Flexible electronics have emerged as an exciting research area in recent years, serving as ideal interfaces bridging biological systems and conventional electronic devices. Flexible electronics can not only collect physiological signals for human health monitoring but also enrich our daily life with multifunctional smart materials and devices. Conductive hydrogels (CHs) have become promising candidates for the fabrication of flexible electronics owing to their biocompatibility, adjustable mechanical flexibility, good conductivity, and multiple stimuli‐responsive properties. To achieve on‐demand mechanical properties such as stretchability, compressibility, and elasticity, the rational design of polymer networks via modulating chemical and physical intermolecular interactions is required. Moreover, the type of conductive components (eg, electron‐conductive materials, ions) and the incorporation method also play an important role in the conductivity of CHs. Electron‐CHs usually possess excellent conductivity, while ion‐CHs are generally transparent and can generate ion gradients within the hydrogel matrices. This mini review focuses on the recent advances in the design of CHs, introducing various design strategies for electron‐CHs and ion‐CHs employed in flexible electronics and highlighting their versatile applications such as biosensors, batteries, supercapacitors, nanogenerators, actuators, touch panels, and displays.image

This study provides genetic evidences at the chromosome, DNA content, DNA fragment and sequence, and morphological levels to support the successful establishment of the polyploid hybrids of red crucian carp 3 blunt snout bream, which belonged to a different subfamily of fish (Cyprininae subfamily and Cultrinae subfamily) in the catalog. We successfully obtained the sterile triploid hybrids and bisexual fertile tetraploid hybrids of red crucian carp (RCC) ($) 3 blunt snout bream (BSB) (#) as well as their pentaploid hybrids. The triploid hybrids possessed 124 chromosomes with two sets from RCC and one set from BSB; the tetraploid hybrids had 148 chromosomes with two sets from RCC and two sets from BSB. The females of tetraploid hybrids produced unreduced tetraploid eggs that were fertilized with the haploid sperm of BSB to generate pentaploid hybrids with 172 chromosomes with three sets from BSB and two sets from RCC. The ploidy levels of triploid, tetraploid, and pentaploid hybrids were confirmed by counting chromosomal number, forming chromosomal karyotype, and measuring DNA content and erythrocyte nuclear volume. The similar and different DNA fragments were PCR amplified and sequenced in triploid, tetraploid hybrids, and their parents, indicating their molecular genetic relationship and genetic markers. In addition, this study also presents results about the phenotypes and feeding habits of polyploid hybrids and discusses the formation mechanism of the polyploid hybrids. It is the first report on the formation of the triploid, tetraploid, and pentaploid hybrids by crossing parents with a different chromosome number in vertebrates. The formation of the polyploid hybrids is potentially interesting in both evolution and fish genetic breeding.

Injectable, self-healing, and pH-responsive hydrogels are great intelligent drug delivery systems for controlled and localized therapeutic release. Hydrogels that show pH-sensitive behaviors in the mildly acidic range are ideal to be used for the treatment of regions showing local acidosis like tumors, wounds and infections. In this work, we present a facile preparation of an injectable, self-healing, and supersensitive pH-responsive nanocomposite hydrogel based on Schiff base reactions between aldehyde-functionalized polymers and amine-modified silica nanoparticles. The hydrogel shows fast gelation within 10 s, injectability, and rapid self-healing capability. Moreover, the hydrogel demonstrates excellent stability under neutral physiological conditions, while a sharp gel−sol transition is observed, induced by a faintly acidic environment, which is desirable for controlled drug delivery. The pH-responsiveness of the hydrogel is ultrasensitive, where the mechanical properties, hydrolytic degradation, and drug release behaviors can alter significantly when subjected to a slight pH change of 0.2. Additionally, the hydrogel's mechanical and pH-responsive properties can be readily tuned by its composition. Its excellent biocompatibility is confirmed by cytotoxicity tests toward human dermal fibroblast cells (HDFa). The novel injectable, self-healing, and sensitive pH-responsive hydrogel serves as a promising candidate as a localized drug carrier with controlled delivery capability, triggered by acidosis, holding great promise for cancer therapy, wound healing, and infection treatment.

Although recent years have witnessed intense efforts and innovations in the design of flexible conductive materials for the development of next-generation electronic devices, it remains a great challenge to integrate multifunctionalities such as stretchability, self-healing, adhesiveness, and sensing capability into one conductive system for practical applications. In this work, for the first time, we have prepared a new electrically conductive elastomer composite that combines all these functionalities by triggering in situ polymerization of pyrrole in a supramolecular polymer matrix cross-linked by multiple hydrogen-bonding 2-ureido-4­[1H]-pyrimidinone (UPy) groups. The polypyrrole (PPy) particles were uniformly dispersed and imparted to the composite desirable conductive properties, while the reversible nature of the dynamic multiple hydrogen bonds in the polymer matrix allowed excellent stretchability, fast self-healing ability, and adhesiveness under ambient condition. The elastomer composite with the incorporation of 7.5 wt % PPy displayed a mechanical strength of 0.72 MPa with an elongation over 300%, where the rapid self-healing of the mechanical and electrical properties was achieved within 5 min. The elastic material also exhibited strong adhesiveness to a broad range of inorganic and organic substrates, and it was further fabricated as a strain sensor for the detection of both large and subtle human motions (i.e., finger bending, pulse beating). The novel PPy-doped conductive elastomer has demonstrated great potential as functional sensors for wearable electronics, which provides a facile and promising approach to the development of various flexible electronic materials with multifunctionalities by combining conductive components with supramolecular polymers.

A self-healing hydrogel ionic conductor has been developed by combining dynamic covalent chemistry with nanofiller reinforcement and micelle crosslinking, and used for sensing of diverse human activities.

The role of miR-26a in cancer cells seemed controversial in previous studies. Until now, the role of miR-26a in gastric cancer remains undefined. In this study, we found that miR-26a was strongly downregulated in gastric cancer (GC) tissues and cell lines, and its expression levels were associated with lymph node metastasis and clinical stage, as well as overall survival and replase-free survival of GC. We also found that ectopic expression of miR-26a inhibited GC cell proliferation and GC metastasis in vitro and in vivo. We further identified a novel mechanism of miR-26a to suppress GC growth and metastasis. FGF9 was proved to be a direct target of miR-26a, using luciferase assay and western blot. FGF9 overexpression in miR-26a-expressing cells could rescue invasion and growth defects of miR-26a. In addition, miR-26a expression inversely correlated with FGF9 protein levels in GC. Taken together, our data suggest that miR-26a functions as a tumor suppressor in GC development and progression, and holds promise as a prognostic biomarker and potential therapeutic target for GC.

Overexpression of hypoxia-induced factor 1α (HIF-1α) has been shown to be involved in the development and progression of hepatocellular carcinoma (HCC). HIF-1α should therefore be a promising molecular target for the development of anti-HCC agents. Metformin, an established antidiabetic drug, has proved to also be effective in treating cancer although the precise underlying mechanisms of this activity are not fully elucidated. The aim of this study was to investigate the effects of metformin on the expression of HIF-1α and oxygen metabolism in HCC. The results showed that metformin inhibited hypoxia-induced HIF-1α accumulation and activation independent of AMP-activated protein kinase (AMPK). Moreover, this decrease in HIF-1α accumulation was accompanied by promotion of HIF-1α protein degradation. In addition, metformin significantly decreased oxygen consumption, ultimately leading to increased intracellular oxygen tension and decreased staining with the hypoxia marker pimonidazole. In vivo studies demonstrated that metformin delayed tumor growth and attenuated the expression of HIF-1α in HCC tumor xenografts. Together, these findings suggest that metformin decreases hypoxia-induced HIF-1α accumulation by actively suppressing mitochondrial oxygen consumption and enhancing cellular oxygenation ability, providing a fundamental mechanism of metformin activity against HCC.

An orientation-mediated zwitterion–Dopa binding mechanism is established as a promising wet adhesion strategy to design zwitterion–Dopa-mediated adhesive materials.