Thyssenkerr4345

Radiation therapy (RT), including external beam radiotherapy (EBRT) and internal radioisotope therapy (RIT), has been an indispensable strategy for cancer therapy in clinical practice in recent years. Ionized atoms and free radicals emitted from the nucleus of radioisotopes can cleave a single strand of DNA, inducing the apoptosis of cancer cells. Thus far, nuclides used for RIT could be classified into three main types containing alpha (α), beta (β), and Auger particle emitters. In order to enhance the bioavailability and reduce the physiological toxicity of radioisotopes, various biomaterials have been utilized as multifunctional nanocarriers, including targeting molecules, macromolecular monoclonal antibodies, peptides, inorganic nanomaterials, and organic and polymeric nanomaterials. Therapeutic radioisotopes have been labeled onto these nanocarriers via different methods (chelating, chemical doping, encapsulating, displacement) to inhibit or kill cancer cells. With the continuous development of research in this respect, more promising biomaterials as well as novel therapeutic strategies have emerged to achieve the high-performance RIT of cancer. In this review article, we summarize recent advances in biomaterial-mediated RIT of cancer and provide guidance for non-experts to understand nuclear medicine and to conduct cancer radiotherapy.The catalytic performances of metal nanoparticles can be widely tuned and promoted by the metal-support interactions. Here, we report that the morphologies and electrocatalytic CO2 reduction reaction (CO2RR) properties of bismuth nanoparticles (BiNPs) can be rationally modulated by their interactions with carbon black (CB) supports by controlling the degree of surface oxidation. Appropriately oxidized CB supports can provide sufficient oxygen-containing groups for anchoring BiNPs with tunable sizes and surface areas, desirable key intermediate adsorption abilities, appropriate surface wettability, and adequate electron transfer abilities. As a result, the optimized Bi/CB catalysts exhibited a promoted CO2RR performance with a Faradaic efficiency of 94% and a current density of 16.7 mA cm-2 for HCOO- at -0.9 V versus a reversible hydrogen electrode. Our results demonstrate the significance of regulating the interactions between supports and metal nanoparticles for both synthesis of the catalyst and electrolysis applications, which may find broader applicability in more electrocatalyst designs.To alter the immunosuppressive tumor microenvironment (TME), we developed an immunostimulatory nanoparticle (NP) to reprogram a tumor's dysfunctional and inhibitory antigen-presenting cells (APCs) into properly activated APCs that stimulate tumor-reactive cytotoxic T cells. Importantly, systemic delivery allowed NPs to efficiently utilize the entire microvasculature and gain access into the majority of the perivascular TME, which coincided with the APC-rich tumor areas leading to uptake of the NPs predominantly by APCs. In this work, a 60 nm NP was loaded with a STING agonist, which triggered robust production of interferon β, resulting in activation of APCs. In addition to untargeted NPs, we employed 'mainstream' ligands targeting fibronectin, αvβ3 integrin and P-selectin that are commonly used to direct nanoparticles to tumors. BI-4020 order Using the 4T1 mouse model, we assessed the microdistribution of the four NP variants in the tumor immune microenvironment in three different breast cancer landscapes, including primary tumor, early metastasis, and late metastasis. The different NP variants resulted in variable uptake by immune cell subsets depending on the organ and tumor stage. Among the NP variants, therapeutic studies indicated that the untargeted NPs and the integrin-targeting NPs exhibited a remarkable short- and long-term immune response and long-lasting antitumor effect.The properties of functional materials are intrinsically linked to their atomic structure. When going to the nanoscale, size-induced structural changes in atomic structure often occur, however these are rarely well-understood. Here, we systematically investigate the atomic structure of tungsten oxide nanoparticles as a function of the nanoparticle size and observe drastic changes when the particles are smaller than 5 nm, where the particles are amorphous. The tungsten oxide nanoparticles are synthesized by thermal decomposition of ammonium metatungstate hydrate in oleylamine and by varying the ammonium metatungstate hydrate concentration, the nanoparticle size, shape and structure can be controlled. At low concentrations, nanoparticles with a diameter of 2-4 nm form and adopt an amorphous structure that locally resembles the structure of polyoxometalate clusters. When the concentration is increased the nanoparticles become elongated and form nanocrystalline rods up to 50 nm in length. The study thus reveals a size-dependent amorphous structure when going to the nanoscale and provides further knowledge on how metal oxide crystal structures change at extreme length scales.Increasing electroluminescene quantum efficiency (EQEEL) of the photoactive layer to reduce non-radiative recombination energy loss (Eloss) has been demonstrated as an effective strategy to improve open-circuit voltage (Voc) of organic solar cells (OSCs). Meanwhile, incorporating a third component into the active-layer film can improve power conversion efficiency (PCE) of resultant ternary OSCs, mostly contributed from increments in short-circuit current density and fill factor but less in the Voc. Herein, we report a highly fluorescent molecule (IT-MCA) as a third component to reduce the Eloss and enhance the Voc for ternary OSCs. Applying the IT-MCA to three binary hosts, a significant increase of Voc (41 mV) is acquired and a best PCE of 16.7% is obtained with outstanding device stability. This work provides a new guideline to design the third-component molecule by enhancing its fluorescence for efficient and stable ternary OSCs with improved Voc.Increasing the energy band gap under the premise to maintain a large nonlinear optical (NLO) response is a challenging issue for the exploration and molecular design of mid-infrared nonlinear optical crystals. Utilizing a charge-transfer engineering method, we designed and synthesized a rare earth chalcogenide, KYGeS4. With an NLO effect as large as that in AgGaS2, KYGeS4 breaks through the limitation of energy band gap, i.e., the "3.0 eV wall", in NLO rare earth chalcogenides, and thus exhibits an excellent comprehensive NLO performance. First-principles electronic structure analysis demonstrates that the large band gap in KYGeS4 is ascribed to the decreased covalency of Y-S bonds by transferring charge from [YS7] to [GeS4] polyhedra. The charge-transfer engineering strategy would have significant implications for the exploration of good-performance NLO crystals.Mixed-valent transition-metal compounds display complex structural, electronic and magnetic properties, which often intricately coexist. Here, we report the new ternary oxide GaV4O8, a structural sibling of skyrmion-hosting lacunar spinels. GaV4O8 contains a vanadium trimer and an original spin-orbital-charge texture that forms upon the structural phase transition at TS = 68 K followed by the magnetic transition at TN = 35 K. The texture arises from the coexistence of orbital molecules on the vanadium trimers and localized electrons on the remaining vanadium atoms. Such hybrid electrons create opportunities for novel types of spin, charge, and orbital order in mixed-valent transition-metal compounds.We design a multiferroic metal that combines seemingly incompatible ferromagnetism, ferroelectricity, and metallicity by hole doping a two-dimensional (2D) ferroelectric with high density of states near the Fermi level. The strong magnetoelectric effect is demonstrated in hole-doped and arsenic-doped monolayer α-In2Se3 using first-principles calculations. Taking advantage of the oppositely charged surfaces created by an out-of-plane polarization, the 2D magnetization and metallicity can be electrically switched on and off in an asymmetrically doped monolayer. The substitutional arsenic defect pair exhibits an intriguing electric field-tunable charge disproportionation process accompanied by an on-off switch of local magnetic moments. The charge ordering process can be controlled by tuning the relative strength of on-site Coulomb repulsion and defect dipole-polarization coupling via strain engineering. Our design principle relying on no transition metal broadens the materials design space for 2D multiferroic metals.Molecular systems can exhibit multi-stimuli switching of their properties, with spin crossover materials having unique magnetic transition triggered by temperature and light, among others. Light-induced room temperature operation is however elusive, as optical changes between metastable spin states require cryogenic temperatures. Furthermore, electrical detection is hampered by the intrinsic low conductivity properties of these materials. We show here how a graphene underlayer reveals the light-induced heating that triggers a spin transition, paving the way for using these molecules for room temperature optoelectronic applications.Moisture-enabled electricity generation as an emerging new energy-harvesting technology is one of the most fascinating and promising candidates for supplying renewable and clean power. However, existing moist-electric generators (MEGs) can only produce intermittent, brief bursts of power with voltage output less than 1 V, severely restricting their practical applications. Therefore, there is an urgent requirement for next-generation MEG devices with high efficiency and continuous energy harvesting properties. In this work, an ion-gradient-enhanced MEG consisting of electrospun nanofiber fabric and porous active electrode was demonstrated to provide a perfect solution for solving instantaneous and low electric output at the same time. The assembled MEG can produce a sustained voltage output of 1.1 V for 40 000 s without any weak signs, reaching the highest level among all reported MEGs. This remarkable performance mainly arises from the higher concentration difference induced by the introduced active electrode which enhances ion diffusion through the porous nanofiber fabric. In addition, the co-existing streaming potential also contributes to the excellent performance. Beyond power generation, the electrospun nanofiber based MEGs also demonstrate successful applications in self-powered sensors, including ammonia leak monitoring and moisture-temperature sensor for forest-fire detection. This study provides insights for the designing of innovative MEGs and opens a pioneering avenue for future energy conversion.A visible-blind ultraviolet (UV) photodetector can detect UV signals and is not interfered with by visible light or infrared light in the environment. In order to realize high-performance visible-blind UV organic photodetectors (OPDs), we design photomultiplication-type (PM-type) OPDs by using a novel strategy. Firstly, wide bandgap organic semiconductor materials, which do not absorb visible light, are selected as donors to absorb UV light. Secondly, a very small amount of C60 is used as an acceptor to trap photogenerated electrons. These accumulating electrons near the Al electrode form a potential, which leads to band bending and narrowing of the interface barrier, thereby assisting hole-tunneling injection to form a multiplication. The fabricated visible-blind UV PM-type OPDs with donor/acceptor doping ratio of 50  1 exhibit a narrowband response with full-width at half-maximum (FWHM) of approximately 36 nm, an ultrahigh external quantum efficiency of 1.08 × 106% and a remarkable specific detectivity of 1.