Results 11 to 20 of about 119,061 (97)
Coded aperture and Compton imaging for the development of 225 Ac-based radiopharmaceuticals. [PDF]
BACKGROUND Targeted alpha-particle therapy (TAT) has great promise as a cancer treatment. Arguably the most promising TAT radionuclide that has been proposed is 225 Ac.
E. Frame +6 more
semanticscholar +1 more source
Background: Actinium-225 (Ac-225) labelled PSMA RLT has been tested recently in metastatic castration-resistant prostate cancer (mCRPC), with encouraging results.
G. Parida +3 more
semanticscholar +1 more source
Overexpression of somatostatin receptors (SSTRs), particularly SSTR2, is found in gastroenteropancreatic neuroendocrine tumors (GEP-NETs), and subsets of other solid tumors such as small cell lung cancer (SCLC). SCLC accounts for approximately 13%-15% of
Guangzhou Han +8 more
semanticscholar +1 more source
Actinium-225 production with an electron accelerator [PDF]
There has been growing clinical evidence of the value of targeted alpha therapy for the treatment of several cancers. The work has been slowed by the lack of availability of the key alpha emitting isotopes, especially Ac-225.
W. Diamond, C. Ross
semanticscholar +1 more source
Recent Innovations and Nano-Delivery of Actinium-225: A Narrative Review
The actinium-225 (225Ac) radioisotope exhibits highly attractive nuclear properties for application in radionuclide therapy. However, the 225Ac radionuclide presents multiple daughter nuclides in its decay chain, which can escape the targeted site ...
Sipho Mdanda +4 more
semanticscholar +1 more source
PURPOSE The anti-CD33 antibody lintuzumab has modest activity against acute myeloid leukemia (AML). To increase its potency, lintuzumab was conjugated to actinium-225 (225Ac), a radionuclide yielding 4 α-particles.
T. Rosenblat +11 more
semanticscholar +1 more source
In vitro dose effect relationships of actinium-225- and lutetium-177-labeled PSMA-I&T
Targeting the prostate-specific membrane antigen (PSMA) using lutetium-177-labeled PSMA-specific tracers has become a very promising novel therapy option for prostate cancer (PCa). The efficacy of this therapy might be further improved by replacing the β-
E. Ruigrok +9 more
semanticscholar +1 more source
Peptide receptor radionuclide therapy (PRRT) has over the last two decades emerged as a very promising approach to treat neuroendocrine tumors (NETs) with rapidly expanding clinical applications. By chelating a radiometal to a somatostatin receptor (SSTR)
Mengqi Shi +6 more
semanticscholar +1 more source
Comparison of PSMA-TO-1 and PSMA-617 labeled with gallium-68, lutetium-177 and actinium-225
Background PSMA-TO-1 (“Tumor-Optimized-1”) is a novel PSMA ligand with longer circulation time than PSMA-617. We compared the biodistribution in subcutaneous tumor-bearing mice of PSMA-TO-1, PSMA-617 and PSMA-11 when labeled with 68 Ga and 177 Lu, and ...
C. Meyer +14 more
semanticscholar +1 more source
Rationale: Small 225Ac-labeled prostate-specific membrane antigen (PSMA)-targeted radioconjugates have been described for targeted alpha therapy of metastatic castration-resistant prostate cancer.
F. Reissig +13 more
semanticscholar +1 more source

