One-step supramolecular co-assembly of lignin into micro-/nanospheres for photostable, sustained-release delivery of photosensitive pesticides

IF 10.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2026-06-22 Epub Date: 2026-05-12 DOI:10.1039/d6gc01679k
Hong-zhen Sun , Hai-xiu Bai , Yu-han Shang , Xin-yao Ye , Min Wang , Wei Xu , Jia-long Wen , Da-xia Zhang , Feng Liu
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引用次数: 0

Abstract

Conventional pesticide formulations face trade-offs among energy-intensive processing, organic-solvent burdens, and poor photostability. While encapsulation strategies offer a remedy, they are invariably hampered by intricate, multi-step fabrication. Herein, we developed a one-step, low-energy platform to prepare aqueous micro-/nanosphere suspensions through cooperative self-assembly between renewable sodium lignosulfonate (SL) and pesticides, exemplified by emamectin benzoate (EB). EB-loaded spheres (EB@MSs and EB@NSs) form in situ at the water/cyclohexanone interface without pre-fabricated carriers or external crosslinking. Multiscale characterization indicates that electrostatic interactions and hydrogen bonding between SL and EB drive the assembly, yielding well-defined, uniform spheres. Remarkably, after 240 min of UV irradiation, EB@MSs and EB@NSs retain approximately 80% of EB, a four-fold enhancement over conventional emulsifiable concentrate (EC) and suspension concentrate (SC) formulations (∼20%). This excellent photostability stems from the protective lignin-based matrix formed during the one-step assembly. Laboratory and field trials against multiple pests demonstrate high efficacy and extended protection, highlighting the potential of this strategy to reduce pesticide dosage. Under the tested conditions, the formulations also showed improved safety toward representative non-target organisms, including Daphnia magna and the predatory mite Amblyseius cucumeris. The strategy also showed preliminary preparative applicability across multiple photosensitive pesticides, which was further supported by functional validation using abamectin (ABM). Overall, this work provides theoretical guidance and a practical framework for the environmentally friendly, low-energy formulation of representative photosensitive pesticides.

Abstract Image

木质素一步超分子共组装成微/纳米微球,用于光敏农药的光稳定缓释递送
传统的农药配方面临着能源密集型加工、有机溶剂负担和光稳定性差的权衡。虽然封装策略提供了一种补救措施,但它们总是受到复杂的多步骤制造的阻碍。在此,我们开发了一个一步、低能的平台,通过可再生木质素磺酸钠(SL)和农药(以苯甲酸埃维菌素(EB)为例)的协同自组装制备水微/纳米球悬浮液。负载eb的球体(EB@MSs和EB@NSs)在水/环己酮界面上原位形成,无需预制载体或外部交联。多尺度表征表明,SL和EB之间的静电相互作用和氢键驱动了组装,产生了定义明确、均匀的球体。值得注意的是,在紫外线照射240分钟后,EB@MSs和EB@NSs保留了大约80%的EB,比传统的乳化浓缩物(EC)和悬浮浓缩物(SC)配方(约20%)提高了四倍。这种优异的光稳定性源于一步组装过程中形成的木质素基保护性基质。对多种害虫的实验室和田间试验表明,该方法具有较高的有效性和较长的保护期,突出了该策略在减少农药用量方面的潜力。在试验条件下,该制剂对水蚤和黄瓜弱绥螨等代表性非目标生物的安全性也有所提高。该策略在多种光敏农药中具有初步的制备适用性,并通过阿维菌素(ABM)进行了功能验证。总体而言,本研究为具有代表性的光敏农药的环保、低能耗配方提供了理论指导和实践框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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