A sugar substitute, or artificial sweetener, is a food additive which duplicates the effect of sugar or corn syrup in taste, but often with less food energy.
An important class of sugar substitutes are known as high intensity sweeteners. These are compounds whose sweetness is many times that of sucrose; accordingly, much less sweetener is required and energy contribution often negligible. The sensation of sweetness caused by these compounds (the "sweetness profile") is sometimes notably different from sucrose, so they are used in complex mixtures that achieve the most natural sweet sensation.
If the sucrose (or other sugar) replaced has contributed to the texture of the product, then a bulking agent is often also needed. This may be seen in soft drinks such as coke labeled as "diet" or "light" which contain artificial sweeteners and often have notably different mouthfeel; or in table sugar replacements which mix maltodextrins with an intense sweetener to achieve satisfactory texture sensation.
In the United States, five artificially derived sugar substitutes have been approved for use. They are saccharin, aspartame, sucralose, neotame and acesulfame potassium. These compounds are all high intensity sweeteners. There is ongoing controversy as to whether artificial sweeteners are health risks. Some studies show that they cause disease in laboratory rats.
The majority of sugar substitutes approved for food use are artificially synthesized compounds. However, some natural sugar substitutes are known — including sorbitol and xylitol, which are found in berries, fruit, vegetables and mushrooms. (Although natural, they may be produced synthetically in bulk food production, to lower production costs.) Other natural substitutes are known but are yet to gain official approval for food use.
Another important group of non-sugar sweeteners are the polyols. These are generally less sweet than sucrose, but have similar bulk properties and can be used in a wide range of food products. Sometimes the sweetness profile is 'fine-tuned' with high intensity sweeteners as described above. As with all food products the development of a formulation to replace sucrose is a complex process.
The reason is very simple: although the profit margins on artificial sweeteners are extremely high for the manufacturers, they still cost the food industry just a fraction of the cost of sugar and corn syrup (which once was introduced by the industry as a low-cost alternative to sugar). So, it's not surprising that the food industry is promoting its "diet" or "light" products heavily, thus moving the customers over to its more profitable, artificially sweetened products.
According to market analysts Mintel, a total of 3,920 products containing artificial sweeteners were launched in the US between 2000 and 2005, whereof 1,649 products in 2004 alone. According to market analysts Freedonia, the US artificial sweetener market is set to grow at around 8.3 % year on year to $189 million in 2008. *.
Aspartame is currently the most popular sweetener in the US food industry, as the price has dropped significantly since the Monsanto patent expired in 1992. However, sucralose may soon replace it, as alternative processes to Tate & Lyle's patent seem to be emerging, which, according to Morgan Stanley, can mean that the price of sucralose drops by 30%. *
However, it should be noted that changing the food energy intake from one food will not necessarily change a person's overall food energy intake, or cause a person to lose weight. No published study has shown this. One study * on WebMD, by the University of Texas Health Science Center at San Antonio, actually showed the opposite, where those who consumed diet soda were more likely to gain weight than those that consumed naturally sweetened soda. However, this study only contains data limited to soda sweetened with aspartame. It is not known if the same results will appear in baked goods and other products sweetened with saccharin, sucralose, or other sugar substitutes.
Saccharin was the first artificial sweetener and was originally synthesized in 1879 by Remsen and Fahlberg and its sweet taste was discovered by accident. It had been created in an experiment with toluene derivatives. A process for the creation of saccharin from phthalic anhydride was developed in 1950 and currently saccharin is created by this process and the original process by which it was discovered. It is 300-500 times as sweet as sugar (sucrose) and is often used to improve the taste of toothpastes, dietary foods, and dietary beverages. The bitter aftertaste of saccharin is often minimized by mixing it with other sweeteners.
Fear about saccharin increased when a 1960 study showed that high levels of saccharin may cause bladder cancer in lab rats. In 1977, Canada banned saccharin due to results from animal research. The FDA in the United States considered banning saccharin in 1977, but after a moratorium was placed on the ban to study the safety of saccharin, the ban was withdrawn in 1991. Likewise, in 2000, the United States repealed a law requiring saccharin products to carry health warning labels. Most other countries also permit saccharin but restrict the levels of use, while other countries have outright banned it.
Initial safety testing suggested that aspartame caused brain tumors in rats; as a result, the additive was held up in the United States for many years in the FDA's approval process. In 1980, the FDA convened a Public Board of Inquiry (PBOI) consisting of independent advisors charged with examining the purported relationship between aspartame and brain cancer. The PBOI's conclusions were unclear whether aspartame causes brain damage, and recommended against approving aspartame at that time, citing unanswered questions about cancer in laboratory rats. In 1981, FDA Commissioner Arthur Hull Hayes, newly appointed by President Ronald Reagan, approved aspartame as a food additive. He was closely associated with the artificial sweetner industry having several close friends, most notably Donald Rumsfeld, the current Secretary of Defense, and then the CEO of G.D. Searle. Hayes cited data from a single Japanese study that had not been available to the members of the PBOI, as his reason for approval. *
Since the FDA approved aspartame for consumption, some researchers have suggested that a rise in brain tumor rates in the United States may be at least partially related to the increasing availability and consumption of aspartame. *," target="_blank" >[http://web.mit.edu/newsoffice/tt/1998/sep16/aspartame.html
One of the many hypotheses about the causes of Gulf war syndrome is that soldiers, after drinking gallons of aspartame-containing soft drinks in the extreme heat, accumulated toxic doses of methanol, formaldehyde, diketopiperazine and formic acid from the breakdown of the sweetener into its component molecules. However, the symptoms do not greatly resemble those of classic methanol poisoning, and the body, in its normal metabolism, produces methanol in quantities comparable to or greater than would be ingested via aspartame, so this theory does not have wide support.
The FDA approved sucralose in 1998. *
The first significant rumblings were in 2000, when osteopathic physician Joseph Mercola wrote an article entitled "The Secret Dangers of Splenda (Sucralose), an Artificial Sweetener". Since then, many others have chimed in.
In December of 2004, five separate false advertising lawsuits were filed against chemical sweetener manufacturer Johnson & Johnson/McNeil for claims made about its artificial sweetener Splenda.
On January 10, 2005, the "Truth About Splenda" website was created by The Sugar Association, an organization representing sugar beet and sugar cane farmers in the United States, in an effort to educate the public on their views.
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