Temma Takashi, Onoe Satoru, Kanazaki Kengo, Ono Masahiro, Saji Hideo
Kyoto University, Graduate School of Pharmaceutical Sciences, Department of Patho-Functional Bioanalysis, 46-29 Yoshida Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Kyoto University, Graduate School of Pharmaceutical Sciences, Department of Patho-Functional Bioanalysis, 46-29 Yoshida Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501, JapanbCanon Inc., Medical Imaging Project, Corporate R&D Headquarters, 3-30-2 Shimomaruko, O.
J Biomed Opt. 2014 Sep;19(9):090501. doi: 10.1117/1.JBO.19.9.090501.
Photoacoustic imaging (PA imaging or PAI) has shown great promise in the detection and monitoring of cancer. Although nanocarrier-based contrast agents have been studied for use in PAI, small molecule contrast agents are required due to their ease of preparation, costeffectiveness, and low toxicity. Here, we evaluated the usefulness of a novel cyanine dye IC7-1-Bu as a PAI contrast agent without conjugated targeting moieties for in vivo tumor imaging in a mice model. Basic PA characteristics of IC7-1-Bu were compared with indocyanine green (ICG), a Food and Drug Administration approved dye, in an aqueous solution. We evaluated the tumor accumulation profile of IC7-1-Bu and ICG by in vivo fluorescence imaging. In vivo PAI was then performed with a photoacoustic tomography system 24 and 48 h after intravenous injection of IC7-1-Bu into tumor bearing mice. IC7-1-Bu showed about a 2.3-fold higher PA signal in aqueous solution compared with that of ICG. Unlike ICG, IC7-1-Bu showed high tumor fluorescence after intravenous injection. In vivo PAI provided a tumor to background PA signal ratio of approximately 2.5 after intravenous injection of IC7-1-Bu. These results indicate that IC7-1-Bu is a promising PAI contrast agent for cancer imaging without conjugation of targeting moieties.
光声成像(PA成像或PAI)在癌症检测和监测方面显示出巨大的潜力。尽管基于纳米载体的造影剂已被研究用于PAI,但由于小分子造影剂易于制备、成本效益高且毒性低,因此仍需要小分子造影剂。在此,我们评估了一种新型花菁染料IC7-1-Bu作为PAI造影剂在小鼠模型体内肿瘤成像中的实用性,该造影剂未偶联靶向部分。在水溶液中,将IC7-1-Bu的基本PA特性与美国食品药品监督管理局批准的染料吲哚菁绿(ICG)进行了比较。我们通过体内荧光成像评估了IC7-1-Bu和ICG的肿瘤蓄积情况。然后,在将IC7-1-Bu静脉注射到荷瘤小鼠体内24小时和48小时后,使用光声断层扫描系统进行体内PAI。与ICG相比,IC7-1-Bu在水溶液中的PA信号高约2.3倍。与ICG不同,IC7-1-Bu静脉注射后显示出高肿瘤荧光。静脉注射IC7-1-Bu后,体内PAI提供的肿瘤与背景PA信号比约为2.5。这些结果表明,IC7-1-Bu是一种有前景的PAI造影剂,可用于未偶联靶向部分的癌症成像。