Cellular absorption of polystyrene nanoplastics with different surface functionalization and the toxicity to RAW264.7 macrophage cells.

Nanoplastics (NPs) are a matter of widespread concern, as they are easily absorbed by a wide variety of organisms and accumulate in biological tissues. While there is evidence that nanoplastics are toxic to various organisms, few studies have investigated the mechanisms underlying the toxicities of NPs with different surface functionalizations to macrophage cells. In this study, mouse mononuclear macrophage (RAW264.7) cells were exposed to polystyrene nanoplastics (PS-NPs) with three different surface functionalizations, namely pristine polystyrene (PS), carboxyl-functionalized polystyrene (PS-COOH), and amino-functionalized polystyrene (PS-NH2), to evaluate the cellular endocytosis, lactate dehydrogenase (LDH) release, cell viability, reactive oxygen species (ROS), mitochondrial membrane potential, apoptosis, and related gene expression. Results showed that all three PS-NPs were endocytosed into cells. However, in the concentration range of 0-100 µg/mL, PS had no effect on cell viability or apoptosis, but it slightly increased cellular ROS and decreased mitochondrial membrane potential. PS-NH2 exhibited the highest cytotoxicity. PS-COOH and PS-NH2 induced ROS production, altered the mitochondrial membrane potential, and caused cell apoptosis regulated by the mitochondrial apoptosis pathway. Results also showed that cell membrane damage induced by PS-NH2 is one of the primary mechanisms of its cytotoxicity to RAW264.7 cells. The results of this study clarify the toxicities of PS-NPs with different surface functionalizations to macrophages, thereby improving the identification of immune system risks related to nanoplastics.

Photocatalytic materials modified with carbon quantum dots for the degradation of organic pollutants under visible light: A review.

In recent years, carbon quantum dots (CQDs) have received widespread attention owing to their non-toxicity, sustainability, excellent photostability, and intrinsic photoluminescence properties. In particular, CQDs have attracted considerable interest for visible-light-driven photocatalysis because of their excellent electron transfer characteristics and high light capture efficiency. Many studies have reported CQDs/photocatalyst composite systems constructed to make full use of the solar spectrum, improving the ability of photocatalytic materials to degrade organic pollutants. Here, we review the recent research on CQDs-based photocatalysts, and their ability to remove environmental pollutants, with a special emphasis on degradation mechanisms. Several improvements in the catalytic response of CQDs to visible light are also included. In addition, we discuss the aspects that should be considered to construct composite materials based on CQD characteristics and the potential applications of CQD-based photocatalysts for efficient utilization of visible light.