Pesticides are widely used to increase agricultural productivity, however, weak adhesion and deposition lead to low efficient utilization. Herein, we prepare a nanopesticide formulation (tebuconazole nanopesticides) which is leaf-adhesive, and water-dispersed via a rapid nanoparticle precipitation method, flash nanoprecipitation, using temperature-responsive copolymers poly-(2-(dimethylamino)ethylmethylacrylate)-b-poly(ε-caprolactone) as the carrier. Compared with commercial suspensions, the encapsulation by the polymer improves the deposition of TEB, and the contact angle on foliage is lowered by 40.0°. Due to the small size and strong van der Waals interactions, the anti-washing efficiency of TEB NPs is increased by 37% in contrast to commercial ones. Finally, the acute toxicity of TEB NPs to zebrafish shows a more than 25-fold reduction as compared to commercial formulation indicating good biocompatibility of the nanopesticides. This work is expected to enhance pesticide droplet deposition and adhesion, maximize the use of pesticides, tackling one of the application challenges of pesticides.

In recent years, electrospun nanofibers have attracted extensive attention due to their large specific surface area, high porosity, and controllable shape. Among the many applications of electrospinning, electrospun nanofibers used in fields such as tissue engineering, food packaging, and air purification often require some antibacterial properties. This paper expounds the development potential of electrospinning in the antibacterial field from four aspects: fiber morphology, antibacterial materials, antibacterial mechanism, and application fields. The effects of fiber morphology and antibacterial materials on the antibacterial activity and characteristics are first presented, then followed by a discussion of the antibacterial mechanisms and influencing factors of these materials. Typical application examples of antibacterial nanofibers are presented, which show the good prospects of electrospinning in the antibacterial field.

To mimic the underwater adhesion of marine mussels, a bioadhesive has been prepared with a poly(acrylic acid) backbone functionalized with 30% catechol appendants. The polyelectrolyte chains can be reversibly crosslinked through metal chelation and irreversibly gelled by oxidative crosslinking. Surprisingly, the reported “poor” metal chelator Zn²⁺ not only imparts this injectable adhesive with superior adhesion after the formation of coacervation compared to the one chelated by a stronger metal crosslinker (e.g. Fe³⁺), but also generates good mechanical performance of the self-healing hydrogel after the oxidation of catechol groups with a pH trigger. Such a pH-responsive material with strong adhesion and good self-healing property at different conditions could be an ideal candidate in biomedical adhesion and tissue engineering.