Department of Chemistry, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, IL 61801, USA.
Acc Chem Res. 2013 Mar 19;46(3):650-61. doi: 10.1021/ar300015b. Epub 2012 Jun 25.
Since the late 1980s, researchers have prepared inorganic nanoparticles of many types--including elemental metals, metal oxides, metal sulfides, metal selenides, and metal tellurides--with excellent control over size and shape. Originally many researchers were primarily interested in exploring the quantum size effects predicted for such materials. Applications of inorganic nanomaterials initially centered on physics, optics, and engineering but have expanded to include biology. Many current nanomaterials can serve as biochemical sensors, contrast agents in cellular or tissue imaging, drug delivery vehicles, or even as therapeutics. In this Account we emphasize that the understanding of how nanomaterials will function in a biological system relies on the knowledge of the interface between biological systems and nanomaterials, the nano-bio interface. Gold nanoparticles can serve as excellent standards to understand more general features of the nano-bio interface because of its many advantages over other inorganic materials. The bulk material is chemically inert, and well-established synthetic methods allow researchers to control its size, shape, and surface chemistry. Gold's background concentration in biological systems is low, which makes it relatively easy to measure it at the part-per-billion level or lower in water. In addition, the large electron density of gold enables relatively simple electron microscopic experiments to localize it within thin sections of cells or tissue. Finally, gold's brilliant optical properties at the nanoscale are tunable with size, shape, and aggregation state and enable many of the promising chemical sensing, imaging, and therapeutic applications. Basic experiments with gold nanoparticles and cells include measuring the toxicity of the particles to cells in in vitro experiments. The species other than gold in the nanoparticle solution can be responsible for the apparent toxicity at a particular dose. Once the identity of the toxic agent in nanoparticle solutions is known, researchers can employ strategies to mitigate toxicity. For example, the surfactant used at high concentration in the synthesis (0.1 M) of gold nanorods remains on their surface in the form of a bilayer and can be toxic to certain cells at 200 nM concentrations. Several strategies can alleviate the toxic response. Polyelectrolyte layer-by-layer wrapping can cover up the surfactant bilayer, or researchers can exchange the surfactant with chemically similar molecules. Researchers can also replace the surfactant with a biocompatible thiol or use a polymerizable surfactant that can be "stitched" onto the nanorods and reduce its lability. In all these cases, however, proteins or other molecules from the cellular media cover the engineered surface of the nanoparticles, which can drastically change the charges and functional groups on the nanoparticle surface.
自 20 世纪 80 年代末以来,研究人员已经制备了多种类型的无机纳米粒子,包括元素金属、金属氧化物、金属硫化物、金属硒化物和金属碲化物,对其尺寸和形状具有出色的控制能力。最初,许多研究人员主要对探索此类材料所预测的量子尺寸效应感兴趣。无机纳米材料的应用最初集中在物理、光学和工程领域,但现已扩展到生物学领域。许多当前的纳米材料可用作生化传感器、细胞或组织成像中的对比剂、药物输送载体,甚至用作治疗剂。在本说明中,我们强调,要了解纳米材料在生物系统中的功能,必须了解生物系统与纳米材料之间的界面,即纳米-生物界面。由于金纳米粒子相对于其他无机材料具有许多优势,因此它可以作为理解纳米-生物界面的出色标准。其体材料化学惰性,成熟的合成方法可让研究人员控制其尺寸、形状和表面化学性质。金在生物系统中的背景浓度较低,这使得在水中以十亿分之几或更低的水平相对容易地测量它。此外,金的大电子密度使相对简单的电子显微镜实验能够在细胞或组织的薄片中定位它。最后,金在纳米尺度上的出色光学性质可通过尺寸、形状和聚集状态进行调整,并为许多有前途的化学传感、成像和治疗应用提供了支持。与金纳米粒子和细胞进行的基本实验包括测量粒子在体外实验中对细胞的毒性。在纳米粒子溶液中除金以外的物质可能是特定剂量下明显毒性的原因。一旦确定了纳米粒子溶液中有毒物质的身份,研究人员就可以采用策略来减轻毒性。例如,在金纳米棒的合成(0.1 M)中高浓度使用的表面活性剂以双层的形式保留在其表面上,并且在 200 nM 浓度下对某些细胞可能有毒。有几种策略可以减轻毒性反应。聚电解质层层包裹可以覆盖表面活性剂双层,或者研究人员可以用化学相似的分子交换表面活性剂。研究人员还可以用生物相容性的硫醇代替表面活性剂,或者使用可聚合的表面活性剂将其“缝合”到纳米棒上,并降低其不稳定性。然而,在所有这些情况下,来自细胞介质的蛋白质或其他分子都会覆盖纳米粒子的工程表面,这会极大地改变纳米粒子表面的电荷和功能基团。