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Sucralose

Non-nutritive sweetener

Sucralose

Summary

Non-nutritive sweetener

| NFPA-H = 1 | NFPA-F = 1 | NFPA-R = 0

Sucralose: (C<sub>12</sub>H<sub>19</sub>Cl<sub>3</sub>O<sub>8</sub>) Black Carbon, White Hydrogen, Green Chlorine, Red Oxygen

Sucralose is an artificial sweetener and sugar substitute. In the European Union, it is also known under the E number E955. It is produced by chlorination of sucrose, selectively replacing three of the hydroxy groups—in the C1 and C6 positions of the fructose portion and the C4 position of the glucose portion—to give a 1,6-dichloro-1,6-dideoxyfructose4-chloro-4-deoxygalactose disaccharide. Sucralose is about 600 times sweeter than sucrose (table sugar), 3 times as sweet as both aspartame and acesulfame potassium, and 2 times as sweet as sodium saccharin.

The commercial success of sucralose-based products stems from its favorable comparison to other low-calorie sweeteners in terms of taste, stability, and safety.

Uses

Sucralose is used in many food and beverage products because it is a non-nutritive sweetener (14 kJ per typical one-gram serving), does not promote dental cavities, is safe for consumption by diabetics and nondiabetics and does not affect insulin levels. The powdered form of the sucralose-based sweetener product Splenda contains the bulking agents – dextrose and maltodextrin. Sucralose content is about 1.1% and remainder is bulking agents.

Sucralose is used as a replacement for (or in combination with) other artificial or natural sweeteners such as aspartame, acesulfame potassium or high-fructose corn syrup. It is used in products such as candy, breakfast bars, coffee pods, and soft drinks. It is also used in canned fruits wherein water and sucralose take the place of much higher-energy corn syrup-based additives. Sucralose mixed with dextrose or maltodextrin (both made from corn) as bulking agents is sold internationally by McNeil Nutritionals under the Splenda brand name.

Cooking

This mixture of granulated sucralose includes fillers, all of which rapidly dissolve in water. Sucralose is not hygroscopic when humidity is below 80%, which can lead to baked goods that are noticeably drier and manifest a less dense texture than those made with sucrose.

Safety evaluation

Sucralose has been accepted as safe by several food safety regulatory bodies worldwide, including the U.S. Food and Drug Administration (FDA), the Joint FAO/WHO Expert Committee Report on Food Additives, the European Union's Scientific Committee on Food, Health Protection Branch of Health and Welfare Canada, and Food Standards Australia New Zealand.

At normal baking temperatures, sucralose is mostly heat-stable, indicating that it retains its sweetness and is suitable as a sugar substitute for use in baked goods. Especially when heating sucralose above 120 °C, chlorinated organic compounds such as polychlorinated dibenzo-p-dioxins (PCDD), polychlorinated dibenzofurans (PCDF), or chloropropanol might form.

Maximum acceptable daily intake

Various assessments have reported different amounts of maximum acceptable daily intake (ADI), usually measured as mg per kg of body weight. According to the Canadian Diabetes Association, the amount of sucralose that can be consumed over a person's lifetime without any adverse effects is 9 milligrams per kilogram of body weight per day. The FDA approval process indicated that consuming sucralose in typical amounts as a sweetener was safe. The intake at which adverse effects are seen is 1500 mg per kilogram of body weight per day, providing a large margin of safety compared to the estimated daily intake. The European Food Safety Authority (EFSA) proposed an ADI of 5 mg per kilogram of body weight, while the FDA established it as 15 mg per kilogram of body weight, that is, 350–1050 mg per day for a person of 70 kg.

Metabolism

Most ingested sucralose is directly excreted in the feces, while about 11–27% is absorbed by the gastrointestinal tract (gut). The amount absorbed from the gut is largely removed from the blood by the kidneys and eliminated via urine, with 20–30% of absorbed sucralose being metabolized.

Possible health effects

In reviewing a 1987 food additive petition by McNeil Nutritionals, the FDA stated that "in the 2-year rodent bioassays ... there was no evidence of carcinogenic activity for either sucralose or its hydrolysis products".

In 2023, the World Health Organization (WHO) conditionally recommended against the use of non-sugar sweeteners, including sucralose, for weight management or preventive care in the general population (except for diabetics). The WHO recommended reducing the intake of sugar, highly processed food and sweetened beverages, and replacing them with minimally processed unsweetened beverages and foods, such as fruits.

, reviews of numerous safety and toxicology studies on sucralose concluded that it is not toxic or carcinogenic, even at levels of daily consumption much larger than those typically used.

History

Sucralose was discovered in 1975 by scientists from Tate & Lyle, working with researchers Leslie Hough and Shashikant Phadnis at Queen Elizabeth College (now part of King's College London). While researching novel uses of sucrose and its synthetic derivatives, mixing sulfuryl chloride with sugar, Phadnis was told to "test" a chlorinated sugar compound. According to an anecdotal account, Phadnis thought Hough asked him to "taste" it, so he did and found the compound to be exceptionally sweet.

Tate & Lyle patented the substance in 1976; as of 2008, the only remaining patents concerned specific manufacturing processes.

A Duke University animal study funded by the Sugar Association found evidence that doses of Splenda (containing ~1% sucralose and ~99% maltodextrin by weight) between 100 and 1000 mg/kg BW/day, containing sucralose at 1.1 to 11 mg/kg BW/day, fed to rats reduced gut microbiota, increased the pH level in the intestines, contributed to increases in body weight, and increased levels of P-glycoprotein (P-gp). These effects have not been reported in humans.

Sucralose was first approved for use in Canada in 1991. Subsequent approvals came in Australia in 1993, in New Zealand in 1996, in the United States in 1998, and in the European Union in 2004. By 2008, it had been approved in over 80 countries, including Mexico, Brazil, China, India, and Japan. In 2006, the FDA amended the regulations for foods to include sucralose as a "non-nutritive sweetener" in food. In May 2008, Fusion Nutraceuticals launched a generic product to the market, using Tate & Lyle patents.

In April 2015, PepsiCo announced that it would be moving from aspartame to sucralose for most of its diet drinks in the U.S. due to sales of Diet Pepsi falling by more than 5% in the U.S. The company stated that its decision was a commercial one, responding to consumer preferences.

In February 2018, PepsiCo went back to using aspartame in Diet Pepsi because of an 8% drop in sales for the previous year.

Chemistry and production

Sucralose is a disaccharide composed of 1,6-dichloro-1,6-dideoxyfructose and 4-chloro-4-deoxygalactose. It is synthesized by the selective chlorination of sucrose in a multistep route that substitutes three specific hydroxyl groups with chlorine atoms. This chlorination is achieved by selective protection of one of the primary alcohols as an ester (acetate or benzoate), followed by chlorination with an excess of any of several chlorinating agent to replace the two remaining primary alcohols and one of the secondary alcohols, and then by hydrolysis of the ester.

Storage

Sucralose is stable when stored under normal conditions of temperature, pressure and humidity. Upon prolonged heating during storage at elevated temperatures (38 °C, 100 °F), sucralose may break down, releasing carbon dioxide, carbon monoxide and minor amounts of hydrogen chloride.

Research

No evidence of an effect of sucralose on long-term weight loss or body mass index has been found, with cohort studies showing a minor effect on weight gain and heart disease risks.

Environmental effects

The majority of ingested sucralose is not metabolized by the human body, but is instead excreted unchanged. It is an emerging environmental contaminant that can not be removed in conventional waste water treatment process.

According to one study, sucralose is digestible by a number of microorganisms and is broken down once released into the environment. However, measurements by the Swedish Environmental Research Institute have shown that sewage treatment has little effect on sucralose, which is present in wastewater effluents at levels of several μg/L (ppb). No ecotoxicological effects are known at such levels, but the Swedish Environmental Protection Agency warns that a continuous increase in levels may occur if the compound is only slowly degraded in nature. When heated to very high temperatures (over 350 °C or 662 °F) in metal containers, sucralose can produce polychlorinated dibenzo-p-dioxins and other persistent organic pollutants in the resulting smoke.

Sucralose has been detected in natural waters, but research indicates that the levels found in the environment are far below those required to cause adverse effects to certain kinds of aquatic life.

References

References

  1. ''[[Merck Index]]'', 11th Edition, '''8854'''.
  2. (3 April 1998). "Food Additives Permitted for Direct Addition to Food for Human Consumption; Sucralose". Federal Register: 21 CFR Part 172, Docket No. 87F-0086.
  3. (25 September 2024). "Aspartame and Other Sweeteners in Food". US Food and Drug Administration.
  4. "A Report on Sucralose from the Food Sanitation Council". The Japan Food Chemical Research Foundation.
  5. (1 April 2019). "Sucralose nutrition information for a one gram portion (pick list)". FoodData Central, US Department of Agriculture.
  6. Food and Drug Administration. (March 2006). "Food labeling: health claims; dietary noncariogenic carbohydrate sweeteners and dental caries. Final rule". Federal Register.
  7. (December 2003). "Lack of effect of sucralose on glucose homeostasis in subjects with type 2 diabetes". Journal of the American Dietetic Association.
  8. (April 2011). "Effects of oral ingestion of sucralose on gut hormone response and appetite in healthy normal-weight subjects". European Journal of Clinical Nutrition.
  9. (2024). "Ingredients: Splenda Sweetener Packets".
  10. (2008). "Splenda alters gut microflora and increases intestinal p-glycoprotein and cytochrome p-450 in male rats". Journal of Toxicology and Environmental Health. Part A.
  11. (2012). "Sweeteners and Sugar Alternatives in Food Technology". Wiley.
  12. (2019-04-09). "BfR-Stellungnahme Nr. 012/2019 des BfR vom 9. April 2019". Bundesinstitut für Risikobewertung.
  13. (September 2008). "Canadian Diabetes Association 2008 Clinical Practice Guidelines for the Prevention and Management of Diabetes in Canada". Canadian Journal of Diabetes.
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  20. (28 November 2002). "Eurekas and Euphorias: The Oxford Book of Scientific Anecdotes". Oxford University Press.
  21. "Tate & Lyle loses sucralose patent case". ap-foodtechnology.com.
  22. (2 September 2008). "New Salvo in Splenda Skirmish". The New York Times.
  23. (2008). "Splenda alters gut microflora and increases intestinal p-glycoprotein and cytochrome p-450 in male rats". Journal of Toxicology and Environmental Health. Part A.
  24. (2 September 2009). "Sucralose safety 'scientifically sound': Expert panel".
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  26. (3 April 2006). "FDA amends regulations that include sucralose as a non-nutritive sweetener in food.". [[FDA Consumer]].
  27. (2015-04-27). "Pepsi to ditch artificial sweetener". BBC News.
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  30. (2012). "From Sugar to Splenda: A Personal and Scientific Journey of a Carbohydrate Chemist and Expert Witness". Berlin: Springer.
  31. {{US patent. 5498709
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  34. (2021-08-01). "Sucralose, a persistent artificial sweetener in the urban water cycle: insights into occurrence, chlorinated byproducts formation, and human exposure". Journal of Environmental Chemical Engineering.
  35. (2024-07-12). "Some artificial sweeteners are forever chemicals that could be harming aquatic life".
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  37. "Measurements of Sucralose in the Swedish Screening Program 2007, Part I; Sucralose in surface waters and STP samples".
  38. (October 2013). "Polychlorinated dibenzo-p-dioxins and dibenzofurans formed from sucralose at high temperatures". Scientific Reports.
  39. (October 2014). "Early life stage (ELS) toxicity of sucralose to fathead minnows, Pimephales promelas". Bulletin of Environmental Contamination and Toxicology.
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