Scholarly article on topic 'Sugar alcohols—their role in the modern world of sweeteners: a review'

Sugar alcohols—their role in the modern world of sweeteners: a review Academic research paper on "Agricultural biotechnology"

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Eur Food Res Technol
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Academic research paper on topic "Sugar alcohols—their role in the modern world of sweeteners: a review"

Eur Food Res Technol

DOI 10.1007/s00217-015-2437-7


Sugar alcohols—their role in the modern world of sweeteners: a review

Matgorzata Grembecka

Received: 31 August 2014 / Revised: 16 December 2014 / Accepted: 13 February 2015 © The Author(s) 2015. This article is published with open access at

Abstract Epidemic obesity and diabetes encouraged the changes in population lifestyle and consumers' food products awareness. Food industry has responded people's demand by producing a number of energy-reduced products with sugar alcohols as sweeteners. These compounds are usually produced by a catalytic hydrogenation of carbohydrates, but they can be also found in nature in fruits, vegetables or mushrooms as well as in human organism. Due to their properties, sugar alcohols are widely used in food, beverage, confectionery and pharmaceutical industries throughout the world. They have found use as bulk sweeteners that promote dental health and exert prebiotic effect. They are added to foods as alternative sweeteners what might be helpful in the control of calories intake. Consumption of low-calorie foods by the worldwide population has dramatically increased, as well as health concerns associated with the consequent high intake of sweeteners. This review deals with the role of commonly used sugar alcohols such as erythritol, isomalt, lactitol, maltitol, mannitol, sorbitol and xylitol as sugar substitutes in food industry.

Keywords Sugar alcohols • Polyols • Bulk sweeteners • Sugar substitution • Sugar-free products


People always tried to use benefits of the nature; however, just recently in the final years of the twentieth century, a gigantic progress in the food technology could have been

M. Grembecka (*)

Department of Food Sciences, Medical University of Gdansk, Al. Gen. J. Hallera 107, 80-416 Gdansk, Poland e-mail:

Published online: 28 February 2015

observed. It was mainly due to the developments in biological studies, the change of a population lifestyle and the increase in the consumer awareness concerning food products. The health quality of food depends mainly on nutrients, but also on foreign substances such as food additives. The presence of foreign substances in the food can be justified, allowed or tolerated only when they are harmless to our health. Epidemic obesity and diabetes encouraged the growth of the artificial sweetener industry. There are more and more people who are trying to lose weight or keeping the weight off; therefore, sweeteners can be now found in almost all food products. There are two main types of sweeteners, i.e., nutritive and artificial ones. The latter does not provide calories and will not influence blood glucose; however, some of nutritive sweeteners such as sugar alcohols also characterize with lower blood glucose response and can be metabolized without insulin, being at the same time natural compounds.

Sugar alcohols (polyols or polyhydric alcohols) are low digestible carbohydrates, which are obtained by substituting and aldehyde group with a hydroxyl one [1, 2]. As most of sugar alcohols are produced from their corresponding aldose sugars, they are also called alditols [3]. Among sugar alcohols can be listed hydrogenated monosaccharides (sorbitol, mannitol), hydrogenated disaccharides (isomalt, maltitol, lactitol) and mixtures of hydrogenated mono-di-and/or oligosaccharides (hydrogenated starch hydrolysates) [1, 2, 4].

Polyols are naturally present in smaller quantities in fruits as well as in certain kinds of vegetables or mushrooms, and they are also regulated as either generally recognized as safe or food additives [5-7]. Food additives are substances that are added intentionally to foodstuffs in order to perform certain technological functions such as to give color, to sweeten or to help in food preservation.

1 Springer

Table 1 Characteristics of sugar alcohols

Sugar alcohol Formula Systematic name Synonyms Functional classes

Erythritol C4H10O4 (2R,3S)-1,2,3,4-Butanetetrol -Erythrite Flavor enhancer

-Meso-erythritol Humectant

-Tetrahydroxybutane Sweetener

Isomalt C12H24O11 6-0-alpha-D-glucopyranosyl-, mixed with -Hydrogenated isomaltulose Anti-caking agent

1-0-alpha-D-glucopyranosyl-D-mannitol -Isomaltitol Bulking agent

Glazing agent




Lactitol C12H24O11 4-O-P-L-Galactopyranosyl-L-glucitol -Lactit Emulsifier

-Lactobiosit Sweetener

-Lactositol Thickener

Maltitol C12H24O11 4-0-a-D-Glucopyranosyl-D-glucitol -D-Maltitol Bulking agent

-Dried maltitol syrup Emulsifier

-Hydrogenated glucose syrup Humectant

-Hydrogenated high maltose content glucose Stabilizer

syrup Sweetener

-Hydrogenated maltose Thickener

-Maltitol syrup powder

Mannitol C6H14O6 D-Mannitol -Mannite Anti-caking agent

-D-Mannitol Bulking agent





Sorbitol C6H14O6 D-Glucitol -D-Glucitol, Bulking agent

-D-Glucitol syrup Humectant

-Sorbit Sequestrant

-D-sorbitol Stabilizer

-Sorbol Sweetener


Xylitol C5HJ2O5 D-erythro-pentitol - Emulsifier

Humectant Stabilizer Sweetener Thickener

polyols must include the advisory statement "excessive consumption may produce laxative effects" [10, 11].

Sugar alcohols' sweetness is usually lower than the one of monosaccharide, and therefore, they are used volume-for-volume like sugar and are called bulk sweeteners. They are often used in combination with other sweeteners to achieve the desired level of sweetness and flavor. Similarly to carbohydrates, they are not only responsible for sweet taste, but they are also responsible for product texture, its preservation, filling, holding moisture and cooling sensation in the mouth [12] (Table 1).

These compounds have a lower nutritional value than sugars (Table 2) [12], due to slower and incomplete absorption from the intestine, which results in indirect metabolism via fermentative degradation by the intestinal flora (Table 3). Products of fermentation include short-chain fatty acids and gases [9]. Sugar alcohols due to lower caloric value might help consumers to reduce their

According to the European Union legislation, all food additives are identified by an E number and must be always stated on the packaging in the ingredient lists. All food additives prior their usage must be authorized by particular legislations such as EU and FDA. There are seven sugar alcohols which are defined as nutritive sweeteners according to EU legislation, i.e., sorbitol (E420), mannitol (E421), isomalt (E953), maltitol (E965), lactitol (E966), xylitol (E967) and erythritol (E968) [8]. They need to be declared on the products label, and when there is only one sugar alcohol present, the specific name may be substituted for "sugar alcohol," e.g., xylitol [5, 7]. Although acceptable daily intake (ADI) dose has not been specified for them, they are known for their potent laxative effect and other gastrointestinal symptoms such as flatulence, bloating, and abdominal discomfort when eaten in excess [1, 9, 10]. Therefore, in order to ensure consumers with adequate information, products containing more than 10 % added

Table 2 Caloric value, sweetness and glycemic index of sugar alcohols

Polyol Sweetnessa Caloric value (kcal/g) US data* European regulations* Glycemic indexb*

Erythritol 0.6-0.8 0.2 2.4 0

Isomalt 0.45-0.65 2.0 9

Lactitol 0.3-0.4 1.9 6

Maltitol 0.9 2.1 35

Mannitol 0.5-0.7 1.6 0

Sorbitol 0.5-0.7 2.7 9

Xylitol 1.0 2.4 13

a Sucrose b Glucose * [1, 8] = 1 [12] = 100 [1, 8]

Table 3 Metabolism of sugar alcohols Sugar alcohol Metabolism

Erythritol Fast absorption through the small intestine, not

metabolized, over 90 % excreted unchanged in the urine; the unabsorbed part is fermented in the large intestine by the colonic microorganisms Well tolerated in human body even up to 80 g when consumed spread over the day [1, 18, 23, 126] Isomalt Slowly and only partly digested and absorbed in the

upper gastrointestinal tract, and the unabsorbed part (~90 %) is fermented by the gut microflora in the colon [1, 40, 44]

Lactitol Small part is absorbed (2 %) by passive diffusion, and

the remainder passes undigested to the colon (the distal part of the large intestine) where is slowly fermented [45-47] Maltitol Partially digested in the intestines, and non-absorbed

part is metabolized by colonic bacteria [1, 60, 64] Mannitol Passively absorbed part is digested in the intestines, and non-absorbed part is metabolized by colonic bacteria in the lower gut [75, 78] Sorbitol Partially absorbed in the upper gastrointestinal tract

where it undergoes digestion, and non-absorbed part is metabolized by colonic bacteria [1, 68, 72, 75, 78]

Xylitol Indirect—fermentative degradation of unabsorbed

xylitol by intestine bacterial flora Direct metabolism via the glucuronic acid-pentose phosphate shunt—a portion of xylitol undergoes metabolic pathway in mammalian liver [47, 108]

energy intake and lose weight [1, 9]. What is more, consumption of products containing polyols do not induce (or to very small extent) an increase in blood glucose or insulin secretion, and thus, such products are recommended for people with diabetes [6, 9, 10, 13; Table 2]. Polyols also act as prebiotics, anti-cariogenic agents and

similar to fiber can help normalize intestine function [1, 9, 10]. Sugar alcohols such as maltitol and lactitol were found to increase mineral bioavailability in human and rats [13, 14].

Nutritive sweeteners are generally recognized as safe, yet concern exists about increasing sweetener intakes relative to optimal nutrition and health. The present review focuses on the role, metabolism and dietary characteristic of the chosen sugar alcohols such as erythritol, isomalt, lac-titol, maltitol, mannitol, sorbitol and xylitol.

Sugar alcohols characteristics


1,2,3,4-Butanetetrol, which is a chemical name of erythritol (Fig. 1), can be naturally found in small quantities in vegetables, fruits (melons, peaches), mushrooms and fermented foods such as wine, beer, sake and soy sauce [15-22]. It can be also found in several human tissues such as semen, lens, cerebrospinal fluid and serum [18, 20, 23]. Erythritol consumption from natural sources is estimated to amount from 25 mg/person/day in the USA to 106 mg/person/day in Japan [23].

Properties and applications

This sugar alcohol characterizes with a high stability in temperature and acid or alkaline environments as well as does not take part in Maillard-type browning reactions [23]. It is also a non-hygroscopic substance. Erythritol is currently used as a low-calorie, tooth-friendly, bulk sweetener, which provides volume, texture as well as microbiological stability in such products as tooth-friendly chewing gums, candy products, ice creams and also ipocaloric beverages [22, 23].

Besides heaving a high digestive tolerance, it is non-glycemic and does not promote tooth decay [3, 21, 24] (Table 4). Erythritol inhibits the growth of mutans streptococci and combined with xylitol may potentially act caries limiting [3, 25]. Moreover, Runnel et al. [25] in a three-year study found that consumption of erythritol-containing candies by initially 7- to 8-year-old children resulted in reduced plaque growth, lower levels of plaque acetic acid and propionic acid.

Erythritol, characterizes with a clean sweet taste, is approximately 70 % as sweet as sucrose, with no aftertaste and a mild cooling effect in the mouth [18, 20, 22, 26]. It can be easily blended with artificial sweeteners such as acesulfame potassium and aspartame or other polyols, i.e., sorbitol and xylitol or other sweeteners such as ste-via to give a similar flavor to the one of table sugar [22,

Fig. 1 Chemical structures of sugar alcohols

27]. Even slight amounts of aspartame or acesulfame K increase erythritol sweetness by about 30 %. It can also improve mouthfeel and mask certain unwanted aftertastes of intense sweeteners [23]. Erythritol was also reported to protect endothelial cells under hyperglycemic conditions (Table 4) [28]. In vitro studies have also shown that erythritol is an excellent radical scavenger with membrane-protecting properties [19, 23]. Moreover, it was also found that simultaneous intake of equimolar amounts of erythritol and fructose results in the impaired absorption of the latter [29].


Based on clinical studies, it was stated that erythritol is well (60-90 %) and rapidly absorbed in the small intestine

and then excreted intact in urine within 24 h (Table 3). Only small amounts are subjected to intestinal fermentation, and thus laxative side effects associated with excessive polyol consumption are unlikely to observe [1, 15, 19, 20, 23]. Gastrointestinal effects were recorded when high doses were consumed, up to 1000 mg/kg body [15]. Oku and Okazaki [18] also stated that women are more resistant to diarrhea resulting from a high ingestion of erythritol than men. What is more, the diarrheal effect of sorbitol is greater than that of erythritol [18]. According to American and Japanese legislation, it provides 0.2 kcal/g, whereas EU directives set this value at 2.4 kcal/g [Table 2; 21]. It has been intensively tested for safe use in both animals and humans, and thus no ADI have been specified for this polyol [30].

Table 4 Biological activities of sugar alcohols

Sugar alcohol Biological activities

Erythritol [1, Non-caloric

19, 23, 24, 29] Non-glycemic

High digestive tolerance


Free radical scavenger


Antioxidative and endothelium-protective proper-

Increases malabsorption of fructose

Isomalt [1, 24, Very low glycemic index

39, 44] Non-cariogenic

Reduced calorie value

Has an effect like dietary fiber in the gut

Lactitol Non-cariogenic

[1, 13, 14, 24, Reduced calorie value

45-48, 50-56] Increases the growth of probiotic bacteria

Reduces the population of putrefactive bacteria

Lowers the intestinal pH

Role in treating encephalopathy and constipation

Increases mineral bioavailability in human and rats

Maltitol [1, 13, Low glycemic index

14, 21, 24, Lower calories

59-62] Non-cariogenic

Increases mineral bioavailability in human and rats

Combination with short-chain fructo-oligosaccha-

rides in sugar-free food product formulations

results in lower postprandial glycemic responses

Mannitol [75, Reduces the rise in blood glucose and insulin levels

81, 82] Low calories


When inhaled is helpful in mucus and cough

clearance in asthmatics and other hypersecretory


Sorbitol [75, 78] Non-cariogenic

Reduced calorie value

Very low glycemic index

Xylitol [3, Non-cariogenic, improves dental health (helps in

26, 95-97, remineralization of tooth enamel)

109-114, 116, Increases saliva production, which helps in treating

117, 127] xerostomia

Protects salivary proteins, has a protein-stabilizing


Improves breath odor

Reduces infections in the mouth and nasopharynx

Low calorie and very low glycemic index

Antiketogenic—decreases serum-free fatty acid

levels and improves peripheral glucose utilization

Favors absorption of calcium and B vitamins

Inhibits yeast growth, including Candida albicans

Decreases glycation of proteins, reduces AGEs

Helps to maintain healthy gut function


Contrary to other polyols, it is not produced by direct catalytic hydrogénation due to the high cost of substrate eryth-rose [31; Table 5]. Its industrial manufacturing is based on fermentation processes led by osmophilic yeasts such as

Table 5 Industrial manufacturing of sugar alcohols Sugar alcohol Industrial manufacturing

Erythritol Fermentative processes led by osmophilic yeasts such as Moniliella pollinis or Trichosporonoides meg-achiliensis [16, 21-23, 26, 32] or some species of lactic acid bacteria, i.e., Oenococcus oeni, Leucon-ostoc mesenteroides and Lactobacillus sanfrancis-cencis [33-35] and Yarrowia lipolytica [36-38] Isomalt Transformation of sucrose into isomaltulose which is

then subsequently hydrogenated [22, 39, 40] Lactitol Hydrogenation of a 30-40 % lactose solution at about

100 °C with a Raney nickel catalyst [45-47] Maltitol Catalytic hydrogenation of maltose or very high

maltose glucose syrup [61] Crystallization from the maltose syrup and hydrogen-ate followed by aqueous or melt crystallization [61] Hydrogenation of maltose syrup and a high-purity liquid maltitol is recovered using liquid chromatog-raphy [61]

Hydrogenation and melt crystallization of maltitol from a maltose syrup with a maltose content in excess of 92-93 % [61] Mannitol Extraction from seaweed in China [75] Fermentation [75]

Catalytic hydrogenation of fructose derived from sugar or starch (more complicated process, but cost-effective) [66, 75, 78] Sorbitol Catalytic hydrogenation of sugar, starch or glucose

syrups, at high temperature (typically, 100-150 C) and high pressure [100-150 bar; 75, 78] Xylitol Nickel catalyzed hydrogenation of wood sugar

(xylose)—four step process that includes xylose isolation, purification, hydrogenation to xylitol and its crystallization [47, 108] Biotechnologically by yeasts such as Candida tropi-calis that metabolize wood sugar [128]

Moniliella pollinis or Trichosporonoides megachiliensis [16, 21, 22, 26, 32] as well as some species of lactic acid bacteria, i.e., Oenococcus oeni, Leuconostoc mesenter-oides and Lactobacillus sanfranciscencis [33-35]. Eythritol can also be produced from glycerol by Yarrowia lipolytica MK1 [36-38].


Isomalt, which is a mixture of two isomeric disaccha-ride alcohols: gluco-mannitol (a-D-gluco-pyranosyl-1-6-mannitol) and gluco-sorbitol (a-D-gluco-pyranosyl-1-6-Sorbitol), was discovered in the 1960s (Fig. 1).


It is produced from sucrose in a two-step process, which makes isomalt chemically and enzymatically more stable than the sucrose. It starts by sugar enzymatic

Table 6 Reported side effects of sugar alcohols

Sugar alcohol Reported side effects

: [125]

Erythritol Non-observed under the anticipated conditions of use; symptoms of over- Not specified

consumption are flatulence and laxation [1, 15, 18-20, 23, 130] Isomalt Excess consumption causes laxative effect [39] Not specified

Lactitol Bloating and flatulence after an intake more than 20 g in a single dose [46] Not specified

Maltitol Abdominal bloating and laxative effect when consumed in large quantities Not specified

[59, 60]

Mannitol In amounts greater than 20 mg/kg body weight may cause abdominal pain, Not specified

excessive gas (flatulence), loose stools or diarrhea [1, 68, 72, 78] Sorbitol Osmotic diarrhea as a result of intestinal malabsorption when ingested dose Not specified

is greater than 50 grams per day [78] Consumption of 20-30 g/day results in abdominal pain [108] Xylitol Occasionally noted temporary laxation and gastrointestinal discomfort [129, Not specified

transglucosidation into maltulose that is subsequently hydrogenated into isomalt, which is a combination of two disaccharide alcohols, 6-0-a-d-glucopyranosyl-d-sorbitol (1,6-GPS) and 1-0-a-d-glucopyranosyl-d-mannitol dihy-drate (1,1-GPM) [39, 40].

Properties and applications

Isomalt is resistant to the loss of sweetness during heating; thus, it can be used in products, which are subjected to high temperatures [41]. Its sweetness depends on concentration, temperature as well the form of product in which it is used; on average it has 45-65 % of the sweetness of sucrose [40, 41]. Besides resembling table sugar physically (white, crystalline and odorless), it is also slightly hygroscopic substance and enhances flavor transfer in foods [40, 41]. Moreover, it does not crystallize as quickly as sucrose, so it can be used for sugar sculptures and other decorative edible products [22]. Contrary to other polyols, it does not give cooling effect in the mouth. It is often combined with non-nutritive sweeteners, because it helps masking the bitter aftertaste of some sweet food additives and bulking agents [40]. Aside from being sweetener, it also acts as a bulking agent, anti-caking agent and glazing agent [42; Table 1]. It is synergistic with other sweeteners, especially those intense ones, is anti-cariogenic and does not increase blood glucose or insulin levels (Table 4). Similarly to other polyols, products sweetened with isomalt may be labeled safe for teeth [10, 43]. What is more, isomalt-containing toothpastes were found to enhance teeth remineralization [43].

It has been available in Europe since the early 1980s and is currently used in a wide variety of products such as hard candies, toffees, chewing gum, chocolates, baked goods, nutritional supplements, cough drops and throat lozenges [42].


Isomalt absorption is very low amounting to 10 % and 90 % of the absorbed part is being fermented [1, 40]. The bacterial fermentation products are short-chain fatty acids, CO2, CH4 and H2 [40]. Due to its partial digestion in the intestines, it supplies only half of the caloric value of sucrose (Table 2). However, it cannot be fermented by a large number of yeasts and other microorganisms found in nature [39]. In vitro studies have demonstrated that this polyol is a good source of butyrate and increases growth of bifidobacteria, which results in prebiotic effect [39, 44].

ADI for isomalt has been established by the Joint Food and Agriculture Organization/World Health Organization Expert Committee on Food Additives (JECFA) as "not specified." When consumed in high amounts may result in laxative effect, which is greater when isomalt is consumed in liquid food. However, its intolerance depends on many factors such as individual sensitivity, the moment and frequency of consumption [Table 6; 39].


It was discovered in 1920 by a French food chemist but not commercially used until 1980's. Lactitol is a disaccha-ride polyol, which is composed of sorbitol and galactose (Fig. 1). It is produced from lactose by a catalytic hydrogenation using Raney nickel as the catalyst [45-47].


Although it is produced from lactose, it is not hydrolyzed by lactase, but is broken down by gut microflora (Table 3). Lactitol is metabolized by bacteria in the large intestine, where it is converted into biomass, carbon dioxide, a small amount of hydrogen and organic acids [45, 47], which are

further metabolized to give energy in the amount of 2-2.4 calories per gram (Table 2). It was also found that lactitol is used as an energy source by special intestinal microflora in the colon, i.e., Bifidobacteria and Lactobacillus spp [47, 48]. Overconsumption might result in laxative effect, which varies depending on the mode and frequency of ingestion, diet, age and general gut health [46].

Properties and applications

Lactitol characterizes with a clean sweet taste and a sweetening power of 40 % of that of sucrose [47]. However, it is used as a sucrose 1:1 substitute in calorie-controlled foods, mainly due to its good solubility. It can be dissolved at lower temperatures than sucrose, which results in saving of energy and processing costs [45, 46]. It does not take part in non-enzymatic browning (Maillard) reactions and can be stored for long periods [46].

Its characteristic mild sweetness helps in better perception of product flavor, and thus, it is usually combined with low-calorie sweeteners such as acesulfame K, aspar-tame, cyclamate, neotame, saccharin, stevia sweeteners and sucralose. Lactitol sweetness increases with the concentration level, but it has a very small cooling effect. This sugar alcohol is non-hygroscopic, stable in high temperatures as well as acidic and alkaline conditions. Besides sweetening, it can be used as a thickener and emulsifier [49]. Lactitol has a negligible effect on blood glucose levels and can be metabolized without insulin [45]. Similarly to other sugar alcohols, it also does not contribute to dental caries [10, 45]. Lactitol also acts as a prebiotic that is capable of promoting the growth of beneficial bacteria in the colon such as Bifidobacteria and Lactobacilli, but also reduces the population of putrefactive bacteria selectively and lowers the intestinal pH as well as the production and absorption of ammonia [45, 46, 48, 50, 51]. Lactitol was also applied in treating encephalopathy and constipation [52-56].

Due to its properties, lactitol is used in certain pharmaceutical applications, in food for diabetics, low-calorie, low-fat and/or sugar-free foods such as ice cream, chocolate, hard and soft candies, baked goods, sugar-reduced preserves, chewing gums and sugar substitutes [49, 52, 57, 58]. However, due to its low sweetness, it is usually mixed with intense sweeteners [47]. Similar to other polyols, it is reckoned as safe and has been allocated an ADI "not specified" by JECFA (Table 6) [45].


Maltitol, also called 4-0-a-D-glucopyranosyl-D-glucitol (Fig. 1), is a disaccharide polyol that consists of glucose and sorbitol in equal parts and is obtained from starch, by

hydrogenating maltose or very high maltose glucose syrup [1, 59, 60].

Properties and applications

Among polyols, maltitol characterizes with properties the most resembling the ones of sucrose [60, 61]. Its sweetness is clean and pleasant and amounts up to 90 % of the one attributed to sucrose, but its caloric value amounts to 2.12.4 kcal/g (Table 2). Maltitol is also a non-cariogenic agent, which characterizes a pleasant sweet taste that is similar to sucrose; however, due to slow absorption, the insulin response associated with its ingestion is significantly reduced [1, 10]. It has been reported that its simultaneous application with short-chain fructo-oligosaccharides in sugar-free food product formulations lowers postprandial glycemic responses [62].

It does not undergo carmelization and browning process, and it cooling effect is negligible when compared with other polyols. Besides replacing sweeteners, it can also be used as a fat substitute, as it gives a creamy texture to food [59-61, 63]. Due to its low hygroscopicity and stability in high temperatures, it is used in many baked products as well as a variety of reduced calorie, reduced fat and sugar-free foods [21, 59, 60].


Maltitol absorption ranges from 5 to 80 %, but is must be preceded by hydrolysis which leads to glucose and sorbitol [1]. It is slowly digested in the small intestine, and the non-absorbed part passes to the colon where is undergoes fermentation by bacteria [64]. Although its ADI was not specified, it reveals laxative effects when consumed in amounts exceeding 25-30 g/kg body weight per day [59].

Currently, its use is approved in most countries including Canada, Europe, Australia, New Zealand and Japan, but awaits approval of Food and Drug Administration (FDA). However, US food manufacturers may use maltitol since FDA has accepted the petition concerning this compound [61].


This 6-carbon sugar alcohol is an isomer of sorbitol (Fig. 1). Mannitol is used as a reserve carbohydrate by some bacteria, fungi, brown seaweeds and some higher plants [65, 66].


Its production is based on the catalytic hydrogenation of glucose/fructose (1:1) mixture, obtained from invert sugar

or starch, at high temperatures and pressure [67-69]. However, this process characterizes with low efficiency yielding only 25 % of mannitol in the obtained mixture and a need of elaborate purification step. Thus, fermentative processes have been researched, especially with the use of heterofermentative lactic acid bacteria, resulting in a complete conversion of D-fructose into D-mannitol in mild conditions [70-73]. Recently, cyanobacteria were found useful for mannitol production, mainly due to the fact that sugars are the primary products of photosynthesis [66]. As it can be found in high amounts in the exudates of certain trees, especially from Manna ash (Fraxinus ornus), figs, olives, larches, edible fungi, yeasts and seaweed, its production through extraction from natural sources is also considered [17, 65, 68, 69, 74, 75].


Mannitol is poorly absorbed, and thus, the rise in blood glucose and demand for insulin is much less than would be experienced after sucrose ingestion. It is only partially absorbed (~25 %) from the small intestine and not metabolized (Table 3). However, in the lower part of the intestinal tract, colonic bacteria can slowly metabolize some of the non-absorbed portion, and thus, consumption of doses exceeding 20 g/day might have a laxative effect [Table 6; 1, 68, 72]. The fermentation yields organic acids production, which can be utilized by human organism [14].

Properties and applications

It is about 50 % as sweet as sucrose and has a desirable cooling effect, which is efficient in masking bitter tastes [1, 17, 68]. Mannitol can be mixed with other ingredients and sweeteners what can result in a synergistic effect of better sweetness and tasting. This sugar alcohol characterizes with a pleasant taste, stability, even in high temperatures, and a high melting point (165-169° C). Thus, it is commonly used in pharmaceuticals and nutritional tablets as well as in food industry, i.e., in chocolate-flavored coating agents for ice cream and confections or "breath-freshening" and "sugar-free" products. Mannitol can be also used as a feedstock for bioethanol production [76]. As mannitol is non-hygroscopic, it is used as a bulking agent for sugar-free coatings and a dusting powder for chewing gum to prevent the gum from sticking to manufacturing equipment and wrappers [68, 77, 78].

It can be also applied as a potent osmotic diuretic and is a well-known antioxidant [17, 19, 31, 68, 69, 79]. Moreover, it acts as a scavenger of hydroxyl radicals and is claimed to protect against the development of colon cancer [68, 80]. Mannitol is also presumed to be health promoting, and thus, its addition to foods can result in extra nutritional

value [72]. When mannitol is inhaled, it helps in mucus and cough clearance in asthmatics and other hypersecretory diseases [81, 82]. Mannitol accompanied with hydration during endovascular aortic aneurysm repair might improve renal function [83].

Besides being non-cariogenic, it is also characterized with a low caloric value (Table 2). As mannitol is not metabolized by humans, it does not induce hyperglycemia and has glycemic and insulinemic indexes of 0 [1, 24, 69, 72].

Similar to other polyols, mannitol is also resistant to oral bacteria which prevents from the increase in the acidity of the mouth after ingestion (Table 4). Thus, according to the US FDA and European Commission, products containing mannitol can have a health claim on the labeling stating "does not promote tooth decay" [10]. FDA as well as JECFA have approved usage of mannitol as a food additive, which is regarded as safe (Table 6).


Sorbitol, which has a systematic name D-glucitol (Fig. 1), is a 6-carbon sugar alcohol that was discovered by a French chemist in the berries of the mountain ash in 1872. This polyol can be naturally found in apples, pears, peaches, apricots and nectarines as well as in dried fruits, such as prunes, dates and raisins and in some vegetables [17, 22, 75, 84-88].


Sorbitol is produced from glucose or sucrose, by a catalytic hydrogenation with hydrogen gas and nickel catalyst at high temperatures [17, 21, 22, 89]. However, it can be also produced by electrochemical reduction of dextrose in alkaline conditions [21, 22]. Although there are known several industrial processes which are used for the production of sorbitol, only a few microorganisms, including three yeast strains and bacteria such as Zymomonas mobilis and Candida boidini, have been suggested as potential sorbitol producers [17, 73, 87, 90-92].

Properties and applications

Sorbitol supplies fewer calories than sugars, and its sweetness amounts to about 60 % of the one assigned to sucrose (Table 2). It also characterizes with a 20-fold higher solubility in water than mannitol. [17, 84, 87]. It is manufactured in both liquid and crystalline form [75, 84]. Similarly to xylitol and erythritol, it has a negative heat of solution, and thus it gives a cooling sensation in the mouth. Sorbitol has a sweet, cool and pleasant taste. Besides acting as a sweetener, it is also an excellent humectant, softener, texturizing and

anti-crystallizing agent [17, 90] (Table 1). It is easily compressible substance but has a great technological disadvantage, which is high hygroscopicity [77, 78]. This polyol is chemically inert and stable, even in high temperatures, and does not undergo Maillard reactions [75, 93, 94]. Sorbitol can combine well with other food components such as sugars, gelling agents, proteins and fats. It also may reveal syn-ergistic effects with other sweeteners that result in greater sweetness and better taste. This sugar alcohol is important for fruits carbon metabolism and affects the quality of starch accumulation and sugar-acid balance [22].

Sorbitol is resistant to digestion by oral bacteria which break down sugars and starches to release acids that may lead to cavities or erode tooth enamel. According to the US FDA and European Commission, products containing this sugar alcohol can have a health claim on the labeling stating "does not promote tooth decay" [10].

Due to its non-cariogenic properties, it is used in products for special nutritional purposes designated for people with diabetes, but it also finds its application in pharmaceuticals and cosmetics. Sorbitol can be added to a wide variety of products, including sugar-free candies, chewing gums and sugar-free foods such as frozen desserts and baked goods. As it prevents loss of moisture content, it is used in the production of confectionery, baked goods and chocolate, which have a tendency to become dry or harden during storage. Sorbitol is also used as an important precursor of the vitamin C production, sorbose as well as surfactants [5, 87, 92]. The worldwide production of sorbitol is estimated to be higher than 500,000 tons/year, and the market is continuously increasing, and about 25 % of that production is used for the synthesis of vitamin C [73, 85, 87]. What is more, 25 % of total sorbitol production is used in manufacturing of syrups [21].

Its safety has been supported by many scientific studies, and JECFA has defined an acceptable daily intake (ADI) for sorbitol as "not specified," and thus, no limits are placed on its use. Similar to other polyols, it might reveal laxative effect when eaten in excess [22; Table 6].


It is a 5-carbon polyol which is produced from D-xylose (Fig. 1). It was discovered in 1891 and since the 1960s has been used as a sweetener. It can be found in nature in many fruits and vegetables, berries, oats and mushrooms and is produced in small quantities in human organism [21, 22, 95-99].


Main substrate for its production is xylan, which is usually obtained from birch trees and other hardwood [95, 97,

100]. Similarly to other sugar alcohols, xylitol is produced by metal catalyzed hydrogenation of a corresponding sugar, i.e., D-xylose [26, 98, 101]. This process starts with xylan isolation from wood material followed by its hydrolysis to xylose. Then xylose is chromatographically purified, and the resulting solution is subjected to hydrogenation in the presence of nickel catalyst. Commercial xylitol production might be also started by xylose solution hydrogenation, its purification and final crystallization in orthorhombic form [21, 99].

However, due to high production cost, biotechnologi-cal production systems from corn cobs, the waste of sugarcane and other fibers were developed, but still they are not introduced on commercial scale [99, 102-106]. It can be also efficiently produced by yeasts that naturally obtain xylitol as an intermediate during D-xylose metabolism [17, 73]. The genus Candida is their best source, but it cannot be used in food industry as it is a pathogenic one [17, 73]. Recombinant microalgae were also reported to produce xylitol [107].


Xylitol is approximately absorbed in 50 % in small intestine and its fermentation, which takes place in large bowel, ranges from 50 to 75 % [1]. It can be metabolized directly in the liver or indirectly by fermentative degradation by intestinal flora (Table 3) [108]. Human tolerance of xylitol amounts to 100 g per day [96].

Properties and applications

Xylitol is the sweetest among all sugar alcohols (Table 2). It characterizes with the same sweetness and bulk as sucrose with one-third fewer calories and no unpleasant aftertaste [21]. Insulin is not required for its metabolism [26, 97]. It quickly dissolves and produces a cooling sensation in the mouth [3, 98, 99].

Xylitol is widely used in biomedical and other applications [3]. Its regular consumption in adequate doses results in the reduction of tooth decay [26, 97, 109]. Besides reducing the development of dental caries, it also plays a role in a decrease in plaque formation as it inhibits the growth and metabolism of Streptococcus mutans and Streptococcus sobrinus, which are responsible for caries and dental plaque acid production, respectively [96, 110-113]. There are results of several clinical studies which confirm that the daily usage of small amounts of xylitol significantly decreases the risk of dental caries [3, 95, 114]. It has been also reported that maternal xylitol consumption results in reduced occurrence of dental caries in children [115]. Xylitol increases pH values in the oral cavity that contributes to teeth remineralization as well as forms

complexes with Ca(II) which is supposed to play a huge role in tooth mineralization [3, 116, 117]. Moreover, xylitol acts as a statherin, which is a polypeptide that provides a protective and stabilized environment for teeth [3]. There is also data implying that xylitol reduces the incidence of ear infections and has an anti-bacterial effect on pneumococ-cal nasal colonization [96, 118-120]. This sugar alcohol is used as an energy source in infusion therapy [121]. It also acts as an antioxidant agent of fish oil [122], as a sanitizer [123] and as a preventive factor of adrenocortical suppression during steroid therapy [121] and phenylenediamine-induced hepatotoxicity [124].

Due to its properties and only few reported side effects, mainly gastrointestinal (Table 6), it is widely used in food, pharmaceuticals and nutraceuticals, especially in such products as chewing gums and candies [98, 99]. FDA approved its use in 1960 s and in Europe, it is known as E967 food additive, which is safe for use with children [95].

Sugar alcohols versus artificial sweeteners

The health and safety agencies from different countries regulate which sweeteners are allowed as well as the maximum amount that can be added to a specific food group. Sweeteners may be used separately or in combination with other sweeteners, and the latter is becoming increasingly popular in recent years owing to technical, health and commercial advantages. The consumption of low-calorie foods by the worldwide population has dramatically increased, as well as health concerns associated with the consequent high intake of sweeteners both nutritive and non-nutritive.

Nutritive sweeteners include refined sugar, honey, high fructose, corn syrup, dextrose and sugar alcohols. There are eight non-nutritive sweeteners included in EU legislation that are allowed for use in food, i.e., acesulfame K (E950), aspartame (E951), cyclamic acid and its Na, Ca salts (E952), saccharin and its Na, K, Ca salts (E954), sucralose (E955), thaumatin (E957), neohesperidine DC (E959) and salt of aspartame-acesulfame K (E962) [11].

One of the most important differences between artificial sugar substitutes and polyols is that the first ones contain zero calories, with the exception of aspartame that provides 4 kcal per gram but is consumed in very small amounts, contributing negligible energy. Sugar alcohols contain from 0.2 to 2.7 calories per gram (Table 2), while common sugars supply 4 kcal/g.

Unlike artificial sweeteners, polyols can raise blood glucose but less than sugars, which is due to their incomplete absorption in human organism. However, particular sugar alcohols are metabolized differently and thus can exhibit various impacts on glucose levels in organism (Table 2).

Polyols are in general partially digested in the intestines, and the non-absorbed part is slowly metabolized by colonic bacteria yielding volatile short-chain fatty acids (Table 3). Most of artificial intense sweeteners are not metabolized (acesulfame potassium), but aspartame is digested to phe-nylalanine, aspartic acid and methanol; thus, people with phenylketonuria, a rare genetic disorder, cannot consume products sweetened with this substance [2, 26].

The sweetness of sugar alcohols varies from 25 to 100 % as compared with table sugar (Table 2), whereas artificial sweeteners are 30 to even 13,000 times sweeter than sucrose [2, 26]. Thus, they can be used in small amounts to achieve desired sweetness in such products as beverages, ice cream chewing gum, chocolate, jams/jellies, yogurt and salad dressings [2]. However, artificial intense sweeteners are used only for sweetening, whereas polyols can be used as anti-caking and glazing agents as well as stabilizers and thickeners (Table 1). Similar to common sugars, they can be also used as bulking agents besides being excellent natural sweeteners. They also help food keep moisture, prevent browning when heated and add a cooling sensation to products. Some artificial sweeteners may leave an aftertaste, but mixing with particular polyols such as erythritol, isomalt or lactitol can result in a similar flavor to the one of table sugar [22, 27, 40].

The use of sugar alcohols in food products is defined in the Regulation (EC) 1333/2008 on food additives, and they are authorized to be added on where quantum satis level for all purposes, i.e., sweetening and others [8; Table 6]. However, each artificial sweetener has been established an acceptable daily intake (ADI) and are used in foods within specified limits [11]. Although there are some controversies over the safety of artificial sweeteners, especially aspar-tame, they have been approved both by the FDA as well as JECFA (The Joint FAO/WHO Expert Committee on Food Additives) [2, 26]. Sugar alcohols have been also associated with few side effects when eaten in excess, which include bloating, abdominal pain and diarrhea (Table 6). However, in reasonable amounts, artificial sweeteners and polyols might be helpful in diabetes and weight control, but tooth decay prevention can be only associated to the latter consumption. Besides that, sugar alcohols exhibit many health protection roles (Table 4).

All in all, both groups of sweeteners can be useful in diabetes management and are good option for people on low-carbohydrate diet. The highest polyol intake can be associated with consumption of confectionery products, fish/meat product and miscellaneous foods. However, such estimates might differ in dependence on scenario adopted for exposure modeling [125]. Overconsumption of polyols can be only of concern in view of digestive comfort, while artificial sweeteners must be always estimated with respect to the maximum amounts allowed, which are considered safe for human

consumption. Therefore, it might be worth using sugar alcohols in food products marketed to patients with diabetes and individuals considering energy restricted diets more frequently but bearing in mind their gastrointestinal effects. However, optimal diet should be based on fresh unprocessed foods with the minimal amounts of food additives, and then the sugar replacers such as sugar alcohols or even artificial sweeteners will not have a significant role in the daily diet.


Due to increasing epidemic of obesity and diabetes, it is important to educate consumers to make reasonable and healthy food choices. Consumption of added sugars has risen dramatically over the past few decades and has negatively contributed to human health. Foods rich in added sugar contribute mainly extra calories to diet usually without nutritional value. Unfortunately, people crave sweetness, and thus, sugar substitutes have drawn attention of consumers as well as producers and dieticians. However, human body response is not identical when we compare artificial sweeteners with those of natural origin, especially sugar alcohols that characterize with many attractive properties not only to producers but also to consumers. As these compounds are new, there is a need for education as products containing polyols are a rapidly growing category of nutraceuticals and functional food. Therefore, there is a constant need for studies regarding sugar alcohols metabolism and physiological effects on human bodies.

Conflict of interest None.

Ethical standards The manuscript does not contain clinical studies or patient data, but it makes references to clinical studies.

Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.


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