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Continuous cell washing and mixing driven by an ultrasound standing wave within a microfluidic channel

机译:在微流体通道内由超声驻波驱动的连续细胞洗涤和混合

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Ultrasound standing wave radiation force and laminar flow have been used to transfer yeast cells from one liquid medium to another(washing)by a continuous field-flow fractionation(FFF)approach.Two co-flowing streams,a cell-free suspending phase(flow rate > 50% of the total flow-through volume)and a yeast suspension,were introduced parallel to the nodal plane of a 3 MHz standing wave resonator.The resonator was fabricated to have a single pressure nodal plane at the centre line of the chamber.Laminar flow ensured a stable interface was maintained as the two suspending phases flowed through the sound field.Initiation of the ultrasound transferred cells to the cell-free phase within 0.5 s.This particle transfer procedure circumvents the pellet formation and re-suspension steps of centrifuge based washing procedures.In addition,fluid mixing was demonstrated in the same chamber at higher sound pressures.The channel operates under negligible backpressure(cross-section,0.25 x 10 mm)and with only one flow convergence and one flow division step,the channel cannot be easily blocked.The force acting on the cells is small;less than that experienced in a centrifuge generating100g.The acoustically-driven cell transfer and mixing procedures described may be particularly appropriate for the increasingly complex operations required in molecular biology and microbiology and especially for their conversion to continuous flow processes.
机译:超声波驻波辐射力和层流已通过连续场流分馏(FFF)方法将酵母细胞从一种液体培养基转移到另一种液体(洗涤)。两股同流,无细胞悬浮相(流)率>总流通量的50%)和酵母悬浮液平行于3 MHz驻波谐振器的节点平面引入。谐振器被制造为在腔室的中心线具有单个压力节点平面层流确保在两个悬浮相流过声场时保持稳定的界面。超声转移的细胞在0.5 s内启动至无细胞相。此颗粒转移程序规避了沉淀的形成和重悬浮步骤基于离心的洗涤程序。此外,在较高的声压下在同一腔室中进行了流体混合。通道在可忽略的反压(横截面为0.25 x 10 mm)下且在仅需一个流会聚和一个分流步骤,就不能轻易阻塞通道。作用在细胞上的力很小;比产生100g离心机所经历的力要小。所述的声驱动细胞转移和混合程序可能特别适合分子生物学和微生物学中日益复杂的操作,尤其是将其转换为连续流动过程的操作。

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