Synthesis and Characterization of 89Zr-Labeled Ultrasmall Nanoparticles

被引:23
|
作者
Truillet, Charles [1 ]
Thomas, Eloise [2 ]
Lux, Francois [2 ]
Huynh, Loc T. [1 ]
Tillement, Olivier [2 ]
Evans, Michael J. [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, 185 Berry St,Lobby 6,Suite 350, San Francisco, CA 94107 USA
[2] Univ Lyon 1, CNRS, Inst Lumiere Matiere, UMR5306, F-69622 Villeurbanne, France
基金
美国国家卫生研究院;
关键词
AGuIX; nanoparticle; positron emission tomography; cancer; GADOLINIUM-BASED NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; PET; CANCER; MRI; BIODISTRIBUTION; PARTICLES; TUMORS;
D O I
10.1021/acs.molpharmaceut.6b00264
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The ultrasmall nanoparticle AGuIX is a versatile platform that tolerates a range of chemical diversity for theranostic applications. Our previous work showed that AGuIX clears rapidly from normal tissues, while durably accumulating within the tumor microenvironment. On this basis, AGuIX was used to detect tumor tissue with Gd3+ enhanced MRI and can sensitize tumors to radiation therapy. As we begin the translation of AGuIX, we appreciated that coupling AGuIX to a long-lived radioisotope would help to more completely measure the magnitude and duration of its retention within the tumor microenvironment. Therefore, we developed Zr-89-DFO-AGuIX. AGuIX was coupled to DFO and then to Zr-89 in similar to 99% radiochemical yield. Stability studies showed that Zr-89-DFO-AGuIX did not dissociate after 72 h. In animals bearing U87MG xenografts, it was detectable at levels above background for 72 h. Lastly, Zr-89-DFO-AGuIX did not accumulate in inflammatory abscesses in vivo, highlighting its specificity for well vascularized tumors.
引用
收藏
页码:2596 / 2601
页数:6
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