磁铁矿阳离子脂质体细胞黏附热纳米颗粒的中温非依赖性细胞毒性及其治疗应用

T. Morino, H. Takase, T. Etani, T. Naiki, N. Kawai, A. Ito, T. Yasui
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引用次数: 3

摘要

利用磁铁矿阳离子脂质体(MCL)作为发热纳米颗粒进行癌症临床研究。采用交变磁场(AMF)照射诱导MCL颗粒在瘤内产生热量,杀死肿瘤附近的癌细胞。其可行性和安全性已得到证实,但在温度升高相似的肿瘤中,其疗效是不同的。为保证疗效,提出热剂量除以肿瘤体积(J/cm3)作为控制临床治疗的候选指标。本研究的目的是研究AMF照射下MCL颗粒的细胞毒性,并讨论所提出的指标的有效性。MCL颗粒在体外以2 ng-MCL/细胞的速度吸附人前列腺癌细胞,这取决于来自阳离子脂质成分的正zeta电位。光学和电镜观察显示,MCL颗粒大部分位于细胞膜上,很少位于细胞质中。MCL颗粒的产热活性以比吸收率(SAR)表示,单位为J/g-MCL·min,并随辐照条件的变化而变化。在提供1.2×10-4 J/细胞热剂量的条件下,发现MCL颗粒在AMF照射下具有细胞毒性,并伴有细胞形态改变和膜破裂。值得注意的是,在这种条件下,培养基没有出现升温现象。MCL颗粒的细胞毒性被认为是由细胞膜(J/cell)局部产生的热量引起的,与介质温度无关。这些结果将支持热剂量指数(J/cm3肿瘤体积)代替肿瘤温度来控制临床治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Medium Temperature Independent Cytotoxicity of Cell-adhesive Heat-generating Nanoparticles Named Magnetite Cationic Liposomes and its Therapeutic Use
Cancer clinical research using heat-generating nanoparticles named magnetite cationic liposomes (MCL) has been conducted. Heat generation from intratumorally injected MCL particles was induced by alternating magnetic field (AMF) irradiation to kill cancer cells nearby located. Its feasibility and safety have been shown but efficacy was variable among tumors whose temperature rises were similarly achieved. To ensure efficacy heat dose divided by tumor volume (J/cm3) has been proposed as candidate index to control clinical treatment. Purpose of this study is to investigate cytotoxicity of MCL particles upon AMF irradiation and discuss validity of the proposed index. MCL particles were shown to adsorb human prostate cancer cells in vitro at 2 ng-MCL/cell, depending on positive zeta potential derived from a cationic lipid component. Optical and electron microscopic observations showed majority of MCL particles located on cell membrane and scarcely in cytosol. Heat generation activities of MCL particles were represented by specific absorption rate (SAR) with unit of J/g-MCL・min and were shown variable due to irradiation conditions. Cytotoxicity of MCL particles upon AMF irradiation was found under a condition supplying heat dose of 1.2×10-4 J/cell with concomitant cellular morphological changes and membrane burst. Notably, temperature rise of culture medium was not observed under this condition. Cytotoxicity of MCL particles was considered to be caused by heat generated locally on cell membrane (J/cell) independently of medium temperature. These results would support the proposed heat dose index (J/cm3 tumor volume) to control clinical treatment instead of tumor temperature.
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