Center for Research at Bio/Nano Interface, Department of Chemistry, Shands Cancer Center, UF Genetics Institute, University of Florida, Gainesville, Florida 32611-7200, USA.
J Am Chem Soc. 2012 Aug 15;134(32):13164-7. doi: 10.1021/ja304115q. Epub 2012 Jul 26.
High quality nanocrystals have demonstrated substantial potential for biomedical applications. However, being generally hydrophobic, their use has been greatly limited by complicated and inefficient surface engineering that often fails to yield biocompatible nanocrystals with minimal aggregation in biological fluids and active targeting toward specific biomolecules. Using chimeric DNA molecules, we developed a one-step facile surface engineering method for hydrophobic nanocrystals. The procedure is simple and versatile, generating individual nanocrystals with multiple ligands. In addition, the resulting nanocrystals can actively and specifically target various molecular addresses, varying from nucleic acids to cancer cells. Together, the strategy developed here holds great promise in generating critical technologies needed for biomedical applications of nanocrystals.
高质量的纳米晶体在生物医学应用中显示出巨大的潜力。然而,由于其普遍的疏水性,其应用受到了极大的限制,因为复杂而低效的表面工程往往无法产生在生物流体中具有最小聚集性和对特定生物分子具有主动靶向性的生物相容性纳米晶体。我们使用嵌合 DNA 分子为疏水性纳米晶体开发了一种一步简便的表面工程方法。该程序简单且通用,可生成具有多种配体的单个纳米晶体。此外,所得的纳米晶体可以主动且特异性地靶向各种分子靶标,从核酸到癌细胞不等。总之,这里开发的策略在生成纳米晶体生物医学应用所需的关键技术方面具有巨大的潜力。