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Investigation of Lysine-Functionalized Dendrimers as Dichlorvos Detoxification Agents. | LitMetric

Investigation of Lysine-Functionalized Dendrimers as Dichlorvos Detoxification Agents.

Biomacromolecules

Laboratory of Asymmetric Synthesis, Chemistry Institute of Natural Resources; Nanobiotechnology Division at University of Talca, Fraunhofer Chile Research Foundation - Center for Systems Biotechnology, FCR-CSB, Talca University, P.O. Box 747, Talca, Chile.

Published: November 2015

AI Article Synopsis

  • Lysine-containing polymers are versatile due to their ability to bind biologically relevant molecules, and this report details the synthesis of polyester dendrimers with lysine groups.
  • The study investigates their stability over time and different pH levels, their toxicity to various cell lines, and their potential as nano-detoxification agents for organophosphate compounds.
  • The dendrimers, designed with 4, 8, and 16 lysine groups, show promise for applications in drug delivery, gene delivery, and removing organic toxins, notably demonstrating effectiveness in capturing the pesticide dichlorvos.

Article Abstract

Lysine-containing polymers have seen broad application due to their amines' inherent ability to bind to a range of biologically relevant molecules. The synthesis of multiple generations of polyester dendrimers bearing lysine groups on their periphery is described in this report. Their hydrolytic stabilities with respect to pH and time, their toxicity to a range of cell lines, and their possible application as nano-detoxification agents of organophosphate compounds are all investigated. These zeroth-, first-, and second-generation water-soluble dendrimers have been designed to bear exactly 4, 8, and 16 lysine groups, respectively, on their dendritic periphery. Such monodisperse bioactive polymers show potential for a range of applications including drug delivery, gene delivery, heavy metal binding, and the sequestration of organic toxins. These monodisperse bioactive dendrimers were synthesized using an aliphatic ester dendritic core (prepared from pentaerythritol) and protected amino acid moieties. This library of lysine-conjugated dendrimers showed the ability to efficiently capture the pesticide dichlorvos, confirming the potential of dendrimer-based antidotes to maintain acetylcholinesterase activity in response to poisoning events.

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Source
http://dx.doi.org/10.1021/acs.biomac.5b00657DOI Listing

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