天美传媒

ISSN: 2167-065X

Clinical Pharmacology & Biopharmaceutics
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A high throughput solubility assay by microscale shake-flask and rapid quantification of UHPLCUV- CLND for drug discovery

7th Annual Global Pharma Summit

Baiwei Lin

Genentech Inc., USA

Posters & Accepted Abstracts: Clin Pharmacol Biopharm

DOI:

Abstract
The rapid determination of key physical properties of lead compounds is essential to the drug discovery process. Solubility is one of the most important properties since good solubility is needed not only for obtaining reliable in vitro and in vivo assay results in early discovery but also to ensure sufficient concentration of the drug being in circulation to get the desired therapeutic exposure at the target of interest. In order for medicinal chemists to tune solubility of lead compounds, a rapid assay is needed to provide solubility data that is accurate and predictive so that it can be reliably used for designing the next generation of compounds with improved properties. To ensure speed and data quality, we developed a high throughput solubility assay that utilizes a single calibration UHPLC-UV-CLND method and a 24 hours shake-flask format for rapid quantification. A set of 46 model compounds was used to demonstrate that the method is accurate, reproducible and predictive. Here we present development of the assay, including evaluation of quantification method, filtration membranes, equilibrium times, DMSO concentrations and buffer conditions. A comparison of thermodynamic solubility results to our high throughput 24 hour shake-flask solubility assay results is also discussed.
Biography

Email: lin.baiwei@gene.com

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