深部肿瘤荧光诊断和光动力治疗的可能途径

V. Loschenov, T. Savelieva, P. Grachev, K. Linkov, Yuliya Maklygina, I. Romanishkin, A. Ryabova, D. Kustov, S. Goryajnov, A. Potapov
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引用次数: 0

摘要

激光辐射对生物组织的有限穿透性阻碍了光诊断和光动力治疗方法在临床实践中的广泛应用。我们研究了深部肿瘤PD和PDT的几种方法:1。激光光谱控制的立体定向活检套管。在PD和PDT中,为了使肿瘤细胞不迁移到脑深部,而是沿着纤维偶尔进行激光照射,开发了用于长期安装在肿瘤切除区域的特殊光纤端口。纤维表面涂有一种特殊的化合物,含有光敏剂(PS)和癌细胞的营养物质。2. 具有视频荧光和光谱分析系统功能的神经外科吸痰器。采用激光激发下5-氨基乙酰丙酸(5-ALA)诱导原卟啉IX (Pp IX)荧光在红光谱范围内进行荧光导航,对500多例不同类型脑肿瘤患者进行了手术。3.。当荧光在红色和近红外范围内被激发时,肿瘤的诊断和导航。采用吲哚菁绿(ICG)作为近红外染料,观察实验动物的血液和淋巴血管。该方法可用于肿瘤床及邻近区域的检查。4. 基于切伦科夫辐射的放射性药物与PS的联合作用。18f -氟脱氧葡萄糖衰变过程中线粒体内Cherenkov辐射激发ppix的PDT机制导致细胞死亡。这个想法在患有C6胶质瘤的大鼠身上取得了很好的效果。用相同剂量的氯e6ps使用这种方法的结果是阴性的。5. 通过光动力灭活肿瘤相关巨噬细胞和小胶质细胞的作用。微创方法测定巨噬细胞(小胶质细胞)表型及其在肿瘤及其邻近原位的极化。这将允许评估治疗的有效性,包括PDT。以Pp IX和酞菁铝纳米颗粒获得了最有希望的结果。研究已经在移植肿瘤的实验动物身上进行,部分研究也在临床的癌症患者身上进行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Possible approaches to fluorescence diagnosis and photodynamic therapy for deep-seated tumors
The limited penetration of laser radiation into biological tissue prevents the widespread distribution of photodiagnostics (PD) and photodynamic therapy (PDT) methods to clinical practice. We have investigated several approaches for PD and PDT of deep-seated tumors: 1. Stereotactic biopsy cannula with a laser spectroscopic control. Special fiber ports for long-term installation in the tumor removal area were developed in order to cause tumor cells to migrate not into the depth of brain but along the fibers with occasional laser irradiation for PD and PDT. The fibers are coated with a special compound containing photosensitizer (PS) and nutrients for cancer cells. 2. Neurosurgical aspirator with the function of video-fluorescence and spectroscopic analysis system. More than 500 patients with various types of brain tumors were operated on using fluorescent navigation based on 5-aminolevulinic acid (5-ALA) induced protoporphyrin IX (Pp IX) fluorescence under laser excitation in red spectral range. 3. Diagnostics and navigation of tumors when fluorescence is excited in the red and near infrared ranges. We used indocyanine green (ICG) as near infrared dye to observe blood and lymph vasculature of laboratory animals. This method could be useful while examining tumor bed and adjacent area. 4. Joint action of radiopharmaceuticals and PS based on Cherenkov radiation. Cell death by PDT mechanism via Pp IX excitation by Cherenkov radiation in mitochondria during 18F-fludeoxyglucose decay. This idea achieved good results on rats with C6 glioma. The results of using this approach with chlorin e6 PS in comparable doses are negative. 5. Action through photodynamic inactivation of tumor-associated macrophages and microglia. Idea of minimally invasive method for determining macrophage (microglia) phenotype and their polarization in tumors and their immediate vicinity in situ. This would allow evaluating the effectiveness of the treatment, including PDT. The most promising results were obtained with Pp IX and aluminum phthalocyanine nanoparticles. Studies have been conducted on experimental animals with grafted tumors and, in part, on cancer patients in the clinic.
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