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Possible approaches to fluorescence diagnosis and photodynamic therapy for deep-seated tumors

机译:深层肿瘤的荧光诊断和光动力疗法的可能方法

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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 thetumor removal area were developed in order to cause tumor cells to migrate not into the depth of brain but along thefibers with occasional laser irradiation for PD and PDT. The fibers are coated with a special compound containingphotosensitizer (PS) and nutrients for cancer cells.2. Neurosurgical aspirator with the function of video-fluorescence and spectroscopic analysis system. More than 500patients with various types of brain tumors were operated on using fluorescent navigation based on 5-aminolevulinicacid (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 usedindocyanine green (ICG) as near infrared dye to observe blood and lymph vasculature of laboratory animals. Thismethod 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 IXexcitation by Cherenkov radiation in mitochondria during 18F-fludeoxyglucose decay. This idea achieved goodresults on rats with C6 glioma. The results of using this approach with chlorin e6 PS in comparable doses arenegative.5. Action through photodynamic inactivation of tumor-associated macrophages and microglia. Idea of minimallyinvasive method for determining macrophage (microglia) phenotype and their polarization in tumors and theirimmediate vicinity in situ. This would allow evaluating the effectiveness of the treatment, including PDT. The mostpromising 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.
机译:激光辐射进入生物组织的渗透受限,阻止了光诊断的广泛分布 (PD)和光动力疗法(PDT)方法的临床实践。 我们研究了深部肿瘤的PD和PDT的几种方法: 1.具有激光光谱控制的立体定向活检插管。特殊的光纤端口,可长期安装在 肿瘤切除区域的发展是为了使肿瘤细胞不迁移到脑深处,而是沿着神经元迁移。 光纤,偶尔用于PD和PDT激光照射。纤维涂有特殊的化合物,其中包含 光敏剂(PS)和癌细胞营养物质。 2.具有视频荧光和光谱分析系统功能的神经外科抽吸器。超过500 使用基于5-氨基乙酰丙酸的荧光导航对患有各种类型脑瘤的患者进行手术 酸(5-ALA)在红色光谱范围内的激光激发下诱导原卟啉IX(Pp IX)荧光。 3.在红色和近红外范围内激发荧光时的肿瘤诊断和导航。我们用了 吲哚菁绿(ICG)作为近红外染料,用于观察实验动物的血液和淋巴管。这 该方法在检查肿瘤床和邻近区域时可能有用。 4.基于契伦科夫辐射的放射性药物和PS的共同作用。通过Pp IX的PDT机制造成的细胞死亡 在18F-氟脱氧葡萄糖衰变过程中线粒体的Cherenkov辐射激发。这个主意取得了不错的成绩 C6神经胶质瘤大鼠的实验结果。将这种方法与可比剂量的二氢卟酚e6 PS一起使用的结果是 消极的。 5.通过光动力学灭活与肿瘤相关的巨噬细胞和小胶质细胞的作用。最小的想法 以确定肿瘤中巨噬细胞(小胶质细胞)表型及其极化的侵入性方法及其 原位紧邻。这将允许评估包括PDT在内的治疗效果。最多 Pp IX和铝酞菁纳米粒子获得了可喜的结果。 已经对具有移植肿瘤的实验动物以及部分在临床上的癌症患者进行了研究。

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