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Abstract Immediate oral implant placement is a widely accepted technique, known for its efficacy in reducing treatment duration, surgical visits, and overall healing time. One of the primary challenges associated with immediate implant placement is the attainment of initial stability. The inevitable loss of bone and soft tissue after extraction poses a risk to implant osseointegration in both vertical and horizontal dimensions. Guided tissue regeneration/guided bone regeneration (GTR/GBR) is a well‐established method for periodontal regeneration. However, current GTR/GBR membranes lack tissue inherent regeneration properties and necessitate combination with grafts to enhance tissue recovery. In this context, biomaterials have emerged as a promising option due to their good biocompatibility, biodegradability, and bioactive properties. They present a potential alternative to standard autologous/allograft procedures. The field of biomaterials for bone regeneration has rapidly evolved, developing new guiding materials and engineering techniques. These advances have become integral in addressing tissue defects at the immediate implant site. Various materials such as bioceramics, natural polymers, and synthetic polymers have been used for tissue repair. This article undertakes an etiological examination of tissue deficiency associated with immediate implant placement. Additionally, it reviews the advantages and disadvantages of a variety of biomaterials, aiming to provide references for clinical treatment and areas for further investigation.

Abstract Human skin moisture is closely related to health and personal care issues. Many creams were developed to claim capable of skin moisturizing. However, people can hardly check their skin moisture status and the moisturizing effect of various creams conveniently, since currently all the skin moisturizing detection rely on large equipment requiring power supply. Herein, we report a power‐supply independent supramolecular film that is able to directly report the moisturizing status of the skin. With the strategy of solid‐phase molecular self‐assembly (SPMSA), the aqueous precipitates formed by commercially available polyelectrolyte and oppositely charged surfactant would transform into a supramolecular film under a mild mechanical pressure, where the hydrophobic surfactant domains bridged by polyelectrolyte merge into hydrophobic mesophases to reduce interfacial energy. The hydrophobic mesophase will greatly retard water diffusion inside the film, so that a humidity gradient is generated as the film is exposed to a humid environment. The film will bend upward automatically in touch with moisture skin, and the bending degree is proportional to the skin moisture status. Therefore, the film can be used as portable smart power‐free skin moisture sensor.

Abstract Across a city, tree communities are spatially heterogenous and vary by land use type. However, it remains unclear how urban tree communities change over time and whether rates of change depend on land use type. To address this knowledge gap, we analyzed urban tree composition using long‐term plot data to examine tree diversity changes across six different urban land use types in 1999, 2004, 2009, and 2014. We found that spatial differences in tree species diversity and community composition among land uses were much greater than changes over time. Number of trees increased over time, being driven by gains of non‐native species. There was also a significant interaction between land use and time, with institutional and transportation land uses having greater community changes over time. Our study can inform site‐specific efforts to promote and preserve urban biodiversity across public and private land uses.

Abstract The tumor microenvironment (TME) is a biological system with sophisticated constituents. In addition to tumor cells, tumor‐associated macrophages (TAMs) and microbiota are also dominant components. The phenotypic and functional changes of TAMs are widely considered to be related to most tumor progressions. The chronic colonization of pathogenic microbes and opportunistic pathogens accounts for the generation and development of tumors. As messengers of cell‐to‐cell communication, tumor‐derived extracellular vesicles (TDEVs) can transfer various malignant factors, regulating physiological and pathological changes in the recipients and affecting TAMs and microbes in the TME. Despite the new insights into tumorigenesis and progress brought by the above factors, the crosstalk among tumor cells, macrophages, and microbiota remain elusive, and few studies have focused on how TDEVs act as an intermediary. We reviewed how tumor cells recruit and domesticate macrophages and microbes through extracellular vehicles and how hijacked macrophages and microbiota interact with tumor‐promoting feedback, achieving a reciprocal coexistence under the TME and working together to facilitate tumor progression. It is significant to seek evidence to clarify those specific interactions and reveal therapeutic targets to curb tumor progression and improve prognosis.