首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >A novel approach for monitoring extracellular acidification rates:based on bead injection spectrophotometry and the lab-on-valve system
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A novel approach for monitoring extracellular acidification rates:based on bead injection spectrophotometry and the lab-on-valve system

机译:一种监测细胞外酸化率的新方法:基于珠粒注射分光光度法和实验室阀门系统

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Monitoring extracellular acidification rates (ECARs) is important for the study of cellular activities, since it allows for the evaluation of factors that alter metabolic function, such as stimulants, inhibitors, toxins as well as receptor and non-receptor mediated events. While the light addressable potentiometric sensor (Cytosensor Microphysiometer) has been the principal tool for ECARs measurement in the past, this work introduces a novel method that exploits an immobilized pH indicator on the surface of microcarrier beads (Sephadex) and is probed with a fiber optic coupled spectrophotometer. Likewise, live cells under investigation were also immobilized on microcarrier beads (Cytopore). These beads are metered, transported and monitored within a microfluidic system, termed as the Lab-on-Valve (LOV). Use of carrier beads in conjunction with Bead Injection Spectrophotometry and a Lab-on-Valve module (BIS-LOV), makes ECAR measurements reliable and automated. The feasibility of the BIS-LOV approach is demonstrated measuring ECARs of the mouse hepatocyte cell line, TABX.2S, grown on Cytopore beads packed within the central channel of the LOV system. These immobilized cells were perfused in a phosphate buffer carrier solution (capacity: 1 mmol L~(-1), pH 7.4). Protons extruded from 10~5 to 10~6 cells were accumulated during a stopped flow period of 220 s followed by a pH measurement, detected by changes in absorbance of the pH indicator bonded to the microcarrier beads. Addition of metabolic inhibitors (sodium azide, oxamic acid) to the carrier buffer solution can induced an increase or decrease of the basal proton extrusion rate in a very reproducible manner. Comparison of the BIS-LOV technique to the Cytosensor microphysiometer and literature confirms the validity of this novel approach, highlighting its advantages and suggesting future improvements that will make the BIS-LOV a practical tool for routine ECARs measurement.
机译:监测细胞外酸化率(ECAR)对于研究细胞活性非常重要,因为它可以评估改变代谢功能的因素,例如刺激剂,抑制剂,毒素以及受体和非受体介导的事件。尽管光寻址电位传感器(Cytosensor Microphysiometer)过去一直是ECAR测量的主要工具,但这项工作引入了一种新方法,该方法利用微载体珠(Sephadex)表面上固定的pH指示剂并用光纤探测耦合分光光度计。同样,被研究的活细胞也被固定在微载体珠(Cytopore)上。这些微珠在称为阀实验室(LOV)的微流体系统中进行计量,运输和监控。结合使用载体微珠,微珠注射分光光度法和阀上实验室模块(BIS-LOV),可确保ECAR测量的可靠性和自动化程度。证明了BIS-LOV方法的可行性,可以测量在堆积在LOV系统中央通道内的细胞孔珠上生长的小鼠肝细胞细胞TABX.2S的ECAR。将这些固定化的细胞灌注在磷酸盐缓冲液载体溶液中(容量:1 mmol L〜(-1),pH 7.4)。在220 s的停止流动期间,从10〜5个细胞挤出到10〜6个细胞的质子积聚,随后进行pH测量,这是通过与微载体珠粒结合的pH指示剂的吸光度变化来检测的。向载体缓冲溶液中添加代谢抑制剂(叠氮化钠,草酰胺酸)可以非常可重复的方式引起基础质子挤出速率的增加或降低。将BIS-LOV技术与细胞传感器微生理仪和文献进行比较,证实了该新方法的有效性,突出了其优势,并提出了未来的改进方法,这些将使BIS-LOV成为常规ECAR测量的实用工具。

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