concept of replacing sucrose in food stuff which are proved to be highly cariogenic TYPES These are of two types:
(A) Non nutritive sweeteners
(B) Nutritive sweeteners
NON NUTRITIVE SWEETNERS These are intense sweeteners, non caloric sweeteners
Much sweeter than sugar
Yield little or no energy,provide no bulk
Used in small quantities in drinks or blended
with sugar substitutes in food & snacks Approved products in market are ASPARTATE SACCHARINE CYCLANATE SUCRALASE ACESULFAME-K
From dental point of view caloric
sweeteners are very useful as they are not fermented to acid by oral bacteria ASPARTATE White, crystalline, odourless, slightly water soluble non carbohydrate powder
About 150 to 200 times sweeter than
sucrose
Used as low calorie sugar substitute in
soft drinks,table sweeteners & other food products SACCHARINE White, crystalline, odourless, slightly water soluble powder produced synthetically 500 times sweeter than sugar in dilute solution Its soluble sodium salt is used as a non caloric sugar substitute Also called as benzosulfimide or gluside Widely used in “diet” soft drinks, dietic foods,mouth washes,medicines & as a sweetener for table use since 1940 DISADVANTAGE
May cause bladder cancer
banned in USA & Canada
CYCLAMATE An organic sweetener
30 times sweeter than sucrose
When ingested,absorbed into
blood streams & excreted almost unchanged in urine However part of it is converted to Cyclohexylamine by microorganism in lower intestinal tract
Banned in USA & Canada as it can cause
cancer
Cyclohexylamine can produce
vasoconstriction & hypertensive effect by affecting sympathetic nervous system NUTRITIVE SWEETENERS Caloric sweetener, carbohydrate sugar substitute
Includes a large number of
monosaccharide & disaccharides, various polyols & starch hydrolysates & hydrogenates
Relative sweetness of these
compounds is only occasionally more than equal to sucrose, in most instances it is lower CLASSIFICATION NUTRITIVE SWEETENERS SUGAR SUGAR ALCOHOL o Glucose Sorbitol o Fructose Mannitol o Lactose Xylitol o Maltose SUGARS Sugars other than sucrose used now a days in a large scale in various food items,reason for this is not dental but rather technological or economical
Lactose used in most of baby foods
Has lower cariogenicity than
sucrose,glucose & fructose Since people can not tolerate its large amount so it has a little practical importance as a sugar substitute
Now palatinose is used as a sugar substitute
It is a disaccharides & “coupling sugar” & a
mixture of various fructose –glucose polymers SUGAR ALCOHOLS Not good substrate for plaque bacteria & therefore produces only a minimal drop in plaque pH
On metabolism it get oxidized to
either to ketose or aldose SORBITOL White, crystalline, water soluble powder
Used as sugar substitute in diabetes
Prepared from glucose by hydrogenation
About half as sweet as sucrose & used alone or with other polyalcohols to provide a sweetener in dairy foods, especially in chewing gums
Following absorption,dietary sorbitol
is oxidised to fructose by “sorbitol dehydrogenase” & further metabolism is like fructose
WHO recommended intake rate of
sorbitol is up to 150mg/kg/day MANNITOL
White ,crystalline,water soluble carbohydrate alcohol XYLITOL Well established that it is non cariogenic & is used in chewing gums
It is one of a sugar sweetner approved for use
in food & other items in many countries
It has specific as well as non specific effects
on oral flora & especially on certain strains of mutans streptococci add to its caries preventive profile PLAQUE 1.non fermentability by plaque organism 2.reduction in plaque quantity 3.selective reduction of mutans streptococci 4.introduction of mutans streptococcus strain with reduced virulence. It has some proposed actions 5.increased conc. Of ammonia in plaque 6.accumulation of xylitol-5PO4 in some plaque streptococci 7.participation in a futile metabolic cycle in some plaque organisms 8.reduced adhesion of plaque flora 9.reduced transmission of mutans streptococci SALIVA 1.changes in quantity & quality of saliva ENAMEL 1.aids remineralisation
Journal of Polymer Science Part A - Polymer Chemistry Volume 38 Issue 23 2000 (Doi 10.1002/1099-0518 (20001201) 38:23-4206::aid-Pola60-3.0.Co 2-E) Michael J. Monteiro Marie Sjöberg Je