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A column classification system for SFC to help with method development has been developed. This article demonstrates how the system can be used to select a column when developing a new SFC method.

Gerstel GmbH & Co. KG (M?lheim an der Ruhr, Germany) and Spark Holland (Emmen, The Netherlands) have announced an original equipment manufacturer (OEM) agreement. The agreement will allow Gerstel to develop and market fully integrated automated dried blood spot (DBS) technology from Spark Holland that recently received a US patent.

Frederic Lynen discusses why LC–MS is the ideal analytical tool for the quantitative analysis of analytes in biological samples, and presents a new HILIC-based SPE approach to improve analyte recovery and sensitivity.

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The advent of ultrahigh-pressure liquid chromatography (UHPLC) and its successful commercialization in the last few years has brought forth a modern high performance liquid chromatography (HPLC) platform capable of higher speed, resolution, precision, and sensitivity. Currently, all major HPLC manufacturers have some type of low-dispersion UHPLC products with upper pressure limits ranging from 15,000 to 19,000 psi (1000 to 1300 bar) on the market. This installment describes a number of popular myths or half-truths in UHPLC and provides data that contradict or even repudiate some of these commonly held beliefs.

Peaks of Interest

Daniel W. Armstrong, a professor of chemistry and biochemistry at the University of Texas Arlington in Arlington, Texas, is to receive the 2014 American Chemical Society Award in Separations Science and Technology.

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Analytica 2014

A look at some highlights for chromatographers at Analytica 2014.

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Currently available methods for the detection of matrix effects in liquid chromatography–mass spectrometry (LC–MS) are tedious and complex; therefore, a simpler method is required. Although there are no methods to completely eliminate matrix effects, the most well-recognized technique available to correct for matrix effects is that of internal standardization using stable isotope–labelled versions of the analytes. As this method can prove expensive, an alternative method of correction is likely to be useful. In this study, a simple method based on recovery is assessed for the detection of matrix effects. Two alternative methods for the rectification of matrix effects in LC–MS are also assessed: Standard addition and the coeluting internal standard method.

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The mechanisms of mixed-mode chromatography are discussed with reference to the parameters that are used to optimize selectivity and retention. Illustrative examples are presented with strategies for column selection and screening to allow this technique to be quickly and effectively adopted by end users.