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The development of lithium–metal batteries (LMBs) has emerged as a mainstream approach for achieving high‐energy‐density energy storage devices. The stability of electrochemical interfaces plays an essential role in realizing stable and long‐life LMBs. Despite extensive and comprehensive research on the lithium anode interface, there is limited focus on the cathode interface, particularly regarding high‐voltage transition metal oxide cathode materials. In this review, the challenges associated with developing stable high‐voltage cathode materials are first discussed. Characterization techniques for understanding the composition and structure of the cathode–electrolyte interphase (CEI) are then introduced. Subsequently, recent developments in electrolyte design and interface modification for constructing a stable CEI are summarized. Finally, perspectives on future research trends for understanding and developing the high‐voltage CEI are discussed. This review can offer valuable guidance for understanding and designing the high‐voltage CEI, pushing forward the development of high‐energy‐density LMBs. [ABSTRACT FROM AUTHOR]

Heat shock is a heat-related pathology characterized by a high body temperature and an obvious change of many enzymatic activities. Carboxylesterase (CE), as the major hydrolase in liver, is responsible for the hydrolysis of many drugs or the detoxification of various toxins from all organs. However, the correlation between heat shock and the CE activity in cells remains unknown, mainly due to the lack of a suitable research approach. Herein, a new water-soluble fluorescence probe, MYO-CE, with a specific bipiperidinyl recognition moiety has been developed for detecting the CE activity. MYO-CE reacted selectively with CE instead of other esterase, causing a large fluorescence off-on response at 560 nm with a detection limit of 0.39 U/mL. The applicability of MYO-CE for cell imaging was demonstrated by monitoring the alteration of the hepatocellular CE activity under inflammation. More importantly, we investigated the change of the CE activity during heat shock, uncovering a significant increase for the first time. This finding was further validated by a commercial colorimetric kit assay. The proposed probe shows a promising prospect for the CE study in cells under different pathological conditions. [ABSTRACT FROM AUTHOR]

Many fluorophores/probes suffer from the interference of albumin in biosystems. Herein, we propose an effective strategy to overcome this interference by virtue of both an albumin‐insensitive fluorophore and its changeable π‐conjugation, and demonstrate the strategy by designing an oxazine‐based fluorogenic probe for aminopeptidase N (APN). The modification on the N atom in the oxazine fluorophore with alanine through a cleavable linker locks the resulting probe in a non‐conjugated, colorless and non‐fluorescent state, so the non‐specific interaction of albumin produces no spectroscopic response. APN can selectively cleave the alanine moiety, restoring the large π‐conjugation and strong fluorescence. The capability of the probe to eliminate the albumin influence has been demonstrated by imaging APN in different cell lines, and by quantitatively determining APN in human serum and mouse urine. The present strategy may be useful for developing more specific fluorogenic probes for other enzymes. [ABSTRACT FROM AUTHOR]

Many fluorophores/probes suffer from the interference of albumin in biosystems. Herein, we propose an effective strategy to overcome this interference by virtue of both an albumin‐insensitive fluorophore and its changeable π‐conjugation, and demonstrate the strategy by designing an oxazine‐based fluorogenic probe for aminopeptidase N (APN). The modification on the N atom in the oxazine fluorophore with alanine through a cleavable linker locks the resulting probe in a non‐conjugated, colorless and non‐fluorescent state, so the non‐specific interaction of albumin produces no spectroscopic response. APN can selectively cleave the alanine moiety, restoring the large π‐conjugation and strong fluorescence. The capability of the probe to eliminate the albumin influence has been demonstrated by imaging APN in different cell lines, and by quantitatively determining APN in human serum and mouse urine. The present strategy may be useful for developing more specific fluorogenic probes for other enzymes. [ABSTRACT FROM AUTHOR]

Anode‐free potassium (K) metal batteries are promising candidates in high‐energy‐density batteries. Nevertheless, the notorious potassium dendrite growth and poor K plating/stripping efficiency originating from the potassiophobicity of conventional Cu current collectors impede their practical applications. Herein, by means of systematically multi‐scale theoretical simulations, the correlations among K deposition morphology, nucleation sites, and potassiophilicity of mediation layers are well illuminated from thermodynamics and dynamics perspectives. As a proof of concept, a potassiophilic alloy Cu6Sn5 layer is constructed on commercial Cu foils via a facile electroless plating approach. The designed Cu6Sn5@Cu can guide the homogeneous distribution of K+ flux and regulate the electronic field, promoting uniform K+ plating and stripping. Meanwhile, a KF‐rich solid electrolyte interphase (SEI) layer with high mechanical strength is electrochemically induced and formed, facilitating the transport of K+ through SEI and enhancing the stability of SEI. Consequently, Cu6Sn5@Cu delivers great performance with durable stability of up to 600 h (1 mA cm−2 and 1 mAh cm−2) in no‐reservoir half‐cells. Benefiting from the unique mediation layer design, a novel anode‐free K‐metal full‐cell prototype demonstrates ameliorative cyclic stability. This work advances a fundamental understanding and establishes the bridge between the potassium deposition morphology and mediation layer properties for anode‐free potassium‐metal batteries. [ABSTRACT FROM AUTHOR]

Metallic Na is a promising metal anode for large‐scale energy storage. Nevertheless, unstable solid electrolyte interphase (SEI) and uncontrollable Na dendrite growth lead to disastrous short circuit and poor cycle life. Through phase field and ab initio molecular dynamics simulation, we first predict that the sodium bromide (NaBr) with the lowest Na ion diffusion energy barrier among sodium halogen compounds (NaX, X=F, Cl, Br, I) is the ideal SEI composition to induce the spherical Na deposition for suppressing dendrite growth. Then, 1,2‐dibromobenzene (1,2‐DBB) additive is introduced into the common fluoroethylene carbonate‐based carbonate electrolyte (the corresponding SEI has high mechanical stability) to construct a desirable NaBr‐rich stable SEI layer. When the Na||Na3V2(PO4)3 cell utilizes the electrolyte with 1,2‐DBB additive, an extraordinary capacity retention of 94 % is achieved after 2000 cycles at a high rate of 10 C. This study provides a design philosophy for dendrite‐free Na metal anode and can be expanded to other metal anodes. [ABSTRACT FROM AUTHOR]

Metallic Na is a promising metal anode for large‐scale energy storage. Nevertheless, unstable solid electrolyte interphase (SEI) and uncontrollable Na dendrite growth lead to disastrous short circuit and poor cycle life. Through phase field and ab initio molecular dynamics simulation, we first predict that the sodium bromide (NaBr) with the lowest Na ion diffusion energy barrier among sodium halogen compounds (NaX, X=F, Cl, Br, I) is the ideal SEI composition to induce the spherical Na deposition for suppressing dendrite growth. Then, 1,2‐dibromobenzene (1,2‐DBB) additive is introduced into the common fluoroethylene carbonate‐based carbonate electrolyte (the corresponding SEI has high mechanical stability) to construct a desirable NaBr‐rich stable SEI layer. When the Na||Na3V2(PO4)3 cell utilizes the electrolyte with 1,2‐DBB additive, an extraordinary capacity retention of 94 % is achieved after 2000 cycles at a high rate of 10 C. This study provides a design philosophy for dendrite‐free Na metal anode and can be expanded to other metal anodes. [ABSTRACT FROM AUTHOR]

Objective. Nanodelivery is a modern technology involving improved delivery methods and drug formulations. The current development and initial applications of nanocarriers are pointing to new directions in the current development of nanomedicine. Researchers are increasingly applying nanodelivery to the delivery of therapeutic or diagnostic agents. This article discusses the preparation and application of nanocomplexes and nanoparticles, as well as their potential future value in clinical research. Through a review and analysis, it is hoped that this will serve as a guide for the future development of various nanodelivery technologies and help researchers learn more about these technologies. Materials and Methods. A literature search was conducted using the keywords "Nano drug delivery" or "Nanomedical materials" or "Nano". A literature search was conducted in three major databases, PubMed, Web of Science, and Google Scholar, using the keywords such as "Nano drug delivery", "Nanomedical materials", or "Nanobubble drug delivery". The initial search was screened by title and abstract. In the full-text review, the titles or abstracts were reviewed according to the selection criteria based on the inclusion criteria. The risk of bias and study quality was assessed according to the Cochrane guidelines, and possible biases such as selection bias and good selection bias were included in the review. Results. A total of 297 studies were included in this study, of which 219 were excluded based on the screening criteria, resulting in the inclusion of 78 studies, the majority of which were original studies and clinical trials, and a small number of which provided design and route of administration analysis of nanomaterial particles and effect fluorograms and were studied in more depth. This paper summarises and reviews the views and directions of the included articles. The main directions include cyclodextrin-based or grafted cyclodextrin nanomaterials, nanobubbles, and stimuli-sensitive and temperature-sensitive nanodelivery systems. Conclusion. The use of innovative, targeted drug delivery systems is effective in cancer drug delivery by summarising the previous studies. However, nanodelivery systems' risks and therapeutic effects need to be evaluated before clinical application. Future research in the field of targeted drug delivery nanosystems should focus on the development of nanocarriers with high in vivo delivery capacity, good synergy with therapeutic agents, and milder short-term and long-term toxicological effects and conduct comprehensive preclinical trials on nanodrug delivery systems with high potential for clinical application as soon as possible, to find nanodrug delivery systems suitable for clinical use and put them into the clinical application as soon as possible. [ABSTRACT FROM AUTHOR]

We developed a photoacoustic and fluorescent dual-mode imaging probe, CCYS, for the detection of cysteine with high selectivity and sensitivity in a living system for the first time. By using CCYS, we found that the limited synthesis of glutathione in pulmonary fibrosis was not caused by cysteine deficiency. [ABSTRACT FROM AUTHOR]

Highlights • A photoacoustic and fluorescence dual-mode probe for LTA 4 H sensing was developed. • Cy-ASP has high selectivity and high sensitivity toward LTA 4 H. • Combined with PA technology, Cy-ASP could image the activity of LTA 4 H in mice without dissection. • The probe Cy-ASP could fast locate the inflammation site in mice. Abstract Inflammation widely occurs in various tissues and organs in the human body. Rapid and accurate diagnosis of inflammation is essential to avoid severe complications. This study aims to obtain a non-destructive, fast, and comprehensive tool for the detection of pathogenic sites of inflammation in vivo. A fluorescence and photoacoustic dual-mode imaging probe, Cy-ASP, was first developed to detect inflammatory biomarker LTA 4 H with good sensitivity and selectivity in living small animal. Furthermore, the relationship between LTA 4 H and NF-κB in an LPS-induced cell was investigated. This work provides a new idea for the clinical diagnosis of pneumonia and hepatitis and revealing the upstream regulatory mechanism of LTA 4 H in the pneumonia model. [ABSTRACT FROM AUTHOR]

As an essential amino acid, cysteine is involved in various biosynthetic and metabolic processes, such as protein synthesis, hormone synthesis, and redox homeostatic maintenance. Inordinate cysteine levels are often associated with serious diseases. Thus, designing and synthesizing a novel fluorescent probe for determining the concentration of cellular cysteine, which could indirectly monitor the prevalence of these diseases, is essential. We developed a florescence probe P−Cy with good sensitivity for cysteine detection in vivo. P−Cy only exhibited good response toward cysteine but did not show response toward other biothiols, such as homocysteine (Hcy) and glutathione (GSH). In this study, we used P−Cy by successfully imaging cellular endogenous and exogenous cysteine levels. Furthermore, P−Cy was also performed in mice to detect cysteine level, indicating that P−Cy is a powerful tool for cysteine detection in situ. No more hiding for Cys: A highly selective fluorescent probe P−Cy is synthesized for the detection of cysteine both in vitro and in vivo. P−Cy shows a weak response to homocysteine and glutathione, which could specifically give a response to cysteine. The probe can be used for the fluorescence imaging of cysteine in cells and in mice with low cytotoxicity. [ABSTRACT FROM AUTHOR]