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Time-Resolved Pharmacological Studies using Automated On-line Monitoring of Five Parallel Suspension Cultures

机译:使用自动在线监测五种平行悬浮培养物的时间分辨药理学研究

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摘要

Early stage pharmacological studies rely on in vitro methodologies for screening and testing compounds. Conventional assays based on endpoint measurements provide limited information because the lack in temporal resolution may not determine the pharmacological effect at its maximum. We developed an on-line, automated system for near real-time monitoring of extracellular content from five parallel suspension cultures, combining cell density measurements with a high-resolution separations every 12 minutes for 4 days. Selector and switching valves provide the fluidic control required to sample from one culture during the analysis of the previous sample from another culture, a time-saving measure that is fundamental to the throughput of the presented system. The system was applied to study the metabolic effects of the drugs rotenone, β-lapachone and clioquinol using lactate as metabolic indicator. For each drug, 96 assays were executed on the extracellular matrix at three concentrations with two controls in parallel, consuming only 5.78 mL of media from each culture over four days, less than 60 μL per analysis. The automated system provides high sample throughput, good temporal resolution and low sample consumption combined with a rugged analytical method with adequate sensitivity, providing a promising new platform for pharmacological and biotechnological studies.
机译:早期药理研究依赖于体外方法来筛选和测试化合物。基于终点测量的常规测定只能提供有限的信息,因为缺乏时间分辨率可能无法最大程度地确定药理作用。我们开发了一种在线自动化系统,用于对来自五种平行悬浮培养物的细胞外含量进行近实时监测,将细胞密度测量与每隔12分钟的高分辨率分离相结合,持续4天。选择器和切换阀提供了在分析另一种培养物的先前样品的过程中从一种培养物进行采样所需的流体控制,这是一种节省时间的措施,对本系统的通量至关重要。该系统以乳酸为代谢指标,用于研究鱼藤酮,β-拉帕酮和氯喹诺醇的代谢作用。对于每种药物,在细胞外基质上以三种浓度与两个对照平行进行96个测定,在四天内仅消耗每种培养物的5.78μmL培养基,每次分析小于60μL。自动化系统可提供高样品通量,良好的时间分辨率和较低的样品消耗,再加上具有足够灵敏度的坚固耐用的分析方法,为药理学和生物技术研究提供了有希望的新平台。

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