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Type I interferons (IFN-I) play pivotal roles in tumor therapy for three decades, underscoring the critical importance of maintaining the integrity of the IFN-1 signaling pathway in radiotherapy, chemotherapy, targeted therapy, and immunotherapy. However, the specific mechanism by which IFN-I contributes to these therapies, particularly in terms of activating dendritic cells (DCs), remains unclear. Based on recent studies, aberrant DNA in the cytoplasm activates the cyclic GMP-AMP synthase (cGAS)- stimulator of interferon genes (STING) signaling pathway, which in turn produces IFN-I, which is essential for antiviral and anticancer immunity. Notably, STING can also enhance anticancer immunity by promoting autophagy, inflammation, and glycolysis in an IFN-I-independent manner. These research advancements contribute to our comprehension of the distinctions between IFN-I drugs and STING agonists in the context of oncology therapy and shed light on the challenges involved in developing STING agonist drugs. Thus, we aimed to summarize the novel mechanisms underlying cGAS-STING-IFN-I signal activation in DC-mediated antigen presentation and its role in the cancer immune cycle in this review. [ABSTRACT FROM AUTHOR]

Salidroside has been widely used in anti-tumor, cardiovascular, and cerebrovascular protection. However, there are few reports of its use for wound repair. Herein, salidroside inflammation-targeted emulsion gel and non-targeted emulsion gel were developed for wound repair. The inflammation-targeted emulsion gels showed an overall trend of better transdermal penetration and lower potential than non-targeted emulsion gels (−58.7 mV and −1.6 mV, respectively). The apparent improvement of the trauma surface was significant in each administration group. There was a significant difference in the rate of wound healing of the rats between each administration group and the model group at days 7 and 14. Pathological tissue sections showed that inflammatory cells in the epidermis, dermis, and basal layer were significantly reduced, and the granulation tissue was proliferated in the inflammation-targeted emulsion gel group and the non-targeted emulsion gel group. Regarding the expressions of EGF and bFGF, the expressions of bFGF and EGF in the tissues of the inflammation-targeted group at days 7, 14, or 21 were significantly higher than that of the non-targeted emulsion gel group and the model group, both of which were statistically significant compared with the model group (p < 0.05). These results demonstrated that salidroside has the potential as an alternative drug for wound repair. [ABSTRACT FROM AUTHOR]

The purpose of this work was to analyze and evaluate the functional properties of a new nanoemulsion that contained cordycepin. Droplet size and distribution were measured, and the stability of the nanoemulsion in different storage conditions was evaluated. We also tested skin irritation caused by the nanoemulsion, cordycepin stability in the nanoemulsion, anti-aging effect, and microbial challenge. The nanoemulsion was homogeneous with proper dispersion stability, and cordycepin was stable for eight months within the cosmetic nanoemulsion. The nanoemulsion did not irritate human hand and face skin, and the cosmetic nanoemulsion was effective in preventing microbial contamination of the product during use and storage. The new nanoemulsion containing cordycepin satisfied provisions of the 2015 Safety and Technical Standards for Cosmetics of the Ministry of Health, People's Republic of China. [ABSTRACT FROM AUTHOR]

Cobalt coordinated covalent organic frameworks have attracted increasing interest in the field of CO2 photoreduction to CO, owing to their high electron affinity and predesigned structures. However, achieving high conversion efficiency is challenging since most Co related coordination environments facilitate fast recombination of photogenerated electron-hole pairs. Here, we design two kinds of Co-COF catalysts with oxygen coordinated Co atoms and find that after tuning of coordination environment, the reported Co framework catalyst with Co-O4 sites exhibits a high CO production rate of 18000 µmol g−1 h−1 with selectivity as high as 95.7% under visible light irradiation. From in/ex-situ spectral characterizations and theoretical calculations, it is revealed that the predesigned Co-O4 sites significantly facilitate the carrier migration in framework matrixes and inhibit the recombination of photogenerated electron-hole pairs in the photocatalytic process. This work opens a way for the design of high-performance catalysts for CO2 photoreduction. A class of inexpensive aminoanthraquinone organic dyes are shown to facilitate visible-light-driven CO2 reduction. Overall reaction efficiencies were found to be optimal when both electron donating and accepting groups were on a single dye molecule. [ABSTRACT FROM AUTHOR]

Designing highly active and durable electrocatalysts remain an ongoing challenge in the oxygen reduction reaction (ORR). Here, the reductive IL/Ti3C2Tx(FA) is produced in a water‐free mixture of formic acid (FA), ionic liquid (IL) and LiF, subsequently, the simultaneous reduction encapsulation trap the Pd nanocatalysts and IL within bilayer carbide‐derived carbon (CDC) to obtain Pd@IL/CDC(FA) with high metal loading up to 69.7%. Thereby, the featured active phases in Pd@IL/CDC(FA) impart potent chemical nanoconfinement to defend metals from dissolution and aggregation, boost mass and electron transfer, and mediate oxidation states and adsorption/desorption of metal Pd in the ORR. Instead of deactivation and Ostwald ripening, the catalytic performances of Pd@IL/CDC(FA) are gradually enhanced in an accelerated durability test up to 20 000 cycles. In a Zn–air battery, the Pd@IL/CDC(FA) cathode gives a specific capacity of 812.6 mAh gZn−1 and a voltage loss of only 41 mV in galvanostatic discharge for 1000 h. The work opens new venues in controllably preparing high activity and durable electrocatalysts from in‐situ generated CDCs. [ABSTRACT FROM AUTHOR]

Ti3C2Tx MXene is regarded as a promising material in energy-related applications; however, the overscreening charge effect of the electric double layer on electrified interfaces, along with "inert" F terminations, limits the electrochemical operation efficiencies. Here, we developed a protocol to harvest a coupled conductor through confining in situ 1-ethyl-3-methylimidazolium ([Emim]+) ions into Ti3C2Tx interlayers. The ionic–electronic coupling does not require any external counterions, but activates terminal F and even sub-surface Ti, and endows the conductor with metal-like and ionophilic characteristics. Different from physically preintercalated or adsorbed ions, the resulting chemically confined [Emim]+ ions offer more accessible electroactive sites, faster electron transport in surface redox, and more efficient channels for ion transfer. Hence, the Ti3C2Tx electrodes present high gravimetric capacitance, rate performance and cycling stability. This work highlights the important roles of the coupling in the design and research of mixed ionic–electronic conductors with high electrochemical activity. [ABSTRACT FROM AUTHOR]

Although significant progress has been made in the synthesis of covalent organic frameworks (COFs) in recent years, the construction of hierarchical pores in such materials remains a great challenge. Herein, we report a facile synthesis of hierarchically porous COFs (HP-COFs) under mild conditions in ionic liquids 1-alkyl-3-methylimidazolium tetrafluoroborates ([Cnmim][BF4], n = 4, 6, 10). It has been found that apart from the inherent micropores, a large mesoporous structure has been produced in the COFs in which the size of pores can be simply tuned by adjusting the alkyl chain length of the ionic liquids. These mesopores have been confirmed by N2 sorption and electron microscopy techniques. Importantly, this approach is applicable for the preparation of various HP-COFs, such as imine and hydrazone based COFs, which are quite difficult to acquire through traditional methods. In addition, these HP-COFs show highly effective catalytic performance for C–C bond formation, especially for large size molecule based C–C coupling reactions in comparison with uni-pore COFs. [ABSTRACT FROM AUTHOR]

Ultraviolet-induced interface reactions are used for the modification of silver nanoparticles (Ag NPs), which is controllable in both the color and the surface chemistry of the nanoparticles. The studies have shown that the color changes are directly related to the chemical components on the surface of Ag NPs and hence the correlation of the colors with the chemical states of main components on the surface of Ag NPs is made during the course of interface reactions.

The critical behavior of relative viscosity and intrinsic viscosity near the gelation point was experimentally examined for 1 g/100 ml alginate solution induced by cupric ions. The critical exponent of relative viscosity was found to be 1.27, which is in good agreement with the prediction of the percolation model based on a Rouse cluster approximation gives the exponent as 1.3. Critical behavior of intrinsic viscosity reveals that the constant of Huggins equation k′ for alginate clusters formed near the gelation point was considerably higher than that of linear alginate polychains in aqueous solution. Typically intramolecular crosslinking between polychains in the low cupric concentration could be detected in the plots of [η] vs molar fraction of cupric ions for the system. The weak divergence of intrinsic viscosity resembles the critical behavior of Zimm clusters predicted by the three-dimensional percolation theory rather than clusters of classical theory. © 1996 American Institute of Physics. [ABSTRACT FROM AUTHOR]

The charge transfer and active sites of metal-free imidazolium-based composites were unveiled by an electrochemical method with high sensitivity and selectivity due to the specific donor–acceptor coupling of imidazolium with NO2−. [ABSTRACT FROM AUTHOR]

With the aid of TiO 2 and Ag/TiO 2 composites with ultrahigh specific surface areas (about 400 m 2 g −1 ), we demonstrated a facile controlled strategy to adjust the photooxidation activity of Ag/TiO 2 in the photocatalysis degradation process of Rhodamine B (RhB). A series of photocatalysis experiment results indicated that the selective oxidation of RhB could be performed through changing irradiation light. When the as-prepared unannealed Ag/TiO 2 was used as photocatalyst, Rh-110 was produced only under visible light irradiation. Instead, RhB would be oxidized completely under ultraviolet irradiation or using the annealing Ag/TiO 2 . Although there were many photocatalysis degradation mechanisms of RhB in previous literatures, we have not found an appropriate mechanism to explain this phenomenon. Radical-trapping tests indicated that the effect of superoxide anion radical was more important than hydroxyl radical in the forming process of Rh-110, and hence the selective oxidation mechanism of Ag/TiO 2 was suggested according to the role changing of Ag nanoparticles on the composites under visible and ultraviolet irradiation. [ABSTRACT FROM AUTHOR]