Development of on-line two-dimensional LCxLC-UV/MS and LCxSFC-UV methods for the analysis of pharmaceutical samples

La chromatographie en phase liquide bidimensionnelle est une technique à fort potentiel, offrant un grand pouvoir de séparation. Après avoir démontré son intérêt dans l’industrie pharmaceutique et présenté les enjeux liés à l’analyse quantitative, une attention particulière est portée sur le développement de méthodes. Dans l’idée de développer une stratégie d’analyse générique, la première étape est de sélectionner un set de trois systèmes 2D par le biais d’une approche développée au laboratoire. La deuxième étape est d’évaluer le potentiel de ces systèmes pour l’analyse quantitative. Ces deux étapes ont conduit à la proposition d’une stratégie d’analyse applicable à l’analyse pharmaceutique dans un contexte industriel. Enfin le potentiel du couplage RPLCxSFC est envisagé dans deux cas de figure différents. Premièrement, dans le but de comparer ce couplage aux séparations RPLCxRPLC développées dans le cadre d’une stratégie analytique générique, en termes de pouvoir de séparation. Deuxièmement, dans le cadre de l’analyse de composés chiraux, en développant un couplage sRPLCxSFC permettant une analyse achirale/chirale simultanée. Les avantages d’une telle approche ont été mis en avant en la comparant aux approches conventionnellesTwo-dimensional liquid chromatography (2D-LC) is a powerful technique considering its high separation power. After showing the advantage of 2D-LC in the pharmaceutical area and presenting the challenges related to quantitative analysis, special attention was paid to method development. With the aim of developing a generic analytical strategy for pharmaceuticals, the first step of our approach consisted in selecting a set of three 2D-systems with the help of a methodology previously developed. In a second step, the potential of these 2D-systems was evaluated for the purpose of quantitative analysis. An analytical strategy able to be applied to pharmaceutical analysis in an industrial context was proposed. Finally, the potential of RPLCxSFC was investigated in two different cases. Firstly, for comparing this on-line two dimensional technique to on-line RPLCxRPLC with respect of the separation power. Secondly, for chiral compounds by developing a selective RPLCxSFC method for simultaneous achiral-chiral analysis. The advantage of such method was highlighted by comparing to conventional approache

Développement de méthodes bidimensionnelles en ligne LCxLC-UV/MS et LCxSFC-UV pour l’analyse de composés pharmaceutiques

Two-dimensional liquid chromatography (2D-LC) is a powerful technique considering its high separation power. After showing the advantage of 2D-LC in the pharmaceutical area and presenting the challenges related to quantitative analysis, special attention was paid to method development. With the aim of developing a generic analytical strategy for pharmaceuticals, the first step of our approach consisted in selecting a set of three 2D-systems with the help of a methodology previously developed. In a second step, the potential of these 2D-systems was evaluated for the purpose of quantitative analysis. An analytical strategy able to be applied to pharmaceutical analysis in an industrial context was proposed. Finally, the potential of RPLCxSFC was investigated in two different cases. Firstly, for comparing this on-line two dimensional technique to on-line RPLCxRPLC with respect of the separation power. Secondly, for chiral compounds by developing a selective RPLCxSFC method for simultaneous achiral-chiral analysis. The advantage of such method was highlighted by comparing to conventional approachesLa chromatographie en phase liquide bidimensionnelle est une technique à fort potentiel, offrant un grand pouvoir de séparation. Après avoir démontré son intérêt dans l’industrie pharmaceutique et présenté les enjeux liés à l’analyse quantitative, une attention particulière est portée sur le développement de méthodes. Dans l’idée de développer une stratégie d’analyse générique, la première étape est de sélectionner un set de trois systèmes 2D par le biais d’une approche développée au laboratoire. La deuxième étape est d’évaluer le potentiel de ces systèmes pour l’analyse quantitative. Ces deux étapes ont conduit à la proposition d’une stratégie d’analyse applicable à l’analyse pharmaceutique dans un contexte industriel. Enfin le potentiel du couplage RPLCxSFC est envisagé dans deux cas de figure différents. Premièrement, dans le but de comparer ce couplage aux séparations RPLCxRPLC développées dans le cadre d’une stratégie analytique générique, en termes de pouvoir de séparation. Deuxièmement, dans le cadre de l’analyse de composés chiraux, en développant un couplage sRPLCxSFC permettant une analyse achirale/chirale simultanée. Les avantages d’une telle approche ont été mis en avant en la comparant aux approches conventionnelle

Two-dimensional liquid chromatography in pharmaceutical analysis. Instrumental aspects, trends and applications

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Comparison of RPLC and SFC for the Analysis of Pharmaceutical Compounds With the Objective of Two-Dimensional Coupling In Order To Achieve Very High Separation Power

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LCxLC-MS separations of protein tryptic digests

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On-line coupling of RPLC and SFC for the analysis of chiral compounds

https://www.ilmexhibitions.com/htc/abstract/On-line+coupling+of+RPLC+and+chiral+SFC+for+the+analysis+of+pharmaceutical+compounds/378/International audienc

On-line achiral RPLCx chiral SFC for the analysis of chiral compounds

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Sélection de systèmes LCxLC en ligne à très haut pouvoir séparatif pour l’analyse de composés pharmaceutiques

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Comprehensive two dimensional liquid chromatography as analytical strategy for pharmaceutical analysis

International audienceComprehensive on-line two-dimensional liquid chromatography (LCxLC) is expected to generate impressive peak capacities, which makes it a method of choice for the analysis of complex samples such as pharmaceuticals. A comparative study of different sets of chromatographic conditions including stationary phase, pH additive and organic modifier was carried out with two real pharmaceutical samples in order to find out the best analytical conditions for implementation of one or several generic on-line LCxLC separations. Our choice was based on the evaluation of both degree of orthogonality and practical sample peak capacity under linear gradient conditions. The potential of 190 combinations of chromatographic systems was compared. A set of 3 RPLCxRPLC configurations was found to be very attractive for both samples and in good agreement with the findings of a previous study carried out with 17 model compounds, thereby supporting the idea of using generic LCxLC conditions in the pharmaceutical area. The three selected 2D-systems were implemented for the on-line RPLCxRPLC-UV/MS analysis of two pharmaceutical samples. It was shown, for each sample, that these 2D-systems were able to generate an effective peak capacity close to 1000 in less than 50min. For each sample, baseline separation was obtained for every known compound and furthermore a large number of unknown impurities could also be separated and identified. Finally, in the proposed conditions, the total number of compounds detected was significantly improved from one RPLC separation to one RPLCxRPLC separation. Only a small additional gain was observed by performing a second RPLCxRPLC separation or even a third one