UV aging may enhance adsorption capacity of Poly (butylene adipate-co-terephthalate) (PBAT) to heavy metals and toxicity to zebrafish.

Compared with the fossil-based plastics, biodegradable plastics are more easily decomposed into small-sized particles (e.g., microplastics). However, the role of aged biodegradable plastics in being vector of co-existed pollutants and potential toxicological effects remain to be elucidated. The present study selected micro-sized biodegradable polymer Poly (butylene adipate-co-terephthalate) (PBAT) as the object, aiming to explore its aging process, environmental behavior with heavy metals (Cu and Pb), and the toxic effects on zebrafish. The results showed that distinct changes such as cracks and severe deformation can be observed on the surface of PBAT after 60 days of UV aging, and the functional groups changed consequently. The maximum adsorption capacity of aged PBAT for Cu and Pb reached 0.967 and 0.939 mg·g-1, which increased by 1.32 and 1.46 times, respectively. The results of 7-day acute toxicology experiments suggested that the adsorption behavior of aged PBAT may alleviate the toxic effects of heavy metals Cu and Pb on zebrafish in short-term exposure, however it could simultaneously cause a serious imbalance of intestinal microorganisms in zebrafish. As demonstrated, the coexistence of aged PBAT and heavy metals (Cu, Pb) can seriously reduce the intestinal microbial diversity and richness of zebrafish, which may induce more serious toxicity and disease in long-term exposure to pollutants. This study could provide fundamental data for better understanding on the adsorption behavior and ecological risk of aged biodegradable plastics with coexisted pollutants.

Effects of biodegradable and conventional microplastics on the intestine, intestinal community composition, and metabolic levels in tilapia (Oreochromis mossambicus).

Despite growing interest in conventional microplastics (CMPs) and their toxicological effects on aquatic species, little is known about biodegradable microplastics (BMPs) and their corresponding implications for aquatic life. Here, tilapia (Oreochromis mossambicus) were semi-statically exposed for 14 days to the bio-based plastic polylactic acid (PLA, 100 µg/L, 2.52 ± 0.46 µm) and the petroleum-based plastic polyvinyl chloride (PVC, 100 µg/L, 1.58 ± 0.36 µm). The results showed that ingesting the above two types of microplastics (MPs) led to oxidative stress in the fish gut, and damage to gut tissues and organelles, and PLA resulted in more obvious gut tissue edema than PVC. Furthermore, PLA caused increased levels of gut microbiota dysbiosis and a decrease in the abundance of the genus Cetobacterium, which is linked to vitamin B-12 synthesis, whereas an opposite relationship was observed on PVC. Metabolomic analysis indicated that PVC caused a significant down-regulation of orotic acid, co-metabolite of folic acid with vitamin B-12, while PLA did not affect orotic acid, which may lead to the accumulation of folic acid in fish. The joint analysis found that MPs disturbed gut metabolism homeostasis, implying that abnormal gut microbiota metabolites may be a key mechanism for MPs to induce tissue damage and oxidative stress in the gut. Overall, this study systematically illustrates the differential toxic effects of BMPs and CMPs on tilapia through gut microbiota and metabolite interactions, which will contribute to assessing the risks of BMPs to organismal health.

Fabrication of inverse-opal lysozyme-imprinted polydopamine/polypyrrole microspheres with near-infrared-light-controlled release property.

The combination of the molecular imprinting technology and porous materials is a promising way to obtain high-efficient selective adsorption and separation materials for bioactive macromolecules. In this work, we developed a novel approach to prepare near-infrared (NIR)-light-response inverse-opal lysozyme (Lyz)-imprinted polydopamine/polypyrrole (IO-PDA/PPy-MIP) composite microspheres using micron-sized SiO2 colloidal crystal microspheres as the sacrificed template. The pore size of the IO-PDA/PPy-MIP microspheres can be tuned from 200 to 800 nm by the size of silica nanoparticles which self-assemble to form the template SiO2 colloidal crystal microspheres. The IO-PDA/PPy-MIP microspheres show a rapid selective adsorption ability for Lyz due to the inverse-opal macroporous structure. The adsorption capacity exceeds 800 mg/g within 20 min, and the imprinting factor is as high as 24. The bound Lyz molecules can be released rapidly from IO-PDA/PPy-MIP microspheres triggered by the irradiation of NIR laser and remain enough bioactivity to decompose Escherichia coli efficiently. The prepared IO-PDA/PPy-MIP microspheres also exhibit excellent structure stability and good recyclability. The adsorption capacity can remain up to 90% of the initial value after 5 times recycle. This work provides not only a method to prepare novel NIR-light-response inverse-opal macroporous molecularly imprinted microspheres, but also a new perspective on the design of selectively separation materials for the fast, high-efficient recognition and separation of biomacromolecules.

CO2-induced microstructure transition of surfactant in aqueous solution: insight from molecular dynamics simulation.

A molecular dynamics simulation study is reported to investigate a CO(2)-induced microstructure transition of surfactant AOT4 in aqueous solution. The lamellar bilayer changes into a spherical micelle induced by CO(2) at ambient temperature, while a thermotropic aggregate transition occurs in the absence of CO(2) above 140 degrees C. In the lamellar bilayer, AOT4 shows a bimodal density distribution. The bilayer thickness and the average area per AOT4 are estimated to be 19.2 A and 83.3 A(2). The AOT4 bilayer possesses a sandwich structure and consists of a hydrophobic region in the center and a hydrated layer on both sides. Upon CO(2) dissolving, the lamellar bilayer is swollen and becomes loose and unstable. CO(2) molecules in the lamellar bilayer are initially near the ester groups of AOT4 and then accumulate in the center of the hydrophobic region. With increasing amounts of CO(2), the AOT4 bilayer expands gradually and the density distribution of each leaflet becomes broader. Driven by surface tension, the lamellar bilayer tends to reduce the surface area. The lamellar bilayer changes into a 3D cubic network in a small simulation box, attributed to the influence of neighboring images. In a sufficiently large box, the lamellar bilayer transforms into spherical micelles. CO(2)-active surfactants such as fluorinated surfactants and oxygenated AOT analogues are proposed to substitute CO(2)-inactive AOT and may reduce the critical pressure in microstructure transition.