Arumuganathar Sumathy, Irvine Scott, McEwan Jean R, Jayasinghe Suwan N
Department of Mechanical Engineering, University College London, Torrington Place, London WC1E 7JE, UK.
Biomed Mater. 2007 Jun;2(2):158-68. doi: 10.1088/1748-6041/2/2/015. Epub 2007 May 17.
We recently demonstrated the ability to use electrified jets under stable conditions for the generation of cell-bearing droplets to the formation of composite threads which are biologically active. Our studies established that processed cells were viable over several generations post-jetting and -threading. These harmless and successful techniques for jet-based cell handling to deployment for precision deposition have great potential and widespread applications in bioengineering and biotechnology. Nonetheless, our investigations into 'bio-electrosprays' and 'cell electrospinning' have elucidated these jets having direct applicability in regenerative and therapeutic medicine to studies in developmental biology. For these very reasons, jet methodologies having the capability to safely handle living organisms for drop and placing are increasingly gaining the interests of life scientists. We now demonstrate yet another technique (a non-electric field-driven approach, previously never explored with jetting living cells), possessing the ability to directly handle the processing of primary living organisms by means of the flow of a cell suspension within a needle placed in a pressure chamber in the presence of an applied pressure difference. The technique we introduce here is referred to as 'aerodynamically assisted bio-jets/-jetting' which is driven completely by aerodynamic forces applied over an exit orifice by way of a differential pressure. Our investigations present an operational window in which stable jetting conditions are achieved for the formation of a near-monodispersed distribution of cell-bearing droplets and droplet residues. Finally, the aerodynamically bio-jetted living primary organisms are assessed (over both short and long time points) for cellular viability by means of FACScan, a flow cytometry technology which quantifies the percentage of living and dead cells. These advanced biophysical and bioengineering studies elucidate the emergence of a non-electric field-driven bio-jetting technology which now joins the cell jetting race.
我们最近展示了在稳定条件下使用带电射流来生成携带细胞的液滴,进而形成具有生物活性的复合纤维的能力。我们的研究表明,经过处理的细胞在喷射和纺丝后的几代中仍具有活力。这些用于基于射流的细胞处理以实现精确沉积的无害且成功的技术在生物工程和生物技术中具有巨大潜力和广泛应用。尽管如此,我们对“生物电喷雾”和“细胞电纺丝”的研究表明,这些射流在再生医学和治疗医学以及发育生物学研究中具有直接适用性。正是由于这些原因,能够安全处理活体以进行滴注和放置的射流方法越来越受到生命科学家的关注。我们现在展示另一种技术(一种非电场驱动的方法,以前从未用于喷射活细胞),它能够通过在存在外加压力差的情况下,使细胞悬浮液在置于压力室中的针内流动,直接处理原生活体的加工过程。我们在此介绍的技术被称为“空气动力学辅助生物射流/喷射”,它完全由通过压差施加在出口孔上的空气动力驱动。我们的研究给出了一个操作窗口,在该窗口中可实现稳定的喷射条件,以形成携带细胞的液滴和液滴残余物的近单分散分布。最后,通过FACScan(一种流式细胞术技术,用于量化活细胞和死细胞的百分比)对空气动力学生物喷射的原生活体在短时间和长时间点进行细胞活力评估。这些先进的生物物理和生物工程研究阐明了一种非电场驱动的生物喷射技术的出现,该技术现已加入细胞喷射竞争行列。