Gold Coated Lanthanide Phosphate Nanoparticles for Targeted Alpha Generator Radiotherapy
Покрытые золотом наночастицы фосфатов лантаноидов для таргетной альфа-генераторной радиотерапии
2013-01-18
SCID: 54.1/eqe2q3ns
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actinium-225lanthanide phosphate nanoparticlesmultilayered nanoparticle-antibody conjugateradioactive daughter containmenttargeted alpha radiotherapy
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Abstract (AI)
Targeted radiotherapies maximize cytotoxicty to cancer cells. In vivo α-generator targeted radiotherapies can deliver multiple α particles to a receptor site dramatically amplifying the radiation dose delivered to the target. The major challenge with α-generator radiotherapies is that traditional chelating moieties are unable to sequester the radioactive daughters in the bioconjugate which is critical to minimize toxicity to healthy, non-target tissue. The recoil energy of the (225)Ac daughters following α decay will sever any metal-ligand bond used to form the bioconjugate. This work demonstrates that an engineered multilayered nanoparticle-antibody conjugate can deliver multiple α radiations and contain the decay daughters of (225)Ac while targeting biologically relevant receptors in a female BALB/c mouse model. These multi-shell nanoparticles combine the radiation resistance of lanthanide phosphate to contain (225)Ac and its radioactive decay daughters, the magnetic properties of gadolinium phosphate for easy separation, and established gold chemistry for attachment of targeting moieties.
Key Findings
1
An engineered multilayered nanoparticle–antibody conjugate delivered multiple alpha particles to biologically relevant receptors in female BALB/c mice.
2
Gadolinium phosphate incorporated magnetic properties enabling easier nanoparticle separation, while gold chemistry enabled attachment of targeting moieties.
3
Radiation-resistant lanthanide phosphate shells provided containment of 225Ac and decay daughters within the targeted radiotherapy construct.
4
The nanoparticle system contained 225Ac and its radioactive decay daughters, addressing daughter radionuclide escape caused by alpha-decay recoil.
5
The platform was designed to reduce radiation toxicity to healthy, non-target tissues by retaining radioactive daughters within the bioconjugate.
Research Object
Engineered multilayered lanthanide phosphate–gold nanoparticle–antibody conjugates containing 225Ac and its radioactive decay daughters in a female BALB/c mouse model
Research Subject
Targeted alpha-generator radiotherapy performance, including delivery of multiple alpha particles to biologically relevant receptors and sequestration of 225Ac decay daughters to limit off-target toxicity
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2013-01-18
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