High-throughput and ultra-high-throughput screening: solution- and cell-based approaches.
By S. Sundberg. Current Opinion in Biotechnology, 2000
402 citations recorded by the source corpus.
Subfields: Biomedical Engineering
View Paper: https://www.semanticscholar.org/paper/fb023ffa634810b17ac638c4e313a5433e8dab90
How researchers see this paper
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In Biomedical Engineering
- David A. Weitz
- Petra S. Dittrich
- Andreas Manz
- M. Himmel
- Roland Zengerle
- S. Haeberle
- Safa A. Damiati
- Leoni A. Kunz-Schughart
Citations in the corpus
- Outlook for cellulase improvement: screening and selection strategies. (2006, methodology): “It is often implemented using 96-well microtiter plates, although some researchers are moving towards 384-well and higher density plate formats with the help of accurate, low-volume dispensing instruments (Sundberg, 2000).”
- Droplet-based microfluidic platforms for the encapsulation and screening of Mammalian cells and multicellular organisms. (2008, background): “Hence, a wide range of commercially available fluorescence-based assays (Gonzalez and Negulescu, 1998; Sundberg, 2000) can potentially be performed in a high-throughput fashion.”
- Ligand–receptor interaction platforms and their applications for drug discovery (2012, background): “In general, these techniques are readily amenable to automation using so-called mix and read assays for many targets, and allow straightforward miniaturization of the assays, so high throughput screening (HTS), even ultra-HTS, can be performed [50,52,56-58].”
- Biosynthesis of anthraquinones in cell cultures of the Rubiaceae (2001, background): “Recently, DNA microarrays, consisting of thousands of individual gene sequences printed in a high-density array on a glass microscope slide, provide an exciting new tool for studying gene expression on a very large scale (Graves, 1999; Sundberg, 2000).”
- Microfluidic lab-on-a-chip platforms: requirements, characteristics and applications. (2010, background): “based assays received increasing interest over the last years [43, 44].”
- Lab-on-a-chip: microfluidics in drug discovery (2006, methodology): “Alternatively, screening assays can be performed in a continuous manner using a flowing system that allows the analysis and isolation of compounds on a single chi”
- The Use of 3-D Cultures for High-Throughput Screening: The Multicellular Spheroid Model (2004, background): “One field of research and development for HTS focuses on automation and miniaturization issues to provide ultra–high-throughput approaches.(1,2) Another field concentrates instead on the design and adaptation of novel, more complex test systems to gain deeper insight into the effects and functions o”
- Microfluidic Devices for Drug Delivery Systems and Drug Screening (2018, background): “This system lowers sample and reagent consumption from the microliter to the nanoliter range and minimizes the multistep liquid handling operation [145].”
- PubChem3D: Biologically relevant 3-D similarity (2011, background): “Background Recent advances in combinatorial chemistry [1-6] and high-throughput screening technology [7-17] have made the synthesis and screening of diverse chemical compounds easier, helping to create a demand in the biomedical research community for archives of publicly available screening data.”