Risk factors and prognosis of sentinel lymph node metastasis in breast-conserving breast cancer: A retrospective study based on the SEER database.

At present, the risk factors and prognosis of sentinel lymph node metastasis (SLNM) are analyzed based on the study of axillary lymph node metastasis, but whether there is a difference between the two is unclear. Therefore, an accurate and appropriate predictive model needs to be proposed to evaluate patients undergoing sentinel lymph node biopsy (SLNB) for breast cancer. We selected 16983 women with breast cancer from the Surveillance Epidemiology and End Results (SEER) database. They were randomly assigned to two cohorts, one for development (n = 11891) and one for validation (n = 5092). multi-factor logistics regression was used to distinguish risk factors affecting SLNM. The potential prognostic factors were identified using the COX regression analysis. The hazard ratio (HR) and 95% confidence interval (95%CI) were calculated for all results. Multiple Cox models are included in the nomogram, with a critical P value of .05. In order to evaluate the model's performance, Concordance index and receiver operating characteristic curves were used. Six independent risk factors affecting SLNM were screened out from the Logistic regression, including tumor location, number of regional lymph nodes (2-5), ER positive, PR positive, tumor size (T2-3), and histological grade (Grade II-III) are independent risk factors for SLNM in patients (P < .05). Eight prognostic factors were screened out in the multivariate COX regression analysis (P < .05): Age: Age 60 to 79 years, Age ≥ 80 years; Race; Histological grading: Grade II, Grade III; No radiotherapy; Tumor size: T2, T3; ER positive:, sentinel lymph node positive, married. Histological grade, tumor location, T stage, ER status, PR status and the number of SLNB are significantly correlated with axillary SLNM. Age, ethnicity, histological grade, radiotherapy, tumor size, ER status, SLN status, and marital status were independent risk factors for Breast cancer specific survival (BCSS). Moreover, the survival rate of patients with 3 positive SLNs was not significantly different from that with one or two positive SLNs, We concluded that patients with stage N1 breast cancer were exempt from axillary lymph node dissection, which is worthy of further study.

Rifampicin-Loaded Polyelectrolyte Complex Eliminates Intracellular Bacteria through Thiol-Mediated Cellular Uptake and Oxidative Stress Enhancement.

The poor accumulation of antibiotics in the cytoplasm leads to the poor eradication of intracellular bacteria. Herein, a polyelectrolyte complex (PECs@Rif) allowing direct cytosolic delivery of rifampicin (Rif) was developed for the treatment of intracellular infections by complexation of poly(α-lipoic acid) (pLA) and oligosaccharide (COS) in water and loading Rif. Due to the thiol-mediated cellular uptake, PECs@Rif delivered 3.9 times higher Rif into the cytoplasm than that of the free Rif during 8 h of incubation. After entering cells, PECs@Rif released Rif by dissociating pLA into dihydrolipoic acid (DHLA) in the presence of intracellular thioredoxin reductase (TrxR). Notably, DHLA could reduce endogenous Fe(III) to Fe(II) and provide a catalyst for the Fenton reaction to produce a large amount of reactive oxygen species (ROS), which would assist Rif in eradicating intracellular bacteria. In vitro assay showed that PECs@Rif reduced almost 2.8 orders of magnitude of intracellular bacteria, much higher than 0.7 orders of magnitude of free Rif. The bacteremia-bearing mouse models showed that PECs@Rif reduced bacterial levels in the liver, spleen, and kidney by 2.2, 3.7, and 2.3 orders of magnitude, respectively, much higher than free Rif in corresponding tissues. The direct cytosolic delivery in a thiol-mediated manner and enhanced oxidative stress proposed a feasible strategy for treating intracellular bacteria infection.

In-Plane Palladium and Interplanar Copper Dual Single-Atom Catalyst in Bulk-Like Carbon Nitride for Cascade CO2 Photoreduction.

Dual single-atom catalysts (DSACs) are promising for breaking the scaling relationships and ensuring synergistic effects compared with conventional single-atom catalysts (SACs). Nevertheless, precise synthesis and optimization of DSACs with specific locations and functions remain challenging. Herein, dual single-atoms are specifically incorporated into the layer-stacked bulk-like carbon nitride, featuring in-plane three-coordinated Pd and interplanar four-coordinated Cu (Pd1-Cu1/b-CN) atomic sites, from both experimental results and DFT simulations. Using femtosecond time-resolved transient absorption (fs-TA) spectroscopy, it is found that the in-plane Pd features a charge decay lifetime of 95.6 ps which is much longer than that of the interplanar Cu (3.07 ps). This finding indicates that the in-plane Pd can provide electrons for the reaction as the catalytically active site in both structurally and dynamically favorable manners. Such a well-defined bi-functional cascade system ensures a 3.47-fold increase in CO yield compared to that of bulk-like CN (b-CN), while also exceeding the effects of single Pd1/b-CN and Cu1/b-CN sites. Furthermore, DFT calculations reveal that the inherent transformation from s-p coupling to d-p hybridization between the Pd site and CO2 molecule occurs during the initial CO2 adsorption and hydrogenation processes and stimulates the preferred CO2-to-CO reaction pathway.

A Dynamically Stable Mixed Conducting Interphase for All-Solid-State Lithium Metal Batteries.

All-solid-state lithium (Li) metal batteries (ASSLMBs) employing sulfide solid electrolytes have attracted increasing attention owing to superior safety and high energy density. However, the instability of sulfide electrolytes against Li metal induces the formation of two types of incompetent interphases, solid electrolyte interphase (SEI) and mixed conducting interphase (MCI), which significantly blocks rapid Li-ion transport and induces uneven Li deposition and continuous interface degradation. In this contribution, a dynamically stable mixed conducting interphase (S-MCI) is proposed by in situ stress self-limiting reaction to achieve the compatibility of Li metal with composite sulfide electrolytes (Li6 PS5 Cl (LPSCl) and Li10 GeP2 S12 (LGPS)). The rational design of composite electrolytes utilizes the expansion stress induced by the electrolyte decomposition to in turn constrain the further decomposition of LGPS. Consequently, the S-MCI inherits the high dynamical stability of LPSCl-derived SEI and the lithiophilic affinity of Li-Ge alloy in LGPS-derived MCI. The Li||Li symmetric cells with the protection of S-MCI can operate stably for 1500 h at 0.5 mA cm-2 and 0.5 mAh cm-2 . The Li||NCM622 full cells present stable cycling for 100 cycles at 0.1 C with a high-capacity retention of 93.7%. This work sheds fresh insight into constructing electrochemically stable interphase for high-performance ASSLMBs.

Splitting phenomenon of ferromagnetic resonance spectra in NiFe films deposited on periodically rippled sapphire substrates.

The splitting phenomenon of ferromagnetic resonance (FMR) spectra of Ni80Fe20 (NiFe) films deposited on periodically rippled sapphire substrates is studied experimentally and with the help of micromagnetic simulation. The analyses show that the splitting of FMR spectra is related to the periodic ripple topography of films. When the applied magnetic field is perpendicular to the ripple direction, the effective field of periodically rippled films becomes inhomogeneous. The splitting of ferromagnetic resonance spectra originates from localized FMR peaks corresponding to different regions with different effective field intensities in the rippled structure. Furthermore, the relative intensity and position between the split mode and the main FMR mode can be changed by designing ripple topography. This work would help understand the splitting phenomenon of FMR spectra for these NiFe films deposited on the periodically rippled sapphire substrates.

Understanding the unique S-scheme charge migration in triazine/heptazine crystalline carbon nitride homojunction.

Understanding charge transfer dynamics and carrier separation pathway is challenging due to the lack of appropriate characterization strategies. In this work, a crystalline triazine/heptazine carbon nitride homojunction is selected as a model system to demonstrate the interfacial electron-transfer mechanism. Surface bimetallic cocatalysts are used as sensitive probes during in situ photoemission for tracing the S-scheme transfer of interfacial photogenerated electrons from triazine phase to the heptazine phase. Variation of the sample surface potential under light on/off confirms dynamic S-scheme charge transfer. Further theoretical calculations demonstrate an interesting reversal of interfacial electron-transfer path under light/dark conditions, which also supports the experimental evidence of S-scheme transport. Benefiting from the unique merit of S-scheme electron transfer, homojunction shows significantly enhanced activity for CO2 photoreduction. Our work thus provides a strategy to probe dynamic electron transfer mechanisms and to design delicate material structures towards efficient CO2 photoreduction.

Emerging strategies of engineering retinal organoids and organoid-on-a-chip in modeling intraocular drug delivery: Current progress and future perspectives.

Retinal diseases are a rising concern as major causes of blindness in an aging society; therapeutic options are limited, and the precise pathogenesis of these diseases remains largely unknown. Intraocular drug delivery and nanomedicines offering targeted, sustained, and controllable delivery are the most challenging and popular topics in ocular drug development and toxicological evaluation. Retinal organoids (ROs) and organoid-on-a-chip (ROoC) are both emerging as promising in-vitro models to faithfully recapitulate human eyes for retinal research in the replacement of experimental animals and primary cells. In this study, we review the generation and application of ROs resembling the human retina in cell subtypes and laminated structures and introduce the emerging engineered ROoC as a technological opportunity to address critical issues. On-chip vascularization, perfusion, and close inter-tissue interactions recreate physiological environments in vitro, whilst integrating with biosensors facilitates real-time analysis and monitoring during organogenesis of the retina representing engineering efforts in ROoC models. We also emphasize that ROs and ROoCs hold the potential for applications in modeling intraocular drug delivery in vitro and developing next-generation retinal drug delivery strategies.

Effect of Functional Group Modifications on the Photocatalytic Performance of g-C3 N4.

In recent years, photocatalysis has received increasing attention in alleviating energy scarcity and environmental treatment, and graphite carbon nitride (g-C3 N4 ) is used as an ideal photocatalyst. However, it still remains numerous challenges to obtain the desirable photocatalytic performance of intrinsic g-C3 N4 . Functional group functionalization, formed by introducing functional groups into the bulk structure, is one of the common modification techniques to modulate the carrier dynamics and increases the number of active sites, offering new opportunities to break the limits for structure-to-performance relationship of g-C3 N4 . Nevertheless, the general overview of the advance of functional group modification of g-C3 N4 is less reported yet. In order to better understand the structure-to-performance relationship at the molecular level, a review of the latest development of functional group modification is urgently needed. In this review, the functional group modification of g-C3 N4 in terms of structures, properties, and photocatalytic activity is mainly focused, as well as their mechanism of reaction from the molecular level insights is explained. Second, the recent progress of the application of introducing functional groups in g-C3 N4 is introduced and examples are given. Finally, the difficulties and challenges are presented, and based on this, an outlook on the future research development direction is shown.

Advances in In Vitro Models of Neuromuscular Junction: Focusing on Organ-on-a-Chip, Organoids, and Biohybrid Robotics.

The neuromuscular junction (NMJ) is a peripheral synaptic connection between presynaptic motor neurons and postsynaptic skeletal muscle fibers that enables muscle contraction and voluntary motor movement. Many traumatic, neurodegenerative, and neuroimmunological diseases are classically believed to mainly affect either the neuronal or the muscle side of the NMJ, and treatment options are lacking. Recent advances in novel techniques have helped develop in vitro physiological and pathophysiological models of the NMJ as well as enable precise control and evaluation of its functions. This paper reviews the recent developments in in vitro NMJ models with 2D or 3D cultures, from organ-on-a-chip and organoids to biohybrid robotics. Related derivative techniques are introduced for functional analysis of the NMJ, such as the patch-clamp technique, microelectrode arrays, calcium imaging, and stimulus methods, particularly optogenetic-mediated light stimulation, microelectrode-mediated electrical stimulation, and biochemical stimulation. Finally, the applications of the in vitro NMJ models as disease models or for drug screening related to suitable neuromuscular diseases are summarized and their future development trends and challenges are discussed.

Tune the resonance of VO2 joined metamaterial dimers by adjacent cut wires.

Two terahertz metamaterials were joined by a conductivity variable VO2 patch to obtain a metamaterial dimer. By applying voltage or heat to the VO2 patches, active modulation of terahertz wave could be achieved. A cut-wire metamaterial was placed adjacent to the VO2 joined dimer to affect its electromagnetic response. It was found that the cut wire could heavily impact the resonance mode of the VO2 joined dimer, which gives dual resonance dips in transmission spectrum for both insulating and conducting states of VO2 patches. As a result, by tuning the conductivity of VO2, active dual band phase modulation could be achieved with high transmission window by this dimer-cut wire coupling system.

Nitroreductase-induced bioorthogonal ligation for prodrug activation: A traceless strategy for cancer-specific imaging and therapy.

Prodrug development is of great interest in cancer therapy. From bio-friendly standpoints, traceless prodrug activation would be an ideal approach for cancer treatment owning to the avoidance of byproduct which might induce side effects in living system. Here, we report a fully traceless strategy for cancer imaging and therapy via a metal-free bioorthogonal ligation triggered by nitroreductase (NTR) overexpressed in solid tumors. The reduction of nitro substrates to amines by NTR and further condensation of amines with aldehydes can be seamlessly combined to yield imine-based resveratrol (RSV) with water as the only byproduct. In comparison with RSV, this precursor exhibited not only the same level of anticancer efficiency both in vitro and in vivo under hypoxia, but also a high sensitivity to hypoxia and much lower perturbation towards normal cells, which holds a great potential of theranostic prodrug for cancer therapy.

Effect of Li+ Doping on Photoelectric Properties of Double Perovskite Cs2SnI6: First Principles Calculation and Experimental Investigation.

Double perovskite Cs2SnI6 and its doping products (with SnI2, SnF2 or organic lithium salts added) have been utilized as p-type hole transport materials for perovskite and dye-sensitized solar cells in many pieces of research, where the mechanism for producing p-type Cs2SnI6 is rarely reported. In this paper, the mechanism of forming p-type Li+ doped Cs2SnI6 was revealed by first-principles simulation. The simulation results show that Li+ entered the Cs2SnI6 lattice by interstitial doping to form strong interaction between Li+ and I-, resulting in the splitting of the α spin-orbital of I-p at the top of the valence band, with the intermediate energy levels created and the absorption edge redshifted. The experimental results confirmed that Li+ doping neither changed the crystal phase of Cs2SnI6, nor introduced impurities. The Hall effect test results of Li+ doped Cs2SnI6 thin film samples showed that Li+ doping transformed Cs2SnI6 into a p-type semiconductor, and substantially promoted its carrier mobility (356.6 cm2/Vs), making it an ideal hole transport material.

Dual-band terahertz all-silicon metasurface with giant chirality for frequency-undifferentiated near-field imaging.

Chiral metasurfaces are widely used in imaging and biosensing due to their powerful light field control capabilities. Most of the work is devoted to achieving the goals of chirality enhancement and tunability, but lacks consideration of design complexity, loss, cost, and multi-band operation. In order to alleviate this situation, we propose a pair of dual-frequency giant chiral structures based on all-silicon, which can achieve excellent and opposite spin-selective transmission around 1.09 THz and 1.65 THz. The giant chirality derives from the in-plane electric and magnetic dipole moments excited in different degrees. Theoretically, the maximum circular dichroism at the two frequencies are both as high as 0.34, and the coverage bandwidths of the two giant chirality are 85.5 GHz and 41.4 GHz, respectively. The experimental results are in good agreement with the simulation results. Based on the dual-band giant chiral patterns, the terahertz near-field imaging of different Chinese character images is demonstrated at two frequencies. The frequency-undifferentiated characteristics, good intensity contrast and three-dimensional imaging information are shown by the results. This work provides new ideas for the design of terahertz devices with simple structure and multi-functions, which are expected to be applied in the field of terahertz imaging or multi-channel communication.

Vacancy tuned coupling in terahertz metamaterial arrays.

Metamaterials have shown great potential for modulation on the amplitude, phase and polarization of the terahertz wave. Here vacancies were introduced into the metamaterial arrays to tune the mutual interaction between the constituent resonators, which could heavily affect the electromagnetic response of the whole metamaterial arrays. We show that the introduced vacancies in the metamaterial arrays can effectively affect the resonance mode of the metamaterial arrays. Based upon the vacancy mediated coupling, a silicon-metal hybrid metamaterial arrays were designed to achieve active modulation of propagating terahertz waves.

Design and Development of a Solar Water Purification System with Graphene-Plasmonic Based Hybrid Nanocomposites: A Review.

Harvesting solar energy for water treatments has been considered a promising solution for a global community. The shortage of water is a great challenge for scientists due to the increased demand of the population-however, the low efficiency of absorber materials obstacles in practical applications. In addition, state-of-the-art conventional technologies require optical concentrators and multiple component-based systems, leading to lower efficiency and higher cost. In this review, a low-cost, more reliable, less energy-intensive, and more eco-friendly solar water purification system based on graphene-plasmonic hybrid nanocomposite has been demonstrated. Graphene-plasmonic-based hybrid nanocomposite has been utilized to achieve pure water from wastewater. Such hybrid nanocomposites have the ability to clean polluted water very efficiently due to their excellent properties such as higher surface area, low concentration, and working ability. Furthermore, the development of a solar water purification system has been achieved through optimized hybrid nanocomposites.

State-of-the-art recent progress in MXene-based photocatalysts: a comprehensive review.

Recently, the emerging two-dimensional material MXene enjoys a high reputation due to its fascinating characteristics and shines in various research fields. Among them, MXene has received increasing attention and favor from the photocatalysis community due to its regular planar structure, outstanding metal conductivity, surface adjustable chemical properties, abundant derivatives, and excellent optical and thermal properties. There is no doubt that the introduction of MXene has endowed the photocatalytic system with extraordinary performance and has made an important impact in the field of advanced catalysis and chemical technology. Herein, on the one hand, we summarize the synthetic route of MXenes and MXene-derived 0D quantum dots (MQDs), and propose the corresponding improved synthetic strategies for the defects of MXenes obtained by the current synthetic methods. On the other hand, recent progress in MXene-based photocatalysts has been reviewed to provide a comprehensive dissection of their designs and applications. It is highly anticipated that these will present researchers with a one-stop point for the state-of-the-art development of MXene-based photocatalysts. Finally, the future opportunities and challenges of MXenes in the flourishing field of photocatalysis are also discussed.

Transition-Metal-Ion (Fe, Co, Cr, Mn, Etc.) Doping of TiO2 Nanotubes: A General Approach.

Transition-metal (TM)-ion-doped TiO2 materials are of great importance for photocatalysis- and photoelectrochemical (PEC)-related applications. We introduced a facile, low-cost, and scalable doping method of TM ions (Cr, Co, Cu, Fe, Mn, etc.) into TiO2 nanotubes (NTs), while maintaining their high-ordered tubular structures (with ∼120 nm outside diameter). Both crystallization and doping processes were simultaneously accomplished in aqueous solution at a temperature as low as ∼90 °C, and the fastest doping process could be accomplished in 30 min for Fe doping. Besides, the surface areas of the doped TiO2 NTs were increased to 129.0 m2/g, and their absorption ranges could be expanded from 380 to >500 nm. This study shed light on a facile method for doping TM ions that is extendable to other semiconductors in the field of PEC water splitting and could improve their efficiencies as well.

Interfacial modification of titanium dioxide to enhance photocatalytic efficiency towards H2 production.

Strong demand for affordable clean energy to support applications ranging from conventional energy supply to space propulsion places spotlight on advanced energy generation using photovoltaic and wind power. Yet, the intermittent nature of solar and wind sources drives the search for energy storage solutions that would permit the needed level of resilience and support further growth in the use of renewable sources of power. Hydrogen generation using sunlight is a promising pathway to decouple demand from supply. Herein, we show how exposure to reactive Ar-H2, Ar-H2-N2, and Ar-O2 plasma environments can notably enhance surface properties of photocatalytic TiO2 nanosheets used in advanced energy generation systems. Treatment using Ar-H2 plasmas produced highly hydrogenated, surface-disordered TiO2 nanosheets with oxygen vacancies, whereas exposure to Ar-H2-N2 plasmas resulted in N doping. Surprisingly, Ar-O2 plasma treatment did not change surface properties of TiO2. Optical emission spectroscopy was used to monitor transient species to further understand surface modification in plasma. Direct measurements demonstrated that among thus-produced samples, hydrogenated TiO2 nanosheets exhibit the highest photocatalytic H2-generation activity under visible-light irradiation, which is also greater than the activity of pure, untreated nanosheets. The mechanism of enhancing the visible-light photocatalytic H2-generation activity on hydrogenated TiO2 nanosheets is also proposed. The level of surface disorder and oxygen vacancies plays an important role in enhancing visible-light absorption and reducing the recombination of photogenerated electrons and holes.

UV Radiation Cumulative Recording Based on Amorphous TiO2 Nanotubes.

Ultraviolet (UV) photochromism is observed from natural light in amorphous TiO2 nanotube arrays (NTAs) for the first time. Surface color of the NTAs film would change from light yellow to dark brown eventually, either under ultraviolet bulb irradiation or basking under natural sunlight. This photochromism is attributed to the appearance of Ti3 + ions in the TiO2 NTAs after UV illumination. Furthermore, a UV radiation cumulative dosimeter is designed and fabricated, consisting of a photochromic film and a colorimetric card, which convert invisible ultraviolet rays into visible color changes. This device helps people to understand intuitively how much UV radiation has been received in total from surrounding environments, which is of great importance for skin safety and public health.

Constructing functionalized plasmonic gold/titanium dioxide nanosheets with small gold nanoparticles for efficient photocatalytic hydrogen evolution.

Small plasmonic Au nanoparticles (NPs)-decorated with TiO2 nanosheets were fabricated to improve the photocatalytic performance. The Au/TiO2 nanosheets with Au NPs of different sizes ranging from ∼3 nm to 28 nm were prepared by using hydrothermally obtained TiO2 nanosheets as substrate via urea and light reduction method. During synthesis, the obtained Au NPs through urea reduction treatment in different calcination temperatures possessed smaller size (∼3-13 nm) than those of the light reduction method (∼28 nm). The introduced Au NPs were tightly loaded on the surface of TiO2 nanosheets through in situ growth reduction process of chloroauric acid. The emergence of smaller Au NPs promoted the photocatalytic performance over Au/TiO2 nanosheets. The as-prepared Au/TiO2 nanosheets with small Au NP sizes of ∼3-5 nm showed the highest photocatalytic rate of hydrogen production (∼230 µmol·h-1) under xenon lamp illumination, exceeding more than twice that of Au/TiO2 nanosheets with loading of larger Au NPs (∼28 nm). The favorable constituents and combination of Au/TiO2 nanosheets provided large surface adsorptive sites for reactant adsorption, introduced plasmonic effects and formed Schottky barrier junction via surface plasmon resonance. The Schottky barrier height was lower due to the presence of smaller Au NPs, thereby enhancing the charge separation through the Schottky transfer hub to neighboring TiO2 nanosheets. The synergistic effect between the plasmonic hot carrier-driven Au NPs and TiO2 nanosheets was discussed. The photocatalytic mechanism was also proposed for the fabrication of visible light-restricted photocatalysts with smaller Au NPs.