In this study, chitosan and alginate were selected to prepare alginate/chitosan nanoparticles to load the drug lovastatin by the ionic gelation method. The synthesized nanoparticles loaded with drug were characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), laser scattering and differential scanning calorimetry (DSC) methods. The FTIR spectrum of the alginate/chitosan/lovastatin nanoparticles showed that chitosan and alginate interacted with lovastatin through hydrogen bonding and dipolar-dipolar interactions between the C-O, C=O, and OH groups in lovastatin, the C-O, NH, and OH groups in chitosan and the C-O, C=O, and OH groups in alginate. The laser scattering results and SEM images indicated that the alginate/chitosan/lovastatin nanoparticles have a spherical shape with a particle size in the range of 50–80 nm. The DSC diagrams displayed that the melting temperature of the alginate/chitosan/lovastatin nanoparticles was higher than that of chitosan and lower than that of alginate. This result means that the alginate and chitosan interact together, so that the nanoparticles have a larger crystal degree when compared with alginate and chitosan individually. Investigations of thein vitrolovastatin release from the alginate/chitosan/lovastatin nanoparticles under different conditions, including different alginate/chitosan ratios, different solution pH values and different lovastatin contents, were carried out by ultraviolet-visible spectroscopy. The rate of drug release from the nanoparticles is proportional to the increase in the solution pH and inversely proportional to the content of the loaded lovastatin. The drug release process is divided into two stages: a rapid stage over the first 10 hr, then the release becomes gradual and stable. The Korsmeyer-Peppas model is most suitable for the lovastatin release process from the alginate/chitosan/lovastatin nanoparticles in the first stage, and then the drug release complies with other models depending on solution pH in the slow release stage. In addition, the toxicity of alginate/chitosan/lovastatin (abbreviated ACL) nanoparticles was sufficiently low in mice in the acute toxicity test. The LD₅₀of the drug was higher than 5000 mg/kg, while in the subchronic toxicity test with treatments of 100 mg/kg and 300 mg/kg ACL nanoparticles, there were no abnormal signs, mortality, or toxicity in general to the function or structure of the crucial organs. The results show that the ACL nanoparticles are safe in mice and that these composite nanoparticles might be useful as a new drug carrier.

Growing wastewater treatment demands drive reliance on polymeric materials to facilitate the process, and traditional fossil-based polymers face limitations, prompting the exploration of sustainable alternatives. Biopolymers derived from renewable sources (chitosan, keratin, and cellulose) offer advantages like biodegradability and enhanced adsorption. This review provides an overview of the potential biopolymer-based composites for removing various pollutants (pesticides, heavy metals, and dyes) and highlights the importance of reusing spent adsorbents for multiple applications.

Determining the hazards posed by microplastics (MPs, <5 mm) requires an understanding of plastic degradation processes when exposed to environmental weathering forces. However, despite their perceived risks, limited information exists on the natural weathering progression of microplastics in marine environments. Our findings from environmentally realistic conditions reveal that long-term marine weathering resulted in significant degradation of plastic surfaces and bulk-phases, which varied by time and plastic polymer type. Plastics displayed biofouling, and an altered surface morphology, thermal stability and chemical signature. Secondary micronanoplastics (MNPs, <1 µm) were formed from weathered plastic surfaces, supported by a significant reduction in the size of PCL and PVC pellets. Using real world data, we reveal that plastic surfaces can degrade at a rate of up to 469.73 µm per year, 12 times greater than previous estimates. Our time-series data contributes valuable information towards developing plastic specific risk assessment frameworks and future plastics policy.

Due to the depletion of fossil fuels and their‐related environmental issues, sustainable, clean, and renewable energy is urgently needed to replace fossil fuel as the primary energy resource. Hydrogen is considered as one of the cleanest energies. Among the approaches to hydrogen production, photocatalysis is the most sustainable and renewable solar energy technique. Considering the low cost of fabrication, earth abundance, appropriate bandgap, and high performance, carbon nitride has attracted extensive attention as the catalyst for photocatalytic hydrogen production in the last two decades. In this review, the carbon nitride‐based photocatalytic hydrogen production system, including the catalytic mechanism and the strategies for improving the photocatalytic performance is discussed. According to the photocatalytic processes, the strengthened mechanism of carbon nitride‐based catalysts is particularly described in terms of boosting the excitation of electrons and holes, suppressing carriers recombination, and enhancing the utilization efficiency of photon‐excited electron–hole. Finally, the current trends related to the screening design of superior photocatalytic hydrogen production systems are outlined, and the development direction of carbon nitride for hydrogen production is clarified.