Hughes Fraser, Cookson Alex, Tamaki Fabio, Bailey Christopher, Gray David W, Wrobel Karolina, Cookson Kirsty, Bell Steve, Tarver Gary
Drug Discovery Unit, School of Life Sciences, University of Dundee, DD1 5EH, United Kingdom.
Drug Discovery Unit, School of Life Sciences, University of Dundee, DD1 5EH, United Kingdom.
SLAS Technol. 2024 Dec;29(6):100204. doi: 10.1016/j.slast.2024.100204. Epub 2024 Oct 11.
Dry DMSO can rapidly pull water vapor out of the air due to its hygroscopic nature. This is a well-documented problem within drug discovery, particularly within high-throughput screening (HTS). This hydration is caused by atmospheric moisture being absorbed each time a compound library is used. This effect becomes increasingly pronounced when a compound library is used routinely. The result of this hydration is a change to both the total volume of solution and the concentration of sample still in solution. This can result in a large amount of variability in the measured biological activity of a sample depending on the library usage. In this paper, we show the detrimental effects the hydration of sample libraries has on the reproducibility of biological data and present a novel way to remove it from HTS library plates. Our approach involves creating a DMSO-rich environment, created by placing anhydrous DMSO in compound storage pods purged with nitrogen, and incubating library plates in this environment for up to 3 days. Quantification via evaporative light scattering detection (ELSD) showed that removing water greatly increased the molarity of solutions, with a greater effect being seen for compounds with poor solubility. We also demonstrated how this approach can restore the inhibitory activity of stock solutions of compounds (pIC) of samples containing ∼30 % water from >30 µM to sub-micromolar after moisture removal. This method improves the reliability of tested compounds in HTS by potentially saving pharmaceutical companies hundreds of thousands of dollars in screening campaigns and increasing the quality of data.
由于其吸湿性,干燥的二甲基亚砜(DMSO)能迅速从空气中吸收水蒸气。这在药物发现领域,尤其是在高通量筛选(HTS)中,是一个有充分文献记载的问题。这种水合作用是由于每次使用化合物库时大气中的水分被吸收所致。当常规使用化合物库时,这种影响会变得越来越明显。这种水合作用的结果是溶液总体积和仍在溶液中的样品浓度都发生变化。这可能导致根据库的使用情况,样品的测量生物活性出现大量变异性。在本文中,我们展示了样品库水合作用对生物数据再现性的有害影响,并提出了一种从HTS库板中去除它的新方法。我们的方法包括通过在充有氮气的化合物储存盒中放置无水DMSO来营造一个富含DMSO的环境,并将库板在该环境中孵育长达3天。通过蒸发光散射检测(ELSD)进行定量分析表明,去除水分极大地提高了溶液的摩尔浓度,对于溶解度差的化合物,效果更为明显。我们还展示了这种方法如何能将含水量约30%的样品中化合物储备溶液(pIC)的抑制活性在去除水分后从大于30µM恢复到亚微摩尔水平。这种方法通过有可能为制药公司在筛选活动中节省数十万美元并提高数据质量,提高了HTS中测试化合物的可靠性。