Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-1088, USA.
Int J Cancer. 2011 Oct 1;129(7):1671-7. doi: 10.1002/ijc.26113. Epub 2011 Jun 18.
Near infrared fluorescence-guidance can be used for the detection of small cancer metastases and can aid in the endoscopic management of cancer. Indocyanine green (ICG) is a Food and Drug Administration (FDA)-approved fluorescence agent. Through non-specific interactions with serum proteins, ICG achieves enhanced permeability and retention (EPR) effects. Yet, ICG demonstrates rapid clearance from the circulation. Therefore, ICG may be an ideal contrast agent for real-time fluorescence imaging of tumors. To evaluate the usefulness of real-time dual fluorescence and white light endoscopic optical imaging to detect tumor implants using the contrast agent ICG, fluorescence-guided laparoscopic procedures were performed in mouse models of peritoneally disseminated ovarian cancers. Animals were administered intravenous ICG or a control contrast agent, IR800-conjugated to albumin. The ability to detect small ovarian cancer implants was then compared. Using the dual view microendoscope, ICG clearly enabled visualization of peritoneal ovarian cancer metastatic nodules derived from SHIN3 and OVCAR5 cells at 6 and 24 hr after injection with significantly higher tumor-to-background ratio than the control agent, IR800-albumin (p < 0.001). In conclusion, ICG has the desirable properties of having both EPR effects and rapid clearance for the real-time endoscopic detection of tiny ovarian cancer peritoneal implants compared to a control macromolecular agent with theoretically better EPR effects but longer circulatory retention. Given that ICG is already FDA-approved and has a long track record of human use, this method could be easily translated to the clinic as a robust tool for fluorescence-guided endoscopic procedures for the management and treatment of cancer.
近红外荧光引导可用于检测小的癌症转移灶,并可辅助癌症的内镜管理。吲哚菁绿(ICG)是一种获得美国食品和药物管理局(FDA)批准的荧光试剂。通过与血清蛋白的非特异性相互作用,ICG 实现了增强的通透性和保留(EPR)效应。然而,ICG 从循环中迅速清除。因此,ICG 可能是实时荧光成像肿瘤的理想对比剂。为了评估使用荧光剂 ICG 进行实时双荧光和白光内镜光学成像检测肿瘤植入物的有用性,在腹膜播散性卵巢癌的小鼠模型中进行了荧光引导腹腔镜手术。动物静脉内给予 ICG 或对照造影剂,即与白蛋白偶联的 IR800。然后比较了检测小卵巢癌植入物的能力。使用双视野微内镜,ICG 可清晰地可视化源自 SHIN3 和 OVCAR5 细胞的腹膜卵巢癌转移性结节,在注射后 6 和 24 小时,肿瘤与背景的比值明显高于对照造影剂 IR800-白蛋白(p < 0.001)。总之,与具有更好的 EPR 效应但循环保留时间更长的对照大分子造影剂相比,ICG 具有 EPR 效应和快速清除的理想特性,可用于实时内镜检测微小的卵巢癌腹膜植入物。鉴于 ICG 已获得 FDA 批准,并且在人类使用方面有着悠久的历史,这种方法可以很容易地转化为临床,作为荧光引导内镜手术管理和治疗癌症的强大工具。