The mechanism of bensulfuron-methyl complexation with β-cyclodextrin and 2-hydroxypropyl-β-cyclodextrin and effect on soil adsorption and bio-activity

• Published in: Scientific reports Vol. 9; no. 1; p. 1882
• Main Authors: Geng, Qianqian, Li, Tian, Wang, Xin, Chu, Weijing, Cai, Mengling, Xie, Jingchan, Ni, Hanwen
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 13-02-2019; Nature Publishing Group
• Subjects: 119/118; 140/131; 639/301/1023/1025; 704/172/4081; Adsorption; Bensulfuron-methyl; Benzene; Biological activity; Herbicides; Humanities and Social Sciences; Hydrophobicity; multidisciplinary; Science; Science (multidisciplinary); Soil adsorption; Solubility; β-Cyclodextrin
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-38234-7

In this work, the inclusion complexes of hydrophobic herbicide bensulfuron-methyl (BSM) with β-cyclodextrin (β-CD) and (2-hydroxypropyl)-β-CD (2-HP-β-CD) were prepared and characterized. Phase solubility study showed that both β-CD and 2-HP-β-CD increased the solubility of BSM. Three-dimensional structures of the inclusion complexes were simulated by the molecular docking method. The docking results indicated that guest BSM could enter into the cavities of host CDs, folded, and centrally aligned inside the inclusion complexes. The benzene ring of the guest molecule was close to the wide rim of the host molecules; the pyrimidine ring and side chains of the guest molecule were oriented toward the narrow rim of the host molecule. The inclusion complexes were successfully prepared by the coprecipitation method. The physiochemical characterization data of
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H NMR, FT-IR, XRD, and DSC showed that the guest and host molecules were well included. BSM had lower soil adsorption and higher herbicidal activity in the complexation form with β-CD or 2-HP-β-CD than in the pure form. The present study provides an approach to develop a novel CDs-based formulation for hydrophobic herbicides.