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Title: Alternative Sweeteners

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Aspartame-Acesulfame: Twinsweet 497<br />

and/or acesulfame released by the salt when it dissolves. Because the salt is a<br />

fixed, equimolar ratio, this is a simple calculation.<br />

At the time of writing, both the U.S. Food and Drug Administration (FDA)<br />

and the Canadian Health Protection Branch regard the marketing of Twinsweet<br />

as being covered by the existing regulations on aspartame and acesulfame-K.<br />

Products containing the salt are required to declare this in their ingredient list as<br />

‘‘aspartame-acesulfame.’’<br />

In June 2000 the Joint WHO/FAO Expert Committee on Food Additives<br />

(JECFA) concluded that the aspartame and acesulfame moieties in Twinsweet<br />

are covered by the acceptable daily intake (ADI) values established previously<br />

for aspartame and acesulfame-K. In the European Union the Scientific Committee<br />

for Food (SCF) also concluded that the use of Twinsweet raises no additional<br />

safety considerations. As a result the product is expected to be included in the<br />

forthcoming amendment of Directive 94/35/EC on sweeteners for use in foodstuffs.<br />

Regulatory clearance is being sought in numerous other countries. This<br />

is principally a matter of administrative process, necessitated because the wording<br />

of regulations in some countries does not encompass the concept of sweetenersweetener<br />

salts.<br />

IX. CONCLUSION<br />

Aspartame-acesulfame is a sweetener-sweetener salt in which the potassium ion<br />

of acesulfame-K has, in effect, been replaced by aspartame. The result is an<br />

intense sweetener combination that can be produced commercially as a pure<br />

and stable solid that possesses highly advantageous properties. Aspartameacesulfame<br />

has a high relative sweetness, about 350 times as sweet as sucrose<br />

in water and 400 times as sweet in pH 3.2 citrate, because it comprises only<br />

synergistic, intensely sweet molecules and contains no significant amounts of<br />

functionless potassium ions or moisture. It dissolves more rapidly than an equimolar<br />

mechanical mix of aspartame and acesulfame-K, yet releases only the same<br />

sweetening molecules as this familiar and widely accepted blend. Also in contrast<br />

to a mixture of aspartame with acesulfame-K, the salt is remarkably immune to<br />

moisture uptake and this, coupled with its rapid dissolution and excellent powder<br />

flow characteristics, makes it an ideal sweetener for use in powder mixes of all<br />

types. In addition, aspartame-acesulfame is stable in low-moisture products that<br />

can offer a challenging environment to aspartame itself through potential reaction<br />

with aldehyde-rich flavors. Not only is the salt resistant to these reactions in<br />

products such as chewing gum, it is also responsible for a marked extension of<br />

the sweetness release of gum, both effects being achieved without the need to<br />

encapsulate the sweetener. Other low-moisture products such as confectionery,<br />

tabletop sweeteners, sugar substitutes, pharmaceutical powders, and tablets are<br />

also likely to benefit from the special attributes of aspartame-acesulfame. Natu-

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