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Related Concept Videos

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Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
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In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
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Direct-acting cholinergic agonists, such as synthetic choline esters and naturally occurring alkaloids, exert their effects by enhancing the actions of acetylcholine and stimulating the parasympathetic nervous system. Synthetic choline esters share structural similarities with acetylcholine. For example, they have a positively charged quaternary ammonium or onium group, contributing to their hydrophilic characteristics. As a result, they are poorly absorbed in the body through oral...
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Related Experiment Video

Updated: Sep 22, 2025

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Amidoxime functionalized chitosan for uranium sequestration in vivo.

Zhiheng Li1, Siyi Wang2, Yipu Dong3

  • 1Department of Pharmaceutical Science, Beijing Institute of Radiation Medicine, Beijing 100850, China.

Ecotoxicology and Environmental Safety
|May 19, 2022
PubMed
Summary

Amidoxime functionalized chitosan (AC) effectively removes uranium in vivo, outperforming commercial drugs. This biocompatible chelator reduces uranium in kidneys and femurs, even when administered hours later.

Keywords:
AmidoximeChitosanSequestrationStructure-activity relationshipUranium

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Area of Science:

  • Biomaterials Science
  • Toxicology
  • Radiochemistry

Background:

  • Uranium contamination poses significant health risks.
  • Effective in vivo uranium chelation therapy is crucial for mitigating toxicity.
  • Chitosan derivatives show promise as biocompatible chelating agents.

Purpose of the Study:

  • To evaluate amidoxime functionalized chitosan (AC) as a chelator for in vivo uranium sequestration.
  • To explore the structure-activity relationship of AC in uranium removal.
  • To compare the efficacy and biocompatibility of AC with ZnNa3-DTPA.

Main Methods:

  • In vivo administration of amidoxime functionalized chitosan (AC) to assess uranium removal.
  • Comparison of AC with ZnNa3-DTPA (a commercial uranium mobilization drug).
  • Quantification of uranium deposition in kidneys and femurs post-treatment.

Main Results:

  • AC demonstrated excellent biocompatibility and high uranium removal efficiency via injection and oral administration.
  • AC reduced uranium deposition in kidneys by up to 43.6% and in femurs by up to 32.3%.
  • AC retained significant uranium mobilization capacity even when administered 72 hours post-exposure.

Conclusions:

  • Amidoxime functionalized chitosan (AC) is a promising biocompatible chelator for in vivo uranium sequestration.
  • AC offers a potentially superior alternative to existing uranium mobilization therapies.
  • Delayed administration of AC remains effective, offering therapeutic flexibility.