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Determination of Mammalian Cell Counts Cell Size and Cell Health Using the Moxi Z Mini Automated Cell Counter

机译:使用Moxi Z Mini自动化细胞计数器测定哺乳动物细胞数细胞大小和细胞健康

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摘要

Particle and cell counting is used for a variety of applications including routine cell culture, hematological analysis, and industrial controls1-5. A critical breakthrough in cell/particle counting technologies was the development of the Coulter technique by Wallace Coulter over 50 years ago. The technique involves the application of an electric field across a micron-sized aperture and hydrodynamically focusing single particles through the aperture. The resulting occlusion of the aperture by the particles yields a measurable change in electric impedance that can be directly and precisely correlated to cell size/volume. The recognition of the approach as the benchmark in cell/particle counting stems from the extraordinary precision and accuracy of its particle sizing and counts, particularly as compared to manual and imaging based technologies (accuracies on the order of 98% for Coulter counters versus 75-80% for manual and vision-based systems). This can be attributed to the fact that, unlike imaging-based approaches to cell counting, the Coulter Technique makes a true three-dimensional (3-D) measurement of cells/particles which dramatically reduces count interference from debris and clustering by calculating precise volumetric information about the cells/particles. Overall this provides a means for enumerating and sizing cells in a more accurate, less tedious, less time-consuming, and less subjective means than other counting techniques6.Despite the prominence of the Coulter technique in cell counting, its widespread use in routine biological studies has been prohibitive due to the cost and size of traditional instruments. Although a less expensive Coulter-based instrument has been produced, it has limitations as compared to its more expensive counterparts in the correction for "coincidence events" in which two or more cells pass through the aperture and are measured simultaneously. Another limitation with existing Coulter technologies is the lack of metrics on the overall health of cell samples. Consequently, additional techniques must often be used in conjunction with Coulter counting to assess cell viability. This extends experimental setup time and cost since the traditional methods of viability assessment require cell staining and/or use of expensive and cumbersome equipment such as a flow cytometer.The Moxi Z mini automated cell counter, described here, is an ultra-small benchtop instrument that combines the accuracy of the Coulter Principle with a thin-film sensor technology to enable precise sizing and counting of particles ranging from 3-25 microns, depending on the cell counting cassette used. The M type cassette can be used to count particles from with average diameters of 4 - 25 microns (dynamic range 2 - 34 microns), and the Type S cassette can be used to count particles with and average diameter of 3 - 20 microns (dynamic range 2 - 26 microns). Since the system uses a volumetric measurement method, the 4-25 microns corresponds to a cell volume range of 34 - 8,180 fL and the 3 - 20 microns corresponds to a cell volume range of 14 - 4200 fL, which is relevant when non-spherical particles are being measured. To perform mammalian cell counts using the Moxi Z, the cells to be counted are first diluted with ORFLO or similar diluent. A cell counting cassette is inserted into the instrument, and the sample is loaded into the port of the cassette. Thousands of cells are pulled, single-file through a "Cell Sensing Zone" (CSZ) in the thin-film membrane over 8-15 seconds. Following the run, the instrument uses proprietary curve-fitting in conjunction with a proprietary software algorithm to provide coincidence event correction along with an assessment of overall culture health by determining the ratio of the number of cells in the population of interest to the total number of particles. The total particle counts include shrunken and broken down dead cells, as well as other debris and contaminants. The results are presented in histogram format with an automatic curve fit, with gates that can be adjusted manually as needed.Ultimately, the Moxi Z enables counting with a precision and accuracy comparable to a Coulter Z2, the current gold standard, while providing additional culture health information. Furthermore it achieves these results in less time, with a smaller footprint, with significantly easier operation and maintenance, and at a fraction of the cost of comparable technologies.
机译:颗粒和细胞计数可用于多种应用,包括常规细胞培养,血液学分析和工业控制 1-5 。细胞/颗粒计数技术的一项关键突破是华莱士·库尔特在50年前开发的库尔特技术。该技术涉及在微米大小的孔上施加电场,并通过孔对单个颗粒进行流体动力学聚焦。颗粒对孔造成的最终阻塞会产生可测量的电阻抗变化,该变化可直接且精确地与细胞大小/体积相关。该方法作为细胞/颗粒计数基准的认可源于其颗粒大小和计数的非凡精度和准确性,特别是与基于手动和成像的技术相比(Coulter计数器的准确性约为98%,而75- 80%用于手动和基于视觉的系统。这可以归因于以下事实:与基于成像的细胞计数方法不同,库尔特技术对细胞/颗粒进行了真正的三维(3-D)测量,可通过计算精确的体积显着减少来自碎片和聚类的计数干扰有关细胞/颗粒的信息。总体而言,这提供了一种比其他计数技术 6 更准确,更乏味,更省时,更省力,更主观的方法来枚举和确定细胞大小。尽管库尔特技术在细胞计数中占有重要地位由于传统仪器的成本和尺寸大,它在常规生物学研究中的广泛使用已被禁止。尽管已经生产出了一种价格较低廉的基于库尔特的仪器,但与更昂贵的同类仪器相比,它在校正“符合事件”时有局限性,在“符合事件”中,两个或多个细胞同时通过孔并同时进行了测量。现有库尔特技术的另一个局限性是缺乏有关细胞样品整体健康状况的指标。因此,必须经常将其他技术与库尔特计数结合使用以评估细胞活力。由于传统的生存力评估方法需要细胞染色和/或使用昂贵且笨重的设备(例如流式细胞仪),因此这延长了实验设置时间和成本。Moxi Z mini自动化细胞计数器是一种超小型台式仪器结合了库尔特原理的精确度和薄膜传感器技术,可根据所使用的细胞计数盒精确地定尺寸和计数3-25微米范围内的颗粒。 M型盒可用于计数平均直径为4-25微米(动态范围2-34微米)的颗粒,S型盒可用于计数平均直径为3-20微米(动态的颗粒)范围2-26微米)。由于系统使用体积测量方法,因此4-25微米对应于34-8,180 fL的晶胞体积范围,而3-20微米对应于14-4200 fL的晶胞体积范围,这在非球形时非常重要正在测量颗粒。为了使用Moxi Z进行哺乳动物细胞计数,首先将要计数的细胞用ORFLO或类似的稀释剂稀释。将细胞计数盒插入仪器中,并将样品装入盒的端口。在8到15秒钟内,成千上万个细胞通过薄膜中的“细胞传感区”(CSZ)被拉入单行。运行后,该仪器将专有曲线拟合与专有软件算法结合使用,以提供巧合事件校正,并通过确定目标群体中细胞数与总菌落数之比来评估整体培养健康状况。粒子。颗粒总数包括收缩的和破裂的死细胞,以及其他碎片和污染物。结果以直方图格式显示,并具有自动曲线拟合功能,可根据需要手动调整闸门数量。最终,Moxi Z能够以与当前的黄金标准Coulter Z2相当的精度和准确性进行计数,同时提供了额外的培养功能健康信息。此外,它以更少的时间,更小的占地面积,显着的操作和维护变得更容易实现这些结果,并且成本仅为同类技术的一小部分。

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