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A S Lister

Publications and source records attributed to A S Lister.

2 recordsLinked to original sources

Gradient elution electrochromatography with a flow-injection analysis interface.

A flow-injection analysis-capillary electrochromatography interface is used for gradient elution capillary electrochromatography giving purely electroosmotic flow through the analytical column. Solvent gradients were generated with a micro-LC system connected to the interface. Injections were carried out on-line using an inert rotary LC valve controlled by an electric actuator. Gradient shape was measured from acetonitrile (5% acetone)-water (50:50, v/v) to (100:0) in open tubular experiments. When compared to conventional instrumentation, peak tailing and peak width increased slightly using the interface. A test mixture of nine solutes was evaluated in isocratic and gradient elution modes. Using the interface, a gradient of MeCN-water (60:40) to (90:10) provided baseline separation of all nine solutes in under 18 min with good band spacing. Reproducibility of retention times in eight replicate injections was found to be better than 2% R.S.D. for all solutes. This interface also allows use of autoinjectors and dramatically lessens movement of the packed column, improving column lifetime.

Chromatography, High Pressure Liquid↗

Behavior and use of nonaqueous media without supporting electrolyte in capillary electrophoresis and capillary electrochromatography.

Five nonaqueous solvents (acetonitrile, methanol, N,N-dimethylformamide, dimethyl sulfoxide, formamide) and deionized water were investigated for their ability to support electroosmotic flow (EOF) without electrolytic additives. In general, flow was found to be equal to or greater than flow with typical CE buffer systems. The magnitude of EOF was determined for each solvent by open tubular capillary electrophoresis (CE) and related to viscosity (eta), dielectric constant (epsilon), and the ratio of dielectric constant to viscosity (eta/epsilon). Zeta potentials (zeta) were derived indirectly from flow data and tabulated. Comparisons of flow behavior and zeta were made between pure solvents and conventional CE buffers, and questions of equilibrium and reproducibility were addressed. Similar experiments were performed using hydroorganic mobile phases (ACN/water, MeOH/water) across the complete compositional range (100% water-100% organic), with flow characteristics and zeta reported for each mobile phase system. Packed capillary columns (5-microns ODS) were evaluated for flow and retention stability under capillary electrochromatographic (CEC) conditions. A separation of 11 polycyclic aromatic hydrocarbons was performed in under 13 min by CEC with an ACN/water mobile phase. Reduced plate heights (h) were calculated between 2.5 and 3.0 for solutes with capacity factors (k') up to 4.5 for the most retained solute.

Acetonitriles↗