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Sugar Substitutes - Acesulfame Potassium Artificial Sweeteners To Save Calories
Acesulfame potassium is a calorie-free artificial sweetener, also
known as Acesulfame K or Ace K, and marketed under the trade names
Sunett and Sweet One. In the European Union it is also known under
the E number (additive code) E950. It was discovered accidentally
in 1967 at Hoechst AG (now Sanofi-Aventis.)
Chemically, acesulfame potassium is the potassium salt of 6-methyl-1,2,3-
oxathiazine-4(3H)-one 2,2-dioxide. It is white crystalline powder
with molecular formula of C4H4NO4KS and molecular weight of 201.24.
Acesulfame K is 100-200 times sweeter than sucrose (table sugar),
or about half as sweet as aspartame or saccharin. Like saccharin,
it has a slightly bitter aftertaste, especially at high concentrations.
Kraft Foods has patented the use of sodium ferulate to mask acesulfame's
aftertaste. Alternatively, acesulfame K is often blended with aspartame
or other sweeteners. These blends are reputed to give a more sugar-like
taste where each sweetener masks the other's aftertaste, and to
exhibit a synergistic effect wherein the blend is sweeter than its
components.
Unlike aspartame, it is stable under heat, even under moderately
acidic or basic conditions, allowing it to be used in baking, or
in products that require a long shelf life.
Popular products containing acesulfame K include Diet Rite Cola,
Pepsi Max, Coca-Cola Zero, Fresca, Diet Coke with Splenda, Trident
gum, Wrigley's Spearmint gum, some SoBe products and sugarfree Jell-O.
In carbonated drinks it is almost always used in conjunction with
another sweetener, such as aspartame or sucralose.
Safety
Acesulfame K has been approved for use in foods in Europe since
1983, in the United States since 1988, and in Canada since 1994.
In 1985, the European Union's Scientific Committee for Food published
a comprehensive assessment of sweetening agents. This committee
of toxicological experts from the EU member countries accepted Acesulfame
K for use in foods and beverages. Safety of usage of Acesulfame
K has also been examined by JECFA, with the conclusion that Acesulfame
K is safe to use, at least at levels less than the acceptable daily
intake of 15 mg/kg of body weight.
However, the studies that purport to show safety have been challenged
by a number of individuals and organizations, most notably the Center
for Science in the Public Interest in the USA. They claim that the
existing studies are inadequate (despite being peer-reviewed), that
there are flaws in the research protocols, dosing, and time length
of the studies, and that as a result the carcinogenicity of acesulfame
K may not be properly understood. In particular they note that there
have not been long-term human studies, so they doubt the studies
which show that acesulfame is rapidly absorbed and then excreted
unchanged (i.e., not metabolized by the human body) are representative
of the long-term.
The EU's Scientific Committee in its re-evaluation of the product
following concerns from CSPI and others concluded that Acesulfame
K is not harmful, as no reproducible mutagenic effects have been
discovered in years of use, noting [1]:
"The Committee considered that although the carcinogenicity
studies are old they could still be used in the safety evaluation
of acesulfame K. Moreover, the Committee does not agree with the
interpretation of the CSPI that there is an indication of possible
carcinogenicity from these studies. The one aberrant, positive mutagenicity
finding in mouse bone marrow cells could not be replicated and all
other mutagenicity findings were negative. No other new data has
appeared indicating potential harmful effects. Thus there is no
reason to require any additional studies of chronic toxicity/carcinogenicity
or mutagenicity."
Currently, the scientific community's official position is that
acesulfame K is safe to consume, which is the view put forth on
the sweetener industry's public relations website, IFIC. IFIC glosses
over the manufacture of acesulfame potassium, stating it is made
from acetoacetic acid, while ignoring its other reactants, possibly
sulfuric acid and ammonia.
An elevation in insulin levels is known to cause an increase in
cravings for food and consequently, weight gain. Sodium saccharin,
sodium cyclamate, stevioside and acesulfame-K are all known to enhance
insulin release even though they are not carbohydrates.
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