Abstract

Lactose is a disaccharide of importance in humans dietary, food products, and the pharmaceutical industry. From the existing isomeric forms, β-lactose is rarely found in nature. Thus, in this work, a simple methodology to obtain anhydrous β-lactose (βL) from α-lactose monohydrate (αL·H2O) is presented. The αL·H2O powder was dispersed into a basic alcoholic solution (72 hours), at controlled conditions of temperature (27, 29, 31, and 32°C), without stirring. The slurry was dried at room temperature and characterized. Fourier transform infrared spectroscopy showed the formation of βL for the samples prepared at 29 and 32°C. Raman spectroscopy confirmed this result and suggested the occurrence of crystalline βL. Rietveld refinement of the X-ray diffraction patterns was employed to identify and quantify the composition of the isomers. The samples prepared at 29 and 31°C showed the formation of pure βL, while those at 27 and 32°C showed the presence of αL·H2O and a mixture of the two isomers, respectively. The morphology of the powders was studied by scanning electron microscopy, observing the formation of irregular shape αL·H2O particles and axe-like βL particles. Clearly, with this methodology, it was possible to obtain pure, crystalline, and anhydrous βL at mild temperature.

Highlights

  • Lactose (4-O-β-D-galactopyranosyl-D-glucopyranose) is found exclusively in the milk of mammals and is composed of molecules of galactose and glucose, linked by a β-glycosidic bond (1,4)

  • Samples prepared at different temperatures were analyzed using the Fourier transform infrared spectrometry (FTIR), to elucidate the formation of the polymorph

  • According to Listiohadi et al (2009) the bands located at 3600–3200 cm−1 correspond to the stretching of the OH groups of the lactose molecule, while the vibrations at 1650 cm−1 are related to the flexion of the OH groups of the crystallized water molecules [18]

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Summary

Introduction

Lactose (4-O-β-D-galactopyranosyl-D-glucopyranose) is found exclusively in the milk of mammals and is composed of molecules of galactose and glucose, linked by a β-glycosidic bond (1,4). Since the anomeric carbon of glucose is free, this disaccharide exhibits the features of reducing sugars; that is, the chain configuration is opened by the formation of an aldehyde group [1]. In the food industry, it is used as a commercial additive because of its texture, flavor, and adhesive properties [2]. When used as excipient in drugs, lactose is the substance where the active ingredient is dispersed and preserved in a stable state [4, 5]. This disaccharide exists in two isomeric forms, α-lactose, and β-lactose, which shows the phenomenon of mutarotation, that is, the interconversion of the stereocenters [6]. Lactose exhibits three polymorphs (anhydrous forms) and a solvate (hydrated form): anhydrous β-lactose (βL), International Journal of Polymer Science

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