通过使用大小可调的纳米粒子,声动力疗法和光动力疗法联合治疗癌症将非常有效。

N Miyoshi, S K Kundu, T Tuziuti, K Yasui, I Shimada, Y Ito
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引用次数: 0

摘要

纳米粒子已被用于纳米科学和光催化表面化学中的许多功能材料。氧化钛纳米粒子作为纳米医学中的敏化剂,可用于激光和/或超声波治疗肿瘤。我们在动物肿瘤模型中研究了光动力疗法和超声动力疗法的联合疗法。口服两种敏化剂氧化钛(0.2%-TiO2 纳米颗粒用于声动力疗法,1 mM 5-aminolevulinic acid 用于光动力疗法)对癌症治疗产生了最佳的联合治疗效果。我们的光镜和拉曼光谱研究显示,钛纳米粒子分布在癌组织的血管内(大小为 1-3 μm)。在这些大小分布广泛的纳米粒子中,只有特定大小的粒子可以穿透癌症组织的血管,而其他粒子可能只对模型小鼠产生副作用。因此,可能有必要分离出最佳尺寸的粒子。为此,我们采用逆流色谱法分离 TiO2 纳米粒子,使用的是浸在超声波浴(42 千赫)中的扁平卷曲柱(内径 1.6 毫米)。分离采用 1-丁醇-乙酸-水两相溶剂系统,体积比为 4:1:5,流速为 0.1 ml/min。逆流色谱分离得到的馏分含有直径分别为 31 纳米和 4400 纳米的颗粒聚集体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Combination of Sonodynamic and Photodynamic Therapy against Cancer Would Be Effective through Using a Regulated Size of Nanoparticles.

Combination of Sonodynamic and Photodynamic Therapy against Cancer Would Be Effective through Using a Regulated Size of Nanoparticles.

Combination of Sonodynamic and Photodynamic Therapy against Cancer Would Be Effective through Using a Regulated Size of Nanoparticles.

Combination of Sonodynamic and Photodynamic Therapy against Cancer Would Be Effective through Using a Regulated Size of Nanoparticles.

Nanoparticles have been used for many functional materials in nano-sciences and photo-catalyzing surface chemistry. The titanium oxide nanoparticles will be useful for the treatment of tumor by laser and/or ultrasound as the sensitizers in nano-medicine. We have studied the combination therapy of photo- and sono-dynamic therapies in an animal tumor model. Oral-administration of two sensitizers titanium oxide, 0.2%-TiO2 nanoparticles for sono-dynamic and 1 mM 5-aminolevulinic acid for photodynamic therapies have resulted in the best combination therapeutic effects for the cancer treatment. Our light microscopic and Raman spectroscopic studies revealed that the titanium nanoparticles were distributed inside the blood vessel of the cancer tissue (1-3 μm sizes). Among these nanoparticles with a broad size distribution, only particular-sized particles could penetrate through the blood vessel of the cancer tissue, while other particles may only exhibit the side effects in the model mouse. Therefore, it may be necessary to separate the optimum size particles. For this purpose we have separated TiO2 nanoparticles by countercurrent chromatography with a flat coiled column (1.6 mm ID) immersed in an ultrasonic bath (42 KHz). Separation was performed with a two-phase solvent system composed of 1-butanol-acetic acid-water at a volume ratio of 4:1:5 at a flow rate of 0.1 ml/min. Countercurrent chromatographic separation yielded fractions containing particle aggregates at 31 and 4400 nm in diameter.

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