Target intelligence / Profile preview

Plutonium-239 ion (Pu-239)

Target
Pu-239
Molecular classification
Other (Radionuclide), Other (Actinide), Other (Heavy metal)
01

Overview

Plutonium-239 is a radioactive isotope of the actinide element plutonium, primarily known for its use in nuclear weapons and reactors. In a biological context, it is a potent toxicant and carcinogen rather than a physiological target like a receptor or enzyme (ATSDR, 2010). Once internalized via inhalation, ingestion, or wound contamination, plutonium-239 ions tend to deposit in the skeleton and liver (CDC, 2014). These ions emit high-energy alpha particles that cause significant DNA damage and increase the risk of cancers such as osteosarcoma and liver cancer (IARC, 2012). Because of its long biological half-life and high radiotoxicity, medical intervention focuses on decorporation therapy. This is achieved using chelating agents like Ca-DTPA and Zn-DTPA, which facilitate the mobilization and renal excretion of the plutonium ions (FDA, 2004). The chemical behavior of plutonium in the body often mimics that of iron, allowing it to be transported by transferrin to various tissues. Management of exposure is a critical concern in nuclear medicine and occupational safety.

Other names
Plutonium-239239PuPu-239 ion
02

Mechanism of action

Chelation therapy: Chelating agents like DTPA bind to the plutonium ion to form a stable, water-soluble complex that is excreted by the kidneys (FDA, 2004).

03

Biological functions

Other (Xenobiotic toxicant)
04

Disease associations

CancerOther (Radiation sickness)Other (Osteosarcoma)Other (Liver cancer)
05

Safety considerations

Alpha radiation-induced DNA damageLong-term retention in bone and liverPotential nephrotoxicity of chelating agents
06

Interacting drugs

Pentetate calcium trisodium (Ca-DTPA)

1 more in the full profile.

07

Biomarkers

Urinary plutonium concentrationFecal plutonium concentrationWhole-body counting

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