Near-infrared fluorophores methylene blue for targeted imaging of the stomach in intraoperative navigation

Near-infrared (NIR) fluorescence imaging-guided surgery is increasingly concerned in gastrointestinal surgery because it can potentially improve clinical outcomes. This new technique can provide intraoperative image guidance for surgical margin evaluation and help surgeons examine residual lesions and small tumors during surgery. NIR fluorophores methylene blue (MB) is a promising fluorescent probe because of its safety and intraoperative imaging in the clinic. However, whether MB possesses the potential to perform intraoperative navigation of the stomach and gastric tumors needs to be further explored. Therefore, the current study mainly validated MB’s usefulness in animal models’ intraoperative imaging of stomach and gastric tumors. NIR fluorophores MB can exhibit specific uptake by the gastric epithelial cells and cancer cells. It is primarily found that MB can directly target the stomach in mice. Interestingly, MB was applied for the NIR imaging of gastric cancer cell xenografts, suggesting that MB cannot specifically target subcutaneous and orthotopic gastric tumors in xenograft models. Thus, it can be concluded that MB has no inherent specificity for gastric tumors but specificity for gastric tissues. Apparently, MB-positive and negative NIR imaging are meaningful in targeting gastric tissues and tumors. MB is expected to represent a helpful NIR agent to secure precise resection margins during the gastrectomy and resection of gastric tumors

Ultrasmall dopamine-coated nanogolds: preparation, characteristics, and CT imaging

<p>Water-dispersible ultrasmall nanogolds (WDU AuNPs) and their dopamine-coated nanogolds (WDU AuNPs@DPAs) were prepared by a reduction method with sodium borohydride as a reducing agent and a stabilised agent of 2-mercaptosuccinic acid in aqueous solution. The effects of these nanoparticles on computed tomography (CT) imaging were evaluated. The size distributions and Zeta potential of the nanoparticles were measured with a Malvern size analyser, and nanoparticle morphology was observed by transmission electron microscopy. These characteristics were confirmed by Fourier transform spectroscopy and ultraviolet/visible spectra. It was found that WDU AuNPs@DPAs were 5.4 nm in size with clear core–shell structure. The 3-(4, 5-Dimethyl-2-thiazolyl)-2, 5-diphenyltetrazolium bromide assay results showed that the WDU AuNPs and WDU AuNPs@DPAs were hypotoxic to different cells. The WDU AuNPs@DPAs showed a much longer circulation time and a larger CT attenuation coefficient than iohexol and could be excreted by the kidney and bladder. These nanoparticles showed considerable potential for future application in CT imaging.</p

Theory on logging interpretation of igneous rocks and its application

Based on the summary of theories and methods of well logging interpretation for igneous rock at home and abroad, a complete interpretation process of well logging is formed, which includes lithology identification, quantitative matrix porosity calculation, quantitative saturation calculation, and fluid nature identification. This paper presents a theory and an application model of porosity and saturation calculation for heterogeneous and complex reservoirs, and establishes a framework for interpreting complex volcanic rock reservoirs; proposes a new method combining ECS with FMI logging for 3-D lithology identification of igneous rocks. Based on the study of the micro-fracture simulation well, this paper puts forward a practical quantitative calculation method for calculating the fracture porosity of heterogeneous reservoirs. By experimenting with core of whole diameter under high temperature and high pressure, the authors studied the influence of fracture on saturation calculation through numerical simulation, and proposed a new method of quantitative saturation calculation. The results of the Xujiaweizi area in the Daqing Oilfield and the Ludong-Wucaiwan area in the Xinjiang Oilfield show that the theory and the method are correct and effective. Key words: igneous rock, well-log interpretation, interpretation model, fracture porosity, saturatio

CsPbBr3 Perovskite Nanocrystal Grown on MXene Nanosheets for Enhanced Photoelectric Detection and Photocatalytic CO2 Reduction.

All-inorganic CsPbX3 (X = Cl, Br or I) perovskite nanocrystals have attracted extensive interest recently due to their exceptional optoelectronic properties. In an effort to improve the charge separation and transfer following efficient exciton generation in such nanocrystals, novel functional nanocomposites were synthesized by the in situ growth of CsPbBr3 perovskite nanocrystals on two-dimensional MXene nanosheets. Efficient excited state charge transfer occurs between CsPbBr3 NCs and MXene nanosheets, as indicated by significant photoluminescence (PL) quenching and much shorter PL decay lifetimes compared with pure CsPbBr3 NCs. The as-obtained CsPbBr3/MXene nanocomposites demonstrated increased photocurrent generation in response to visible light and X-ray illumination, attesting to the potential application of these heterostructure nanocomposites for photoelectric detection. The efficient charge transfer also renders the CsPbBr3/MXene nanocomposite an active photocatalyst for the reduction of CO2 to CO and CH4. This work provides a guide for exploration of perovskite materials in next-generation optoelectronics, such as photoelectric detectors or photocatalyst

Stable Luminous Nanocomposites of Confined Mn2+-Doped Lead Halide Perovskite Nanocrystals in Mesoporous Silica Nanospheres as Orange Fluorophores.

Creating highly stable inorganic perovskite nanocrystals (CsPbX3, where X = Cl, Br, and I) with excellent optical performance is challenging because their optical properties depend on their ionic structure and its inherent defects. Here, we present a facile and effective synthesis using a nanoconfinement strategy to grow Mn2+-doped CsPbCl3 nanocrystals embedded in dendritic mesoporous silica nanospheres (MSNs). The resulting nanocomposite is abbreviated as Cs(Pb x/Mn1- x)Cl3@MSNs and can serve as the orange emitter for white light-emitting diodes (WLEDs). The MSN matrix was prepared via a templated sol-gel technique as monodispersed center-radial dendritic porous particles, with a diamater of ∼105 nm and an inner pore size of ∼13 nm. The MSN was then utilized as the matrix to initiate the growth of Mn-doped perovskite nanocrystals (NCs). The NCs in the resulting composite have an average diameter of 8 nm and a photoluminescence quantum yield of &gt;30%. In addition, the optical properties of the Cs(Pb x/Mn1- x)Cl3@MSNs can be tuned by varying the Mn2+ doping level. The resulting composites presented a significantly improved resistance to ultraviolet (UV) light, temperature, and moisture compared to that of bare Cs(Pb0.72/Mn0.28)Cl3. Finally, we fabricated down-converting WLEDs by using Cs(Pb x/Mn1- x)Cl3@MSNs as the orange-emitting phosphor deposited onto UV-emitting chips, demonstrating their promising applications in solid-state lighting. This work provides a valuable approach to fabricating stable orange luminophores as replacements for traditional emitters in light-emitting diode devices

Stable and Recyclable Photocatalysts of CsPbBr3@MSNs Nanocomposites for Photoinduced Electron Transfer RAFT Polymerization

All-inorganic metal halide perovskite CsPbX3(X = Cl, Br, I) nanocrystals (NCs) have demonstrated attractive optoelectronic characteristics. However, their photocatalytic properties are limited by their poor stability and easy recombination of photogenerated carriers. Herein, we introduced a CsPbBr3@MSNs nanocomposite (CsPbBr3NCs embedded in dendritic mesoporous silica nanospheres (MSNs)) as photocatalysts for photoinduced electron transfer reversible addition-fragmentation chain transfer (PET-RAFT) polymerization. The CsPbBr3nanocrystals (∼8.1 nm; PLQY of 62 ± 2.1%) were embedded in dendritic MSNs using a nanoconfinement strategy. PET-RAFT polymerization was successfully initiated using the CsPbBr3@MSNs nanocomposite as the photocatalyst. Reaction variables, such as catalyst loading, monomer composition, and excitation light wavelengths, were varied to yield polymers with the desired control of molecular weight and dispersity as well as block copolymers with high chain-end fidelity. In addition, the perovskite-based photocatalysts could be readily separated and purified, which allowed effective and rapid recycling of the nanocomposites for multiple polymerization cycles

Insight into a Bentonite-Based Hydrogel for the Conservation of Sandstone-Based Cultural Heritage: In Situ Formation, Reinforcement Mechanism, and High-Durability Evaluation

Conservation of sandstone-based cultural heritage has attracted a great deal of interest. We propose herein a novel protecting strategy, via in situ fabrication of bentonite-based hydrogels (B-H) inside sandstones, where the bentonite-based hydrogels serve as the underlying cement. To create bentonite-based hydrogels with controllable structure, possessing good mechanical and anti-swelling properties, we have optimized forming time, appearance, and viscosity. The hydrogel precursor penetrated into the pores of the sandstone; the hydrogel would then form within 3–5 h. As found by employing a fluorescent tracer, the precursor remained controllably in place without any apparent change in the sandstone morphology. The bentonite-based hydrogels that formed inside the sandstones presented strong hydrogen bonding, coordination, and ionic bonding, as well as strong mechanical interlocking to the sandstone matrix. As a result, the sandstones possessed enhanced mechanical compressive strength and excellent resistance to acid, salt, and freeze–thaw cycles. Our approach provides for a non-destructive, eco-friendly, easy-to-use, and long-term strategy for cultural preservation, one with excellent protection effects

General Strategy for the Preparation of Stable Luminous Nanocomposite Inks Using Chemically Addressable CsPbX₃ Peroskite Nanocrystals

The potential optoelectronic applications of perovskite nanocrystals (NCs) are primarily limited by major material instability arising from the ionic nature of the NC lattice. Herein, we introduce a facile and effective strategy to prepare extremely stable CsPbX₃ NC–polymer composites. NC surfaces are passivated with reactive methacrylic acid (MA) ligands, resulting in the formation of homogeneous nanocubes (abbreviated as MA-NCs) with a size of 14–17 nm and a photoluminescence quantum yield above 80%. The free double bonds on the surface then serve as chemically addressable synthetic handles, enabling UV-induced radical polymerization. Critically, a bromide-rich environment is developed to prevent NC sintering. The composites obtained from copolymerizing MA-NCs with hydrophobic methyl methacrylate and methacrylisobutyl polyhedral oligomeric silsesquioxane monomers exhibit enhanced properties compared to previously reported encapsulated NCs, including higher quantum yields, remarkable chemical stability toward water, and much enhanced thermal stability. The good solubility of the composite in organic solvent further enables its use as a solution-processable luminescent ink, used here for fabrication of white-light-emitting diodes with high luminous efficiency and excellent color-rendering index. The resulting fluorescent and stable NC ink opens the door to potential scalable and robust optoelectronic applications