Beilstein J. Org. Chem.2017,13, 417–427, doi:10.3762/bjoc.13.45
of the agents. The degradation efficiency was found to be dependent on the relative position of the heterocycle towards the reactive group as well as on the nature of the organophosphorus derivative.
Keywords: cyclodextrin; decontamination; enzyme mimic; nerve agents; organophosphoruspesticides
hydrophobic molecules. In particular, these macromolecular structures display the interesting capability to include organophosphoruspesticides into their cavity [13][14][15][16][17]. However, their intrinsic ability to transform these compounds into low or non-toxic metabolites at physiological pH is weak
soman and organophosphoruspesticides having an aromatic group were not hydrolyzed with the same efficiency by the scavengers. In fact, this efficiency is highly substrate-dependent and it is difficult to strictly correlate the hydrolysis profiles to the cyclodextrin structures of the prepared
Beilstein J. Org. Chem.2016,12, 204–228, doi:10.3762/bjoc.12.23
on the current use of cyclodextrins against organophosphorus compound intoxications. Organophosphoruspesticides and nerve agents play a determinant role in the inhibition of cholinesterases. The cyclic structure of cyclodextrins and their toroidal shape are perfectly suitable to design new chemical
potential immunogenic risks associated to proteins such as hydrolases [37].
This review focuses on the various aspects of the detoxification process mediated by CD derivatives: (1) the ability of CDs and their derivatives to form inclusion complexes with organophosphoruspesticides and G nerve agents; (2
guest might weaken the hydration water binding, as revealed in DSC experiments by the lower endothermic fusion peak, specific to a dehydration process. X-ray powder diffraction analysis finally confirmed the complex formation.
All these studies proved that organophosphoruspesticides are able to