Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Langmuir. 2010 Jun 15;26(12):9328-33. doi: 10.1021/la100253k.
Gold nanorods were synthesized using a seed-mediated wet chemical approach with a quaternary ammonium surfactant, cetyltrimethylammonium bromide (CTAB), that forms a bilayer on the surface of the nanorods. The CTAB molecules in the bilayer were exchanged with a similar polymerizable analog, 11-(acryloyloxy) undecyltrimethyl ammonium bromide (p-CTAB). Mass spectrometric analysis of the degree of exchange of CTAB for p-CTAB, after gold digestion, gave 77 +/- 3 and 23 +/- 1% for p-CTAB and CTAB, respectively. On-rod polymerization with a cationic free-radical initiator was confirmed by FTIR analysis and did not induce aggregation as judged by ultraviolet-visible spectroscopy, transmission electron microscopy, and dynamic light scattering measurements after polymerization. In contrast to the nanorods before polymerization, the nanorods with a polymerized bilayer showed improved stability against dialysis as well as enhanced biocompatibility as measured using a viability assay on cultured human cells. Our results indicate that (1) CTAB molecules on the surface of the gold nanorods are exchangeable with similar surfactants that have a positively charged headgroup and (2) surfactant polymerization on the surface of the gold nanorods enhances both the stability and biocompatibility of these nanomaterials, probably by decreasing the degree of surfactant desorption from the surface.
金纳米棒是通过种子介导的湿化学方法合成的,使用的是季铵盐表面活性剂十六烷基三甲基溴化铵(CTAB),它在纳米棒表面形成双层。双层中的 CTAB 分子被类似的可聚合类似物 11-(丙烯酰氧基)十一烷基三甲基溴化铵(p-CTAB)取代。金消解后,通过质谱分析 CTAB 与 p-CTAB 的取代程度,分别得到 77 +/- 3%和 23 +/- 1%的 p-CTAB 和 CTAB。通过傅里叶变换红外光谱分析证实了在棒上的阳离子自由基引发剂引发的聚合反应,并且聚合后通过紫外-可见光谱、透射电子显微镜和动态光散射测量判断没有诱导聚集。与聚合前的纳米棒相比,具有聚合双层的纳米棒在透析过程中表现出更好的稳定性,并且在培养的人细胞活力测定中表现出增强的生物相容性。我们的结果表明:(1)金纳米棒表面的 CTAB 分子可以与具有正电荷头基的类似表面活性剂交换;(2)金纳米棒表面的表面活性剂聚合增强了这些纳米材料的稳定性和生物相容性,可能是通过减少表面活性剂的解吸程度。
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