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IndianJDairySci69(3),2016
239
REVIEW ARTICLE
Polydextrose as a functional ingredient and its food applications: A review
Veena N, Surendra Nath B and Sumit Arora
Received:16August2015/Accepted:08November2015
VeenaN
1
(),SurendraNathB
2
andSumitArora
3
1
DairyChemistryDepartment,CollegeofDairyScienceandTechnology,
GuruAngadDevVeterinaryandAnimalSciencesUniversity,Ludhiana,
Punjab,India.
2
DairyChemistryDepartment,NationalDairyResearchInstitute,Southern
RegionalStation,Bengaluru,Karnataka,India.
3
DairyChemistryDivision,NationalDairyResearchInstitute,Karnal,
Haryana,India
VeenaN
1
DairyChemistryDepartment,CollegeofDairyScienceandTechnology,
GuruAngadDevVeterinaryandAnimalSciencesUniversity,Ludhiana,
Punjab,India.
Email:veena.ndri@gmail.com;Mobile:+919855886831
Abstract: Polydextrose(PD) is alowcalorie, sugar free, low
glycemiccarbohydratethathasavarietyoffunctionalproperties
includinghighwatersolubility,highglasstransitiontemperature,
prebioticproperties,goodstabilityatelevatedtemperatureand
overabroadrangeof pHandiswidelyrecognizedassoluble
dietaryfibre.PDinducesphysiologicaleffects,suchasincreasing
fecalbulking,softeningstools,decreasingfecalpH,increasing
shortchainfattyacidconcentrationsandreducestheconcentration
ofcarcinogenicsubstancesinthecolon.Italsoaidsbloodglucose
homeostasis and can decrease lowdensity lipoprotein (LDL)
cholesterol and totalcholesterollevels inbloodserum.These
functionalandphysiologicalbenefitshaveledtoconsiderable
interestfromthefoodindustrytousePDinthedevelopmentof
newhealthyproducts.PDiswidelyusedinfoodapplications
such as bake d goods , ice cr eam, bev erages , confe ctione ry,
chocolate, yoghurt, and salad dressings, amongmany others.
ThereisnomaximumestablishedlimitforPD.However,good
manufacturingpractices(GMP)limitthequantitytotheamount
necessarytoaccomplishintendedpurposeinthefood.Thisreview
describestheproductionprocess,chemistry,functionalproperties,
physiologicalfunctions,foodapplications,safetyandtolerance,
andregulatoryandlabelinginformationofPD.
Keywords:Polydextrose,functional properties,physiological
functions,foodapplications,safetyandtolerance
Introduction
Thelevelofhealthawarenessamongtheconsumersworldwide
has in crease d and th e conce pt of f ibre-r ich die t is gai ning
importanceduetoitswellknowndigestivehealthbenefits.In
therecentyears,manylow-caloriefibrefoodshavebecomea
partofthe consumer’sdailydiet.Amongthose,PDhas been
iden tified as a source of solub le dieta ry fibre i n foods a nd
beveragesinmanycountries(Wangetal.2014).
PDiscomprised
of90%solublefibreandanenergyvalueofonly1kcal/g.Itisa
non-digestiblepolysaccharidecomposedofrandomlycross-linked
glucose.Duetoitsgoodprocessingperformanceandpotential
healthbenefits,itiswidelyusedaslow-caloriebulkingagentin
avarietyoffoods andapartialreplacement for fatandsugar
(Černáetal.2003).PDhasbeenapprovedasadirectfoodadditive
(21CFR172.841)bytheUSFoodandDrugAdministrationfor
useasanutrientsupplement,texturizer,stabilizerorthickener,
formulation aid and humectants(Burdock and Flamm,1999).
Previousclinicalandin vitrostudiesrevealedthatPDinduces
physiologicaleffects,suchasincreasingfecalbulking,softening
stools,decreasingfecalpH,reducestransittime,increasingshort
chai n fatt y acid ( SCFA) co ncent ration s and th e amoun t of
beneficialbacteria(e.g.LactobacillusandBifidobacterium)(Jie
etal.2000;Probertetal.2004;Lahtinenetal.2010;Raninenet
al. 2011; Tiihonen et al. 2011).In addition, PDfermentation
reducesthe concentrationofcertain putrefactive/carcinogenic
substances(e.g.indole and p-cresol)inthecolon(Endoetal.
1991).PDalsoaidsbloodglucosehomeostasisbecauseofits
lowglycemicindexcomparedtothereferenceglucose(Foster-
Powelletal.2002)andcandecreaseLDLcholesterolandtotal
cholesterolvaluesinhumanblood(LiuandTsai,1995).Thehigh
toleranceandfunctionalpropertiesofPDallowthedevelopment
of food products with avariety of nutritional improvements
withoutcompromisingtasteandtextureprofile(Tiihonenetal.
2011).Thepresentreviewfocusesonthestructure,functional
properties,physiologicalfunctions,foodapplications,safetyand
toleranceandregulatoryandlabelinginformationofPD.
Productionprocess
PD is prepared by a vacuum m elt process involving
polycondensationofglucoseinthepresenceofsmallamountsof
IndianJDairySci69(3),2016
240
sorbitoland citricacid/phosphoric acid in the ratio 89:10:1,
respectively.Sorbitol actsasaplasticizerandcitric acidasa
catalystinthepolymerization(Rennhard,1973;Radostaetal.
1992).Typically,cornglucose isused.Itisimportantthatthe
molecularsizeofthepolymeriscontrolled(MWabout5,000)
duringthemanufacturingprocessinordertorestricttheformation
oflargemolecularweightmolecules.Thiscontrolpreventsthe
formationofinsolublematerialsandresultsinthehighlywater
solublenatureofPD(Beereboom,1981;Allingham,1982).The
polymerissubjectedtovariousclean-upprocedurestoproduce
severalqualitiesofPD.TheprocesswaspatentedbyRennhard
in1975.Itisavailableintwoforms:PD-A(acidform)andPD-
N(neutralisedform), the latterbeingapracticallyneutralised
productobtained bythe addition ofpotassium hydroxide or
carbonatetoasolutionofPD-A(BurdockandFlamm,1999).It
tastesbitter,astringentandsourandthatiswhyitismodifiedby
refinement (e.g.removal ofcitrate esters, neutralization and
reduc tion) to remove un desirab le charac teristic s. It may be
neutralizedwithanyfood-gradebaseand/ordecolourizedand
deionisedforfurtherpurification.Thebittertastecouldalsobe
remediedbypassingthefinalPD,inaqueoussolution,through
anion-exchangeresinandthision-exchangeprocedureremoves
theboundacid.CommercialPDismorepurifiedformavailable
underbrandnamessuchasSta-Lite
®
byTate&Lyle,Decatur;
Litesse
®
byDani sco, New Cent ury, Kan., no w a division o f
Du Pont N utr iti on and Hea lth; a nd Tr imcal
®
fr omC& H
Ingredients,Farington,UK.
Chemistryofpolydextrose
PDisdescribedinitsFoodsChemicalsCodex(FCC)monograph
(Anonymous,2004)asarandomlybondedcondensationpolymer
of D-g lucose, so rbitol an d citric ac id. Commer cial PD al so
containssmallamountsoffreeglucose,sorbitol,citricacid,and
1,6-anhydro-D-glucose(levoglucosan).PDishighlybranched,
withadegreeofpolymerisationbetween2and110(onaverage
approximately12glucoseunits),andwithanaveragemolecular
weightof~2,000Daltons(Allingham,1982;Murray,1988).
All
possi ble linkag es with the glycosidi c carbon of glucose ar e
present:α-andβ-(1,2),(1,3),(1,4)and(1,6)withthe(1,6)linkage
predominating(Auerbachetal.2007).Arepresentativestructure
ofPDisgiveninFigure1anditsphysico-chemicalproperties
aresummarizedinTable1.
Technicalandfunctionalproperties
PD is an odourless, neutraltaste,white tocream amorphous
powderwithvirtuallynosweetness. Itishighlysolubleinwater
(approximately80%w/wat20
o
C)andsolutionshaveahigher
visco sity than suc rose or sorbi tol s olut ions at e quiv alent
concentrationsandtemperatures.ThischaracteristicenablesPD
toprovidethedesirablemouthfeelandtexturalqualitieswhen
replacing sugarsandfats (Mitchel,1996). PD can beused to
replacebothsucroseandfatinchocolateandtoffeeconfectionery.
Thishasled to thedevelopmentof light, reducedcalorie and
tooth-friendlyproductswhichutilisehydrogenatedPDthatdoes
notcontainresidualcariogenicmonosaccharides.PDalsoexhibits
excellent stability over awide rangeof temperaturesand pH
conditions.ModelsystemcontainingPDhaveindicatedverygood
stabilityagainsthydrolysisoverbroadrangeofpH4.5-6.0and
temperaturemakingitidealforuseinmanybeverageapplications,
even those atlowerpH. No significant hydrolysis would be
expectedatanystoragetemperaturewhenpHishigherthan4.0
(Beeretal.1991).
AnimportantcharacteristicofPDisthatithaswateractivity
closelyresemblingthatofsucroseandcanfunctionashumectants
helpingtoslowdownundesirablechangesinthemoisturecontent
offoods(Mitchel,1996).Thisprolongsshelf-lifeandisespecially
importantforbakedgoods.Inshortcrustpastry,thefatcontent
can be reduced by up to 50% with the additionof PDwhile
maintainingthetexturenormallyassociatedwithtraditionalfull-
fatpastry(Murphy,2001).
PDisafunctionalfoodadditiveduetoitsprebioticproperties
(Kolidaetal.2002;Srisuvoretal.2013).Itcontributesonly25
percentofthecaloriesofsugar(1kcal/gversus4kcal/g)and
only11percentofthecaloriesoffat(9kcal/g).Thelowcalorie
contentof PD isaresult of itspoordigestibilityinthe small
intes tine and i ncomple te ferment ation in the large i ntestine
(Oliveria etal. 2009).The random bonds inthe PD polymer
preventmammaliandigestiveenzymesfromreadilyhydrolysing
the m olecule (Murphy, 20 01). This propert y has led t o the
acceptanceofPDasadietaryfibreinmanycountries(Craiget
al.1999;Floodetal.2004).Thefunctionalityofthisprebioticis
beneficialtohumansandincludessuchaspectsaspromotingthe
growthofhealthybacteriaandstimulatingtheimmunesystem
(Gibson,2004;Srisuvoretal.2013).
Theamount ofwater in a foodsystem greatly influencesPD
functionality andits subsequent effecton the glass transition
tempera ture (T g) of th e compo site fo od. PD p owder i s an
amorphousglasswithananhydrousglasstransitiontemperature
of110°C,whichissignificantlyhigherthanthatofmostother
carb ohydrat es and is partly a functio n of its r elative ly low
molecularweight.ThishighTgofPDcanbehelpfulinraising
thecompositeTgoffoods (Stowell, 2009).Whenusedinice
creamandfrozenproducts,thefreezingpointdepressionfactor
permitsthetextureofthefinishedproducttobebalancedtocreate
a rich, creamy smoothness.Products stored in a freezercan
undergo deleterious changes intexture(e.g.ice- and solute-
crystallization,starchretrogradation),structure(e.g.collapseand
shrinkage),and chemicalcomposition (e.g.oxidation flavor/
colourdegradation).PDmay do thisbyinterruptingsugaror
polyolre-crystallizationand/orstarchretrogradation,byproviding
structureand/orraisingthe compositeTg which isthe glass
transitiontemperatureofamaximallyfreezeconcentratedsolution
(Craigetal.1994).TheTgvalues(whereicecannolongerform)
IndianJDairySci69(3),2016
241
oflactose(-28
o
C),sucrose(-32
o
C),fructose(-42
o
C),glucose(-
43
o
C)andsorbitol(-43.5
o
C)arealllowerthanPD(-24
o
C).This
mean s that rep lacemen t of thes e sugars with PD ra ises the
compositeTgofafood(SladeandLevine,1995).Italsoimproves
storagestabilitybynarrowingthedifferencebetweenthestorage
temperatureandthecompositeglasstransitiontemperatureof
maximallyfrozenconcentratedsolutionsforfrozendesserts.
Intransparentbeverages,PDisamagnificentchoiceofdietary
fibre.Highsolubility,clarityandrheologicalpropertiessimilar
tosucrosemakePDversatileenoughtoaddadesirabletexture
toavarietyofliquids,includingdairydrinksandyogurts,sauces
anddressings,whilereducingcaloriesfromfatorsugar.PDworks
particularly well infoods that requirebulkingagentsorthose
thataretraditionallysweetorrichinfat.Itisabletomaintainthe
textureandmouthfeelthatoftenislostintheprocessofremoving
sugarandfattoreducecalories.Sometimesithelpstomaskoff-
flavorsthatmightbegettingfromvitaminsorminerals(Beristain
et al. 2006). Being a humectant,stabilizer,thickening agent,
sol uble f ibre a nd a pr oven p rebio tic su bstan ce, PD offers
opportunitiesforcreatingnewfoodswithmorediversesensory
characteristics.
Physiologicalfunctions
Digestivehealth:fibreandprebioticaction
PD is h ard ly d ige ste d in the sma ll i nte sti ne a fte r or al
administration,with60%ofthePDexcretedinfecesand30%
fermentedinthelowergutbyintestinalmicroflora(Figdorand
Rennhard,1981).TheslowandincompletefermentationofPD
ensuresminimalproductionofgasincomparisontoothermore
quicklyfermentableoligosaccharides(Hernotetal.2009).PD
produ ces v olat ile f atty aci ds (V FA) c ause d by micr obia l
fermentation in the large intestineandlowersthepHoflarge
intestinalcontents.Theuniquearrangementofglycosidiclinkages
of PD makes it resist ant to hy drolys is by hu man dige stive
enzymes.Thishasbeendeterminedusing[
14
C]labeledPDinrat
andhuman intervention studies(Figdor andRennhard, 1981;
FigdorandBianchine,1983).AfteringestionPDpassesintact
into thecolonwhere it is partiallyfermented by the colonic
microflora.TheslowandconsistentfermentationofPDwasfirst
demonstrated usinganin vitrocolonsimulator (Probertetal.
Figure 1. ChemicalStructureofPD
Molecularweightrange 162-5000(90%)
Appearance White-cream
amorphouspowder
Odour None
Meltingpoint 130
o
C
Solubility(25
o
C) 80%w/w
Viscosity(25
o
C,50%w/w) 33.3centipoise
Heatofsolution 9kcal/g
Wateractivity(20%w/w) 0.992
pHinwater(100g/litre) 2.5-3.5
Titratableacidity 0.14-0.16meq/g
Caloricvalue 1kcal/g
Relativesweetness None
Water Max4%
Sorbitol Max2%
(anhydrousashfreebasis)
Glucose Max4%
Table 1 Thephysico-chemicalpropertiesofgenericPD
IndianJDairySci69(3),2016
242
2004;Mäkivuokkoetal.2005)andsubsequentlyconfirmedina
studyontheeffectof PD on intestinalmicrobesand immune
functionsinpigs(Favaetal.2007).Ithasalsobeenshownin
vitro thatthe microbes that ferment PD prefer branched and
espe ciall y singl e-bran ched PD r esidue s over n on-bra nched
residues,especiallythe(1,6)pyranosemoietiesaresubjectedto
microbialdegradationoverothertypesofglycosidiclinkagesin
themolecule(Lahtinenetal.2010).
InahumaninterventionstudybyEndoetal. (1991) inwhich
eighthealthyvolunteerswerefedadietrichincholesteroland
hadadailyintakeof15gofPDfor6weeks,changesincolonic
florawereaccompaniedbyadecreaseinfecalconcentrationsof
Clostridium spp.Inanotherhumanstudy,significantincreasesin
thenumbersofculturableBifidobacteriaandLactobacillitogether
withdecreasedBacteroidesnumbershavebeendemonstratedin
aplacebo-controlled,randomized,double-blindinterventionstudy
comp rising 1 20 subj ects (Ji e et al. 20 00). Imp roved bo wel
functionwasalsodemonstratedinthesamestudywithdailyintake
of4-12gPDwithnoadverseeffects,suchasabdominaldistention,
crampsordiarrheareported.SupplementationwithPDat5g/
day and a probiotic mixture tog ether was fo und to incre ase
cul turab le fec al Bifidobacteria over s upplemen tatio n with
probioticmixturealonewhencomparedovera2weekperiodin
twentyhumansubjects(Tiihonenetal.2008).Also,shortened
oro-fecaltransittime,implicatingtheroleofPDinalleviating
constipation,hasbeenshown(Hengstetal.2009).Thesefindings
suggestthatdietaryPDisasolubledietaryfibre-likesubstance
andshownprebioticpropertieslikemodificationofthemicrobiota
composition,activityandhealthbenefits.
Digestivehealth:bowelfunctionandfecalcharacteristics
Fivehumaninterventionstudies(TomlinandRead,1988;Endo
etal.1991;Archouretal.1994;Jieetal.2000;Floodetal.2004)
andonestudyinrats(Okuetal.1991)haveallreportedincreased
fecalweightinconjugationwithdietarysupplementationwith
PD.Nakagawaetal.(1990)andTomlinandRead(1988)reported
stoolsoftening,andJieetal(2000)reportedimprovedeaseof
defecationincombinationwithPDsupplementation.Twohuman
studieshavereportedincreasedstoolfrequencyonconsumption
ofPD(Endoetal.1991;Jieetal.2000)whiletwootherstudies
haveshownnoeffect(TomlinandRead,1988;Nakagawaetal.
1990).Aratstudy(Okuetal.1991)showedreducedtransittime
inassociationwithPDconsumptionwhiletwohumanstudies
showednoeffect(TomlinandRead,1988;Archouretal.1994).
DecreasedcolonicpH,associatedwiththeincreasedproduction
ofSCFAs,hasbeenconsistentlyreportedinstudies inhuman
(Endoetal.1991;Jieetal.2000),rats(Peuranenetal.2004;
Yoshiokaetal.1994),andintwoin vitrostudiessimulatinghuman
colonicdigestion(Probertetal.2004;Mäkivuokkoetal.2005).
Hence, the abilit y of PD to fa vorably aff ect gut pH is well
documented.
Serumcholesterolandtriglyceridelevels
PDisafermentablenon-viscousfibre,andhasbeenshownto
exhibitlipidmetabolismregulatingeffects(Raninenetal.2011).
Typicallytheseeffectshavebeenassociatedwithtwophysico-
chemicalpropertiesofsolublefibres:viscosityandfermentability.
PDhasbeenreportedtoconferlipidmodulatingeffectsinhuman
clinicalinterventionstudies,aswellasinanimalstudies.Intwo
ratsfeedingstudiesinwhichPDwereaccompaniedwithalipid
load,reducedlipidlevelswerereported.Inoneofthestudy,rats
weregiventwodifferentdosagesofcornoil,10%and20%,to
representamoderateorhigh-fatdiet,for8weeks,withorwithout
5% PD. Rat s in the PD group showed de creased serum
triglyceridesascomparedtoaguargumcontrolinthehigh-fat
diet, in creased leve ls of serum HDL c holesterol b oth in the
moderatefatandhighfatdiet(Choeetal.1992).Anotherstudy
hasbeendonewithgerbilsfor4-weeks,thegerbilswerefedwith
0.15%cholesterolwith30%oftheenergycomingfromfatand
withinclusionof6%PD.Liverandplasmatotalcholesterolas
wellasfreeandesterifiedcholesterolfromliverdecreasedinthe
PDgroup(PronczukandHayes,2006).Theacuteresponseof
PDonserumlipidvalueshasalsobeenstudiedinrats,buttogether
withlactitol(Shimomuraetal.2005).Theratsshowedreduced
serumtriglyceridelevels,andanincreaseinluminaltriglyceride
levelsinthececumafter150minutesofingestionofPD,which
wouldindicatethatthecombinationofPDandlactitolreduced
eithertheleveloffatabsorptionintheearlierpartofsmallintestine
or pro mote d the transi t tim e of f at th roug h the intest ine
(Shimomuraetal.2005).
In human study withnormal healthy adults withno reported
hypercholesterolemiaareductionintheamountoftotalHDLby
administrationof15gofPDfortwomonthswithconcomitant
decreaseinapolipoproetinA-I,whichisthemaincomponentof
HDLcholesterol,hasbeenobserved(Sakuetal.1991).Inanother
studywithhealthyadults,administrationof10gofPDfor18
dayswasshowntodecreaseLDLcholesterolandtotalcholesterol
valueswithnoeffectonHDLcholesterolortriglycerides(Liu
andTsai,1995).Therearealsocontradictoryresultswithhealthy
humans,asadministrationofPDinanamountfrom4to12gper
dayfor29daysdidnotaffecttriacylglycerol,orcholesterol(Jie
etal.2000).Authorsreportedthatduetorelativelylowfatcontent
(20%ofenergyfromfat)inChinesediet,theydidnotexpectto
measureaneffectofPDonbloodlipids.Inhypocholesterolemic
individuals,theeffectofPDhasbeenstudiedina4-weekstudy
withadministrationof15gand30gPD daily (Pronczukand
Hayes,2006).Inthisstudyitwasnotedthat5ofthe6individuals
ingesting30gofPDwereinaseparaterespondergroup,andin
thirdgrouptheLDLcholesterolvaluesdeclined significantly,
andtherewasatendencyforreducedtotalcholesterol,butno
changeinHDLcholesterol.However,whenall6individualswere
studiedtogether,nochangecomparedtocontrolwasobserved.
Another studyinvestigated the effect of PD on postprandial
triglyceride(TG)responsesinthreeindependenttrialsincluding
IndianJDairySci69(3),2016
243
a nor molipi demic, obese and hyp erlipi demic s ubject s. The
maximumpostprandialTGconcentrationwasmorepronounced
inhyperlipidemicgroupcomparedtonormolipidemic(p<0.001)
orobesegroups(p<0.01).ThemodeledTGresponseanalysis
showed that ir respective of the s tudy po pulation, PD
supplementation was one of the factors significantlyreducing
triglycerideresponsecomparedtotheplacebotreatment(p<0.05)
(Tiihonenetal.2015).
TheeffectofPDonlipidvalueshasbeenofinterestintwostudies
withindividualsshowingabnormalglucosemetabolismortype-
2diabetes.Insubjectswithimpairedglucosemetabolism,PD
administeredfor12weeksat16g/dayhasbeenobservedtolower
LDLcholesterol,increaseHDLcholesterolandcausenochange
intriglycerides(Schwabetal.2006).Inacombinationstudywith
7gPDand3goligofructoseadministereddailyfor6weeksin
adultswithtype-2diabetes,adecreaseintotalcholesterol,TG,
VLD L chol ester ol, an d rati os of t otal c holes terol to HDL
cho leste rol, a nd LDL cholest erol t o HDL c holes terol was
observed,whileHDLcholesterolincreased(Ciceketal.2009).
Inadoubleblindandrandomizedstudy,nineteenhealthyyoung
adultsconsumedtwiceastandardhamburgermealwithorwithout
acoladrinkcontaining PD (12.5g).Postprandialtriglyceride
responsewasmeasuredupto360minafterthemeal.Thearea
underthecurvewas25%inthePDtrialthanontheplacebotrial
(VasankariandAhotupa,2005).Aspostprandialhyperlipidemia
isbelievedtobeanindependentriskfactorfortheatherosclerotic
vasculardiseases,PDmayprovidenewdietaryconcepttoreduce
riskfactor.
Glycemiccontrolandinsulinresponse
TheeffectofPDingestiononglucoseandpostprandialinsulin
responsehasbeeninvestigatedinseveralstudies.PDhasavery
lowglycemicindex(4to7)withglycemicloadof1comparedto
thereferenceglucose(100)(Foster-Powelletal.2002).Based
onarecentEFSAscientificopinion,PDissuitableforthosewho
wanttofollowalowglycemicdietwhenitisusedas asugar
replacer(EFSA,2011).PDhasbeenreportedtoattenuate the
bloodglucoseraisingpotentialofglucose,astheglycemicindex
ofglucosewasreducedfrom100to88when12gofPDwas
ingestedtogetherwithglucosebyhealthyadults(Jieetal.2000).
Similarresultswereobservedinastudywithhealthyadultswhen
14gwasingestedtogetherwith50gofglucoseor106gofbread
(Shimomuraetal.2004).Plasmaglucoselevelsweredecreased
by28%and35%,comparedtoglucoseandbreadwithoutPD,
respectivelywithsignificantlyreducedseruminsulinlevelsin
theglucoseplusPDgroup.TheseobservationsindicatethatPD
couldreducetheabsorptionofglucose.WhentheeffectofPD
wasstudiedwithhumansubjectswithimpairedglucosetolerance
or impairedfasting glucose, no changein plasma glucoseor
insulinhasbeenobserved(Schwabetal.2006).DiurnallyPD
didnotseemtochangeplasmasugarlevels,butadecreasein
insulinaftermealswasnoted(Ozawaetal.1993).Indogs,PD
showedanattenuatedpostprandialglycemicandlowerrelative
insulinresponsesthanthecontrolsugarmaltitol(Knappetal.
2008).
Inoneofstudy investigatedtheeffects of a lactose-freemilk
drink,PD-enrichedmilkdrink(fat-andlactosefree),andregular
fat-free milkon fasting insulinand glucose levels in healthy
sub jects ( Lummel a et al. 200 9). The i nsuli n respo nse wa s
significantlylowerforthefibre-enrichedmilkdrinkthanitwas
fortheothermilkproductsandhowever,nodifferencesinthe
responseforglucose.PDhasbeenalsostudiedintrialsinwhich
thereferencegroupreceivedanormalmeal/snackwithglucose,
andtheinterventiongroupthesamebutwiththeglucose,andthe
interventiongroupthesamebutwiththeglucosepartiallyreplaced
withPD.Involunteerswithtype-2diabetes,cranberrieswith10
gofPDshowedattenuatedplasmaglucoseandinsulinresponse
comparedtocranberrieswithglucose (Wilsonetal.2010).In
onestudywithhealthyadults,significantlylowerpostprandial
glucoselevelswereobservedafteringestionofstrawberryjam
with40%PDthanafteringestionofstrawberryjamsweetened
with sugar, cornsyrup, orapple juice, butthis studydid not
measur e insulin (K urotobi et a l. 2010). Thes e above resul ts
indicatethat PDmight havea roleindecreasingpostprandial
glucoseabsorptionandinsulinresponse.
Anti-carcinogenicactivity
Cecalfermentationmaybeanimportantfactorininhibitingcancer
formation, because the fermentationproduct butyrate isanti-
carcinogenic(Perrinetal.1994).Animalstudyhasshownthat
theingestionofPDhassignificantsuppressiveeffectonformation
ofaberrantcryptfoci(ACF)inducedby1,2-dimethylhydraine
(DMH).TheinhibitoryeffectofdietaryPDwassignificantonly
in th e case tha t the PD w as fed fr om 1 week b efore DM H
indicationwhencomparedwithday0,1and7,indicatingthe
timingofinterventionwiththePD-containingdietiscriticalfor
theinhibitoryeffectonACFdevelopmentandtheeffectwasmost
pronouncedintherectum(Ishizukaetal.2003).Theseresults
suggest that th e inges tion of PD ma y preve nt colo rectal
carcinogenesis.
Balancingimmuneresponsesinthelargeintestineisespecially
importantforreducingtheriskofcoloncancerdevelopment.A
possiblemechanismforreductionincancerdevelopmentinvolves
theregulationofmucosalgeneexpression.Overexpressionof
thecyclooxygenage-2(cox-2)geneisrelatedtoearlystagesof
coloncancerdevelopmentandchronicinflammatorydiseasesin
theintestine.Mäkivuokkoetal.(2005)combinedtwodifferent
in vi tro sy stems, n amely a four-st age sim ulator of colo nic
fermentationandacell-culture-basedmodelofhumanintestinal
epithelialfunction,inordertostudytheeffectsofPDoncolon
cancerdevelopment.Adose-dependentdecreasingeffectoncox-
2expressionwasobservedinCaco-2cells(ahumancoloncancer
cellline).Thisreductionofcox-2expressionassociatedwiththe
IndianJDairySci69(3),2016
244
colonicfermentationofPDfurthersuggestsaprotectiveroleof
PDagainstcoloncancer.Recently,theeffectsofPDfermentation
metabolitesoncoloncancercellsandtheirgeneexpressionwere
investigatedinwhole-genomescaleusingAffymetrixgenechips
(Putaalaet al. 2011). Inthisstudy, itwas observed that PD
fermen tation met abolites i ncreased c aspase-2 an d caspase- 3
activation,whichisahallmarkofapoptosis,increasedthelevel
ofapoptosis aswell as diminished cell proliferation ofcolon
cancercells.ThesestudiescombinedindicatethatPDmightbe
beneficialinpreventingriskfactorsassociatedwithcolorectal
carcinogenesis,whichcouldrelatetoitsabilitytopromoteSCFAs
production(Makelainenetal.2007).
Mineralabsorption
Prebiotics likePD contribute toa reducedpH of the colonic
digestathroughtheirfermentationandtherebytoanenhanced
solubilizationtobothcalciumandmagnesium.Animalstudies
hav e shown tha t PD im proves calci um abs orpti on both in
gastrectomizedratsandnormalrats(Haraetal.2000;Santoset
al.2009),wheretheformerprovideamodelforseverelyhampered
calciumabsorption.Innormalrats,PDincreasedtheamountof
calciumandmagnesiuminbone(Haraetal.2000),withincrease
intotalandfemoralbonemineraldensityandcorticalareaand
thickness(Weaveretal.2010).Ironisnormallyabsorbedinthe
small intestine with thestomachplayingan essential role in
improvingthebiologicalavailabilityofiron.Ingastrectomized
rats,PDhasbeenshowntoimproveapparentironabsorptionto
levelsapproachingthoseofnormalrats.Also,innormalrats,
ironabsorptionwasshowntobeimprovedbyPD(Santosetal.
2010).Thestudydemonstratedtheeffectsofcomponentsfroma
typicalJapanesediet(isoflavones,teacatechinordietaryfibre)
on e quol (i s a metab olite of the i soflav one dia dzein ( Dz))
productionandbonemetabolisminovariectomised(OVX)mice.
Dietaryfibre(PDorraffinose)increasedequolproductionand
inhibitbonelossinOVXmice.Thiseffectwasgreaterthanthat
ofDzaloneforpreventingbonelossinmice.PDthusseemsto
beabletoplayaroleinimprovingmineralstatus.
Foodapplications
ThefunctionalbenefitsofPDhaveledtoconsiderableinterest
fromthefoodindustry,leadingtotheuseofthisingredientinthe
developmentofnewhealthyproducts(Murphy,2001).PDallows
thedevelopmentoffoodproductswithawidevarietyofnutritional
impr ovemen ts such as preb iotic, f ibre fo rtific ation, calori e
red uction , reduc ed gly cemic l oad as w ell as s ugar a nd fat
reduc tion. The t echnolo gical pro perties o f PD facil itate th e
productionofproductswithatasteandtextureprofilesimilarto
thatofstandardproducts.InUnitedStates,PDisapprovedby
FoodandDrugAdministration(FDA)foruseinthefollowing
product categories: Chewing gum, confections andfrostings,
dressingsforsalads,frozendairydessertsandmixes,gelatins,
puddingsandfillings,hardcandy,softcandy,bakedgoodsand
bakingmixes,fruitspread,peanutspreads,toppingsandsweet
sauces.
Bakedgoods
PDiswidelyusedasalow-caloriebulkingagentthatcanreplace
partofthesugarsandsomeofthefatinlow-caloriefoodswhile
maintainingapleasanttextureandmouthfeelofbreads,rolls,
cracke rs, flour tor tillas, pita bread, pizza crust, and muff ins
(Mitchelletal.2001;Chaudharyetal.2013).Itwouldfunction
primarilyasahumectantandwaterbindingingredienttohelp
slowdowntheeffects of undesirablechangesinthe moisture
contentandhenceprolongtheshelflifeoftheseproducts.
Martínez-Cervera et al. (2012) evaluatedthe suitability ofa
mixtureofsucraloseandPDtoreplacedifferentpercentagesof
sucroseinmuffins.Low-sucrosemuffinsinwhichthesucrose
hadbeen totally or partially replaced(25%, 50%, 75%)by a
sucralose:PDmixture(1:1012).Thestructuralcharacteristicsof
themuffinsbattersandofthebakedmuffinswerestudiedthrough
rheomet ry, microsco py, image anal ysis and text ure analysis.
Replacementof25%sucrosebyamixtureofPD-sucralosealtered
noneoftheeatingqualitypropertiesofthereformulatedmufûns.
FurtherreplacementofsucrosebyPD-sucraloseprogressively
affectedthebatterstructure,bothbeforeandduringthebaking
process. Thereplacement of sucrose decreased the viscosity,
viscoelasticiyandspecificgravityoftherawmuffinsbatter.It
furtherresultsinamuffinswithlessheightandfewerfinalair
cellsasthe sucrosewasreplaced, and withlowhardness and
spring iness. For 50 % sucrose rep lacement, th e appearance ,
colour,texture,favourandsweetnessandgeneralacceptability
weresimilartothoseofthecontrol.Significantlylessacceptable
muffinswereobtainedwith75and100%sucrosereplacement.
Inasubsequentstudy,muffinswereproducedwhere30%sucrose
oftheformulationwasreplacedagainstaniso-sweetamountof
Steviolglycosides (or rebaudiosideAfromStevia rebaudiana
Bertonileaves)incombinationwithseveralfibres(peafibre,oat
fibre,wheatfibre,wheatbran,applefibre,cellulose,maltodextrin,
PD and inulin) ( Zahn et al . 2013). Mu ltivari ate analys is of
instrumental and sensorydataindicatesthat acombinationof
inu lin or PD with r ebaudi oside A res ults i n produ cts wi th
characteristicsclosetothatofareference.Theuseofwheatbran
orapplefibreasbulkreplacerforsucrosegivesproductswhich
mainlydeviateincrumbcolourandarecharacterisedbyawhole
meal off-tast e, wher eas incr eased c rumblin ess and reduced
elasticityistheconsequenceofpartialsucrosereplacementby
oat,peaorwheatfibre,celluloseormaltodextrin.Comparedto
thereferencemuffinwith1.3goffibre/100g,thereplacementof
30%sugarbyinulinincreasesfibreinmuffinsto4.6g/100gso
thatitallowstheclaim“sourceoffibre”(EC,2006).Muffins
withPDcanberegardedas“highfibre”(7.1g/100 g) source
(Zahnetal.2013).
IndianJDairySci69(3),2016
245
PDcanbeusedtomakefat-reducedpastry.Inshortcrustpastry,
thefatcontentcanbereducedbyupto50%withtheadditionof
PD whi le maint aining th e textur e normall y associa ted with
traditionalfull-fatpastry.Studieshaveshownthattheadditionof
PDtoshortcrustpastryincreasedthecripsiness;reducedpastry
shrinkage; improved themachinabilityof verythin sheets of
dough; causedbrowning under microwavereheat conditions;
reducedamountofsugarsandfatsinshortcrustpastrywithout
affectingtheorganolepticqualityoftheproduct.UsingPD,the
fatcontentofshortcrustpastrycanbereducedtoaslittleas13to
15% of dou gh weight whil e maintainin g acceptable se nsory
characteristics(Mitchel,1996).
Beveragesanddairydrinks
PDwouldbeusedtoreplacesugarand/orfatintheseproductsas
lowcaloriebulkingagenttoimprovecreaminessandmouthfeel.
PDcanbeusedinvarietyofbeveragesincludingcarbonatedand
non-carbonated,concentratedandready-to-drink,hotandcold
beverages.Itisusedindairydrinks;neutralorflavoured,orlow
pH, pa steurized , or UHT and in many oth er clear be verage
formats.PDimprovethemouthfeel,givingthetasteexperience
ofaproduct of a muchhigherfatcontent;thisisparticularly
noticeableinlow-fatdairydrinkapplications(Anonymous,1991).
PDisalsoaddedtobeveragesasasourceofdietaryfibreasitis
verysoluble,formingclearsolutions,andisverystableovershelf
life.
Chocolateconfectionary
Thedevelopmentofchocolateandcompositechocolateproducts
withreducedcalories,sugarandfibreenrichmentispossiblewith
PD.PDfunctionstoreplacesugarandprovidewarm,creamy
textureinthechocolatematrixwithoutcontributingmouthcooling
effectorscratchyaftertaste(Mitchel,1996).PDcompletesthe
chocol ate flavor thr ough the form ation of smal l amounts of
caramelduringprocessing.Itslowresidualacidityensuresthat
thedelicate cocoaandsweetflavors are broughtforwardand
maintained(Renauldetal.2003).PDmaybeaddedtochocolate
asanediblecarbohydrateandintensesweetener(Afoakwaetal.
2007).Gomesetal.(2007)obtainedadietchocolateusingvarious
bulkingagentsassucrosesubstitutes.Thebulkingagentsinthe
studywerePD(24.14–48.27%),inulin,fructooligosaccharides,
lactitol andmaltitol and sucralose used with a high intensity
sweetener.TheformulationscontainingPD,PDandlactitol,and
PDandmaltitol wereevaluated for a sensoryanalysis due to
theirgoodtechnologicalperformanceandadequatemachinability
of the chocolate mass atdifferent stages of the process. The
sensoryanalysisrevealednosignificantdifferenceinthethree
evaluatedformulationsintermsofaroma,hardness,meltingin
themouthandflavorandtherewasnosignificantdifferencein
the i ntenti on to pur chase t he thre e chocol ate for mulatio ns,
althoughapreferencewasshownfortheformulationcontaining
PD(32.60%)andmaltitol(15.57%).
The productionof alow-sugar milk chocolate with prebiotic
propertiesofinulin was evaluatedbyFarzanmehrandAbbasi
(2009).Variousratiosofinulin,PDandmaltodxetrin(MD)along
withsucralose (0.04%w/w) wereusedinstead ofsucrose. In
general,formulationswithhighratiosofPDandMDweremoister
andsofterthancontrol.Thelowestmoisturecontentandhighest
hardnesswereobservedforthemoderateratios.Inaddition,MD
inducedtheleastdesirablesensorialeffects,whereasPDandinulin
pronouncedlyimprovedtheoverallacceptability.PDhasbeen
reportedasagoodoptionsasbulkingagenttoimprovetheoverall
acceptability of low-sugarmilk chocolates (Farzanmehr and
Abbasi,2009).Thediabeticprototypesofmilk-chocolateswere
preparedbysubstitutingsucrosewithhigh-intensitysweeteners,
sucraloseor stevioside, anda PD/lactitol (60/40) blend asa
bulkingagent(Meloetal.2010).
PDandlactitolareusuallywell
toleratedbutmayalsohavesomedose-relatedundesirableeffects
owi ng to their n atura l osmo tic p otent ial and/ or exc essiv e
fermentation (Marteauand Flourié,2001). Shahetal. (2010)
studiedthedevelopmentofasucrose-freechocolatesweetened
withStevia rebaudianaextractandcontainingPDandinulinasa
bulkingagent.Aidooetal.(2014)examinedoptimumconditions
forthe use of inulinand PD mixturesassucrose replacersin
sug ar-fr ee cho colat e, an d effec ts on rheol ogical, phy sical
propertiesandmicrostructurewasalsostudied.TheCassonplastic
viscos ity increase d with increas ing inulin co ncentration and
reductionin PD, whilstCassonyieldstress was reduced.The
propertiesofchocolateformulatedwith100%PDor100%inulin
werecompared.Chocolateformulatedwith100%PDrevealed
largecrystals withdensesmaller particles and minimalinter-
particlespacescomparedtolargecrystalswithmorevoidspaces
inchocolatesformulatedwith100%inulin.Chocolateformulation
consistingof75.3594%PDand24.6406%inulinwasfoundas
the o ptimum c oncentra tions pr oducing the most accepta ble
rheologicalandphysicalqualitycharacteristics.Inasubsequent
study,Aidooetal.(2015)investigatedtherheologicalproperties,
meltingbehavioursandotherphysicalqualitycharacteristicsof
sugar-freechocolatesprocessedfrominulinandPDmixtures(36
and12,%w/w)(ratioof25:75)asbulkingagentssweetenedwith
stevia(0.24%w/w)andthaumatin(0.06%w/w)extracts.The
sugar-freechocolates(steviaandthaumatin)showedsimilarflow
(rheological)andmeltingpropertiesascomparedtothereference
chocolatecontaining48percentsucrose.Sugar-freechocolates
showedsignificantlyhigherviscositythanthereferencechocolate.
Therewerehowever nosignificant differencesinthemelting
beha viour an d textu re of the sugar-f ree choc olates and the
reference.Chocolatescontainingthesugarsubstitutesrecorded
low er onse t tempe rature s and hi gher p eak wid ths tha n the
referencesample.AuthorsconcludedthatinulinandPDmixtures
cou ld be used for s ugar- free cho cola te manuf acture w ith
satisfactoryphysico-chemicalpropertieswhensweetenedwith
steviaorthaumatinextracts.
IndianJDairySci69(3),2016
246
Pastaandnoodles
Fibreenhancementofnoodleandpastaproductsispossiblewith
PDaswellassomeprocessimprovementbenefitstomechanical
propertiesofthedough.TheadditionofPDtothedoughimproves
thefirmnessthatcanaidformingnoodleorspaghettistrandsor
pastashapes.Thetextureofthecookedproductisnotsignificantly
alteredbyadditionofPDand95%oftheaddedPDremainsin
thepastaornoodlesaftercooking(Matsuda,2006).
Fishandmeatapplications
PDwouldbeusedtoreplacenutritivesweetenersorpolyolsin
surimi(myofibrillarproteinconcentrate)andothercomminuted
fishandmeatproductssuchaschickenfingers,salmonpatties,
etc.Itisaneffectivecryoprotectant,whichunlikesorbitolorcorn
syrupdoesnotaddsweetnesstotheproduct(MacDonaldand
Lanier,1991).Toprotectthemuscleproteinsfromdenaturation
andsoimprovethe technologicalproperties of frozenmuscle
tissuecryoprotectivesubstancesareoftenused.PDcanbeused
inmeatproductssuchaschickennuggetstobindmoistureinthe
meatpatty.Moisturelossisreducedduringcookingaswellas
moisturemigrationtothebatterandbreadcrumbcoating.This
hastheeffectofkeepingthechickennuggetmoistandjuicywhile
thecrispnessofthecoatingisimprovedandstayscrispierfor
longer after cooking (Satsuba andOkuma, 1995).
Park etal.
(1993) foundthatthefunctionalqualityofsaltedpre-rigormince
treatedwithPDascryoprotectantandstoredfor6monthsat-
28°Cwasabout equal tothatofpost-rigor freshmuscle.Itis
possiblethatcryoprotectantscouldhelpmaintainthefunctional
propertiesofpre-rigorsaltedminceduringlong-termchilledor
frozenstorage.SadlerandSwan(1997)investigatedthefunctional
propertiesofmincedbeefthatwassaltedpre-rigorwithorwithout
addedPD, then stored,chilled inavacuum pack oracarbon
dioxidecontrolledatmospherepack,orstored frozen.Adding
PD (2.6%)to salted mince improved batter strain and stress
comparedwiththenon-additiveandsalt-onlysamplesandthus
helpedinmaintainingthemeat’sfunctionality.Tomaniaketal.
(1998)studiedtheeffectsofcryoprotectants(sucrose,D-sorbitol,
malto dextrin a nd PD) on fro zen red me at from sl aughtere d
domesticmammals.TheysuggestedthatPDasthecryoprotectant
ofchoiceinredmeat.Dueitsleastsweetness,tastewasdistinctly
suppressedbymeat,itsdurationofsweetnesswastheshortest
anditstotalflavourimpact(thetotalareaunderthetimeintensity
curve)wasthesmallest.
Insurimi andreformed meatproducts,PDmay beused as a
cryoprotectanttomodifytheglasstransition(Tg)ofthefrozen
matrixandprotectmyofibrillarproteinsfromcolddenaturation
duringfrozen storage(Okada,1992). Kovačevićetal.(2011)
investigatedthecryoprotectiveeffectsofPDonchickensurimi
usingtwodifferentthermalanalysistechniques.Thesamplesof
chickensurimiweremixedwithdifferentmassfractionsofPD
(w=2-10%)plusκ-carrageenan(w=0.5%),PD(w=2-10%)
plus sodium chloride (w= 2%),and PD (w= 2 - 10%). The
additionofPDresultsinstabilizationofmyofibrillarproteins.
Theshiftinthethermaltransitiontemperaturesofmyosinand
actintohighertemperatures,increaseofenthalpiesofmyosin
andactintransition,andshiftofinitialfreezingpointtolower
valuesasthemassfractionofPDincreases,indicatingthatPD
actsinaccordancewithcryoprotectingmechanismandinteracts
with proteinsin chickensurimi. Nopianti et al. (2012) used
different types oflow calorie sweetnesssugar (lactitol,MD,
palati nit, PD and tre halose) as a cr yoprotecta nt on physico -
chemicalpropertiesofthreadfinbream(Nemipterusspp)surimi
duringsixmonthsofstoragewasinvestigated.Theyreportedthat
surimi treate d with a cryoprotect ant exhi bits better
physicochemicalpropertiescomparedwithrawsurimi.PDwas
abletomaintainbetterphysico-chemicalproperties(waterholding
capa city, fold ing test , gel st rength e tc.) th an the ot her low
sweetnesssugarsandsucroseduringsixmonthsoffrozenstorage
an d hence sug gested that, PD as a po tential al ternative
cryoprotectanttoreplaceotherlow-sweetnesssugars(Nopianti
etal.2012).
Frozendairydesserts
PDreplacesthebulk,creaminess,smoothness,andmouthfeelof
sugarandfatand enablingtheformation of high-quality,low
calorieandreduced-fatproducts(Kappas,1998).Ithasgreater
visc osity i n solut ion tha n sucro se or so rbitol at equi valent
concentrationsanditsroleinfreezing-pointdepressionhelpsin
achievingcreamy,palatablefrozendesserts.Adessertcanreadily
beformulatedwithPDtoachievea50%caloriereductionwhen
usedwithahigh intensitysweetener.GoffandJordan(1984)
usedPDandaspartame(0.06to0.1%)assugarsubstitutesina
frozendessertsystem.Smoothnessandacceptability,asevaluated
bysensorymethods,indicatedthatsubstitutionofPDfornomore
than12%ofthe14%totalcarbohydratesinthemixproduced
acceptableproducts.Layereddessertsandyoghurtshavebeen
successfullyformulatedusingPDasalow-caloriebulkingagent
(BarranatesandTamime,1993).SpecterandSetser(1994)studied
theeffectsof milkfatandsucrosesubstitutesonphysicaland
sensory propertiesof a frozendessert systemby sensoryand
instrumentalmethods.Twocomplexcarbohydratefatreplacers,
tapioca dextrinand potato maltodextrin, and aPD-aspartame
sweetening system were evaluated. PD-aspartame effectively
com pensa ted fo r func tiona l prop ertie s that norma lly we re
conferredbysucroseandmilkfat.Replacementofmilkfatwith
tapiocadextrinorpotatomaltodextrinincreasedcoarsenessand
waterinessanddecreasedcreaminessrelativetothecontrol.
Rolandetal.(1999)demonstratedtheeffectsoffatreplacerson
thephysical andsensory properties offat-free icecream. Ice
creams(0.5%milk fat) were formulatedwithmaltodextrin,
mil k prot ein co ncent rate, or PD. Lacto se-re duced , free ze-
concentratedskimmilkwasusedtoprepareaicecreammix.Ice
creamswith10or0.1%fatwerepreparedascontrols.Theaddition
IndianJDairySci69(3),2016
247
offatreplacerstofat-freeicecreamdecreasedtheamountofice
intheproduct.Whencomparedwith0.1%faticecream,these
fatreplacersimprovedtheappearanceandtextureoftheicecream
butdidnotmatchtheattributesimpartedby10%milkfat.The
samplecontainingonlymaltodextrinhadthegreatestcreamflavor
and th e bes t tex tura l cha ract eris tics comp ared to sa mple
containingPDormilkproteinconcentrate.Inasubsequentstudy,
lowcalorieicecreamsampleswere producedbymixingmilk
powder(2,4,6or8%)witheithermaltodextrin(10%),PD(10%)
oramixturecontainingequalratiosofmaltodextrin-PD(5%+
5%)onweight basisandartificial sweeteners(aspartame and
asesulfame-K) wereadded tomixes withreduced fatcontent
(Güzeler etal. 2011). Maltodextrin added icecream samples
meltedlateordidnevermelt.However,meltingofsampleswith
PDtakesplaceearlier.Therefore,PDhasapositiveeffectonthe
physicalpropertiesoficecreamthanmaltodextrin.Butsample
containingPDreceivedlowersensoryscoresthanothers.Authors
demonstratedthattheuseofequalmixtureofPDandmaltodextrin
hadpositiveimpactbothonthephysicalandsensoryproperties
oficecreams.
Cultureddairyproducts
Yoghurtisahealthyfoodduetothebeneficialaspectsofitshigh
proteinandcalciumcontents(McKinley,2005).PDcanbeused
asfatandsugarsubstitutesinlow-fatdairyproductsowingto
theiradvantageousfunctionality.Numerousresearchershavetried
toimprovetexturalandfunctionalpropertiesoflow-fatyoghurt
byusingthisfatreplacer.Whenusedasfatreplacer,theygive
fat-likemouthfeelandtexture(Hellandetal.2004).Allgeyeret
al. (2 010) demo nstrated the effect of adding prebioti cs and
prob iotics i nto yogh urt drin k (stirre d yoghu rt) syste m. The
prebioticsinulin,solublecornfibre,andPDwereshowntoalter
thesensorypropertiesoftheyoghurtdrinkwhenincorporatedat
differentlevels.Whenprobiotics(Bifidobacterium lactis Bb-12
and La ctobacillus acidophilus LA-5 ) wer e inc orpo rated,
add itiona l senso ry cha nges we re iden tifie d. Tota l varia nce
explainedbytheprincipalcomponentanalysisbiplotoffactors1
and2was65%,whichshowedyoghurtdrinkswithsolublecorn
fibreandinulinvaryingbythesweetversussourattributesand
yoghurtdrinkswithPDvaryingbythemouthfeelattributes.Based
ontheresultsofthisstudy,onlythePDtreatmentwouldbean
acceptablevehicletodelivertheprobiotichealtheffectsatthe
endofthe30daysstorageperiod.Srisuvoretal.(2013)studied
theeffectsoftwoprebiotics(inulinandPDasfatreplacer,each
at1,2or3g/100mLofreconstitutedmilk)onphysico-chemical
andsensorypropertiesoflow-fatsetyoghurt.Theadditionof
eachprebioticcouldimprovephysicalandsensorypropertiesof
theyoghurtand2gofPD/100mLwasthemostsuitablelevel.
Further,theprobiotic-cultured(withLactobacillus paracasei
Lpc-37)bananapuréewaspreparedandusedasfruitbaseofthe
prod uct a nd some physi coch emical and microb iolo gical
characteristicsweremonitoredduring21daysofstorage.The
numberoftheprobioticswasstillhighlyacceptableat8.86log
CFU/gduringthe entire storageperiod;however,itsphysical
propertiesgraduallydeterioratedafter14days.Authorsconcluded
that theuse ofbananapurée as a source ofnutrientsfor the
probioticandthePDasafatsubstituteinthesetyoghurtwas
beneficialbothfortheconsumersandthemanufacturers.
Cakes
Therearesomestudiesreportedthereplacementofsucrosein
spongecakesbyPD,withorwithoutnonnutritivesweeteners.
Thetextureofyellowlayercakeswasoptimized by Frye and
Setser(1991)usingsixbulkingagents:sorbitol,hydrogenated
sta rch hy drolysate mixture, la ctito l, iso malt, 18-de xtros e-
equivalent maltodextrinand PD incombinations tototally or
partially replace sucrose. Sorb itol at 100% level result ed in
moderatemouthdryingcomparedtoPDwhichcausedlongand
severemouthdrying,whilealessprolongeddryingoccurredfrom
themixtureofthePDwithmaltodextrin,sorbitolorisomalt. Attia
etal.(1993)studiedtheeffectofreplacingsucrosewithfructose,
acesulfame-Koraspartame,withorwithouttheadditionofPD,
onthephysicalpropertiesofcakes.Theresultsindicatedthat
addingPDcausedanimprovementintexturalpropertieswhich
ledtospongecakeswithsimilaracceptabilitytothatofsugar
cake with a40% reduction incalories. Pateras et al. (1994)
demonstratedtheeffectofsucrosereplacementbyPDonfoam
characteristicsofcakebatters.PDcausedanincreaseinthemean
sizeofairbubbles,andintroducedalargervariationinbubble
sizedistributioninthecakebatter.Hicsasmazetal.(2003)studied
theeffectofPDsubstitutiononahigh-ratiocakesystem.Authors
foundthesameincreaseinthemeanbubblesizeandshowedthat
PDwascapableofimitatingthesucrosecakebatterintermsof
bubblesize distribution.Also,theyfoundthatincrease inPD
resultedinasignificantdecreaseincakeheightandasensible
changeinthelightnessandinthecrumbcolourhue.Rondaetal.
(2005)evaluatedtheeffectonspongecakevolume,colourand
texturepropertiesoftotalreplacementofsucrosebysevenbulking
agents. Several polyols - maltitol, mannitol, xylitol, sorbitol,
isomaltoseandtwooligosaccharides-PDandoligofructosewere
testedasbulkingagents.Bestresultswereobtainedwithxylitol
andmaltitol,leadingtospongecakesmoresimilartothecontrol
onemanufacturedwithsucroseandwiththehighestacceptance
levelinsensoryevaluations.Panelistsassignedthelowestscore
in overall acceptabi lity t o mannitol cakes, f ollowed by
oligofructoseandPDones.Thepoorsensoryscoresgiventothe
oligofructoseand PDcakes were mainlyrelatedto taste and
aftertaste.SitiFaridahandNoorAziah(2012)preparedreduced
caloriechocolatecakewithjackfruitseedflourandPD.Optimized
productwasobtainedbypartiallyreplacingsucrosewithPDat
11%andresultedin34%caloriereductionascomparedtothe
controlcake.
Safety
IndianJDairySci69(3),2016
248
ThesafetyofPDinthehumandiethasbeencomprehensively
demonstrated(BurdockandFlamm,1993).BoththeJointFAO
andWHOexpertcommitteeonfoodadditives(JECFA)andthe
EuropeanCommision,ScientificCommitteeonFood(EU/SCF)
haveassignedanacceptabledailyintake(ADI)“notspecified”,
meaningthatneitheragencyfounditnecessarytostipulatean
upperlevelofsafeintakebecauseexcessiveconsumptionisa
matteroftoleranceratherthansafety(JECFA,1987;EC/SCF,
1990).Therefore,PDispermittedforuseinanyfoodatanylevel
withoutrestrictionotherthanGMPinmostmarkets.WhilePDis
notconsideredtoxicathighdosages,laxationeffectshavebeen
observedwhenintakesareelevated,similartoothernondigestible
carbohydrates.Childrenareconsiderednomoresensitivethan
adultstoPDwhengivenatthesamelevelonaperbodyweight
basis (Flood et al. 2004) .As r eported i n a compend ium by
BurdockandFlamm(1999),anextensivearrayoftoxicological
studies,conductedinavarietyofanimalmodels(i.e.mice,rats,
rabbits,dogs)forextensiveperiodsoftime(3–24months),have
fully supporte d the safe ty of two fo rms of PD ( acidic an d
neutralizedforms)asfoodingredients.
Tolerance
Floodetal.(2004)havereviewednineclinicalstudiesinadults
andchildrenwereconductedwithPDtoevaluatetheextentof
gastrointestinalsymptoms.ThesestudiesdemonstratedthatPD
isnotlikelytoinducediarrheainadultsatdoseslessthan50g
perday(apracticalno-effectdose),andmostindividualsmay
onlyexperiencediarrheafrommuchhigherdoses.Thesestudies
showedthatPDisbettertoleratedthanmostotherlow-digestible
carbo hydr ates . The fac t tha t les s gas is pr oduc ed du ring
fermentationislikelyacontributingfactor(Hernotetal.2009;
VesterBoleretal.2009).ThediarrheainducedbyPDisisolated
andtransient.Clinicalchemistryandmetabolicbalancestudies
haveshownnotreatmentrelatedeffectfromingestionofhigh
dosesofPD(Floodetal.2004).PDiswelltolerated,andamean
laxativethresholdof90g/day(1.3g/kgbw)or50gasasingle
dosehasbeengiven(JECFA,1987).TheSCFrapporteurpointed
out,however,thatsuchestimatesareonlyprovidedasaguide
andshouldnotbeusedtoestablishmaximumlevelsofuse(Van
Esch,1987).
Regulatoryandlabelingguidelines
The use of PD in foods has receive d approval i n numerous
countries.Itisapprovedforuseinfoodsin57countries,56of
whompermituseof1kcal/genergyvalueforlabeling(Auerbach
etal.2006).PDhasbeenapprovedasafoodadditiveintheUS
since1982(FoodandDrugAdministration21CFR172.841).In
the EU, PD is appro ved under the Miscel laneous Addit ives
Directive -Annex I, permitting the useof PD in virtually all
foodstuffsfollowingthequantum satisprincipleandislistedas
E1200.InJapan,theMinistryofHealthandWelfare(MOHW)
recognizesPDasafood(Mitchell,2001;Stowell,2009).InIndia,
according to the Food Safety and Standards(FoodProducts
StandardsandFoodAdditives)Regulations(2011),PD(INSNo.
120 0) ma y be us ed as bulki ng ag ent, s tabi lizer, thic kner,
humectantandtexturizerinicecream,frozendesserts, cakes,
biscuits,yoghurt,whiptopping,sugarboiledconfectionary,jam,
fruitjellyandtraditionalIndiansweets(carbohydratebasedand
milkbased)asperGMPlevels(FSSA,2006).
FoodscontainingPDdesignedforspecialdietaryuse,suchas
reducedorlowcaloriefoods,mustbelabeledinaccordancewith
21CFRPart105.Theingredientstatementoffoodscontaining
PD(eitherthepowderorthe70%solutionpartiallyneutralized
withpotassiumhydroxide)shouldincludetheofficialrecognized
nameoftheingredientPD.Foodscontaininginexcessofthe50
mgspotassiumperservingmustalsodeclarepotassiumhydroxide
intheingredientstatement.Aclarifyingstatementmustalsofollow
suchas“forneutralization”or“toadjustpH”.FDArecognizes
thatPDcontainsonlyonecaloriepergramanddoesnotobject
totheuseofthisvalueforpurposeofdeterminingthecaloric
contentoffoodsformulated with PD(Smiles, 1982).
TheUS,
however,allowsPDuseasafoodadditiveinspecificfoodsonly,
andrequiresthat‘Thelabelandlabelingoffood,asingleserving
ofwhichwouldbeexpectedtoexceed15goftheadditive’shall
bear th e statement : ‘Sensiti ve individu als may expe rience a
laxativeeffectfromexcessiveconsumptionofthisproduct’(Flood
et al. 2 004). According t o FSSAI regula tions in Ind ia, food
containingmorethan10%PDshallbearthelabelonpackage
“PDmayhavelaxativeeffects”.
Conclusions
PD is added tofoods for itsphysiological andtechnological
reasons.Itshighstabilityinheatandacidicenvironments,low
viscosity,high solubility in water,and bulkingand texturing
propertiesandblandtastelendsitselftoawidevarietyoffood
and be verage form ulations. PD can impro ve mineral s tatus,
attenuatepostprandialbloodtriglycerides,maintainsbloodsugar
levels,regulates bowel function,softenedthefeces, improves
the ease of defe cation and hel ps in prevention of colon
carcinogenesis.InthisregardPDallowsthedevelopmentoffood
productswithawidevarietyofnutritionalimprovementssuchas
prebiotic,fibrefortification,caloriereduction,reducedglycemic
loadaswellassugarandfatreduction.Hence,PDisaversatile
foodingredientthatcanbeusedtoimprovethenutritionalprofile
ofawiderangeofprocessedfoods.
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