Abstract

Here, we report an accurate and versatile method for the simultaneous determination of 17 sugars (arabinose, erythrose, fructose, galactose, glucose, isomaltulose, lactose, lyxose, maltose, maltotriose, mannose, raffinose, rhamnose, ribose, sucrose, sorbose and xylose), seven polyols (erythritol, inositol, lactitol, maltitol, mannitol, sorbitol and xylitol), five ions (K+, Br−, Cl−, NO3− and SO42−) and the pseudosaccharide acarbose. For compound separation, hydrophilic interaction chromatography (HILIC) coupled to a corona charged aerosol detector (CAD) was used. The method was validated for linearity, precision, reproducibility, retention factor and optimal injection volume. Standards were measured in the range of 1–1000 mg L−1 and showed good intraday and interday repeatability, as well as precision (relative standard deviation (RSD) < 5%). The LODs and LOQs for the 30 analytes were in the range of 0.032–2.675 mg L−1 and 0.107–8.918 mg L−1, respectively. This method exhibited correlation coefficients of at least R2 > 0.97 for all analytes. The method was tested in 24 food and beverage samples to validate the separation efficiency and sensitivity in natural food matrices and to show the practicability of its use for routine food analysis.

Highlights

  • With the development of refractive index detectors (RIDs), carbohydrate analysis via high-performance liquid chromatography (HPLC) has become popular, enabling detection limits in the range of 0.34 ± 0.18 g L−1 [1]

  • HPLC-RID offers fast and simple analysis of carbohydrates, polyols and substances that change the refractive index of the solvent, such as metal cations and hydrocarbons [2,3,4]

  • We present a new hydrophilic interaction chromatography (HILIC)-charged aerosol detector (CAD) method to separate a total of 30 different analytes, including 17 sugars, seven sugar alcohols, five ions and one pseudo saccharide

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Summary

Introduction

With the development of refractive index detectors (RIDs), carbohydrate analysis via high-performance liquid chromatography (HPLC) has become popular, enabling detection limits in the range of 0.34 ± 0.18 g L−1 [1]. HPLC-RID offers fast and simple analysis of carbohydrates, polyols and substances that change the refractive index of the solvent, such as metal cations and hydrocarbons [2,3,4]. UV/VIS detection by HPLC-DAD (diode array detector) offers similar detection limits as HPLC-RID but requires the derivatization of carbohydrates and most polyols pre- or postinjection onto the column [6]. Fluorescence and HPLC-FLD (fluorescence detector) is a technique that further enhances the sensitivity and selectivity of detection compared to those of HPLC-DAD [7]

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