Reverse-phase liquid chromatography precision

From the literature there is evidence that in GC on polar phases and in normal-phase (adsorption) liquid chromatography (HPLC and TLC) the chemically specific, molecular size-independent intermolecular interactions play the main retention-determining role. For example, the HPLC retention parameters determined for substituted benzenes on porous graphite are described by QSRR equations comprising polarity descriptors but containing no bulk descriptors [93-95]. Because, in general, it is difficult to quantify the polarity properties precisely, the QSRR for GC on polar phases and for normal-phase HPLC are usually of lower quality than in the case of GC on non-polar phases and in the case of reversed-phase liquid chromatography. 

The retention time of phenolic compounds in reversed-phase liquid chromatography was predicted via molecular interaction energy values calculated using the MM2 program. The precision of the capacity ratios predicted by this new method was equivalent to a former method in which the retention time was predicted by log P calculated using the MOPAC program. Furthermore, the prediction of capacity ratios of phenolic compounds in reversed-phase... 

As an example, Urakova et al. compared the analysis of chlorogenic acid in green coffee bean extracts by thin layer chromatography on silica (i.e. normal-phase liquid chromatography) and by reversed-phase HPLC The validation data (LOD, LOQ, repeatability, and various precision parameters), the recoveries and the quantitative results were totally comparable. It can be assumed that both methods find the true value. Either method can be used, depending on the preference or instrumentation of a laboratory. 

As a consequence of the previous considerations Kieber et al. [75] have developed an enzymic method to quantify formic acid in non-saline water samples at sub-micromolar concentrations. The method is based on the oxidation of formate by formate dehydrogenase with corresponding reduction of /3-nicotinamide adenine dinucleotide (j6-NAD+) to reduced -NAD+(/3-NADH) jS-NADH is quantified by reversed-phase high performance liquid chromatography with fluorimetric detection. An important feature of this method is that the enzymic reaction occurs directly in aqueous media, even seawater, and does not require sample pre-treatment other than simple filtration. The reaction proceeds at room temperature at a slightly alkaline pH (7.5-8.5), and is specific for formate with a detection limit of 0.5 im (SIN = 4) for a 200 xl injection. The precision of the method was 4.6% relative standard deviation (n = 6) for a 0.6 xM standard addition of formate to Sargasso seawater. Average re-... 

Reversed-phase HPLC is widely utilized to generate a peptide map from digested protein, and the MS online method provides rapid identification of the molecular mass of peptides. The HPLC-MS-FAB online system is a sensitive and precise method for low-MW peptides (<3000 Da) even picomol quantities can be detected. However, as the MW of the analytes increases, the ionization of peptides becomes more difficult and decreases the sensibility of the FAB-MS (112). Electrospray ionization (ESI-MS) was found to be an efficient method for the determination of molecular masses up to 200,000 Da of labile biomolecules, with a precision of better than 0.1%. Molecular weights of peptide standards and an extensive hydrolysate of whey protein were determined by the HPLC-MS-FAB online system and supported by MALDI-TOF (112). Furthermore, HPLC-MS-FAB results were compared with those of Fast Performance Liquid Chro-motography (FPLC) analysis. Mass spectrometry coupled with multidimensional automated chromatography for peptide mapping has also been developed (9f,l 12a). 

In principle, h.p.Lc. arose from conventional liquid column chromatography, following the development of g.l.c. and realisation that it was a rapid and accurate analytical method. This led to a reappraisal of the liquid column chromatographic system, which in turn resulted in research developments in instrument design and in the manufacture of column-packing materials. These now have precise specifications to make them suitable for adsorption, normal and reversed phase partition, ion exchange, gel permeation, and more recently affinity chromatography. 

This consists of a solvent delivery for isocratic reversed phase and gel filtration chromatography. The isocratic system (Fig. 1.1) provides an economic first step into high performance liquid chromatography techniques. The system is built around a high performance, dual-piston, pulse-free pump providing precision flow from 0.01 to 5mL min-1. 

Kerr el. al. [307] employed high performance liquid chromatography for the determination of uranium in groundwaters. The sample was passed through a small reversed phase enrichment cartridge, to separate the uranium from the bulk of the dissolved constituents. The uranium was then back flushed from the cartridge onto a reversed phase analytical column. The separated species were monitored spectrophotometrically after reaction with arsenazo(III). The detection limit was in the 1-2gg L 1 range with a precision of approximately 4%. 

Elhawary, N.A., Shawky, R.M., and Elsayed, N. High-precision DNA microsatellite genotyping in Duchesne muscular dystrophy families using ion-pair reversed-phase high perfonnance liquid chromatography. Clin. Biochem. 2006, 39, 758-761. 

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