Synthesis and Preclinical Evaluation of Folate-NOTA-Al18F for PET Imaging of Folate-Receptor-Positive Tumors

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• 作者：Qingshou Chen ; Xiangjun Meng ; Paul McQuade ; Daniel Rubins ; Shu-An Lin ; Zhizhen Zeng ; Hyking Haley ; Patricia Miller ; Dinko González Trotter ; Philip S. Low
• 刊名：Molecular Pharmaceutics
• 出版年：2016
• 出版时间：May 2, 2016
• 年：2016
• 卷：13
• 期：5
• 页码：1520-1527
• 全文大小：437K
• 年卷期：0
• ISSN：1543-8392

文摘

Folate-receptor-targeted PET radiotracers can potentially serve as versatile imaging agents for the diagnosis, staging, and prediction of response to therapy of patients with folate-receptor (FR)-expressing cancers. Because current FR-targeted PET reagents can be compromised by complex labeling procedures, low specific activities, poor radiochemical yields, or unwanted accumulation in FR negative tissues, we have undertaken to design an improved folate-PET agent that might be more amenable for clinical development. For this purpose, we have synthesized a folate-NOTA-Al¹⁸F radiotracer and examined its properties both in vitro and in vivo. Methods: Radiochemical synthesis of folate-NOTA-Al¹⁸F was achieved by incubating ¹⁸F^– with AlCl₃ for 2 min followed by heating in the presence of folate-NOTA for 15 min at 100 °C. Binding of folate-NOTA-Al¹⁸F to FR was quantitated in homogenates of KB and Cal51 tumor xenografts in the presence and absence of excess folic acid as a competitor. In vivo imaging was performed on nu/nu mice bearing either FR+ve (KB cell) or FR-ve (A549 cell) tumor xenografts, and specific accumulation of the radiotracer in tumor and other tissues was assessed by high-resolution micro-PET and ex vivo biodistribution in the presence and absence of excess folic acid. Image quality of folate-NOTA-Al¹⁸F was compared with that of ^99mTc-EC20, a clinically established folate-targeted SPECT imaging agent. Results: Total radiochemical synthesis and purification of folate-NOTA-Al¹⁸F was completed within 37 min, yielding a specific activity of 68.82 ± 18.5 GBq/μmol, radiochemical yield of 18.6 ± 4.5%, and radiochemical purity of 98.3 ± 2.9%. Analysis of FR binding revealed a K_d of ∼1.0 nM, and micro-PET imaging together with ex vivo biodistribution analyses demonstrated high FR-mediated uptake in an FR+ tumor and the kidneys. Conclusions: Folate-NOTA-Al¹⁸F constitutes an easily prepared FR-targeted PET imaging agent with improved radiopharmaceutical properties and high specificity for folate receptor expressing tumors. Given its improved properties over ^99mTc-EC20 (i.e., higher resolution, shorter image acquisition time, etc.), we conclude that folate-NOTA-Al¹⁸F constitutes a viable alternative to ^99mTc-EC20 for use in identification, diagnosis, and staging of patients with FR-expressing cancers.