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DIFFERENTIAL TUMOR CELL CYTOTOXICITY VIA CONTACT WITH COATED CERIUM OXIDE NANOPARTICLES

机译:通过与包覆的氧化铈纳米粒子接触而获得的不同的肿瘤细胞毒性

摘要

Differential surface-charge-dependent localization of nanoceria in normal cells and cancer cells plays a critical role in the toxicity profile of a nanoceria particle. Engineered surface-coated cerium oxide nanoparticles with different surface charges that are positive, negative and neutral provide therapeutic results for normal and cancer cell lines. Results show that nanoceria with a positive or neutral charge enters most of the cell lines studied, while nanoceria with a negative charge internalizes mostly in the cancer cell lines. Moreover, upon entry into the cells, nanoceria is localized to different cell compartments (e.g. cytoplasm and lysosomes) depending on the nanoparticle surface charge. The internalization and subcellular localization of nanoceria plays a key role in the nanoparticle cytotoxicity profile, exhibiting significant toxicity when they localize in the lysosomes of the cancer cell lines. In contrast, minimal toxicity is observed when they localize into the cytoplasm or do not enter the cells.
机译:纳米氧化铈在正常细胞和癌细胞中的不同表面电荷依赖性定位在纳米氧化铈颗粒的毒性谱中起关键作用。具有正,负和中性不同表面电荷的工程表面涂层二氧化铈纳米颗粒可为正常和癌细胞系提供治疗效果。结果表明,带有正电荷或中性电荷的纳米氧化铈进入大多数研究的细胞系,而带有负电荷的纳米氧化铈主要在癌细胞系中内化。而且,一旦进入细胞,取决于纳米粒子的表面电荷,纳米氧化铈被定位于不同的细胞区室(例如细胞质和溶酶体)。纳米氧化铈的内在化和亚细胞定位在纳米颗粒细胞毒性谱中起关键作用,当它们定位在癌细胞系的溶酶体中时表现出显着的毒性。相反,当它们位于细胞质中或不进入细胞时,观察到最小的毒性。

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