Cascade-Gates Guarded Asymmetrical Nanochannel Membrane: An Interference-Free Device for Straightforward Detection of Trace Biomarker in Undiluted Serum.

Accurate detection of trace biomarkers in biological samples is a key task in diagnostic testing, but it remains challenging due to the high concentration of other physiologically relevant interferences. This work presents a new electrochemiluminescence (ECL) sensing device based on a bio-inspired nanochannel membrane (NM) guarded with two differential gates. The recognition event at the aptamer gate is followed by the permitting of stimulator transport toward the metal-organic framework (MOF) gate. Proof of concept application is evaluated using cytochrome C (Cytc) as the analyte, and glucose, a commonly existing nutriment as the stimulator. The oxidase-mimic plasmonic nanoparticles induce an effective release of ECL luminophore from the MOF gate. This cascade-gates guarded NM can effectively separate biological matrices from the detection cell. Consequently, the proposed system can achieve direct sensing of 1.0 nm Cytc in undiluted serum within the threshold concentrations of leukemia and lymphoma, making it attractive for point-of-care applications.

Plasmon-Mediated Peroxidase-like Activity on an Asymmetric Nanotube Architecture for Rapid Visual Detection of Bacteria.

Rapid and sensitive detection of bacteria from a complex real media remains a challenge. Herein, we report a visual bacterial sensing assay with excellent specificity, anti-interference ability, and sensitivity based on a surface plasmon resonance (SPR)-enhanced peroxidase (POD) mimetic. The POD mimetic based on Pt nanoparticles (NPs) asymmetrically decorated on Au/TiO2 magnetic nanotubes (Au/Pt/MTNTs) is designed by combining the intrinsic photocatalytic activity of TiO2 and the limited transport depth of light. It is revealed that the localized surface plasmon resonance (LSPR) effect of the asymmetric nanotubes is more effective in facilitating the generation of hot electrons, which are subsequently transferred to Pt and MTNTs, thus greatly promoting the catalytic performance. Using Staphylococcus aureus (S. aureus) as a model of Gram-positive bacteria, the dependence of the colorimetric reaction on the active sites of the POD mimetic is used for the sensing of target bacteria. Owing to the specific recognition between S. aureus and peptide, the fluorescein isothiocyanate (FITC) labeled peptide probes are captured by S. aureus and removed from the Au/Pt/MTNTs, leading to the recovery of POD-like activity and fluorescence emission of S. aureus. Particularly, benefiting from the Au-SPR effect and the magnetic feature of the Au/Pt/MTNTs, the recovery of catalytic activity induced an improved colorimetric assay with a wider linear response for S. aureus qualification and a detection limit of four cells, as well as satisfactory selectivity and feasibility for application in real samples. The plasmon-enhanced POD activity would provide a simple-yet-effective approach to achieve a colorimetric bioassay with high efficiency and sensitivity. This asymmetric design can also be utilized to engineer nanozymes in colorimetric assays for the specific detection of biotoxins, biomarkers, and cancer cells.

Deployment of MIL-88B(Fe)/TiO2 Nanotube-Supported Ti Wires as Reusable Electrochemiluminescence Microelectrodes for Noninvasive Sensing of H2O2 from Single Cancer Cells.

As one of the significant intracellular signaling molecules, hydrogen peroxide (H2O2) regulates some vital biological processes. However, it remains a challenge to develop noninvasive electrodes that can be used for sensing trace H2O2 at the cellular level. Here, we evaluated a high-performance solid-state electrochemiluminescence (ECL) H2O2 sensor based on MIL-88B(Fe) nanocrystal-anchored Ti microwires. Semiconducting TiO2 nanotubes (TiNTs) vertically grown around a Ti wire via an anodization technique act as an intrinsic ECL luminophore. By integrating with MIL-88B(Fe), the synergistic effect of the TiO2 luminophore and the remarkable peroxidase-like activity of MIL-88B(Fe) enable the resulting H2O2 sensor an ultrahigh sensitivity featuring a minimum detection limit of 0.1 nM (S/N = 3), long-term stability, high durativity, and wide-range linear response to a concentration of up to 10 mM. To demonstrate the concept of a MIL-88B(Fe)@TiO2 microelectrode for single-cell sensing, the electrode was used to detect intracellular H2O2 in a single cell. Moreover, benefiting from the heterojunction of MIL-88B(Fe)/TiO2, the microelectrode was found to exhibit excellent photocatalytic activity in the visible-light range, that is, the sensor surface can be self-cleaning after a short visible-light treatment. These advanced sensor characteristics involving easy reusability reveal that the MIL-88B(Fe)@TiO2 microelectrode is a new platform for cytosensing. This study provides a new strategy to design semiconductor materials with arbitrary shape and size, allowing for profound applications in biomedical and clinical analysis.

Wireless Battery-Free Generation of Electric Fields on One-Dimensional Asymmetric Au/ZnO Nanorods for Enhanced Raman Sensing.

Wearable electronics have great potential in enhancing health monitoring, disease diagnosis, and environmental pollution tracking. Development of wearable surface-enhanced Raman spectroscopy (SERS) substrates with target sampling and sensitive sensing functions is a promising way to obtain physical and chemical information. This study describes a facile and effective approach for constructing an electrically modulated SERS (E-SERS) substrate as a wearable and wireless battery-free substrate with improved sensitivity. By integrating zinc oxide nanorods (ZnO NRs) with asymmetric gold decoration, controllable enhanced piezoelectric potentials were achieved using magnets to supply the adjustable pressure force. Owing to spatially oriented electron-hole pair separation on the asymmetric NRs, the local hotspot intensity at the Au tips is significantly improved, increasing the SERS signal by 6.7 times. This mechanism was quantitatively analyzed using Raman spectra by in situ formation of Prussian blue (PB). As a proof-of-concept, the E-SERS substrate was further used as a wearable flexible device to directly collect the sweat on a runner's skin and then monitor the lactate status of the runner. This study offers new insight into the development of E-SERS substrates and provides new design options for the construction of wearable sampling and sensing devices for the noninvasive monitoring of metabolites in healthcare and biomedical fields.

Asymmetrically coating Pt nanoparticles on magnetic silica nanospheres for target cell capture and therapy.

A Janus cargo has been developed via the combination of magnetic mesoporous silica (MMS) with asymmetric decoration of Pt nanoparticles (PtNPs). Mesoporous morphology of MMS provides plenty of space for loading photosensitizers and targeting agents; the magnetic feature endows the as-formed nanospheres with satisfactory isolation function in removal of low abundant target cells. The excellent catalytic ability of PtNPs can effectively alleviate the hypoxia condition of tumor microenvironment via the decomposition of hydrogen peroxide (H2O2), as well as an O2-drived nanomotor for highly efficient drug release. Using CCRF-CEM as the model target cell, the Janus cargo is demonstrated to possess significantly improved performance in cell capture and photodynamic therapy. Specially, owing to the patchy Pt decoration, the loaded photosensitizers exhibit a more efficient release behavior. More importantly, asymmetric O2-emission from one side of the nanocargo acts as a driving force, which could effectively accelerate the motion ability of cargo in cell media, thus leading to an enhanced therapeutic effect compared with the traditionally symmetric nanocargo. This Janus cargo would offer a new paradigm to design highly efficient drug carrier for gaining an improved photodynamic therapy in hypoxic cancer cells.

Development of a pulse-induced electrochemical biosensor based on gluconamide for Gram-negative bacteria detection.

Pathogenic bacteria can cause the outbreaks of disease and threaten human health, which stimulates the development of advanced detection techniques. Herein, a specific and sensitive electrochemical biosensor for Gram-negative bacteria was established based on the conductive polymer with artificial muscle properties.  The effective recognition was achieved through the specific carbohydrate-carbohydrate interaction between gluconamide and lipopolysaccharide.  The application of impulse voltage enhances the efficiency of recognition and shortens the detection time through the temporary deformation of the electrode surface, with a limit of detection (LOD)  of 1 × 100 CFU/mL and a linear range of 1 × 100 - 1 × 106 CFU/mL for Escherichia coli (E. coli). In addition  to the merits of low cost, high efficiency, and rapidity,  the developed label-free electrochemical biosensor can also be applicable for other Gram-negative bacteria, owning promising potential in the application of portable devices and paving a potential way for the construction of electrochemical biosensors.

Intracellular Metal-Organic Frameworks: Integrating an All-In-One Semiconductor Electrode Chip for Therapy, Capture, and Quantification of Circulating Tumor Cells.

Capture, analysis, and inactivation of circulating tumor cells (CTCs) have emerged as important issues for the early diagnosis and therapy of cancer. In this study, an all-in-one sensing device was developed by integrating magnetic metal-organic framework (magMOF) nanoparticles (NPs) and TiO2 nanotube arrays (TiNTs). The magMOF NPs are composed of a magnetic Fe3O4 core and a MIL-100(Fe) shell, which is loaded with glucose oxidase (GOD) and provides an intensive starvation therapy by catalyzing the consumption of cellular nutrients, thus accelerating the generation of intracellular iron ions by MIL-100(Fe) dissolution. Importantly, these iron ions not only lead to an intensive Fenton-like reaction but also establish an excellent correlation of electrochemical intensities with cancer cell numbers. Owing to the intracellular magMOF NPs, the CTCs were magnetically collected onto TiNTs. The exogenous ·OH radicals generated by TiNT photocatalysis trigger iron ions to be rapidly released out and subsequently detected via differential pulse voltammetry using TiNTs as the electrode. An excellent correlation of differential pulse voltammetry intensities with CTC numbers is obtained from 2 to 5000 cell mL-1. This nanoplatform not only paves a way to combine starvation therapy agents with Fenton-like reaction for chemodynamic therapy but also opens up new insights into the construction of all-in-one chips for CTC capture and diagnosis.

In Situ Monitoring of the "Point Discharge" Induced Antibacterial Process by the Onsite Formation of a Raman Probe.

Electroporation induced by the "point discharge" effect is an effective technique for bacteria inactivation. Rapidly monitoring the electroporation-induced inactivation process is important for screening nanomaterials with high antimicrobial performance. In this study, we develop a facile strategy to in situ monitor the electroporation induced antimicrobial mechanism based on the surface-enhanced Raman scattering (SERS) effect of the Au-nanotip arrays. Owning to the high local-electric field (∼107 V m-1) generated on the Au nanotips, the bacteria are rapidly electroporated and effectively inactivated with ≥99.9% reduction in bacteria colony counts by only applying an external voltage of +0.8 V for 10 s. The related inactivation mechanism is directly verified by the formation of the Prussian blue (PB) nanocrystals by leaking of the uptaken [Fe(CN)6]3- ions from the cleavage area on the cell membrane. These [Fe(CN)6]3- ions react with Fe2+ to form PB nanocrystals onsite as soon as they leak out. The characteristic peak of PB in the cellular Raman-silent region provides a collective monitoring approach for the destruction of microorganisms. The present strategy not only develops a facial method for future use in evaluating electroporation materials, but also paves a rapid way for offering accurate information on some antibacterial and antitumor processes.

Microstructure and interaction in aluminum hydrides@polydopamine composites and interfacial improvement with GAP adhesive.

The reduction of interfacial interaction and the deterioration of processing properties of aluminum hydrides (AlH3) is the main challenges preventing its practical application. Here, a simple and effective core-shell structure aluminum hydrides@polydopamine (AlH3@PDA) complex was constructed through in-situ polymerization. The evolution of element states on the surface of AlH3 conducted by X-ray photoelectron spectroscopy indicated the successful introduction of PDA to form the core@shell structure, the thickness of the PDA coated layer increased with the increasing PDA dosage from 0.1 to 1.6% in mass fraction, and the maximum of thickness is 50 nm in TEM testing. Py GC/MS results proved that the increase of dopamine concentration leads to higher proportions of self-assemble units, whereas lower dopamine concentrations favor higher levels of chemical bonded components. Regarding whether PDA is a covalent polymer or a noncovalent aggregate of some species, the formation of intermediates, such as dopaminechrome and 5,6-dihydroxyindole played an important role to coordination interaction with AlH3 in FTIR, Raman, and UV-Vis spectra testing. Compared with pure AlH3, the formation of organic PDA coating improved AlH3 heat resistance. The adhesion work with GAP adhesive was also improved from 107.02 J/m2 of pure AlH3 to 111.13 mJ/m2 of AlH3@PDA-5 complex. This paper provides well support for further practical application of AlH3 in solid propellants.

Construction of High-Active SERS Cavities in a TiO2 Nanochannels-Based Membrane: A Selective Device for Identifying Volatile Aldehyde Biomarkers.

The accurate, sensitive, and selective on-site screening of volatile aldehyde biomarkers for lung cancer is of utmost significance for preclinical cancer diagnosis and treatment. Applying surface-enhanced Raman scattering (SERS) for gas sensing remains difficult due to the small Raman cross section of most gaseous molecules and interference from other components in exhaled breath. Using an Au asymmetrically coated TiO2 nanochannel membrane (Au/TiO2 NM) as the substrate, a ZIF-8-covered Au/TiO2 NM SERS sensing substrate is designed for the detection of exhaled volatile organic compounds (VOCs). Au/TiO2 NM provides uniformly amplified Raman signals for trace measurements in this design. Importantly, the interfacial nanocavities between Au nanoparticles (NPs) and metal-organic frameworks (MOFs) served as gaseous confinement cavities, which is the key to enhancing the capture and adsorption ability toward gaseous analytes. Both ends of the membrane are left open, allowing gas molecules to pass through. This facilitates the diffusion of gaseous molecules and efficient capture of the target analyte. Using benzaldehyde as a typical gas marker model of lung cancer, the Schiff base reaction with a Raman-active probe molecule 4-aminothiophene (4-ATP) pregrafted on Au NPs enabled trace and multicomponent detection. Moreover, the combination of machine learning (ML) and Raman spectroscopy eliminates subjective assessments of gaseous aldehyde species with the use of a single feature peak, allowing for more accurate identification. This membrane sensing device offers a promising design for the development of a desktop SERS analysis system for lung cancer point-of-care testing (POCT).

Engineering hierarchical FeS2/TiO2 nanotubes on Ti mesh as a tailorable flow-through catalyst belt for all-day-active degradation of organic pollutants and pathogens.

The increasing organic and microbiological pollutions in fresh water caused by human activities and industrial development have become a global concern nowadays. In this study, three-dimensional (3D) hierarchical FeS2/TiO2 structures with nanotube geometries were grown on a Ti mesh (M-TNTAs-FeS2). Benefitting from the abundant available reactive sites on the open 3D micro/nanoporous structures, excellent photocatalytic activity of FeS2/TiO2 heterostructure in solar light, and satisfactory Fenton activity of FeS2, the obtained M-TNTAs-FeS2 exhibits outstanding performance as an all-day-active catalyst. Importantly, flexible meshes can be easily tailored and enveloped into fluorinated ethylene propylene (FEP) pockets in a series as a flow-through belt for large-capacitance applications (998 L m-2 at a flow rate of 417 L m-2 h-1 for a four-pockets belt), as indicated by the degradation of azo dyes, antibiotics, pesticides, and pathogens. This study may inspire a new tailorable catalyst design for a promising point-of-use purification device.

Understanding of chiral site-dependent enantioselective identification on a plasmon-free semiconductor based SERS substrate.

Chiral differentiation is an important topic in diverse fields ranging from pharmaceutics to chiral synthesis. The improvement of sensitivity and the elucidation of the mechanism of chiral recognition are still the two main challenges. Herein, a plasmon-free semiconductive surface-enhanced Raman spectroscopy (SERS) substrate with sensitive chiral recognition ability is proposed for the discrimination of enantiomers. A homochiral environment is constructed by typical π-π stacking between l-tryptophan (l-Trp) and phenyl rings on well-aligned TiO2 nanotubes (TiO2 NTs). Using 3,4-dihydroxyphenylalanine (DOPA) enantiomers as the targets and the chelating interaction of Fe3+-DOPA for the onsite growth of Prussian blue (PB), the enantioselectivity difference between l-DOPA and d-DOPA on the homochiral substrate can be directly monitored from PB signals in the Raman-silent region. By combining the experimental results with molecular dynamic (MD) simulations, it is found that satisfactory enantioselective identification not only requires a homochiral surface but also largely depends on the chiral center environment-differentiated hydrogen-bond formation availability.

Synthesis and Characterization of a Novel Aqueous Glycidyl Azide Polymer Emulsion.

The current domestic and foreign research on azide polymers such as glycidyl azide polymers (GAP) mainly focuses on the design, synthesis, modification, and performance of elastomers; it is difficult to prepare the GAP/NC (nitrocellulose) blends, and they have poor mechanical properties. Here, we developed a green and safe strategy for the blending and compounding of azide binder and NC by blending the emulsion with NC in water and demulsifying. Considering the structural characteristics of GAP, a novel energetic aqueous GAP-E (energetic elastomer) emulsion was prepared by anionic self-emulsion polymerization using 2,2-dimethylol propionic acid as the hydrophilic chain extender, 1,4-butanediol as the chain extender, and triethylamine as a neutralizer. Furthermore, the GAP-E emulsion/triethylene glycol dinitrate/nitrocellulose blends (GAP-E/TEGN/NC) with different proportions were prepared in aqueous phase by the precipitation method. The related properties of the emulsion were studied by gel permeation chromatography, Fourier transform infrared, universal material testing machine, dynamic mechanical analyzer, thermogravimetric analysis, and scanning electron microscopy (SEM). Our results indicated the emulsion exhibited good stability with the number average molecular weight of 76,600. The GAP-E film showed a tensile strength of 17.8 MPa, elongation at break of 415%, glass transition temperature of -28.5 °C, and initial degradation temperature of 242 °C. The GAP-E emulsion and TEGN/NC can be blended in the aqueous phase by the demulsification method to prepare a homogeneous GAP-E/TEGN/NC blend. Fourier transform infrared spectroscopy (FTIR) showed that there was a certain hydrogen bond interaction between GAP-E and TEGN/NC molecules, which was conducive to the improvement of the mechanical properties. The results of SEM indicated that GAP-E could obviously soften the rigid fiber structure of TEGN/GN, and the blends were well mixed with good interfacial compatibility between the GAP-E (5%) and TEGN/NC. When the mass fraction of GAP-E was 5%, the tensile strength and the elongation at break of the blend reached up to 32.1 MPa and 54.4%, which were improved by 33 and 46% compared to those of the TEGN/NC blend system, respectively. The transition temperature remained at -21.6 °C with obvious enhancement on the mechanical properties.

Designing ultrafine PdCo alloys in mesoporous silica nanospheres with peroxidase-like activity and catalase-like activity.

Nanomaterial-based artificial enzyme mimetics have attracted increasing attention because of their robust stability, adjustable activity, and cost-effectiveness. In this study, we developed a simple and effective method for the synthesis of highly dispersed ultrafine PdCo alloys with peroxidase- and catalase-like activities. The aberration-corrected transmission electron microscopy analysis verified that the cyanogel precursor in the mesoporous silica nanospheres (MSNs) was converted to PdCo alloy in NH3 at a high temperature. The PdCo alloy was homogenously distributed in MSNs as ultrafine and monodispersed particles. By selectively removing the Co species from the binary alloy through an acid-leaching approach, the role of each component in the enzyme-like mimetics was systematically studied. Using glutathione (GSH) as the model analyte, the potential application of PdCo@MSNs in GSH detection from complex cell media was confirmed via colorimetric assay. The ultrafine alloy size, double mimetic activities, and abundant loading space of PdCo@MSNs make them promising not only in clinical diagnosis but also in overcoming hypoxia-induced photodynamic therapy resistance in tumor treatment.

Rapid Capture and Photocatalytic Inactivation of Target Cells from Whole Blood by Rotating Janus Nanotubes.

Effective isolation and removal of target tumor cells from patients' peripheral blood are of great importance to clinical prognosis and recovery. However, the extremely low quantity of target cells in peripheral blood becomes one of the challenges in this respect. Herein, we design and synthesize an innovative nanostructure based on magnetic TiO2 nanotubes with Pt nanoparticles' asymmetrical decoration for effectively capturing and inactivating target cells. Using CCRF-CEM as the model cell, the resulting nanotubes with accurate modification of recognition probes exhibit high selectivity and cell-isolation efficiency upon real blood samples. Particularly, the target cells are selectively captured at a low concentration with a recovery rate of 73.0 ± 11.5% at five cells per milliliter for whole blood samples. Consequently, benefitting from the remarkable photocatalytic activity of the Janus nanotubes, these isolated cells can be rapidly inactivated via light-emitting diode (LED) irradiation with an ignorable effect on normal cells. This work offers a new paradigm for high-efficient isolating/killing target cells from a complex medium.

Numerical Analysis of the Heating Characteristics of Magnetic Oscillation Arc and the Fluid Flow in Molten Pool in Narrow Gap Gas Tungsten Arc Welding.

Magnetic oscillation arc (MOA) technology was developed to avoid insufficient fusion defects appearing at the sidewalls in narrow gap gas tungsten arc welding (NG-GTAW). In this work, a unified model was developed to simulate the process of MOA assisted NG-GTAW. The model included the MOA, welding pool, workpiece and the coupling interaction between them. The heating characteristic of the MOA and the flow of liquid metal were simulated, and the mechanism of forming a uniform welding bead under MOA was investigated. It was found that if the magnetic flux density increased to 9 mT, the MOA could point to the sidewall directly; the maximum heat flux at the bottom declined by almost half and at the side, it increased by more than ten times. Additionally, the heat flux was no longer concentrated but dispersed along the narrow groove face. Under the effect of MOA, there were mainly two flow vortexes in the molten pool, which could further increase the heat distribution between the bottom, sidewall and corner, and was beneficial for the formation of a good-shape weld. The model was validated by experimental data.

NIR Light-Driven Photocatalysis on Amphiphilic TiO2 Nanotubes for Controllable Drug Release.

Titanium dioxide (TiO2) nanomaterials have attracted much interest in life science and biological fields because of their excellent photocatalytic activity and good biocompatibility. However, owing to its wide band gap, photocatalysis of TiO2 can be only triggered by UV light. The limited transparent depth of UV light and the generated reactive oxygen species (ROSs) cause inflammation response of skin tissue, thus posing two major challenges in the photocatalytic application of TiO2-based materials in drug delivery and other biotechnology fields. Here, we propose an upconversion-related strategy to enable the photocatalytic activity of TiO2 nanotubes in near-infrared light and apply the system as a controllable drug delivery platform. More importantly, the ROS-induced cytotoxicity and the preleaching of payloads are significantly reduced on the as-proposed amphiphilic TiO2 nanotubes. The hydrophobic monolayers are served as a "cap" to provide protection for ROS-induced inflammation and long-term storability. This amphiphilic drug delivery system broadens the potential applications of TiO2-based nanomaterials in biomedicine.

Introducing graphitic carbon nitride nanosheets as supersandwich-type assembly on porous electrode for ultrasensitive electrochemiluminescence immunosensing.

Biomarkers in blood or tissue provide essential information for clinical screening and early disease diagnosis. However, increasing the sensitivity of detecting biomarkers remains a major challenge in a wide variety of electrochemical immunoassays. Herein, we present an electrochemiluminescence (ECL) immunosensing strategy with 1: Nn amplification ratio (target-to-signal probe) for biomarkers detection on a porous gold electrode. The high porosity of the electrode surface provides enough bonding sites for capturing the target biomolecules and thus many DNA labels can be introduced. On the basis of this concept, a great number of graphitic carbon nitride (g-C3N4) nanosheets are employed to create a supersandwich-type assembly on a porous electrode via the DNA hybridization process. Furthermore, compared with the traditional sandwich immunoassay (the ratio of target-to-signal probe is 1 : 1), the supersandwich construction can introduce a large number of signal probes, thus resulting in a highly improved sensitivity. The proposed ECL immunosensor exhibits an excellent performance in a concentration range from 0.01 fg mL-1 to 1 µg mL-1 with an ultralow detection limit of 0.001 fg mL-1 (S/N = 3) and excellent selectivity. This sensing strategy could be developed into a real-time assay for the disease-related molecular targets, with many practical applications in biotechnology and life science.

Protein Shell-Encapsulated Pt Clusters as Continuous O2-Supplied Biocoats for Photodynamic Therapy in Hypoxic Cancer Cells.

As a highly oxygen-dependent process, the effect of photodynamic therapy is often obstructed by the premature leakage of photosensitizers and the lack of oxygen in hypoxic cancer cells. To overcome these limitations, this study designs bovine serum albumin protein (BSA)-encapsulated Pt nanoclusters (PtBSA) as O2-supplied biocoats and further incorporates them with mesoporous silica nanospheres to develop intelligent nanoaggregates for achieving improved therapeutic outcomes against hypoxic tumors. The large number of amino groups on BSA can provide sufficient functional groups to anchor tumor targeting agents and thus enhance the selective cellular uptake efficiency. Owing to the outstanding biocompatibility features of BSA and the state-of-the-art catalytic activity of Pt nanoclusters, the nanocomposites have lower dark cytotoxicity, and O2 continuously evolves via the decomposition of H2O2 in a tumor microenvironment. Both in vivo and in vitro experiments indicate that the resulting nanocomposites can effectively relieve hypoxic conditions, specifically induce necrotic cell apoptosis, and remarkably hinder tumor growth. Our results illuminate the great potential of BSA-encapsulated Pt nanoclusters as versatile biocoats in designing intelligent nanocarriers for hypoxic-resistant photodynamic therapy.

Potential field cellular automata model for pedestrian flow.

This paper proposes a cellular automata model of pedestrian flow that defines a cost potential field, which takes into account the costs of travel time and discomfort, for a pedestrian to move to an empty neighboring cell. The formulation is based on a reconstruction of the density distribution and the underlying physics, including the rule for resolving conflicts, which is comparable to that in the floor field cellular automaton model. However, we assume that each pedestrian is familiar with the surroundings, thereby minimizing his or her instantaneous cost. This, in turn, helps reduce the randomness in selecting a target cell, which improves the existing cellular automata modelings, together with the computational efficiency. In the presence of two pedestrian groups, which are distinguished by their destinations, the cost distribution for each group is magnified due to the strong interaction between the two groups. As a typical phenomenon, the formation of lanes in the counter flow is reproduced.