Orchid-flower-shaped ZnO nanomaterials were successfully synthesized via green synthesis and an eco-friendly approach using an aqueous extract of Lycium chinense fruit as a reducing and capping agent. The synthesized Lycium chinense orchid-flower-shaped ZnO (LC-ZnO/OF) nanoparticles (NPs) were characterized using different analytical methods through X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), photoelectron spectroscopy (XPS), and photoluminescence (PL). The FE-TEM analysis revealed the orchid flower shape of the nanoparticles, and the elemental composition was confirmed via XPS analysis. The photocatalytic activity of the nanoparticles was determined by the degrading cationic dye methylene blue (MB) and the anionic dye Eosin Y (EY) under visible light irradiation at (400 w) within 180 min time, where it showed a significant ability to degrade both cationic and anionic dye by almost 50%. The LC-ZnO/OF photocatalyst was also used to check the toxicity level in human cancer cells, where it exhibited remarkable cytotoxicity to the human lung cancer (A549 cell line) and human gastric adenocarcinoma hyperdiploid (AGS cell line). The present investigation suggests that LC-ZnO/OF has the potential photocatalytic ability to degrade toxic dye as well as have anti-cancer effects. These preliminary results suggest that LC-ZnO/OF could have a significant impact on the environmental and biomedical fields.

This study focused on developing Panos nanoemulsion (P-NE) and enhancing the anti-inflammatory efficacy for the treatment of inflammation. The effects of P-NE were evaluated in terms of Nitric oxide (NO production) in Lipopolysaccharide (LPS), induced RAW 264.7 cells, Reactive oxygen species (ROS) generation using Human Keratinocyte cells (HaCaT), and quantitative polymerase chain reaction (qPCR) analysis. Sea buckthorn oil, Tween 80, and span 80 were used and optimize the process. Panos extract (P-Ext) was prepared using the fermentation process. Further high-energy ultra-sonication was used for the preparation of P-NE. The developed nanoemulsion (NE) was characterized using different analytical methods. Field emission transmission electron microscopy (FE-TEM) analyzed the spherical shape and morphology. In addition, stability was analyzed by Dynamic light scattering (DLS) analysis, where particle size was analyzed 83 nm, and Zeta potential −28.20 ± 2 (mV). Furthermore, 90 days of stability was tested using different temperatures conditions where excellent stability was observed. P-NE are non-toxic in (HaCaT), and RAW264.7 cells up to 100 µg/mL further showed effects on ROS and NO production of the cells at 50 µg/mL. The qPCR analysis demonstrated the suppression of pro-inflammatory mediators for (Cox 2, IL-6, IL-1β, and TNF-α, NF-κB, Ikkα, and iNOS) gene expression. The prepared NE exhibited anti-inflammatory effects, demonstrating its potential as a safe and non-toxic nanomedicine.

Alternative splicing (AS) is a widely recognized post-transcriptional regulatory mechanism that plays a crucial role in plant evolution and environmental adaptation. In this study, five representative Panax species were systematically analyzed to examine the evolutionary conservation and functional characteristics of AS events. Results revealed an expansion in the number of AS events and associated genes across the Panax species, accompanied by a genome-wide shift in splicing types from a dominance of intron retention (IR) to an increase in exon skipping (ES), alternative donor (A5), and alternative acceptor (A3) events. Splicing preferences were also found to diverge among allotetraploid species, which exhibited more complex AS patterns. The genomic features of IR and ES events, such as GC content and length of the sequence involved in AS, were highly conserved among Panax species of different ploidy levels (diploid vs. allotetraploid). Genes harboring conserved IR events across all five species were identified, and functional annotation indicated that these genes are primarily involved in chromatin modification and RNA splicing-related processes. This study elucidates the dynamic remodeling of AS during the evolution of Panax and provides important insights into the evolutionary adaptive mechanisms of AS in plants.