We have examined the clinical characteristics and treatment of ectopic meningiomas (EMs). Samples from 17 patients with EMs were analyzed, and their clinical characteristics, mechanism, and treatment were studied in combination with the literature. The main clinical manifestations of EMs included increased intracranial pressure, epilepsy, local mass, and local occupying effects, but diagnosis of EMs depended on the pathology. Surgical removal can achieve the double objectives of confirmed diagnosis and treatment of tumors. The clinical characteristics of EMs vary with the sites of tumors. Operation is the treatment of first choice. Prognosis is better than that of typical meningiomas.

The utilization of high‐voltage LiCoO2 is imperative to break the bottleneck of the practical energy density of lithium‐ion batteries. However, LiCoO2 suffers from severe structural and interfacial degradation at >4.55 V. Herein, a novel lattice‐matched LiCoPO4 coating is rationally designed for LiCoO2 which works at 4.6 V (vs Li/Li+) or above. This LiCoPO4 coating, derived by an in situ chemical reaction, grows epitaxially on LiCoO2 crystallite with strong bonding and complete coverage to LiCoO2, ensuring a stable cathode–electrolyte interface with fewer side reactions and alleviated intergranular cracking and phase collapse during repeated high‐voltage lithiation/delithiation processes. In addition, the formed strong covalent P–O tetrahedron configuration at the interface effectively decreases the surface oxygen activity of LiCoO2, further suppressing oxygen release and irreversible phase transition. Therefore, the LiCoPO4‐LiCoO2ǁLi cells display excellent capacity retention of 87% after 300 cycles at 4.6 V and stable operation at 4.6 V/55 °C or 4.7 V/30 °C. The strategy of lattice‐matching growth affords a new way to impact the development of high‐voltage LiCoO2 and beyond.

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Glioblastoma (GBM) is the most common and lethal type of malignant brain tumor in adults. Currently, interventions are lacking, the median overall survival of patients with GBM is less than 15 months, and the postoperative recurrence rate is greater than 60%. We proposed an innovative local chemotherapy involving the construction of gene therapy-based iron oxide nanoparticles (IONPs) as a treatment for patients with glioblastoma after surgery that targeted ferroptosis and apoptosis to address these problems. The porous structure of IONPs with attached carboxyl groups was modified for the codelivery of small interfering RNA (siRNA) targeting glutathione peroxidase 4 (si-GPX4) and cisplatin (Pt) with high drug loading efficiencies. The synthesized folate (FA)/Pt-si-GPX4@IONPs exerted substantial effects on glioblastoma in U87MG and P3#GBM cells, but limited effects on normal human astrocytes (NHAs). During intracellular degradation, IONPs significantly increased iron (Fe 2+ and Fe 3+ ) levels, while Pt destroyed nuclear DNA and mitochondrial DNA, leading to apoptosis. Furthermore, IONPs increased H 2 O 2 levels by activating reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX). The Fenton reaction between Fe 2+ , Fe 3+ , and intracellular H 2 O 2 generated potent reactive oxygen species (ROS) to initiate ferroptosis, while the co-released si-GPX4 inhibited GPX4 expression and synergistically improved the therapeutic efficacy through a mechanism related to ferroptosis. As a result, superior therapeutic effects with low systemic toxicity were achieved both in vitro and in vivo, indicating that our nanoformulations might represent safe and efficient ferroptosis and apoptosis inducers for use in combinatorial glioblastoma therapy.

Phloem-mobile insecticides are efficient for piercing and sucking insect control. Introduction of sugar or amino acid groups to the parent compound can improve the phloem mobility of insecticides, so a glycinergic−fipronil conjugate (GlyF), 2- (3-(3-cyano-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-((trifluoromethyl)sulfinyl)-1H-pyrazole-5-yl)ureido) acetic acid, was designed and synthesized. Although the "Kleier model" predicted that this conjugate is not phloem mobile, GlyF can be continually detected during a 5 h collection of Ricinus communis phloem sap. Furthermore, an R. communis seedling cotyledon disk uptake experiment demonstrates that the uptake of GlyF is sensitive to pH, carbonyl cyanide m-chlorophenylhydrazone (CCCP), temperature, and p-chloromercuribenzenesulfonic acid (pCMBS) and is likely mediated by amino acid carrier system. To explore the roles of amino acid transporters (AATs) in GlyF uptake, a total of 62 AAT genes were identified from the R. communis genome in silico. Phylogenetic analysis revealed that AATs in R. communis were organized into the ATF (amino acid transporter) and APC (amino acid, polyaminem and choline transporter) superfamilies, with five subfamilies in ATF and two in APC. Furthermore, the expression profiles of 20 abundantly expressed AATs (cycle threshold (Ct) values <27) were analyzed at 1, 3, and 6 h after GlyF treatment by RT-qPCR. The results demonstrated that expression levels of four AAT genes, RcLHT6, RcANT15, RcProT2, and RcCAT2, were induced by the GlyF treatment in R. communis seedlings. On the basis of the observation that the expression profile of the four candidate genes is similar to the time course observation for GlyF foliar disk uptake, it is suggested that those four genes are possible candidates involved in the uptake of GlyF. These results contribute to a better understanding of the mechanism of GlyF uptake as well as phloem loading from a molecular biology perspective and facilitate functional characterization of candidate AAT genes in future studies.

Sulfide-based all-solid-state lithium-ion batteries (ASSLIBs) are promising candidates in the next generation of energy storage technology; the voltage mismatch and the resulting side reactions at the interface between the cathode...

Extending the charge cutoff voltage of cathode (e.g., LiCoO2) is a promising way to increase the energy density of Li-ion batteries, but critical challenges lie in the threats triggered by structural distortion and an unstable electrode/electrolyte interface. The general approach to enhance the stability of the cathode/electrolyte interface (CEI) consists of replacing the decomposition or sacrificing sources of carbonate solvents (e.g., EC) with concentrated or fluorinated electrolyte strategies. Herein, without following typical replacement strategies, we introduce a trace electrolyte additive and refine the dehydrogenation process of the original carbonate solvents, resulting in an enhanced CEI and long-term cycling stability of LiCoO2 up to 4.65 V. We demonstrate that cathode structure distortion, LiPF6 hydrolysis, and Co dissolution and shuttling have been simultaneously restrained. With the achievement of a long-life 250 and 270 Wh/kg pouch cells (assembled with a commercial graphite and SiO anodes), the refinement of the “old-school” electrolyte additive strategy opens up avenues toward the design of practical high-voltage full-cell systems.

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