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The safety and regulatory process for low calorie sweeteners in the United States.

Authors :
Roberts A
Source :
Physiology & behavior [Physiol Behav] 2016 Oct 01; Vol. 164 (Pt B), pp. 439-444. Date of Electronic Publication: 2016 Feb 27.
Publication Year :
2016

Abstract

Low calorie sweeteners are some of the most thoroughly tested and evaluated of all food additives. Products including aspartame and saccharin, have undergone several rounds of risk assessment by the United States Food and Drug Administration (FDA) and the European Food Safety Authority (EFSA), in relation to a number of potential safety concerns, including carcinogenicity and more recently, effects on body weight gain, glycemic control and effects on the gut microbiome. The majority of the modern day sweeteners; acesulfame K, advantame, aspartame, neotame and sucralose have been approved in the United States through the food additive process, whereas the most recent sweetener approvals for steviol glycosides and lo han guo have occurred through the Generally Recognized as Safe (GRAS) system, based on scientific procedures. While the regulatory process and review time of these two types of sweetener evaluations by the FDA differ, the same level of scientific evidence is required to support safety, so as to ensure a reasonable certainty of no harm.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-507X
Volume :
164
Issue :
Pt B
Database :
MEDLINE
Journal :
Physiology & behavior
Publication Type :
Academic Journal
Accession number :
26930537
Full Text :
https://doi.org/10.1016/j.physbeh.2016.02.039