Archive |
Stem Cell applications and opportunities in drug discovery
By Dr Mark A. Thiede
The high attrition rate of late stage drug candidates has led the pharmaceutical and biotech industries to a reassess the in vitro models used to select and validate drug targets and subsequent lead molecules.
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The microplate market past, present and future
By Dr Peter Banks
Microplates and the peripheral markets of liquid handling and detection technologies exist within almost all laboratories performing assays. This article discusses what, if any, are their growth expectations and whether there are new technologies on the horizon that could make the microplate obsolete.
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Letting the target determine your compound acquisition strategy
By Dr John Harris
With compound libraries likely to remain the cornerstone of hit and lead discovery for the foreseeable future, this paper seeks to summarise current and future approaches to optimal library design and compound acquisition, using examples and experimental evidence of the success, limitations and weaknesses of target-led approaches in comparison with diversity-screening alternatives.
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High throughput screening, high content screening, primary and stem cells new techniques now converging
By Dr Richard M. Eglen
Over the past decade, the use of cell-based assays has accelerated in modern drug discovery. Indeed, the majority of assays in either target validation or lead identification/optimisation all now employ cell-based technologies.
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Livening up HCS IMAGING
By Dr John Comley
With the aid of recent end-user feedback, this article investigates interest in and use of live cell and kinetic HCS imaging; most wanted application areas: advantages of live cell HCS imaging; live cell HCS assays of greatest interest; what’s limiting live cell HCS; what is most needed to grow the live cell and kinetic imaging market; assay requirements; and preferred HCS instrument configuration.
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Predicting transporter-mediated drug-drug interactions based on in vitro cell permeability assays
By Dr Chris Bode
Drugs may fail in clinical development or post-marketing for a variety of reasons: they may simply not be as effective as anticipated; poor pharmacokinetic properties may prevent them from reaching their intended target in therapeutic doses; or they are proven unsafe.
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Generation II DNA sequencing technologies
By Dr Stephen F. Kingsmore, Dr Jenny C. van Velkinburgh, Dr Joann Mudge, and Dr Gregory D. May
Generation II DNA sequencing has been widely heralded as a disruptive technology, generating tens of millions of random short sequences at efficiencies up to 20,000-fold greater than Generation I (Sanger) sequencing. This review addresses the technical specifications of the leading Generation II sequencing technologies and current applications of relevance to drug discovery and development. more...