Improvements in Gold Nanorod Biocompatibility with Sodium Dodecyl Sulfate Stabilization

Rossana Terracciano, A. Zhang, Mathieu L. Simeral, D. Demarchi, J. Hafner, Carly S. Filgueira
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引用次数: 5

Abstract

Due to their well-defined plasmonic properties, gold nanorods (GNRs) can be fabricated with optimal light absorption in the near-infrared region of the electromagnetic spectrum, which make them suitable for cancer-related theranostic applications. However, their controversial safety profile, as a result of surfactant stabilization during synthesis, limits their clinical translation. We report a facile method to improve GNR biocompatibility through the presence of sodium dodecyl sulfate (SDS). GNRs (120 × 40 nm) were synthesized through a seed-mediated approach, using cetyltrimethylammonium bromide (CTAB) as a cationic surfactant to direct the growth of nanorods and stabilize the particles. Post-synthesis, SDS was used as an exchange ligand to modify the net surface charge of the particles from positive to negative while maintaining rod stability in an aqueous environment. GNR cytotoxic effects, as well as the mechanisms of their cellular uptake, were examined in two different cancer cell lines, Lewis lung carcinoma (LLC) and HeLa cells. We not only found a significant dose-dependent effect of GNR treatment on cell viability but also a time-dependent effect of GNR surfactant charge on cytotoxicity over the two cell lines. Our results promote a better understanding of how we can mediate the undesired consequences of GNR synthesis byproducts when exposed to a living organism, which so far has limited GNR use in cancer theranostics.
十二烷基硫酸钠稳定金纳米棒生物相容性的改进
由于其明确的等离子体性质,金纳米棒(GNR)可以在电磁光谱的近红外区域制造出最佳的光吸收,这使其适用于癌症相关的治疗应用。然而,由于表面活性剂在合成过程中的稳定性,它们有争议的安全性限制了它们的临床应用。我们报道了一种通过十二烷基硫酸钠(SDS)存在来改善GNR生物相容性的简单方法。以十六烷基三甲基溴化铵(CTAB)为阳离子表面活性剂,通过种子介导的方法合成了GNRs(120×40nm),以引导纳米棒的生长并稳定颗粒。合成后,使用SDS作为交换配体,将颗粒的净表面电荷从正改性为负,同时在水性环境中保持棒的稳定性。在两种不同的癌症细胞系Lewis肺癌(LLC)和HeLa细胞中检测了GNR的细胞毒性效应及其细胞摄取机制。我们不仅发现GNR处理对细胞活力的显著剂量依赖性影响,而且发现GNR表面活性剂电荷对两种细胞系的细胞毒性的时间依赖性影响。我们的研究结果有助于更好地理解我们如何在暴露于活体时介导GNR合成副产物的不良后果,这迄今为止限制了GNR在癌症治疗中的应用。
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