Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York 10065, United States.
Department of Electrical and Computer Engineering, University of Cyprus, Nicosia, Cyprus.
Theranostics. 2019 Aug 13;9(20):5899-5913. doi: 10.7150/thno.36321. eCollection 2019.
: The goal of imaging tumors at depth with high sensitivity and specificity represents a significant challenge in the field of biomedical optical imaging. 'Surface enhanced Raman scattering' (SERS) nanoparticles (NPs) have been employed as image contrast agents and can be used to specifically target cells By tracking their unique "fingerprint" spectra, it becomes possible to determine their precise location. However, while the detection of SERS NPs is very sensitive and specific, conventional Raman spectroscopy imaging devices are limited in their inability to probe through tissue depths of more than a few millimetres, due to scattering and absorption of photons by biological tissues. Here, we combine the use of "Spatially Offset Raman spectroscopy" (SORS) with that of "surface-enhanced resonance Raman spectroscopy" (SERRS) in a technique known as "surface enhanced spatially offset resonance Raman spectroscopy" (SESO(R)RS) to image deep-seated glioblastoma multiforme (GBM) tumors in mice through the intact skull. : A SORS imaging system was built in-house. Proof of concept SORS imaging was achieved using a PTFE-skull-tissue phantom. Imaging of GBMs in the RCAS-PDGF/N-tva transgenic mouse model was achieved through the use of gold nanostars functionalized with a resonant Raman reporter to create SERRS nanostars. These were then encapsulated in a thin silica shell and functionalized with a cyclic-RGDyK peptide to yield integrin-targeting SERRS nanostars. Non-invasive SORS image acquisition of the integrin-targeted nanostars was then performed in living mice under general anesthesia. Conventional non-SORS imaging was used as a direct comparison. : Using a low power density laser, GBMs were imaged via SESORRS in mice (n = 5) and confirmed using MRI and histopathology. The results demonstrate that via utilization of the SORS approach, it is possible to acquire clear and distinct Raman spectra from deep-seated GBMs in mice through the skull. SESORRS images generated using classical least squares outlined the tumors with high precision as confirmed via MRI and histology. Unlike SESORRS, conventional Raman imaging of the same areas did not provide a clear delineation of the tumor. : To the best of our knowledge this is the first report of SESO(R)RS imaging. In a relevant brain tumor mouse model we demonstrate that this technique can overcome the limitations of conventional Raman imaging with regards to penetration depth. This work therefore represents a significant step forward in the potential clinical translation of SERRS nanoparticles for high precision cancer imaging.
: 用高灵敏度和特异性在深度对肿瘤进行成像代表了生物医学光学成像领域的一个重大挑战。“表面增强拉曼散射”(SERS)纳米粒子(NPs)已被用作造影剂,并可用于特异性靶向细胞。通过跟踪它们独特的“指纹”光谱,可以确定它们的精确位置。然而,虽然 SERS NPs 的检测非常灵敏和特异,但由于生物组织对光子的散射和吸收,传统的拉曼光谱成像设备在探测深度超过几毫米时受到限制。在这里,我们将“空间偏移拉曼光谱”(SORS)与“表面增强共振拉曼光谱”(SERRS)结合使用,在一种称为“表面增强空间偏移共振拉曼光谱”(SESO(R)RS)的技术中,对通过完整颅骨对深部多形性胶质母细胞瘤(GBM)肿瘤进行成像。: 我们内部构建了一个 SORS 成像系统。使用 PTFE-颅骨-组织体模实现了概念验证 SORS 成像。通过使用功能化有共振拉曼报告器的金纳米星来创建 SERRS 纳米星,对 RCAS-PDGF/N-tva 转基因小鼠模型中的 GBM 进行成像。然后将它们封装在薄的二氧化硅壳中,并功能化环肽 RGDyK 以产生整合素靶向 SERRS 纳米星。然后在全身麻醉下对活鼠进行非侵入性 SORS 靶向纳米星图像采集。常规非 SORS 成像用作直接比较。: 使用低功率密度激光,通过 SESORRS 在小鼠中对 GBM 进行成像(n = 5),并通过 MRI 和组织病理学进行确认。结果表明,通过利用 SORS 方法,通过颅骨可以从小鼠深部 GBM 中获得清晰而独特的拉曼光谱。使用经典最小二乘法生成的 SESORRS 图像高精度勾勒出肿瘤,通过 MRI 和组织学进行确认。与 SESORRS 不同,对同一区域的常规拉曼成像不能清楚地区分肿瘤。: 据我们所知,这是 SESO(R)RS 成像的第一个报告。在相关的脑肿瘤小鼠模型中,我们证明该技术可以克服传统拉曼成像在穿透深度方面的限制。因此,这项工作在将 SERRS 纳米粒子用于高精度癌症成像的临床转化方面迈出了重要的一步。