Abstract

Water activity is a key factor in the development of pharmaceutical, cosmetic, and food products. In aqueous solutions of nonelectrolytes, the Norrish model provides a simple and effective way to evaluate this quantity. However, it contains a parameter, known as the Norrish constant, that must be estimated from experimental data. In this study, a new strategy is proposed for the prediction of water activity in the absence of experimental information, based on the use of theoretical molecular descriptors for characterizing the effects of a solute. This approach was applied to the evaluation of water activity in the presence of sugars (glucose, fructose, xylose, sucrose) and polyols (sorbitol, xylitol, glycerol, erythritol). The use of two descriptors related to the constitutional and connectivity properties of the solutes was first investigated. Subsequently, a new theoretical descriptor, named the global information index (G), was developed. By using this index, the water activity curves in the binary systems were reconstructed. The positive results obtained support the proposed strategy, as well as the possibility of including, in a single information index, the main molecular features of a solute that determine its effects on water activity.

Highlights

  • Water activity is one of the most important factors influencing the quality and stability of food, cosmetic, and pharmaceutical products [1,2,3]

  • The most popular is that of “free water”, according to which water activity reflects its availability as a solvent or reagent, which results from the interactions between water molecules [8]

  • The aim of this study was to investigate whether the activity of water in the presence of polyols or sugars could be predicted using some theoretical descriptors of the solutes

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Summary

Introduction

Water activity is one of the most important factors influencing the quality and stability of food, cosmetic, and pharmaceutical products [1,2,3]. Most of the studies on water activity have been carried out on food products, since this quantity has a significant effect on microbial stability, shelf life, and organoleptic characteristics [4]. The most popular is that of “free water”, according to which water activity reflects its availability as a solvent or reagent, which results from the interactions between water molecules [8]. Another explanation attributes its origin to the structuring or ordering of water molecules induced by a solute [9]. A further interpretation is based on the concepts of solute clustering and hydration number, that is, the number of water molecules close to the solute [10]

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