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Cyclodextrins and Their Complexes: Chemistry, Analytical Methods, Applications
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The ability of cyclodextrins, CyDs, to form inclusion complexes with a wide variety of hydrophobic guest molecules has been used in agriculture.Their ability to alter the physical, chemical, and biological properties of guest molecules has been used for the preparation of new formulations of pesticides.CyDs form complexes with a wide variety of agricultural chemicals including herbicides, insecticides, fungicides, repellents, pheromones, and growth regulators [1,2].Each CyD has its own ability to form inclusion complexes with specific pesticides, depending on a proper fit of the pesticide molecule into the hydrophobic CyD cavity.The principal advantage is that the binding of pesticide molecules within the host molecule is not fixed or permanent but rather is a dynamic equilibrium.Dissociation of the inclusion complex is a relatively rapid process usually driven by a large increase in the number of water molecules in the surrounding environment [3].aAQ16.3.1aSimilarly to CyD applications in the pharmaceutical (Chapters 14 and 15) and other industries, the most common benefits of CyD applications in agriculture include, among others, alterations of the solubility of the pesticide, stabilization against the effects of light or biochemical degradation, and a reduction of volatility.In some applications, more than one benefit is obtained by complexation with CyDs.However, the application of these hosts in pesticide formulations is very modest, and represents less than 1% of the CyD literature [4].Moreover, most of these publications are not directly practice oriented.Instead they deal with the preparation of pesticides@CyD complexes using different oligosaccharides and processing methods and their characterization using a wide variety of techniques.Among these papers, some are more or less theoretical papers dealing with the correlation between the properties of the new complexes obtained and the properties of the CyDs, pesticides, or external parameters used.Viernstein et al.
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Comprehensive supramolecular chemistry
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American society for testing and materials
Mather, B., & Etris, S. F. (2006) · Encyclopedia of Earth Science · doi:10.1007/0-387-30720-6_5 · Cited by 5,558
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Cyclodextrins as pharmaceutical solubilizers
Brewster, M. E., & Loftsson, T. (2007) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2007.05.012 · Cited by 1,882
Fluorescent Dyes and Their Supramolecular Host/Guest Complexes with Macrocycles in Aqueous Solution
Dsouza, R. N., Pischel, U., & Nau, W. M. (2011) · Chemical Reviews · doi:10.1021/cr200213s · Cited by 1,117
A review on the use of cyclodextrins in foods
Astray, G., Gonzalez-Barreiro, C., Mejuto, J. C., Rial-Otero, R., & Simal-Gándara, J. (2009) · Food Hydrocolloids · doi:10.1016/j.foodhyd.2009.01.001 · Cited by 911
Structure, Energy, Synergy, Time—The Fundamentals of Process Intensification
Van Gerven, T., & Stankiewicz, A. (2009) · Industrial & Engineering Chemistry Research · doi:10.1021/ie801501y · Cited by 600
Environmental applications of water-insoluble β-cyclodextrin–epichlorohydrin polymers
Morin-Crini, N., & Crini, G. (2013) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2012.06.005 · Cited by 434
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- Wiley eBooks
- Publisher
- Wiley
- Published
- 2006-05-22
- OpenAlex
- W1916802147
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- 728
- References
- 2
- FWCI
- 15.93
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- book
- Language
- en
- Open access
- green
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