Evaluation of supercritical fluid chromatography for testing of PEG adducts in pharmaceuticals

•Reaction between PEG 400 and 2 APIs resulted in formation of PEG adducts.•Separation of PEG adducts was performed with supercritical fluid chromatography.•Cetirizine was more reactive towards PEG 400 than indomethacin.•Detection with mass spectrometry is well-suited for identification of PEG adduct...

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Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2014-01, Vol.88, p.256-261
Hauptverfasser: Schou-Pedersen, Anne Marie V., Østergaard, Jesper, Johansson, Mats, Dubant, Stephane, Frederiksen, Rune B., Hansen, Steen Honoré
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container_issue
container_start_page 256
container_title Journal of pharmaceutical and biomedical analysis
container_volume 88
creator Schou-Pedersen, Anne Marie V.
Østergaard, Jesper
Johansson, Mats
Dubant, Stephane
Frederiksen, Rune B.
Hansen, Steen Honoré
description •Reaction between PEG 400 and 2 APIs resulted in formation of PEG adducts.•Separation of PEG adducts was performed with supercritical fluid chromatography.•Cetirizine was more reactive towards PEG 400 than indomethacin.•Detection with mass spectrometry is well-suited for identification of PEG adducts. Drug formulations containing polyethylene glycol may give rise to formation of reaction products between the aforementioned and the active pharmaceutical ingredient. Supercritical fluid chromatography has recently achieved new interest and improved instrumentation is now available. Here, supercritical fluid chromatography has been evaluated for its possible use for determination of reactions products formed between polyethylene glycol and active pharmaceutical ingredients. A mixture of polyethylene glycols with average molecular weights of 400–6000Da was separated with supercritical fluid chromatography using silica columns and carbon dioxide modified with methanol as mobile phase. Satisfactory resolution (Rs=1.2) of the individual oligomers up to a molecular weight of 1000Da was obtained using evaporative light scattering as detection technique. The active pharmaceutical ingredients, cetirizine or indomethacin were investigated in a reaction mixture containing polyethylene glycol 400 after incubation at 80°C for 120h. Polyethylene glycol esters formed upon reaction with both active pharmaceutical ingredients were observed as polymeric patterns with ultraviolet detection and identified with mass spectrometry. Cetirizine was observed to be more reactive than indomethacin. The observed difference in reactivity is due to differences in polar and steric effects between cetirizine and indomethacin. Evaporative light scattering, ultraviolet absorbance and mass spectrometric detection were investigated and each detection technique has its own advantages and disadvantages, but in order to be able to detect selected impurities in the complex mixture of impurities formed, mass spectrometry is superior.
doi_str_mv 10.1016/j.jpba.2013.08.039
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Drug formulations containing polyethylene glycol may give rise to formation of reaction products between the aforementioned and the active pharmaceutical ingredient. Supercritical fluid chromatography has recently achieved new interest and improved instrumentation is now available. Here, supercritical fluid chromatography has been evaluated for its possible use for determination of reactions products formed between polyethylene glycol and active pharmaceutical ingredients. A mixture of polyethylene glycols with average molecular weights of 400–6000Da was separated with supercritical fluid chromatography using silica columns and carbon dioxide modified with methanol as mobile phase. Satisfactory resolution (Rs=1.2) of the individual oligomers up to a molecular weight of 1000Da was obtained using evaporative light scattering as detection technique. The active pharmaceutical ingredients, cetirizine or indomethacin were investigated in a reaction mixture containing polyethylene glycol 400 after incubation at 80°C for 120h. Polyethylene glycol esters formed upon reaction with both active pharmaceutical ingredients were observed as polymeric patterns with ultraviolet detection and identified with mass spectrometry. Cetirizine was observed to be more reactive than indomethacin. The observed difference in reactivity is due to differences in polar and steric effects between cetirizine and indomethacin. 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Drug formulations containing polyethylene glycol may give rise to formation of reaction products between the aforementioned and the active pharmaceutical ingredient. Supercritical fluid chromatography has recently achieved new interest and improved instrumentation is now available. Here, supercritical fluid chromatography has been evaluated for its possible use for determination of reactions products formed between polyethylene glycol and active pharmaceutical ingredients. A mixture of polyethylene glycols with average molecular weights of 400–6000Da was separated with supercritical fluid chromatography using silica columns and carbon dioxide modified with methanol as mobile phase. Satisfactory resolution (Rs=1.2) of the individual oligomers up to a molecular weight of 1000Da was obtained using evaporative light scattering as detection technique. The active pharmaceutical ingredients, cetirizine or indomethacin were investigated in a reaction mixture containing polyethylene glycol 400 after incubation at 80°C for 120h. Polyethylene glycol esters formed upon reaction with both active pharmaceutical ingredients were observed as polymeric patterns with ultraviolet detection and identified with mass spectrometry. Cetirizine was observed to be more reactive than indomethacin. The observed difference in reactivity is due to differences in polar and steric effects between cetirizine and indomethacin. 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Drug formulations containing polyethylene glycol may give rise to formation of reaction products between the aforementioned and the active pharmaceutical ingredient. Supercritical fluid chromatography has recently achieved new interest and improved instrumentation is now available. Here, supercritical fluid chromatography has been evaluated for its possible use for determination of reactions products formed between polyethylene glycol and active pharmaceutical ingredients. A mixture of polyethylene glycols with average molecular weights of 400–6000Da was separated with supercritical fluid chromatography using silica columns and carbon dioxide modified with methanol as mobile phase. Satisfactory resolution (Rs=1.2) of the individual oligomers up to a molecular weight of 1000Da was obtained using evaporative light scattering as detection technique. 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subjects Carbon Dioxide - chemistry
Cetirizine
Cetirizine - chemistry
Chemistry Techniques, Analytical
Chemistry, Pharmaceutical
Chromatography, High Pressure Liquid
Chromatography, Supercritical Fluid
Drug–excipient interaction
Indomethacin
Indomethacin - chemistry
Light
Mass Spectrometry
Methanol - chemistry
Polyethylene glycol
Polyethylene Glycols - chemistry
Polymers - chemistry
Scattering, Radiation
SFC
Time Factors
title Evaluation of supercritical fluid chromatography for testing of PEG adducts in pharmaceuticals
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