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开发和验证一种自动化微流控灌注平台,用于体外平行筛选化合物。

Development and validation of an automated microfluidic perfusion platform for parallelized screening of compounds in vitro.

机构信息

Elvesys - Microfluidic Innovation Center, Paris, France.

Center for Physiology and Pharmacology, Institute of Pharmacology, Medical University of Vienna, Vienna, Austria.

出版信息

Basic Clin Pharmacol Toxicol. 2023 Nov;133(5):535-547. doi: 10.1111/bcpt.13940. Epub 2023 Sep 17.

Abstract

Monoamine transporters are of great interest for their role in the physiological activity of the body and their link to mental and behavioural disorders. Currently, static well-plate assays or manual perfusion systems are used to characterize the interaction of psychostimulants, antidepressants and drugs of abuse with the transporters but still suffer from significant drawbacks caused by lack of automation, for example, low reproducibility, non-comparability of results. An automated microfluidic platform was developed to address the need for more standardized procedures for cell-based assays. An automated system was used to control and drive the simultaneous perfusion of 12 channels on a microfluidic chip, establishing a more standardized protocol to perform release assays to study monoamine transporter-mediated substrate efflux. D-Amphetamine, GBR12909 (norepinephrine transporter) and p-chloroamphetamine, paroxetine (serotonin transporter) were used as control compounds to validate the system. The platform was able to produce the expected releasing (D-Amphetamine, p-chloroamphetamine) or inhibiting (GBR12909, paroxetine) profiles for the two transporters. The reduction of manual operation and introduction of automated flow control enabled the implementation of stronger standardized protocols and the possibility of obtaining higher throughput by increasing parallelization.

摘要

单胺转运体在体内生理活动及其与精神和行为障碍的联系方面备受关注。目前,静态微孔板测定法或手动灌注系统用于表征精神兴奋剂、抗抑郁药和滥用药物与转运体的相互作用,但仍然存在由于缺乏自动化而导致的显著缺陷,例如重现性低、结果不可比。开发了一种自动化微流控平台来满足对更标准化细胞测定程序的需求。自动化系统用于控制和驱动微流控芯片上 12 个通道的同时灌注,建立更标准化的方案来进行释放测定以研究单胺转运体介导的底物外排。D-苯丙胺、GBR12909(去甲肾上腺素转运体)和对氯苯丙胺、帕罗西汀(血清素转运体)被用作对照化合物来验证该系统。该平台能够产生两种转运体的预期释放(D-苯丙胺、对氯苯丙胺)或抑制(GBR12909、帕罗西汀)特征。减少手动操作并引入自动化流量控制,使实施更强的标准化方案成为可能,并通过增加并行化获得更高的通量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf58/10952622/d9c08f7afa74/BCPT-133-535-g004.jpg

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