Elevation and Human Disturbance Interactively Influence the Patterns of Insect Diversity on the Southeastern Periphery of the Tibetan Plateau.

The maintenance of biodiversity and ecological balance heavily relies on the diversity of insects. In order to investigate the impacts of elevation and human disturbance, as well as their interactions on insect diversity, we conducted an intensive survey of insects in the Hengduan Mountain Range, which is situated on the southeastern periphery of the Tibetan Plateau in China. A total of 50 line transects were established in this study to investigate the impact of elevation and human disturbance on insect diversity and distribution patterns.

Macrophages-mediated delivery of protoporphyrin for sonodynamic therapy of rheumatoid arthritis.

Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease characterized by infiltration of inflammatory cells, hyperplasia of synovium, and destruction of the joint cartilage. Owing to the low drug delivery efficiency and limited immunosuppression effect, complete cure for RA remains a formidable challenge. Here, we show that live macrophages (Mφs) carrying protoporphyrin-loaded FeO nanoparticles can migrate to the RA tissues and inhibit the inflammation by sonodynamic therapy.

Tween 80 Micelles Loaded with FeO Nanoparticles and Artemisinin for Combined Oxygen-Independent Ferroptosis Therapy of Cancer.

Artemisinin has an endoperoxide bridge structure, which can be cleaved by ferrous ions to generate various carbonyl radicals in an oxygen-independent manner, highlighting its potential for treating hypoxic tumors. In our study, we fabricated Tween 80 micelles loaded with FeO nanoparticles and artemisinin for cancer therapy. The synthesized FeO nanoparticles and drug-loaded micelles have particle sizes of about 5 nm and 80 nm, respectively, both exhibiting excellent dispersibility and stability.

Synthesis of novel cholesterol-based ionizable lipids for mRNA delivery.

The safe and effective delivery of messenger ribonucleic acid (mRNA) is crucial for its therapeutic effects in vivo. In this study, we developed a new type of ionizable lipid S-1, which contains an amino head, a cholesterol matrix, and a long hydrophobic carbon tail. We employed microfluidics to rapidly mix an ethanol phase containing S-1 lipid with an aqueous mRNA to form mRNA/S-1 lipid nanoparticles (LNPs, 100-200 nm).