-based hydrophobic substrate induced aggregation of gold nanoparticles (Au NPs) to generate ''hot spots'' for SERS and to drive analytes to the hot-spot areas for more sensitive detection. The obtained SERS signal intensity was 5-fold higher than that obtained using common paper, and a detection limit (LOD) of 4.3 × 10-10 M for rhodamine 6G (R6G) was achieved. Randomly selected points on the substrate and different batches of substrates all exhibited high reproducibility, and the relative standard deviation (RSD) at 1362 cm-1 is approximately 11%. A further application of the hydrophobic substrate was demonstrated by the detection of cytochrome C within a linear detection range of 3.90 × 10-8 M-1.25 × 10-6 M. In addition, the prepared substrate can obtain identifiable SERS spectra of cancer cells and non-cancer cells because a large number of AuNP or Au NPs clusters can adhere to cells, resulting in the construction of a 3D hotspot matrix. The disposable hydrophobic paper substrate eliminates the problem of solution diffusion, and also provides an effective platform for biomolecular screening detection.

Recyclable three-dimensional Ag nanorod arrays decorated with O-g-C3N4 for highly sensitive SERS sensing of organic pollutants.

A three-dimensional (3D) substrate was developed by assembling a monolayer of graphitic carbon nitride (O-g-C3N4) on Ag nanorod arrays (Ag NRs) for sensitive and recyclable surface enhanced Raman scattering (SERS) detection. The prepared Ag NRs/O-g-C3N4 substrate not only generated a significant Raman enhancement effect as a result of the strong π-π stacking interaction between O-g-C3N4 and the analytes but also possessed excellent self-cleaning property via visible-light irradiation that was attributed to its outstanding catalytic performance. Highly sensitive SERS detection could be achieved with a LOD of 8.2 × 10-10 M for R6 G, and the substrate could be used repeatedly for at least four cycles with tolerable intensity attenuation. In addition, the 3D substrate exhibited long-term stability originating from the electron-donor effect of O-g-C3N4 and high reproducibility due to the uniform decoration of O-g-C3N4 on the Ag NRs through the strong interaction. Furthermore, using Ag NRs/O-g-C3N4, the recyclable detection of antibiotics in a water sample was demonstrated with high sensitivity, which indicates that the 3D Ag NRs/O-g-C3N4 substrate is a promising candidate for eliminating the challenges of single-use SERS substrates and building a portable SERS platform to sense organic molecular species.

Removal of Antibiotics From Water with an All-Carbon 3D Nanofiltration Membrane.

Recent industrial developments and increased energy demand have resulted in significantly increased levels of environmental pollutants, which have become a serious global problem. Herein, we propose a novel all-carbon nanofiltration (NF) membrane that consists of multi-walled carbon nanotubes (MWCNTs) interposed between graphene oxide (GO) nanosheets to form a three-dimensional (3D) structure. The as-prepared membrane has abundant two-dimensional (2D) nanochannels that can physically sieve antibiotic molecules through electrostatic interaction. As a result, the prepared membrane, with a thickness of 4.26 µm, shows both a high adsorption of 99.23% for tetracycline hydrochloride (TCH) and a high water permeation of 16.12 L m- 2 h- 1 bar- 1. In addition, the cationic dye methylene blue (MB) was also removed to an extent of 83.88%, indicating broad applications of the prepared membrane.

Effective Removal of Tetracycline Antibiotics from Water using Hybrid Carbon Membranes.

Antibiotic residues in drinking water have become a global problem, especially in developing countries. However, effective purification of water contaminated by antibiotics remains a great challenge. Here, we investigated the removing of tetracycline by carbon nanomaterials with different structures and surface functionalities. The result shows that a membrane of thick graphene oxide (GO) and activated carbon (AC) with a thickness of 15 µm can effectively remove 98.9% of tetracycline hydrochloride (TCH) from water by vacuum filtration. Structural analysis indicated that the AC nanoparticles were uniformly inserted into the GO interstitial sites without any aggregations. Also, GO sheets were loosened by the encapsulated AC nanoparticles, leading to the formation of numerous tiny pores (3-10 nm) that acted as channels for fluid passage, whereas the carbons and chemical groups on the GO surface adsorbed TCH. GO/AC membrane exhibits the best adsorption efficiency among the investigated materials, including pure GO, AC, carbon nanotube (CNT), and CNT/AC and GO/CNT hybrids.

Highly Reproducible Ag NPs/CNT-Intercalated GO Membranes for Enrichment and SERS Detection of Antibiotics.

The increasing pollution of aquatic environments by antibiotics makes it necessary to develop efficient enrichment and sensitive detection methods for environmental antibiotics monitoring. In this work, silver nanoparticles and carbon nanotube-intercalated graphene oxide laminar membranes (Ag NPs/CNT-GO membranes) were successfully prepared for enrichment and surface-enhanced Raman scattering (SERS) detection of antibiotics. The prepared Ag NPs/CNT-GO membranes exhibited a high enrichment ability because of the π-π stacking and electrostatic interactions of GO toward antibiotic molecules, which enhanced the sensitivity of SERS measurements and enabled the antibiotics to be determined at sub-nM concentrations. In addition, the nanochannels created by the intercalation of CNTs into GO layers resulted in an 8-fold enhancement in the water permeance of Ag NPs/CNT-GO membranes compared to that of pure GO membranes. More importantly, the Ag NPs/CNT-GO membranes exhibited high reproducibility and long-term stability. The spot-to-spot variation in SERS intensity was less than 15%, and the SERS performance was maintained for at least 70 days. The Ag NPs/CNT-GO membranes were also used for SERS detection of antibiotics in real samples; the results showed that the characteristic peaks of antibiotics were obviously recognizable. Thus, the sensitive SERS detection of antibiotics based on Ag NPs/CNT-GO offers great potential for practical applications in environmental analysis.

Synthesis of MnO2 nanoparticles from sonochemical reduction of MnO4(-) in water under different pH conditions.

MnO2 was synthesized by sonochemical reduction of MnO4(-) in water under Ar atmosphere at 20°C, where the effects of solution pH on the reduction of MnO4(-) were investigated. The obtained XRD results showed that poor crystallinity δ-MnO2 was formed at pH 2.2, 6.0 and 9.3. When solution pH was increased from 2.2 to 9.3, the morphologies of δ-MnO2 changed from aggregated sheet-like or needle-like structures to spherical nanoparticles and finally to cubic or polyhedron nanoparticles. After further irradiation, MnO2 was readily reduced to Mn(2+). It was confirmed that H2O2 and H atoms formed in the sonolysis of water acted as reductants for both reduction for MnO4(-) to MnO2 and MnO2 to Mn(2+). The optimum irradiation time for the effective synthesis of MnO2 was 13 min at pH 2.2, 9 min at pH 6.0, 8 min at pH 9.3, respectively.

Sonochemical fabrication of gold nanoparticles-boron nitride sheets nanocomposites for enzymeless hydrogen peroxide detection.

A simple sonochemical route was developed for the preparation of gold nanoparticles/boron nitride sheets (AuNPs/BNS) nanocomposites without using reducing or stabilizing agents. Transmission electron microscopy, scanning electron microscopy, X-ray diffraction, and UV-vis absorption spectra were used to characterize the structure and morphology of the nanocomposites. The experimental results showed that AuNPs with approximately 20nm were uniformly attached onto the BNS surface. It was found that the AuNPs/BNS nanocomposites exhibited good catalytic activity for the reduction of H2O2. The modified electrochemical sensor showed a linear range from 0.04 to 50mM with a detection limit of 8.3µM at a signal-to-noise ratio of 3. The findings provide a low-cost approach to the production of stable aqueous dispersions of nanoparticles/BNS nanocomposites.

One-step simple sonochemical fabrication and photocatalytic properties of Cu2O-rGO composites.

An easy, one-step synthesis of Cu2O-reduced graphene composites (Cu2O-rGO) was developed using a simple sonochemical route without any surfactants or templates. The morphology and structure of the Cu2O-rGO composites were characterised using techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). The results indicated that the Cu2O sphere is approximately 200 nm in diameter and composed of small Cu2O particles approximately 20 nm in diameter. The morphology and composition of the Cu2O-rGO composites could be well controlled by simply changing the mole ratio of the reactants under ultrasonic irradiation. The Cu2O-rGO composites displayed better photocatalytic performance for the degradation of methyl orange (MO) than pure Cu2O spheres, which may have potential applications in water treatment, sensors, and energy storage.

Sonochemical fabrication of twinned ZnO hollow ellipses for electrochemical biosensing.

Twinned ZnO hollow ellipses (ZnO HEs) have been successfully fabricated by a one-step template-free sonochemical route. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results showed that the ZnO HEs had a hexagonal wurtzite structure, the wall of which was composed of ZnO nanorods. A possible growth mechanism for the formation of ZnO HEs was proposed, in which sonication played a crucial role. The highly efficient H2O2 electrochemical biosensor was fabricated using the film immobilized with hemoglobin, ZnO HEs and chitosan on glassy carbon electrode. The biosensor showed high stability and excellent electrocatalytic activity toward H2O2 with a linear range from 0.5 to 250 microM and a detection limit of 0.15 microM.

Fabrication of a boron nitride-gold nanocluster composite and its versatile application for immunoassays.

A multifunctional boron nitride-gold nanocluster composite was fabricated using poly-diallyldimethylammonium chloride as a stabilizer and a linker. The as-fabricated composite could be used as a fluorescent or an electrochemical label for immunosensing in the sensitive detection of interleukin-6.

Aqueous synthesis of color-tunable CuInS2/ZnS nanocrystals for the detection of human interleukin 6.

In this Article, we present a facile microwave-assisted synthesis route for the preparation of water-soluble and high-quality CuInS2/ZnS nanocrystals (NCs) with glutathione as the stabilizer. The as-prepared CuInS2/ZnS NCs exhibited small particle sizes (~3.3 nm), long photoluminescence lifetimes, and color-tunable properties ranging from the visible to the near-infrared by varying the initial ratio of Cu/In in the precursors. The low-toxicity, highly luminescent and biocompatible CuInS2/ZnS NCs were applied to cell imaging, showing that they could be used as promising fluorescent probes. Furthermore, the CuInS2/ZnS NCs were used as the signal labels for a fluoroimmunoassay of the biomarker IL-6, showing their great potential for use as reliable point-of-care diagnostics for biomarkers of cancer and other diseases.

Microwave-assisted synthesis of highly luminescent AgInS2/ZnS nanocrystals for dynamic intracellular Cu(ii) detection.

Low-toxicity, highly luminescent, and water-soluble AgInS2/ZnS nanocrystals (NCs) have been synthesized via a microwave-assisted approach. The structure and optical features of the AgInS2/ZnS NCs were characterized by X-ray diffraction, high resolution transmission electron microscopy, Fourier transform infrared spectroscopy, ultraviolet visible absorption spectroscopy and photoluminescence (PL) spectroscopy. The as-synthesized AgInS2/ZnS NCs exhibited high PL quantum yields (40%) and long PL lifetimes (424.5 ns). Furthermore, the dynamic changes of the intracellular copper(ii) levels in HeLa cells were monitored using the AgInS2/ZnS NCs as fluorescent probes. The results showed that the AgInS2/ZnS NCs as promising fluorescent probes can be used in the detection of intracellular copper ions in living cells.

Ultrasensitive multianalyte electrochemical immunoassay based on metal ion functionalized titanium phosphate nanospheres.

A novel multianalyte electrochemical immunoassay was developed for ultrasensitive detection of human cardiopathy biomarkers cardiac troponin I (cTnI) and human heart-type fatty-acid-binding protein (FABP) using metal ion functionalized titanium phosphate nanospheres (TiP-metal ion) as labels. The metal ions could be detected directly through square wave voltammetry (SWV) without metal preconcentration, and the distinct voltammetric peaks had a close relationship with each sandwich-type immunoreaction. The position and size of the peaks reflected the identity and level of the corresponding antigen. The large amount of metal ions loading on the TiP nanospheres greatly amplified the detection signals, and the good biocompatibility of graphene nanoribbons (GONRs) retained good stability for the sandwich-type immunoassay. The proposed immunoassay exhibited high sensitivity and selectivity for the detection of cTnI and FABP. The linear relationships between electrochemical signals and the concentrations of cTnI and FABP were obtained in the range of 0.05 pg/mL-50 ng/mL and 0.05 pg/mL-50 ng/mL, respectively. The detection limits of cTnI and HIgG were 1 and 3 fg/mL (S/N = 3), respectively. Moreover, the immunoassay accurately detected the concentrations of cTnI and FABP in human serum samples, which were demonstrated to have excellent correlations with the standard enzyme linked immunosorbent assay (ELISA) method. The results suggested that the electrochemical immunoassay would be promising in the point-of-care diagnostics application of clinical screening of acute myocardial infarction (AMI) biomarkers.