Department of Biomedical Engineering, Washington University, Saint Louis, Missouri 63130, USA.
Acc Chem Res. 2011 Oct 18;44(10):914-24. doi: 10.1021/ar200061q. Epub 2011 Apr 29.
Gold nanostructures have garnered considerable attention in recent years for their potential to facilitate both the diagnosis and treatment of cancer through their advantageous chemical and physical properties. The key feature of Au nanostructures for enabling this diverse array of biomedical applications is their attractive optical properties, specifically the scattering and absorption of light at resonant wavelengths due to the excitation of plasmon oscillations. This phenomenon is commonly known as localized surface plasmon resonance (LSPR) and is the source of the ruby red color of conventional Au colloids. The resonant wavelength depends on the size, shape, and geometry of the nanostructures, providing a set of knobs to manipulate the optical properties as needed. For in vivo applications, especially when optical excitation or transduction is involved, the LSPR peaks of the Au nanostructures have to be tuned to the transparent window of soft tissues in the near-infrared (NIR) region (from 700 to 900 nm) to maximize the penetration depth. Gold nanocages represent one class of nanostructures with tunable LSPR peaks in the NIR region. These versatile nanostructures, characterized by hollow interiors and ultrathin, porous walls, can be prepared in relatively large quantities using a remarkably simple procedure based on the galvanic replacement between Ag nanocubes and aqueous chloroauric acid. The LSPR peaks of Au nanocages can be readily and precisely tuned to any wavelength in the NIR region by controlling their size, wall thickness, or both. Other significant features of Au nanocages that make them particularly intriguing materials for biomedical applications include their compact sizes, large absorption cross sections (almost five orders of magnitude greater than those of conventional organic dyes), and their bio-inertness, as well as a robust and straightforward procedure for surface modification based on Au-thiolate chemistry. In this Account, we present some of the most recent advances in the use of Au nanocages for a broad range of theranostic applications. First, we describe their use as tracers for tracking by multiphoton luminescence. Gold nanocages can also serve as contrast agents for photoacoustic (PA) and mutimodal (PA/fluorescence) imaging. In addition, these nanostructures can be used as photothermal agents for the selective destruction of cancerous or diseased tissue. Finally, Au nanocages can serve as drug delivery vehicles for controlled and localized release in response to external stimuli such as NIR radiation or high-intensity focused ultrasound (HIFU).
金纳米结构因其具有通过其有利的化学和物理性质促进癌症诊断和治疗的潜力,近年来受到了广泛关注。Au 纳米结构在实现这种多样化的生物医学应用中的关键特征是其吸引人的光学性质,特别是在共振波长处光的散射和吸收,这是由于等离子体激元振荡的激发。这种现象通常称为局域表面等离子体共振(LSPR),是常规 Au 胶体呈现红宝石红色的原因。共振波长取决于纳米结构的尺寸、形状和几何形状,提供了一组旋钮,可以根据需要调节光学性质。对于体内应用,特别是涉及光学激发或转换时,Au 纳米结构的 LSPR 峰值必须调谐到近红外(NIR)区域的软组织透明窗口(700 至 900nm),以最大化穿透深度。金纳米笼是一类具有可调谐 LSPR 峰值的纳米结构。这些多功能纳米结构具有空心内部和超薄多孔壁的特点,可以使用基于 Ag 纳米立方体和水合氯金酸之间的电置换的非常简单的程序相对大量地制备。通过控制其尺寸、壁厚度或两者,Au 纳米笼的 LSPR 峰值可以很容易且精确地调谐到 NIR 区域中的任何波长。Au 纳米笼作为生物医学应用特别有趣的材料的其他重要特征包括其紧凑的尺寸、大的吸收截面(比常规有机染料大几乎五个数量级)和生物惰性,以及基于 Au-硫醇化学的稳健和简单的表面修饰程序。在本综述中,我们介绍了 Au 纳米笼在广泛的治疗应用中使用的一些最新进展。首先,我们描述了它们作为多光子荧光跟踪示踪剂的用途。金纳米笼也可用作光声(PA)和多模态(PA/荧光)成像的造影剂。此外,这些纳米结构可用作光热剂,用于选择性破坏癌性或患病组织。最后,Au 纳米笼可用作药物输送载体,以响应外部刺激(如 NIR 辐射或高强度聚焦超声(HIFU))进行控制和局部释放。