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Method of localized removal of cells using a bolt‐clamped Langevin transducer with an ultrasonic horn

机译:使用带超声变幅杆的螺栓固定兰格文换能器局部去除细胞的方法

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摘要

Cell isolation by eliminating undesirable cell aggregations or colonies with low activity is essential to improve cell culture efficiency. Moreover, when creating tissues from induced pluripotent stem cells, residual undifferentiated cells must be removed to prevent tumor formation in vivo. Here, we evaluated the use of ultrasonic irradiation, which can apply energy locally without contact, and proposed a method to eliminate cells in a small area of culture by ultrasonic irradiation from a Langevin transducer. We constructed a device that incorporated a bolt‐clamped 19.84 kHz Langevin transducer with an ultrasonic horn and determined the optimal conditions for stable elimination of cells in small areas of a 35‐mm culture dish. The optimal conditions were as follows: number of cycles = 400, clearance distance = 1 mm, volume of medium = 4 mL, and distance from the center of culture surface = 0 mm. The mean cell elimination area under these conditions was 0.097 mm . We also evaluated the viability of neighboring cells after ultrasonic irradiation by fluorescent staining and found that most cells around the elimination area survived. These findings suggest that the proposed method has potential for localized elimination of cells without the need for contact with the cell surface.
机译:通过消除低活性的不良细胞聚集或集落来分离细胞对于提高细胞培养效率至关重要。而且,当从诱导的多能干细胞创建组织时,必须去除残留的未分化细胞以防止体内肿瘤形成。在这里,我们评估了超声辐照的使用,该超声辐照可以在不接触的情况下局部施加能量,并提出了一种通过Langevin换能器进行超声辐照以消除培养的小区域中细胞的方法。我们构建了一种结合了螺栓固定式19.84 kHz Langevin换能器和超声变幅杆的设备,并确定了稳定消除35 mm培养皿小面积细胞的最佳条件。最佳条件如下:循环数= 400,清除距离= 1 mm,培养基体积= 4 mL,离培养表面中心的距离= 0 mm。在这些条件下的平均细胞消除面积为0.097mm。我们还通过荧光染色对超声波照射后的邻近细胞进行了评估,发现消除区域周围的大多数细胞都可以存活。这些发现表明,所提出的方法具有在不与细胞表面接触的情况下局部消除细胞的潜力。

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