Popoff Alexandre, Fichou Denis
CEA-Saclay, Organic Nanostructures and Semiconductors Lab CNRS-CEA-UPMC, Bât. 462, SPCSI, 91191 Gif-sur-Yvette, France.
Colloids Surf B Biointerfaces. 2008 May 1;63(1):153-8. doi: 10.1016/j.colsurfb.2007.11.003. Epub 2007 Nov 19.
We show here by means of scanning tunneling microscopy (STM) at the liquid/solid interface that paracetamol and benzocaine molecules bearing a long aliphatic chain can be immobilized on highly oriented pyrolitic graphite (HOPG) as perfectly ordered two-dimensional domains extending over several hundreds of nanometers. In both cases, high-resolution STM images reveal that compounds 1 and 2 self-assemble into parallel lamellae having a head-to-head arrangement. The paracetamol heads of 1 are in a zigzag position with entangled n-dodecyloxy side chains while benzocaine heads of compound 2 are perfectly aligned as a double row and have their palmitic side chains on either sides of the head alignment. We attribute the very long-range ordering of these two pro-drug derivatives on HOPG to the combined effects of intermolecular H-bonding on one side and Van der Waals interactions between aliphatic side chains and graphite on the other side. The 2D immobilization of pro-drug derivatives via a non-destructive physisorption mechanism could prove to be useful for applications such as drug delivery if it can be realized on a biocompatible substrate.
我们在此通过液体/固体界面的扫描隧道显微镜(STM)表明,带有长脂肪链的对乙酰氨基酚和苯佐卡因分子可以作为延伸数百纳米的完美有序二维域固定在高度取向的热解石墨(HOPG)上。在这两种情况下,高分辨率STM图像显示化合物1和2自组装成具有头对头排列的平行薄片。化合物1的对乙酰氨基酚头部呈锯齿状排列,n-十二烷氧基侧链相互缠结,而化合物2的苯佐卡因头部完美排列成双排,其棕榈酸侧链位于头部排列的两侧。我们将这两种前药衍生物在HOPG上的超远程有序排列归因于一方面分子间氢键的综合作用,另一方面是脂肪族侧链与石墨之间的范德华相互作用。如果前药衍生物能够在生物相容性底物上实现,那么通过无损物理吸附机制将其二维固定化对于药物递送等应用可能是有用的。