We study coacervation upon mixing two aqueous solutions of polyelectrolytes (PEs) with opposite charge, by considering asymmetric effects of PE composition and charge valency. The phase behavior, interfacial structure, and coacervate composition are investigated by a classical densityfunctional theory. We find two types of coacervation that are different in their density. Supernatant phase in low-density coacervation (LDCA) fully consists of small ions, while in high-density coacervation (HDCA) it contains a considerable amount of PE chains. Asymmetric PE composition could generate an electric double layer at the interface of coacervate. For HDCA, ion density changes monotonically, while for LDCA it shows a global minimum at the double layer, giving a low tension value. Charged species of high charge valency enhance the existence of double layer. Our results explained the coacervate structure of low interfacial tension, which is important for experiments and industrial applications.
Humans and animals may be exposed to increasing contaminant lithium (Li) concentrations in the environment with the use and disposal of Li-containing products.Meanwhile, Li plays a key role in the treatment of human mental disorders, while the excessive accumulation of Li salts in the body can cause renal damage and nephrotic syndrome. In this study, the mechanism of renal inflammatory reaction induced by Li excessive intake was studied by establishing mice models in vitro and in vivo. The results of histopathology staining and TdT-mediated dUTP nick-end labeling assay showed that high Li condition (Lithium carbonate, 20 mg/kg/twice a day, i.e., for 30 consecutive days) caused inflammatory damage and apoptosis in kidney tissue cells. Western blot, qPCR, and immunohistochemical analysis were used to further study. In the vivo experiments, we found that Li reduced antioxidant enzyme capacity (glutathione peroxidase, total superoxide dismutase, total antioxidant capacity, and catalase) and induced the production of reactive oxygen species (ROS). Moreover, excessive Li activated nuclear factor kappa-B (NF-κB) signaling pathway and nucleotide-binding oligomerization domain-like receptors domains-containing protein 3 (NLRP3) inflammasome, resulting in activation of inflammatory factors tumor necrosis factor-α and IL-1β in the kidney of mice. In the vitro study, ROS as an upstream signal phosphorylated IκBα and NF-κB, up-regulated the NLRP3 inflammasome, increased caspase3, 6, 7, and 9 to exaggerate inflammation response, finally inducing pyroptosis in renal cells.
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