skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: From early prophylaxis to delayed treatment: Establishing the plutonium decorporation activity window of hydroxypyridinonate chelating agents

Journal Article · · Chemico-Biological Interactions
 [1];  [1];  [1];  [1]
  1. Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Chemical Sciences Division

The potential consequences of a major radiological event are not only large-scale external radiation exposure of the population, but also uncontrolled dissemination of, and internal contamination with, radionuclides. When planning an emergency response to radiological and nuclear incidents, one must consider the need for not only post-exposure treatment for contaminated individuals, but also prophylactic measures to protect the workforce facing contaminated areas and patients in the aftermath of such events. In addition to meeting the desired criteria for post-exposure treatments such as safety, ease of administration, and broad-spectrum efficacy against multiple radionuclides and levels of challenge, ideal prophylactic countermeasures must include rapid onset; induce minimal to no performance-decrementing side effects; be compatible with current military Chemical, Biological, Radiological, Nuclear, and Explosive countermeasures; and require minimal logistical burdens. Hydroxypyridinone-based actinide decorporation agents have shown the most promise as decorporation strategies for various radionuclides of concern, including the actinides plutonium and americium. The studies here probe the extent of plutonium decorporation efficacy for two chelating agents, 3,4,3-LI(1,2-HOPO) and 5-LIO(Me-3,2-HOPO), from early pre-exposure time points to a delay of up to 7 days in parenteral or oral treatment administration, i.e., well beyond the initial hours of emergency response. Despite delayed treatment after a contamination event, both ligands clearly enhanced plutonium elimination through the investigated 7-day post-treatment period. In addition, a remarkable prophylactic efficacy was revealed for 3,4,3-LI(1,2-HOPO) with treatment as early as 48 h before the plutonium challenge. This work provides new perspectives in the indication and use of experimental actinide decorporation treatments.

Research Organization:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
SC-22.1 USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22). Chemical Sciences, Geosciences & Biosciences Division; National Institutes of Health (NIH)
Grant/Contract Number:
AC02-05CH11231; RAI087604Z
OSTI ID:
1458488
Alternate ID(s):
OSTI ID: 1397624
Journal Information:
Chemico-Biological Interactions, Vol. 267, Issue C; Related Information: © 2016 Elsevier Ireland Ltd; ISSN 0009-2797
Publisher:
ElsevierCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 25 works
Citation information provided by
Web of Science

References (19)

A Public Health Perspective on the U.S. Response to the Fukushima Radiological Emergency journal January 2015
Radiation Drugs-A Hot Topic: Radiation Drugs journal August 2012
Use of DTPA for Increasing the Rate of Elimination of Plutonium-238 and Americium-241 from Rodents after their Inhalation as the Nitrates journal November 1985
Medical Countermeasures against Nuclear Threats: Radionuclide Decorporation Agents journal October 2008
Treatment of human contamination with plutonium and americium: would orally administered Ca- or Zn-DTPA be effective? journal June 2007
Treatment of actinide exposures: a review of Ca-DTPA injections inside CEA-COGEMA plants journal June 2007
Action of DTPA on Hepatic Plutonium: III. Evidence for a Direct Chelation Mechanism for DTPA-Induced Excretion of Monomeric Plutonium into Rat Bile journal October 1979
238 Pu elimination profiles after delayed treatment with 3,4,3LI(1,2HOPO) in female and male Swiss-Webster mice journal August 2014
Lauriston s. Taylor Lecture: the Quest for Therapeutic Actinide Chelators journal January 2008
Actinide chelation: biodistribution and in vivo complex stability of the targeted metal ions journal October 2012
Biomimetic Actinide Chelators: an Update on the Preclinical Development of the Orally Active Hydroxypyridonate Decorporation Agents 3,4,3-Li(1,2-Hopo) and 5-Lio(Me-3,2-Hopo) journal January 2010
Significance of Single Variables in Defining Adequate Animal Models to Assess the Efficacy of New Radionuclide Decorporation Agents: Using the Contamination Dose as an Example: Animal Models for Chelating Agents Efficacy journal August 2012
Dose-Dependent Efficacy and Safety Toxicology of Hydroxypyridinonate Actinide Decorporation Agents in Rodents: Towards a Safe and Effective Human Dosing Regimen journal February 2013
Gross Composition and Plasma and Extracellular Water Volumes of Tissues of a Reference Mouse journal January 1992
Structure of a Single Model to Describe Plutonium and Americium Decorporation by dtpa Treatments journal January 2010
Biodistribution of the Multidentate Hydroxypyridinonate Ligand [ 14 C]-3,4,3-LI(1,2-HOPO), a Potent Actinide Decorporation Agent : BIODISTRIBUTION OF 3,4,3-LI(1,2-HOPO) journal April 2015
In Vitro Metabolism and Stability of the Actinide Chelating Agent 3,4,3-LI(1,2-HOPO) journal May 2015
Simplified Structure of a New Model to Describe Urinary Excretion of Plutonium after Systemic, Liver or Pulmonary Contamination of Rats Associated with Ca-DTPA Treatments journal June 2009
Development of the Plutonium-DTPA Biokinetic Model journal January 2015

Cited By (3)

Simple measurement of actinides in urine using solid-state scintillation journal July 2019
Evaluating the potential of chelation therapy to prevent and treat gadolinium deposition from MRI contrast agents journal March 2018
Multiple Patients With Burn Injury Induced by a Chemical Explosion Managed by Physician-Staffed Helicopters journal January 2019

Figures / Tables (5)