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Surface charge modulates the internalization vs. penetration of gold nanoparticles: comprehensive scrutiny on monolayer cancer cells, multicellular spheroids and solid tumors by SERS modality

机译:表面电荷调节内化vs。金纳米粒子的渗透:全面审查单层癌症细胞,多细胞球状体和实体肿瘤ser形态

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摘要

Precise control over the dynamics of nanoparticles (NPs) in a tumor microenvironment is highly warranted for the development of an efficient nanotheranostic agent. Even though inductively coupled plasma mass spectrometry can provide a quantitative assessment regarding the uptake efficiency of metal NPs, enumeration of deep tissue penetration capacity remains as a challenge. Herein, we have demonstrated an accurate tracking of the uptake efficiency and penetration phenomenon of gold nanoparticles (AuNPs: 40-50 nm) with respect to three different surface charges in monolayer (2D) cells, multicellular spheroids (3D) and in vivo tumors by surface-enhanced Raman spectroscopy (SERS). While positively charged AuNPs showed around two-fold increased internalization in monolayer cells, SERS-tag-based line scanning on multi-layered tumor spheroids illustrated almost nine-fold superior penetration capability with negatively charged AuNPs. Further, the enhanced solid tumor distribution contributed by the negatively charged AuNPs could appreciably escalate its clinical utility in cancer management.
机译:精确控制纳米粒子的动力学肿瘤微环境是高度(NPs)保证为一个有效的发展nanotheranostic代理。耦合等离子体质谱法可以提供关于吸收定量评估金属NPs效率,枚举的深组织穿透能力仍然是一挑战。准确的跟踪效率和吸收金纳米粒子的渗透现象(AuNPs: 40 - 50 nm)对三种不同在单层表面电荷(2 d)细胞,多细胞球状体(3 d)和体内肿瘤通过表面增强拉曼光谱(ser)。而带正电AuNPs显示双重的增加了单层的内化细胞,SERS-tag-based线扫描多层肿瘤插图近球状体9倍优越的渗透能力带负电荷的AuNPs。固体肿瘤分布造成的带负电荷的AuNPs可以明显升级其在癌症临床效用管理。

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