A near-infrared fluorescent heptamethine indocyanine dye with preferential tumor accumulation for in vivo imaging

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• 作者：Chao Zhang ; Tao Liu ; Yongping Su ; Shenglin Luo ; Ying Zhu ; Xu Tan ; Song Fan ; Lilong Zhang ; Yue Zhou ; Tianmin Cheng ; Chunmeng Shi
• 关键词：In vivo test ; Fluorescence ; Tumor targeting ; Heptamethine dye
• 刊名：Biomaterials
• 出版年：2010
• 出版时间：September 2010
• 年：2010
• 卷：31
• 期：25
• 页码：6612-6617
• 全文大小：1019 K

文摘

Near-infrared (NIR) fluorescence imaging holds great promise for tumor imaging due to low tissue autofluorescence and deep tissue penetration. However, most tumor-targeting fluorescent probes require combination of targeting agents and fluorescent reporters. In this study, we described a NIR heptamethine cyanine dye, IR-780 iodide, with preferential accumulation in multiple tumor cells without the necessity of chemical conjugation. The IR-780 iodide was found to retain in tumors but not normal cells in multiple tumor xenografts in nude mice and chemically-induced lung tumors in C57BL/6 mice. The fluorescent signal of tumors could persist at least 20 days with a significant signal-to-backgroud ratio. As a lipophilic cation, a predominant accumulation of IR-780 iodide was shown in the mitochondria of tumor cells owing to the high magnitude of mitochondrial membrane potential in tumor cells than normal cells. We further showed that the transportation of IR-780 iodide into tumor cells was mediated by the organic anion transporter peptides (OATPs) because the dye accumulation was significantly inhibited by sulfobromophthalein (BSP), a competitive inhibitor of OATPs. Our study shows that IR-780 iodide that preferentially accumulates in tumor cells and is natively NIR fluorescent would be useful in tumor detection.