Actinium-225 for Targeted α Therapy: Coordination Chemistry and Current Chelation Approaches

被引:119
作者
Thiele, Nikki A. [1 ]
Wilson, Justin J. [1 ]
机构
[1] Cornell Univ, Dept Chem & Chem Biol, Ithaca, NY USA
关键词
actinides; actinium-225; coordination chemistry; macrocyclic ligands; radiopharmaceuticals; targeted alpha therapy; RESISTANT PROSTATE-CANCER; PARAMETRIC CORRELATION; STABILITY-CONSTANTS; PARTICLE THERAPY; AQUEOUS-SOLUTION; AC-225; LIGANDS; IONS; RADIOIMMUNOTHERAPY; COMPLEXES;
D O I
10.1089/cbr.2018.2494
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The alpha-emitting radionuclide actinium-225 possesses nuclear properties that are highly promising for use in targeted alpha therapy (TAT), a therapeutic strategy that employs alpha particle emissions to destroy tumors. A key factor, however, that may hinder the clinical use of actinium-225 is the poor understanding of its coordination chemistry, which creates challenges for the development of suitable chelation strategies for this ion. In this article, we provide an overview of the known chemistry of actinium and a summary of the chelating agents that have been explored for use in actinium-225-based TAT. This overview provides a starting point for researchers in the field of TAT to gain an understanding of this valuable therapeutic radionuclide.
引用
收藏
页码:336 / 348
页数:13
相关论文
共 111 条
  • [11] The influence of EDTMP-concentration on the biodistribution of radio-lanthanides and 225-Ac in tumor-bearing mice
    Beyer, GJ
    Offord, R
    Kunzi, G
    Aleksandrova, Y
    Ravn, U
    Jahn, S
    Barker, J
    Tengblad, O
    Lindroos, M
    [J]. NUCLEAR MEDICINE AND BIOLOGY, 1997, 24 (05) : 367 - 372
  • [12] Production of actinium-225 for alpha particle mediated radioimmunotherapy
    Boll, RA
    Malkemus, D
    Mirzadeh, S
    [J]. APPLIED RADIATION AND ISOTOPES, 2005, 62 (05) : 667 - 679
  • [13] Borchardt PE, 2003, CANCER RES, V63, P5084
  • [14] Water soluble diaza crown ether derivative: Synthesis and barium complexation studies
    Boubekeur-Lecaque, Leila
    Souffrin, Clement
    Gontard, Geoffrey
    Boubekeur, Kamal
    Amatore, Christian
    [J]. POLYHEDRON, 2014, 68 : 191 - 198
  • [15] ACTINIDE THERMODYNAMIC PREDICTIONS .3. THERMODYNAMICS OF COMPOUNDS AND AQUO IONS OF THE 2+, 3+, AND 4+ OXIDATION-STATES AND STANDARD ELECTRODE-POTENTIALS AT 298.15 K
    BRATSCH, SG
    LAGOWSKI, JJ
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1986, 90 (02) : 307 - 312
  • [16] Density functional theory studies of actinide(III) motexafins (An-Motex2+, An = Ac, Cm, Lr).: Structure, stability, and comparison with lanthanide(III) motexafins
    Cao, XY
    Li, QS
    Moritz, A
    Xie, ZZ
    Dolg, M
    Chen, XB
    Fang, WH
    [J]. INORGANIC CHEMISTRY, 2006, 45 (08) : 3444 - 3451
  • [17] Functionalized TiO2 nanoparticles labelled with 225Ac for targeted alpha radionuclide therapy
    Cedrowska, Edyta
    Pruszynski, Marek
    Majkowska-Pilip, Agnieszka
    Meczynska-Wielgosz, Sylwia
    Bruchertseifer, Frank
    Morgenstern, Alfred
    Bilewicz, Aleksander
    [J]. JOURNAL OF NANOPARTICLE RESEARCH, 2018, 20 (03)
  • [18] Synthesis, conjugation, and radiolabeling of a novel bifunctional chelating agent for 225Ac radioimmunotherapy applications
    Chappell, LL
    Deal, KA
    Dadachova, E
    Brechbiel, MW
    [J]. BIOCONJUGATE CHEMISTRY, 2000, 11 (04) : 510 - 519
  • [19] Chen XY, 1999, SYNLETT, P1784
  • [20] Carboxylate-derived calixarenes with high selectivity for actinium-225
    Chen, XY
    Ji, M
    Fisher, DR
    Wai, CM
    [J]. CHEMICAL COMMUNICATIONS, 1998, (03) : 377 - 378