SUPA, School of Physics and Astronomy, University of St Andrews, St Andrews, Fife, UK. ya10@st‑andrews.ac.uk
Opt Lett. 2013 Sep 1;38(17):3402-5. doi: 10.1364/OL.38.003402.
The cell selective introduction of therapeutic agents remains a challenging problem. Here we demonstrate spatially controlled cavitation instigated by laser-induced breakdown of an optically trapped single gold nanoparticle of diameter 100 nm. The energy breakdown threshold of the gold nanoparticle with a single nanosecond laser pulse at 532 nm is three orders of magnitude lower than water, which leads to nanocavitation allowing single cell transfection. We quantify the shear stress to cells from the expanding bubble and optimize the pressure to be in the range of 1-10 kPa for transfection. The method shows transfection of plasmid DNA into individual mammalian cells with an efficiency of 75%.
细胞选择性引入治疗剂仍然是一个具有挑战性的问题。在这里,我们展示了通过激光诱导的直径为 100nm 的单个金纳米粒子的光阱破坏引发的空间控制空化。直径为 100nm 的单个金纳米粒子在 532nm 的单个纳秒激光脉冲下的能量破坏阈值比水低三个数量级,这导致了允许单细胞转染的纳米空化。我们从膨胀气泡中定量计算了对细胞的剪切力,并将压力优化在 1-10kPa 的范围内用于转染。该方法显示将质粒 DNA转染到单个哺乳动物细胞中的效率为 75%。