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Title: Alternative Sweeteners

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<strong>Alternative</strong> <strong>Sweeteners</strong>:<br />

An Overview<br />

Lyn O’Brien Nabors<br />

Calorie Control Council, Atlanta, Georgia<br />

The use of low-calorie sugar-free products tripled in the final two decades of the<br />

20th century. In the United States alone, more than 150 million people use these<br />

products regularly. Even though hundreds of good-tasting low-calorie, sugar-free<br />

products are now available, most light product consumers say they would like<br />

to have additional low-calorie sugar-free products available. Of particular interest<br />

are baked goods and desserts (1).<br />

A number of events that occurred in the late 1990s are expected to facilitate<br />

providing additional good-tasting, low-calorie, sugar-free products. The approval<br />

of acesulfame potassium for soft drinks and aspartame and sucralose as general<br />

purpose sweeteners in the United States and recognition by regulatory agencies<br />

around the world that polyols have reduced caloric values compared with sucrose<br />

are examples. (A general purpose sweetener may be used in accordance with<br />

good manufacturing practices to sweeten any food when a standard of identity<br />

does not preclude its use.) These events should expand the use of sweeteners<br />

alone and in combination as well.<br />

On the scientific front, after more than 100 years of use, scientists around<br />

the world are publicly acknowledging that saccharin is safe for humans. For example,<br />

in 1997, a special International Agency for Research on Cancer (IARC)<br />

panel determined the bladder tumors in male rats resulting from the ingestion of<br />

high doses of sodium saccharin are not relevant to man. And, in late 1998, IARC<br />

downgraded saccharin from a Category 2B substance, possible carcinogenic to<br />

humans, to Category 3, not classifiable as to its carcinogenicity to humans. Agents<br />

for which the evidence of carcinogenicity is inadequate in humans but sufficient<br />

in experimental animals may be placed in Group 3 when strong evidence exists<br />

that the mechanism of carcinogenicity in experimental animals does not operate<br />

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