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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Near infrared fluorescence-guided real-time endoscopic detection of peritoneal ovarian cancer nodules using intravenously injected indocyanine green.
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Near infrared fluorescence-guided real-time endoscopic detection of peritoneal ovarian cancer nodules using intravenously injected indocyanine green.

机译:使用静脉注射吲哚菁绿的近红外荧光引导的实时内窥镜检查腹膜卵巢癌结节。

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摘要

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.
机译:近红外荧光引导可用于检测小癌转移,并有助于内窥镜检查癌症。吲哚菁绿(ICG)是美国食品药品监督管理局(FDA)批准的荧光剂。通过与血清蛋白的非特异性相互作用,ICG获得了增强的通透性和保留(EPR)效果。但是,ICG展示了迅速从发行中清除的机会。因此,ICG可能是用于肿瘤实时荧光成像的理想造影剂。为了评估实时双重荧光和白光内窥镜光学成像对使用造影剂ICG检测肿瘤植入物的有用性,在腹膜扩散性卵巢癌的小鼠模型中进行了荧光引导的腹腔镜检查。给动物静脉注射ICG或与白蛋白偶联的对照造影剂IR800。然后比较了检测小卵巢癌植入物的能力。使用双视角显微内窥镜,ICG可以在注射后6和24小时清楚地观察到源自SHIN3和OVCAR5细胞的腹膜卵巢癌转移结节,其肿瘤背景比明显高于对照剂IR800-白蛋白(p <0.001 )。总之,与理论上具有更好的EPR效果但循环保留时间更长的对照大分子药物相比,ICG具有理想的特性,即具有EPR效果和快速清除率,可用于实时内窥镜检查微小卵巢癌腹膜植入物。鉴于ICG已经获得FDA批准,并且在人类使用方面已有很长的记录,因此该方法可以轻松地作为荧光引导内窥镜程序用于癌症治疗和治疗的强大工具,应用于临床。

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