12November/ December 2009 interpretation of gradient or isocratic conditions. Small scale purifications can be expedited by reproducing the gradient method of choice on automated laboratory Flash- LC equipment. Often however, isocratic conditions are favoured for use with simpler or larger scale flash purification equipment. Isocratic conditions for any particular analyte can be estimated from its retention time ( see Figure 2). The reported gradient profile is engineered so that the estimated solvent composition that it predicts, results in the analyte having a retention factor under those isocratic conditions that is suitable for a preparative purification process. For absolute confidence in the selected method it is advisable to run one TLC to confirm the suitability of the solvent system and to estimate the sample loading prior to transferring the separation to a preparative process. Speed and simplicity are key factors towards successful implementation of this screening approach with the end user. A standard screen of six methods takes approximately 45 minutes. The Chemstation software running the instrument is operated with Easy- Access software to facilitate open- access sample login and to build the method screen. It then automatically generates a report and emails it to the users. It is important to note that UV detection can be an issue when working with normal phase solvents, especially those that have a very high UV cut- off ( e. g. toluene or acetone). Alternative HPLC detectors such as evaporative light scattering detection ( ELSD) provide complementary information to UV when solvent UV background is prohibitive or because the analyte lacks a significant chromophore. Reverse Phase Flash method screening Bonded Flash silica, including C18 bonded silica for Reverse Phase Flash- LC, is readily available in pre- packed commercial columns ( Crane et al. 4). It offers a useful complementary method to the normal phase separation mode as analyte selectivity can be very different, as can the solvent compatibility and solubility ( e. g. for alkanes, ethyl acetates, ketones or ethers). Moreover, since reverse phase HPLC is often used as an analytical technique of choice to follow chemical reactions, this analytical method can often provide the foundation for perfectly reasonable RP Flash purification and an integrated purification workflow. A method screening system was designed and built using standard HPLC equipment that enabled an unskilled user to quickly assess the feasibility of a reverse phase Flash purification. The screen comprises four sets of conditions performed on a scaling Flash column ( 4.6mm x 250mm) using a generic gradient ( see Table 3). The same generic gradient is pre- installed on the automated laboratory Flash instrument to allow for simple transfer. The screening system is designed to scout for, or verify, RP phase conditions as well as provide an estimate of the preparative loading for a successful Flash purification. This negates the need for a loading study and facilitates a rapid purification workflow. The preparative loading is estimated from the resolution between critical components of choice on the chromatogram. For absolute ease of use by the end users, the resolution is expressed in time units ( e. g. T in minutes) and the preparative loading expressed as percent weight on ( RP) silica ( see Figure 3). This approach has been implemented and is particularly well suited to enabling rapid purification workflows on the laboratory scale ( see Figure 4). Again, speed and simplicity are key factors towards successful implementation of this technique with the end user. A standard screen of four methods takes approximately 90 minutes. Automation of the method screening, method verification and loading study combined with automated laboratory Flash- LC equipment makes for a RP Flash purification workflow that is light, reliable and rapid. Conclusion Method screening systems have been put in place to facilitate the use of preparative Flash- LC in order to realise efficiency gains and achieve quality specifications in the chemistry laboratory compared to traditional approaches. Comprehensive and automated method screening gives facile and rapid access to optimal separation conditions. Any chemist is capable of accessing consistent and optimal purification conditions independent of their depth of knowledge in Flash- LC method development. The implementation of an automated and integrated Flash- LC method screen has had a significant impact on working practices in our research and development laboratories. The approach has removed technical barriers for the chemists which has resulted in greater uptake of the technique. It has enabled the development of higher quality methods in shorter timeframes so increasing the speed to and quality of purifications run by Flash- LC in our laboratories. At laboratory scale, an integrated approach combines automated screening and purification equipment to facilitate rapid access to pure materials. For large scale Flash chromatography ( e. g. pilot scale) the method screening approach consistently generates methods with a strong foundation for further optimisation, reducing the overall method development time. In this way, appropriate application of Flash- LC method development has realised increases in the individual chemist's and the overall project's productivity. References 1. W. C. Still, M. Kahn, A. Mitra; J. Org. Chem.; 43 ( 1978) 2923 2. L. R. Snyder, J. L. Glajch, J. J. Kirkland; J. Chromatogr.; 218 ( 1981) 299 3. J. L. Glajch, J. J. Kirkland, L. R. Snyder; J. Chromatogr.; 238 ( 1982) 269 4. L. J. Crane, M. Zief, J. Horvath; Amer. Lab.; 13 ( 1981) 128 Figure 4: A schematic of the workflow for a laboratory scale RP- Flash purification: 1. Feasibility step, if a reversed HPLC method is used to monitor a chemical reaction it can be used to assess feasibility by demonstrating selectivity for critical components; 2. Verification and optimisation step, the same sample is run on the Reverse Phase Flash screen, suitability of the RP Flash silica is confirmed and optimal loading can be estimated; 3. Run purification, the sample is loaded on the Flash reverse phase cartridge and exhibits the expected scale- up, enabling predictable peak tracking and collection of the desired product( s). Figure 3: A chart used to estimate preparative loading expressed as percent weight on ( RP) silica from a chromatogram produced by the RP Flash method screening system.

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