The present invention relates to a seed coating composition comprising at least: (a) a polyvinyl acetate binder, (b) activated carbon powder, and (c) at least two minerals from the group of calcium carbonate, micro-mica, vermiculite or a silicon-comprising clay. The present invention is furthermore related to the method for producing seed pellets, comprising blending the components (a) to (c), water and seeds to be coated in a pelletizer such that the seeds are coated, and, and drying the coated seeds to obtain seed pellets, and, optionally, sieving the thus obtained seed pellets.

The present invention relates to a seed coating composition comprising at least: (a) a polyvinyl acetate binder, (b) activated carbon powder, and (c) at least two minerals from the group of calcium carbonate, micro-mica, vermiculite or a silicon-comprising clay. The present invention is furthermore related to the method for producing seed pellets, comprising blending the components (a) to (c), water and seeds to be coated in a pelletizer such that the seeds are coated, and, and drying the coated seeds to obtain seed pellets, and, optionally, sieving the thus obtained seed pellets.

The present invention relates to a seed coating composition comprising at least: (a) a polyvinyl acetate binder, (b) activated carbon powder, and (c) at least two minerals from the group of calcium carbonate, micro-mica, vermiculite or a silicon-comprising clay. The present invention is furthermore related to the method for producing seed pellets, comprising blending the components (a) to (c), water and seeds to be coated in a pelletizer such that the seeds are coated, and, and drying the coated seeds to obtain seed pellets, and, optionally, sieving the thus obtained seed pellets.

Disclosed herein are compositions (e.g., sprays, paints, etc.) that comprise antimicrobial zeolite nanoparticles. Also provided are hemostatic compositions comprising zeolite nanoparticles, dryer sheets comprising zeolite nanoparticles, and textiles comprising zeolite nanoparticles. Also disclosed are compositions (e.g., sprays) that include a binder polymer to improve coating adherence. In some cases, the zeolite nanoparticles can further comprise an optical tracer (e.g., a fluorophore) associated with the zeolite nanoparticles. The optical tracer can be interrogated to confirm presence of the zeolite nanoparticles (or a coating comprising the zeolite nanoparticles) on a surface. Also provided are methods of forming viricidal coatings using compositions that comprise zeolite nanoparticles dispersed in a carrier.

Disclosed herein are compositions (e.g., sprays, paints, etc.) that comprise antimicrobial zeolite nanoparticles. Also provided are hemostatic compositions comprising zeolite nanoparticles, dryer sheets comprising zeolite nanoparticles, and textiles comprising zeolite nanoparticles. Also disclosed are compositions (e.g., sprays) that include a binder polymer to improve coating adherence. In some cases, the zeolite nanoparticles can further comprise an optical tracer (e.g., a fluorophore) associated with the zeolite nanoparticles. The optical tracer can be interrogated to confirm presence of the zeolite nanoparticles (or a coating comprising the zeolite nanoparticles) on a surface. Also provided are methods of forming viricidal coatings using compositions that comprise zeolite nanoparticles dispersed in a carrier.

A plastic material for extended release of a bio-active agent, the plastic material comprising a structural polymer, at least one bio-active ingredient embedded within the structural polymer as solid islands, a liquid binding material embedded within the structural polymer as granules, and a carrier liquid absorbed within the liquid-absorbent material. The carrier liquid may be sufficiently non-compatible with the structural polymer so that at least a portion of the carrier liquid is released from the liquid-absorbent material through the structural polymer to an outer surface of the plastic material over a period of time, such as a week or more, a month or more, or about three months. The bio-active agent comprised in the at least one bio-active ingredient may be sufficiently soluble in the carrier liquid at room or body temperature so that the carrier liquid released to the outer surface comprises the bio-active agent in solution.

A plastic material for extended release of a bio-active agent, the plastic material comprising a structural polymer, at least one bio-active ingredient embedded within the structural polymer as solid islands, a liquid binding material embedded within the structural polymer as granules, and a carrier liquid absorbed within the liquid-absorbent material. The carrier liquid may be sufficiently non-compatible with the structural polymer so that at least a portion of the carrier liquid is released from the liquid-absorbent material through the structural polymer to an outer surface of the plastic material over a period of time, such as a week or more, a month or more, or about three months. The bio-active agent comprised in the at least one bio-active ingredient may be sufficiently soluble in the carrier liquid at room or body temperature so that the carrier liquid released to the outer surface comprises the bio-active agent in solution.

An antimicrobial composition comprising: a) C2-C8 alkylated polyvinylpyrrolidone polymer; and b) biocidal agent selected from the group consisting of quaternary ammonium compounds, chlorohexidine salts, polymeric biguanides, organic acids, hydrogen peroxide, tertiary alkyl amines, iodophors and mixtures thereof.

An antimicrobial composition comprising: a) C2-C8 alkylated polyvinylpyrrolidone polymer; and b) biocidal agent selected from the group consisting of quaternary ammonium compounds, chlorohexidine salts, polymeric biguanides, organic acids, hydrogen peroxide, tertiary alkyl amines, iodophors and mixtures thereof.

Disclosed herein are methods of making pure chalcogenide (e.g., selenium, tellurium, or selenium/tellurium) nanoparticles by irradiating chalcogenide pellets by nano-second laser ablation using chitosan as a capping agent to form chitosan chalcogenide nanoparticles (CS-CgNPs). CS-CgNPs and methods of using such particles are also disclosed herein, such as antimicrobials and antimicrobial coatings effective against biofilms.