A model of COVID-19 pandemic with vaccines and mutant viruses.

This paper proposes a compartment model (SVEIHRM model) based on a system of ordinary differential equations to simulate the pandemic of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).Emergence of mutant viruses gave rise to multiple peaks in the number of confirmed cases. Vaccine developers and WHO suggest individuals to receive multiple vaccinations (the primary and the secondary vaccinations and booster shots) to mitigate transmission of COVID-19. Taking this into account, we include compartments for multiple vaccinations and mutant viruses of COVID-19 in the model. In particular, our model considers breakthrough infection according to the antibody formation rate following multiple vaccinations. We obtain the effective reproduction numbers of the original virus, the Delta, and the Omicron variants by fitting this model to data in Korea. Additionally, we provide various simulations adjusting the daily vaccination rate and the timing of vaccination to investigate the effects of these two vaccine-related measures on the number of infected individuals. We also show that starting vaccinations early is the key to reduce the number of infected individuals. Delaying the start date requires increasing substantially the rate of vaccination to achieve similar target results. In the sensitivity analysis on the vaccination rate of Korean data, it is shown that a 10% increase (decrease) in vaccination rates can reduce (increase) the number of confirmed cases by 35.22% (82.82%), respectively.

Physciosporin suppresses the proliferation, motility and tumourigenesis of colorectal cancer cells.

BACKGROUND: Lichens, which represent symbiotic associations of fungi and algae, are potential sources of numerous natural products. Physciosporin (PHY) is a potent secondary metabolite found in lichens and was recently reported to inhibit the motility of lung cancer cells via novel mechanisms. PURPOSE: The present study investigated the anticancer potential of PHY on colorectal cancer (CRC) cells. METHODS: PHY was isolated from lichen extract by preparative TLC. The effect of PHY on cell viability, motility and tumourigenicity was elucidated by MTT assay, hoechst staining, flow cytometric analysis, transwell invasion and migration assay, soft agar colony formation assay, Western blotting, qRT-PCR and PCR array in vitro as well as tumorigenicity study in vivo. RESULTS: PHY decreased the viability of various CRC cell lines (Caco2, CT26, DLD1, HCT116 and SW620). Moreover, PHY elicited cytotoxic effects by inducing apoptosis at toxic concentrations. At non-toxic concentrations, PHY dose-dependently suppressed the invasion, migration and colony formation of CRC cells. PHY inhibited the motility of CRC cells by suppressing epithelial-mesenchymal transition and downregulating actin-based motility markers. In addition, PHY downregulated ß-catenin and its downstream target genes cyclin-D1 and c-Myc. Moreover, PHY modulated KAI1 C-terminal-interacting tetraspanin and KAI1 expression, and downregulated the downstream transcription factors c-jun and c-fos. Finally, PHY administration showed considerable bioavailability and effectively decreased the growth of CRC xenografts in mice without causing toxicity. CONCLUSION: PHY suppresses the growth and motility of CRC cells via novel mechanisms.

Potassium usnate, a water-soluble usnic acid salt, shows enhanced bioavailability and inhibits invasion and metastasis in colorectal cancer.

Usnic acid (UA), a lichen secondary substance, has considerable anticancer activity in vitro, whereas its effect in vivo is limited. Here, potassium usnate (KU) was prepared by the salinization of UA to enhance its water solubility. KU showed increased bioavailability compared with UA in the tumor, liver, and plasma of a CT26 syngeneic mouse tumor xenograft model after oral administration, as determined by LC-MS/MS analysis. KU exhibited potent anticancer effects on colorectal cancer cells and inhibited liver metastasis in an orthotopic murine colorectal cancer model. KU treatment downregulated the epithelial-mesenchymal markers Twist, Snail, and Slug and the metastasis-related genes CAPN1, CDC42, CFL1, IGF1, WASF1, and WASL in cells and tumor tissues. The present results suggest the potential application of the water-soluble form of UA, KU, in anticancer therapy.

Spontaneous deposition of gold nanoparticle nanocomposite on polymer surfaces through sol-gel chemistry.

A aminosilica nanocomposite layer containing a monolayer of gold nanoparticles (d = 18-22 nm) with a well-defined spacing was spontaneously deposited on an unmodified polystyrene surface via a sol-gel reaction when the reduction reaction was carried out under 1:8 molar ratio (gold(III):aminosilane). The amount of aminosilica and spacing between gold nanoparticles were found to be a function of the aminosilane:water molar ratio, which contributes to the plasmonic property of the films with its absorption wavelength ranging between 701 and 548 nm. Furthermore, the nanocomposite film that consists of a monolayer of nanoparticles in aminosilica has also been deposited on the surface of polystyrene beads. This core-shell structure was found capable of storing electrostatic charges and forming a well-separated 2D array.

Self-assembly of silver-aminosilica nanocomposites through silver nanoparticle fusion on hydrophobic surfaces.

Silver-nanoparticle-embedded aminosilica colloids synthesized via aminosilane-induced spontaneous reduction reaction exhibit selective adhesion properties on hydrophobic surfaces and have been utilized as a simple and one-step procedure to create patterned nanocomposite film with silver to aminosilica mole ratio at 0.9:1. Substrates that enable self-assembly of the colloids include silicon wafer, polydimethylsiloxane, and microscope slide, where patterns of hydrophilic surface were either created using oxygen plasma treatment or stamped with chemical ink using microcontact printing. Upon substrates being immersed in a solution containing silver-aminosilica colloids, particles attach to hydrophobic surfaces and continuously self-assemble onto the deposited film, allowing us to fabricate nanocomposite patterns with controllable thickness (approximately 200 nm).