PubMed HealthSearch

PubMed · 9586230

High performance liquid chromatography mobile phase composition optimization for the quantitative determination of a carboxylic acid compound in human plasma by negative ion electrospray high performance liquid chromatography tandem mass spectrometry.

Abstract

A systematic investigation was undertaken to study the effects of varying concentrations of additives in the acetonitrile/water high performance liquid chromatography mobile phase, especially formic acid and ammonium formate, on the negative ion electrospray response of a carboxylic acid compound. The study showed that the response progressively decreased with increase in the formic acid concentration. While such a decrease in the response could be qualitatively explained by the decrease in the concentration of the ionized form of the carboxylic acid compound due to the lower pH of the mobile phase, the change in response was not as large as expected from the change of the concentration of the ionized form. The response also progressively decreased with increase in the ammonium formate concentration but the decrease cannot be explained by the change in the pH of the mobile phase. Although the best negative ion electrospray response was obtained with a water/acetonitrile mobile phase that contained no additives at all, the retention time of the analyte was not found to be adequately reproducible on repeated injections. Thus, this mobile phase was deemed unacceptable for practical, routine use. Comparing formic acid against ammonium formate, the former was preferable since it caused a smaller attenuation of the negative ion response. Equally important was the fact that addition of formic acid had the desirable effect of maintaining a reasonably high capacity factor (k') for the analyte even at a relatively high acetonitrile concentration. A concentration of 1 mM formic acid in the mobile phase was large enough to achieve the reproducible elongated retention time for the analyte, with a loss in the analyte response of about 60% only. It should be noted that the sensitivity achieved with the 1 mM formic acid mobile phase, in which the carboxylic acid is expected to be about 10% in the ionized form, is about 9 times better than the sensitivity achieved in the 1 mM ammonium formate mobile phase, in which the carboxylic acid is expected to be about 99% in the ionized form.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

M Jemal, Z Ouyang, D S Teitz. 1998. High performance liquid chromatography mobile phase composition optimization for the quantitative determination of a carboxylic acid compound in human plasma by negative ion electrospray high performance liquid chromatography tandem mass spectrometry.. https://doi.org/10.1002/(sici)1097-0231(19980430)12%3A8%3C429%3A%3Aaid-rcm179%3E3.0.co%3B2-i

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Retention behaviours and separation of carboxylic acids by ion-exchange chromatography.

The use of high-performance suppressed ion chromatography for the separation of aliphatic carboxylic acids has become an attractive and viable method during the past years. This paper summarises and critically concludes that some new results have been achieved in separation and detection of low-molecular-mass organic anions. Theoretical and practical considerations of ion-exchange selectivity to control retention behaviour are presented. The major factors that determine the separation ability of ion-exchange chromatography (pKa values, the aliphatic nature and valency of solutes, eluent pH and the chemical composition of stationary phases) are discussed. The question of isocratic vs. gradient elution and different separation modes are examined briefly. The potentials and limitations of the developed methods and their specific application areas are outlined.

Carboxylic Acids

Carboxylic acids: prediction of retention data from chromatographic and electrophoretic behaviours.

A review of the main results reached in the prediction of retention data of carboxylic acids, inferred by their chromatographic and electrophoretic behaviour, is presented. Attention has been focused on the main separation methods used in carboxylic acids analysis, that is ion-exclusion, anion-exchange, reversed-phase (RP) liquid chromatography and capillary electrophoresis. Papers proposing mechanistic models as well as chemometric and multilayer feed-forward neural network analysis of ion chromatography (IC) and RP chromatographic retention data were reviewed. Principal component analysis, PCA, sequential simplex method and simultaneous modelling of response surfaces through simple nonlinear models (not related to equilibria involved in retention) have been considered. Computer simulations for the prediction of retention data have also been discussed. A quick overlook on the prediction of capacity factors of analytes by less common determination methods such as thin-layer, gas chromatography and supercritical fluid chromatography has also been done.

Carboxylic Acids

Chromatographic separations of aromatic carboxylic acids.

The purpose of this review is to present methods of chromatographic analysis of aromatic carboxylic acids. The separation, identification and quantitative analysis of aromatic carboxylic acids are necessary because of their importance as non-steroid antiphlogistic drugs, semi-products of biosynthesis of aromatic amino-acids in plants (phenolic acids), metabolites of numerous toxic substances, drugs and catecholamines. HPLC separation of ionic samples tends to be more complicated than separation of non-ionic compounds. The review describes the dependence of the retention of ionic solutes on pH and solvent composition as well as on the ionic strength of a mobile phase. The application of the ion-suppressing RP-HPLC method using organic modifiers (aqueous buffer solutions) as eluents in aromatic carboxylic acid analysis is also presented. In more difficult cases of analysis the addition of an ion-pairing reagent, such as the quaternary alkylammonium ion, is necessary to obtain satisfactory separations. Hypotheses of ion-pair formation in reversed-phase systems as well as the influence of various agents on the separation of ionic solutes in IP-RP systems are explained. Examples of the application of ion-pair liquid chromatography to the analysis of aromatic carboxylic acids have also been reviewed. The principles and application of ion-exchange chromatography to the purification, isolation and less frequently, to chromatographic analysis are discussed. Polar adsorbents and polar bonded stationary phases are also widely used in carboxylic acid separation in normal-phase systems, mainly by TLC, often coupled with densitometry. The review also shows examples of separation of chiral benzoic acids and their derivatives in LC systems. The possibilities of application of gas chromatography preceded by derivatisation or pyrolysis of acidic compounds and applications of GC-MS and Py-GC-MS coupled methods in identification and quantitation of aromatic carboxylic acids is also reviewed.

Carboxylic Acids