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Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin

The herbicide diuron is hardly soluble in water and most organic solvents and is usually made into a wettable powder or mixed with soil when used, which causes environmental risk and a reduction in herbicidal efficacy. In this study, the physicochemical properties were changed by using β-cyclodextri...

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Autores principales: Gao, Shuang, Jiang, Jing-Yu, Liu, Yan-Yan, Fu, Ying, Zhao, Li-Xia, Li, Chun-Yan, Ye, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780809/
https://www.ncbi.nlm.nih.gov/pubmed/31450656
http://dx.doi.org/10.3390/polym11091396
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author Gao, Shuang
Jiang, Jing-Yu
Liu, Yan-Yan
Fu, Ying
Zhao, Li-Xia
Li, Chun-Yan
Ye, Fei
author_facet Gao, Shuang
Jiang, Jing-Yu
Liu, Yan-Yan
Fu, Ying
Zhao, Li-Xia
Li, Chun-Yan
Ye, Fei
author_sort Gao, Shuang
collection PubMed
description The herbicide diuron is hardly soluble in water and most organic solvents and is usually made into a wettable powder or mixed with soil when used, which causes environmental risk and a reduction in herbicidal efficacy. In this study, the physicochemical properties were changed by using β-cyclodextrin (β-CD) to encapsulate diuron to form an inclusion complex. Some key technologies, including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and nuclear magnetic resonance ((1)H NMR), were used to characterize the inclusion complex. The stoichiometry of the inclusion complex was determined by recording the (1)H NMR spectrum or by using a diagram of inclusion ratios. A phase solubility study proved that the formed inclusion complex exhibited higher water solubility. Thermogravimetric analysis (TGA) demonstrated that the formed inclusion complex exhibited better thermal stability. Biological activity studies indicated that the herbicidal activity, in terms of herbicide removal, of the formed inclusion complex was higher than that of the original diuron. In general, the formation of the inclusion complex could reduce the environmental damage caused by diuron and enhance its herbicidal activity, providing an environmentally friendly method for using diuron.
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spelling pubmed-67808092019-10-30 Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin Gao, Shuang Jiang, Jing-Yu Liu, Yan-Yan Fu, Ying Zhao, Li-Xia Li, Chun-Yan Ye, Fei Polymers (Basel) Article The herbicide diuron is hardly soluble in water and most organic solvents and is usually made into a wettable powder or mixed with soil when used, which causes environmental risk and a reduction in herbicidal efficacy. In this study, the physicochemical properties were changed by using β-cyclodextrin (β-CD) to encapsulate diuron to form an inclusion complex. Some key technologies, including X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and nuclear magnetic resonance ((1)H NMR), were used to characterize the inclusion complex. The stoichiometry of the inclusion complex was determined by recording the (1)H NMR spectrum or by using a diagram of inclusion ratios. A phase solubility study proved that the formed inclusion complex exhibited higher water solubility. Thermogravimetric analysis (TGA) demonstrated that the formed inclusion complex exhibited better thermal stability. Biological activity studies indicated that the herbicidal activity, in terms of herbicide removal, of the formed inclusion complex was higher than that of the original diuron. In general, the formation of the inclusion complex could reduce the environmental damage caused by diuron and enhance its herbicidal activity, providing an environmentally friendly method for using diuron. MDPI 2019-08-25 /pmc/articles/PMC6780809/ /pubmed/31450656 http://dx.doi.org/10.3390/polym11091396 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gao, Shuang
Jiang, Jing-Yu
Liu, Yan-Yan
Fu, Ying
Zhao, Li-Xia
Li, Chun-Yan
Ye, Fei
Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin
title Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin
title_full Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin
title_fullStr Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin
title_full_unstemmed Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin
title_short Enhanced Solubility, Stability, and Herbicidal Activity of the Herbicide Diuron by Complex Formation with β-Cyclodextrin
title_sort enhanced solubility, stability, and herbicidal activity of the herbicide diuron by complex formation with β-cyclodextrin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780809/
https://www.ncbi.nlm.nih.gov/pubmed/31450656
http://dx.doi.org/10.3390/polym11091396
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