Azhdari Suna, Linders Jürgen, Coban Deniz, Stank Tim Julian, Dargel Carina, Gojzewski Hubert, Hellweg Thomas, Gröschel André H, Wurm Frederik R
Institute for Physical Chemistry and Center for Soft Nanoscience (SoN), University of Münster, Corrensstraße 28-30, 48149, Münster, Germany.
Sustainable Polymer Chemistry (SPC), Department of Molecules and Materials, MESA+ Institute for Nanotechnology, Faculty of Science and Technology, University of Twente, P.O. Box 217, Enschede, 7500 AE, Netherlands.
Adv Mater. 2024 Sep;36(38):e2406831. doi: 10.1002/adma.202406831. Epub 2024 Jul 28.
Microplastic pollution and the urgent need for sustainable agriculture have raised interest in developing degradable carriers for controlled agrochemical release. Porous polymeric particles are particularly promising due to their unique release profiles compared to solid or core-shell carriers. However, creating degradable, mesoporous (2-50 nm) microparticles is challenging, and their potential for agrochemical delivery is largely unexplored. A straightforward self-assembly method is demonstrated for fully degradable porous polymer cubosomes (PCs), showcasing their ability to load and release agrochemicals. Using fully degradable block copolymers (BCPs), poly(ethyl ethylene phosphate)-b-polylactide (PEEP-b-PLA), PCs are synthesized in water with high inner order and open pores averaging 19 ± 3 nm in diameter. During the self-assembly process in the presence of the hydrophobic fungicide tebuconazole, polymersomes transform into PCs by enriching the hydrophobic polymer domain and altering the BCP packing parameter. After self-assemby, highly porous and fungicide-loaded PCs are obtained. Fungicide-loaded PCs show high antimycotic activity against Botrytis cinerea (grey mold), adhere to Vitis vinifera Riesling leaves even after simulated rain, and release the fungicide continuously over several days with different release-kinetics compared to solid particles. PCs hydrolyze completely into lactic acid and phosphate derivatives, highlighting their potential as microplastic-free agrochemical delivery systems for sustainable agriculture.
微塑料污染以及对可持续农业的迫切需求引发了人们对开发用于控制农用化学品释放的可降解载体的兴趣。与固体或核壳载体相比,多孔聚合物颗粒因其独特的释放特性而特别有前景。然而,制备可降解的介孔(2-50纳米)微粒具有挑战性,并且它们在农用化学品递送方面的潜力在很大程度上尚未得到探索。本文展示了一种用于完全可降解多孔聚合物立方液晶相(PCs)的直接自组装方法,展示了它们负载和释放农用化学品的能力。使用完全可降解的嵌段共聚物(BCPs),聚(乙基乙烯磷酸酯)-b-聚丙交酯(PEEP-b-PLA),在水中合成了具有高内部有序性且平均孔径为19±3纳米的开孔的PCs。在疏水性杀菌剂戊唑醇存在下的自组装过程中,聚合物囊泡通过富集疏水性聚合物域并改变BCP堆积参数而转变为PCs。自组装后,获得了高度多孔且负载杀菌剂的PCs。负载杀菌剂的PCs对灰葡萄孢(灰霉病)表现出高抗真菌活性,即使在模拟降雨后仍能附着在雷司令葡萄叶片上,并且与固体颗粒相比,能以不同的释放动力学在数天内持续释放杀菌剂。PCs完全水解成乳酸和磷酸盐衍生物,突出了它们作为无微塑料的农用化学品递送系统用于可持续农业的潜力。