Design and Implementation of High Throughput Screening Assays for Drug Discoveries

F. Bokhari, A. Albukhari
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引用次数: 2

Abstract

The process of drug discovery is challenging and a costly affair. It takes about 12 to 15 years and costs over $1 billion dollars to develop a new drug and introduce the finished product in the market. With the increase in diseases, virus spread, and patients, it has become essential to invent new medicines. Consequently, today researchers are becoming interested in inventing new medicines faster by adopting higher throughput screening methods. One avenue of approach to discovering drugs faster is the High-Throughput Screening (HTS) method, which has gained a lot of attention in the previous few years. Today, High-Throughput Screening (HTS) has become a standard method for discovering drugs in various pharmaceutical industries. This review focuses on the advancement of technologies in High-Throughput Screening (HTS) methods, namely fluorescence resonance energy transfer (FRET), biochemical assay, fluorescence polarization (FP), homogeneous time resolved fluorescence (HTRF), Fluorescence correlation spectroscopy (FCS), Fluorescence intensity distribution analysis (FIDA), Nuclear magnetic resonance (NMR), and research advances in three major technology areas including miniaturization, automation and robotics, and artificial intelligence, which promises to help speed up the discovery of medicines and its development process.
药物发现的高通量筛选试验的设计和实施
药物发现的过程是具有挑战性和昂贵的事情。开发一种新药并将其推向市场,大约需要12到15年的时间,耗资超过10亿美元。随着疾病、病毒传播和病人的增加,发明新药变得至关重要。因此,今天的研究人员越来越有兴趣通过采用更高通量的筛选方法来更快地发明新药。一种更快发现药物的方法是高通量筛选(HTS)方法,在过去的几年里得到了很多关注。如今,高通量筛选(HTS)已成为各个制药行业发现药物的标准方法。本文综述了高通量筛选(HTS)方法的研究进展,即荧光共振能量转移(FRET)、生化分析、荧光极化(FP)、均匀时间分辨荧光(HTRF)、荧光相关光谱(FCS)、荧光强度分布分析(FIDA)、核磁共振(NMR),以及小型化、自动化和机器人技术三大技术领域的研究进展。还有人工智能,它有望帮助加快药物的发现和开发过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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