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用于近红外荧光成像应用的新型靶向FAP的七甲川花菁

Novel FAP-Targeted Heptamethine Cyanines for NIRF Imaging Applications.

作者信息

Rizzo Rebecca, Capozza Martina, Conti Laura, Avalle Lidia, Poli Valeria, Terreno Enzo

机构信息

Department of Molecular Biotechnology and Health Sciences, University of Turin, Piazza Nizza 44/bis, Turin 10126, Italy.

DISIT, University of Eastern Piedmont, Viale Teresa Michel 11, Alessandria 15121, Italy.

出版信息

Mol Pharm. 2025 Mar 3;22(3):1518-1528. doi: 10.1021/acs.molpharmaceut.4c01232. Epub 2025 Feb 15.

Abstract

Fibroblast activation protein (FAP) is a pan-cancer target that is useful for imaging, ideally all epithelial cancers. This work aimed to develop, characterize, and validate two novel FAP-targeted probes for optical imaging, both in and . IRDye800CW and FNIRTag heptamethine cyanines were conjugated to the NH precursor of the well-known FAP inhibitor FAPI-46, which is widely employed in nuclear medicine. In addition to synthesis, the dyes were characterized in terms of physicochemical properties, biodistribution, and imaging performances in a breast cancer tumor model. FAPI-FNIRTag showed a stronger fluorescence and higher photostability compared to FAPI-IRDye800CW. Notably, both compounds exhibited strong tumor accumulation in TUBO breast cancer-bearing mice 24 h postadministration, suggesting potential for further investigation as fluorescence-guided surgery (FGS) agents.

摘要

成纤维细胞活化蛋白(FAP)是一种泛癌靶点,对成像很有用,理想情况下适用于所有上皮癌。这项工作旨在开发、表征和验证两种用于光学成像的新型FAP靶向探针,包括体内和体外研究。IRDye800CW和FNIRTag七甲川花菁与核医学中广泛使用的著名FAP抑制剂FAPI-46的NH前体偶联。除了合成外,还对染料的物理化学性质、生物分布和在乳腺癌肿瘤模型中的成像性能进行了表征。与FAPI-IRDye800CW相比,FAPI-FNIRTag显示出更强的荧光和更高的光稳定性。值得注意的是,两种化合物在给药后24小时在荷TUBO乳腺癌小鼠中均表现出强烈的肿瘤蓄积,表明它们作为荧光引导手术(FGS)试剂具有进一步研究的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e32d/11881144/cb82ef523062/mp4c01232_0001.jpg

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