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本文引用的文献

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Sentinel lymph node mapping with type-II quantum dots.使用II型量子点进行前哨淋巴结定位
Methods Mol Biol. 2007;374:147-59. doi: 10.1385/1-59745-369-2:147.
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J Biomed Opt. 2006 Jan-Feb;11(1):014007. doi: 10.1117/1.2170579.
3
Sentinel lymph node mapping of the gastrointestinal tract by using invisible light.利用不可见光进行胃肠道前哨淋巴结定位
Ann Surg Oncol. 2006 Mar;13(3):386-96. doi: 10.1245/ASO.2006.04.025. Epub 2006 Jan 31.
4
High-affinity near-infrared fluorescent small-molecule contrast agents for in vivo imaging of prostate-specific membrane antigen.用于前列腺特异性膜抗原体内成像的高亲和力近红外荧光小分子造影剂。
Mol Imaging. 2005 Oct-Dec;4(4):448-62. doi: 10.2310/7290.2005.05163.
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Organic alternatives to quantum dots for intraoperative near-infrared fluorescent sentinel lymph node mapping.用于术中近红外荧光前哨淋巴结映射的量子点有机替代物
Mol Imaging. 2005 Jul-Sep;4(3):172-81. doi: 10.1162/15353500200505127.
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A comparison of transit-time flowmetry and intraoperative fluorescence imaging for assessing coronary artery bypass graft patency.用于评估冠状动脉旁路移植血管通畅性的渡越时间血流测定法与术中荧光成像的比较。
J Thorac Cardiovasc Surg. 2005 Aug;130(2):315-20. doi: 10.1016/j.jtcvs.2004.11.033.
7
Engineering InAs(x)P(1-x)/InP/ZnSe III-V alloyed core/shell quantum dots for the near-infrared.用于近红外的工程化InAs(x)P(1-x)/InP/ZnSe III-V族合金核壳量子点
J Am Chem Soc. 2005 Aug 3;127(30):10526-32. doi: 10.1021/ja0434331.
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Contrast-enhanced sonographic imaging of lymphatic channels and sentinel lymph nodes.淋巴管和前哨淋巴结的超声造影成像
J Ultrasound Med. 2005 Jul;24(7):953-65. doi: 10.7863/jum.2005.24.7.953.
9
Sentinel lymph node mapping of the pleural space.胸膜腔前哨淋巴结定位
Chest. 2005 May;127(5):1799-804. doi: 10.1378/chest.127.5.1799.
10
Intraoperative identification of esophageal sentinel lymph nodes with near-infrared fluorescence imaging.术中利用近红外荧光成像识别食管前哨淋巴结
J Thorac Cardiovasc Surg. 2005 Apr;129(4):844-50. doi: 10.1016/j.jtcvs.2004.08.001.

使用不可见光的图像引导肿瘤手术:前哨淋巴结 mapping 的临床前开发已完成。

Image-guided oncologic surgery using invisible light: completed pre-clinical development for sentinel lymph node mapping.

作者信息

Tanaka Eiichi, Choi Hak Soo, Fujii Hirofumi, Bawendi Moungi G, Frangioni John V

机构信息

Division of Hematology/Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA.

出版信息

Ann Surg Oncol. 2006 Dec;13(12):1671-81. doi: 10.1245/s10434-006-9194-6. Epub 2006 Sep 29.

DOI:10.1245/s10434-006-9194-6
PMID:17009138
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2474791/
Abstract

BACKGROUND

Invisible near-infrared (NIR) fluorescent light permits high sensitivity, real-time image-guidance during oncologic surgery without changing the look of the surgical field. In this study, we complete pre-clinical development of the technology for sentinel lymph node (SLN) mapping using a large animal model of spontaneous melanoma.

METHODS

Sinclair swine with spontaneous melanoma metastatic to regional lymph nodes were used because of their similarity to human melanoma. Organic lymphatic tracers tested included FDA-approved indocyanine green adsorbed non-covalently to human serum albumin (HSA), and NIR fluorophore CW800 conjugated covalently to HSA (HSA800). The inorganic/organic hybrid tracer tested was type II NIR quantum dots with an anionic coating. Primary tumors received four peri-tumoral injections of each tracer, with a fluorophore dose of 100 pmol to 1 nmol per injection. SLN mapping and image-guided resection were performed in real-time.

RESULTS

Each of the 3 lymphatic tracers was injected into n = 4 separate primary melanomas in a total of 6 animals. All 12 injections resulted in identification of the SLN(s) and their associated lymphatic channels within 1 minute in 100% of cases, despite highly pigmented skin and black fur. Hydrodynamic diameter had a profound impact on tracer behavior in vivo.

CONCLUSIONS

This study completes the pre-clinical development of NIR fluorescence-guided SLN mapping and provides insight into imaging system optimization and tracer choice for future human clinical trials. The technology is likely to eliminate the need for radioactive and colored tracers, permits real-time image guidance throughout the procedure, and assists the pathologist in tissue analysis.

摘要

背景

不可见近红外(NIR)荧光可在肿瘤手术期间实现高灵敏度实时图像引导,且不会改变手术视野外观。在本研究中,我们利用自发黑色素瘤的大型动物模型完成了前哨淋巴结(SLN) mapping技术的临床前开发。

方法

选用有区域淋巴结转移的自发黑色素瘤的辛克莱猪,因为它们与人类黑色素瘤相似。测试的有机淋巴示踪剂包括经FDA批准的与人类血清白蛋白(HSA)非共价吸附的吲哚菁绿,以及与HSA共价偶联的NIR荧光团CW800(HSA800)。测试的无机/有机混合示踪剂是具有阴离子涂层的II型NIR量子点。原发性肿瘤在肿瘤周围注射每种示踪剂4次,每次注射的荧光团剂量为100 pmol至1 nmol。实时进行SLN mapping和图像引导切除。

结果

在总共6只动物中,将3种淋巴示踪剂中的每一种分别注射到4个单独的原发性黑色素瘤中。尽管皮肤色素沉着严重且有黑色皮毛,但所有12次注射均在1分钟内100%的病例中识别出了前哨淋巴结及其相关淋巴通道。流体动力学直径对示踪剂在体内的行为有深远影响。

结论

本研究完成了NIR荧光引导的SLN mapping的临床前开发,并为未来人类临床试验的成像系统优化和示踪剂选择提供了见解。该技术可能无需放射性和有色示踪剂,在整个手术过程中实现实时图像引导,并协助病理学家进行组织分析。