Using Diels–Alders (DA) chemistry as a dynamic-covalent linkage, we explored the kinetic growth mechanism of polymer structures including starlike materials and nanogels. The use of reversible addition–fragmentation chain transfer (RAFT) polymerization allows for precise control of DA linkages within the polymer backbone. Controlling the competition between intra- and intermolecular cross-linking reactions allows for the preparation of polymer structures that can expand their volume after cleavage of the DA linkages as determined by dynamic light scattering (DLS). Macroscopically, this would be analogous to untying a rope ball knot, commonly termed a “monkey’s fist”.

As virus outbreaks continue to pose a challenge, a nonspecific viral inhibitor can provide significant benefits, especially against respiratory viruses. Polyglycerol sulfates recently emerge as promising agents that mediate interactions between cells and viruses through electrostatics, leading to virus inhibition. Similarly, hydrophobic C60 fullerene can prevent virus infection via interactions with hydrophobic cavities of surface proteins. Here, two strategies are combined to inhibit infection of SARS‐CoV‐2 variants in vitro. Effective inhibitory concentrations in the millimolar range highlight the significance of bare fullerene's hydrophobic moiety and electrostatic interactions of polysulfates with surface proteins of SARS‐CoV‐2. Furthermore, microscale thermophoresis measurements support that fullerene linear polyglycerol sulfates interact with the SARS‐CoV‐2 virus via its spike protein, and highlight importance of electrostatic interactions within it. All‐atom molecular dynamics simulations reveal that the fullerene binding site is situated close to the receptor binding domain, within 4 nm of polyglycerol sulfate binding sites, feasibly allowing both portions of the material to interact simultaneously.

Inhibition of SARS‐CoV‐2 Variants In the article number 2206154, Ievgen S. Donskyi and co‐workers describe effective SARS‐CoV‐2 inhibitor. Low molecular weight polyglycerol sulfate works in tandem with a single hydrophobic fullerene to prevent the infection in vitro. Investigated through plaque reduction assays, microscale thermophoresis (MST) binding studies, and molecular dynamics (MD) simulations, fullerene appears to nestle in to a solvent accessible hydrophobic pocket on the S1 spike protein.

The production scalability and increasing demand for nanoblack phosphorus materials (nano-BPs) inevitably lead to their environmental leakage, thereby raising the risk of human exposure through inhalation, ingestion, dermal, and even intravenous pathways. Consequently, a systematic evaluation of their potential impacts on human health is necessary. This Review outlines recent progress in the understanding of various biological responses to nano-BPs. Attention is particularly given to the inconsistent toxicological findings caused by a wide variation of nano-BPs' physicochemical properties, toxicological testing methods, and cell types examined in each study. Additionally, cellular uptake and intracellular trafficking, cell death modes, immunological effects, and other biologically relevant processes are discussed in detail, providing evidence for the potential health implications of nano-BPs. Finally, we address the remaining challenges related to the health risk evaluation of nano-BPs and propose a broader range of applications for these promising nanomaterials.