Sei sulla pagina 1di 4

7/7/2015

EvaluationofantimicrobialefficacyofAloeveraanditseffectivenessindecontaminatingguttaperchacones

JConservDent.2012JulSep15(3):246248.

PMCID:PMC3410334

doi:10.4103/09720707.97949

EvaluationofantimicrobialefficacyofAloeveraanditseffectivenessin
decontaminatingguttaperchacones
PrakashPAthiban,BikashJyotiBorthakur,SGanesan,andBSwathika
DepartmentofConservativedentistryandEndodontics,MahatmaGandhiPostGraduteInstituteofDentalSciences,(Govt.ofPuducherryInstitution),
Puducherry,India
Addressforcorrespondence:Dr.PrakashPAthiban,DepartmentofConservativedentistryandEndodontics,MahatmaGandhiPostGraduteInstitute
ofDentalSciences,(Govt.ofPuducherryInstitution),IndiraNagar,Gorimedu,Puducherry605006,IndiaEmail:prakash4bds@gmail.com
Received2012Jan26Revised2012Mar10Accepted2012Mar13.
Copyright:JournalofConservativeDentistry
ThisisanopenaccessarticledistributedunderthetermsoftheCreativeCommonsAttributionNoncommercialShareAlike3.0Unported,whichpermits
unrestricteduse,distribution,andreproductioninanymedium,providedtheoriginalworkisproperlycited.

ThisarticlehasbeencitedbyotherarticlesinPMC.

Abstract

Goto:

Aim:

TheaimofthisstudywastoevaluatetheantimicrobialefficacyofAloeveraandtodetermineitseffectivenessin
decontaminatingguttaperchacones.
MaterialsandMethods:

AconcentratedextractofAloeverawasusedtocheckfortheantimicrobialefficacyusingtheagarwelldiffusion
method.PresenceofzonesofdiffusionwasidentifiedagainstthreecommonGPcontaminantsnamely,E.coli,
E.faecalisandStaph.aureus.NewGPCones,freshlytakenoutofthepacketwerethendecontaminatedfor
1minuteusingAloeveragelandthenplacedinthioglycolatebrothtocheckforthepresenceofturbidity.
Results:

Thezonesofinhibitionontheagarplateweremeasuredas24mm,21mmand24mmrespectively.Thebroth
remainedclearevenafter48hoursofincubation.
Conclusion:

WeconcludethatAloeveraisindeedeffectiveasaGPdecontaminantanditholdsapromisingfutureasamedium
forstorageofGPcones.
Keywords:Aloevera,decontamination,guttaperchacones
INTRODUCTION

Goto:

Theprimaryobjectiveofendodontictherapyistomaintainanasepticchainrightfromtheaccessopeningtothe
permanentcoronalrestorationofthetooth.Eliminatingordecreasingthenumberofmicroorganismsisof
considerableimportanceforendodonticsuccess.Guttapercha(GP)isadriedcoagulatedextractofplantsof
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410334/

1/4

7/7/2015

EvaluationofantimicrobialefficacyofAloeveraanditseffectivenessindecontaminatingguttaperchacones

palaquiamoftheblancogenusofsapotaceaefamily,andwasintroducedtodentistryin1847byEdwinTruman.
[1,2]Itstillcontinuestomaintainitspositionasanimportantdentalmaterialandhasemergedastheprimeroot
canalfillingmaterial.TheSSWhiteCompanybeganmarketingGPpointsfordentalusein1887.GPsupplied
commerciallyisnotusuallysterilizedordecontaminatedbeforeobturation.Also,itcannotbesterilizedbymoistor
dryheatasthiscarriesariskofphysicaldeformation.However,chairsidedecontaminationpriortoobturation
cannotbeignored.Manychemicalssuchas,hydrogenperoxide,chlorhexidine,ethylalcohol,polyvinylpyrolidone
iodine,quartenaryammoniumcompoundshavebeentriedforGPdecontamination.Recently,theuseofelectron
beamsterilizationhasalsobeentried.However,noneofthesemethodshavebeenprovenasfullyeffective.The
recommendedmethodfordecontaminationofGPpointsconsistsoftreatingtheconesusinga1%Sodium
hypochloritefor1minute(Milton'ssolution),or0.5%Sodiumhypochloritefor5minutes(Dakin'ssolution).[3]
Here,theriskofSodiumhypochloritecausingcrystaldepositionwithinthecanalswhichcanimpedetheobturation
cannotbeignored.Thepurposeofthisstudywastoevaluatetheeffectivenessofaherbalalternative,Aloeveragel
forrapiddecontaminationofguttaperchacones.
AloebarbadensisMill,isashortsucculentherbresemblingacactus,withgreendaggershapedfleshy,spinyand
marginatedleaves,filledwithaclearviscousgel.Aloeverahaspotentantibacterial,antifungal,andantiviral
properties.[4,5]TheantimicrobialeffectsofAloeverahavebeenattributedtotheplant'snaturalanthraquinones
whichhavedemonstratedinvitroinhibitionofMycobacteriumtuberculosisandBacillussubtilis.Aloejuicehas
beenfoundtobebacteriostaticagainstStaphylococcusaureus,StreptococcuspyogenesandalsoSalmonella
paratyphi.[6,7]InaninvitrodiscdiffusionstudybySuleymanetalStreptococcusfaecalisandCandidaalbicans
wereculturedtocontain108109CFUmL/1levelsoforganism.A100%Aloeverajuiceobtainedfromthecold
pressedleavesoftheplantwereusedandtheresultsobtainedshowedsignificantzonesofinhibitionof20mmand
30mmagainstboththeseorganisms[8].Aloeveraisalsoknowntobevirucidal,especiallyagainstherpesvirus.
MATERIALSANDMETHODS

Goto:

Testorganisms

ReferencestrainsofthreemostcommonGPcontaminants,Eschericiacoli,Enterococcusfaecalisand
StaphylococcusaureuswereobtainedfromtheDepartmentofMicrobiology,JIPMER,Puducherry.
Preparationoftheextract

Theleavesoftheplantwerewashedwithdistilledwater,cutopened,andfreshpulpwascollected.Thegelwas
driedinanovenat80Cfor48hoursandthenpowdered.Anethanolextractwasobtainedbydissolving20grams
ofthepowderin200mlofethanol.ThecontentswerethenfilteredthroughWhatmannfilterpaperno1,andthe
filtratewasevaporatedfordryness.
AntimicrobialactivityofAloevera

TheantibacterialactivityoftheextractwastestedusingAgarwelldiffusiontechnique.Thereferencestrainswere
culturedovernightinthioglycolatebroth,andtheculturewasstreakedonaplateofbloodagar.Threewellsof5
mm5mmmeasureweremadewiththehelpofatemplateonthesurfaceoftheagarplate.About0.1mlofthe
extractwasdeliveredintothewellusingamicropipette.Theothertwowellswerefilledwith5.25%ofsodium
hypochloriteand0.9%normalsalineaspositiveandnegativecontrols,respectively.Theywerethenincubatedat
37Cfor24hours,andcloselymonitoredforthedevelopmentofclearzonesaroundtheextracts.Theantibacterial
activitywasassessedbythediameteroftheinhibitionzone.Aclearzoneofinhibitionwasobtainedagainstallthe
threeorganisms.
GuttaPerchadecontamination

AnewpackofDiaProTplus(DiadentEurope.B.V,Almere,Netherlands)F2SizeProtaperguttaperchapoints
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410334/

2/4

7/7/2015

EvaluationofantimicrobialefficacyofAloeveraanditseffectivenessindecontaminatingguttaperchacones

wereusedfortheprocedure.Thepackwasopenedundersterileconditionsandfourpointsweretakenoutusinga
steriletweezer.Thepointswerethenplacedinsidethefreshlypreparedthioglycolatebroth,andincubatedfor24
hours.Simultaneously,fournewGPconeswereremoved,anddecontaminatedforoneminutein90%Aloevera
gel.Theconeswerethenremovedfromthegel,andcleanedfreeofthegelusingasterilegauze,andthen
incubatedinthioglycolatebrothfor24hours.Boththetubeswerethencloselymonitoredforthedevelopmentof
turbidity.
RESULTS

Goto:

Theantimicrobialefficacywasassessedbythepresenceofzonesofinhibition.Escherichiacoli,Enterococcus
faecalis,Staphylococcusaureusshowed24mm,21mmand24mminhibitionzonesrespectively,whichwas
almostequivalentto5.25%Sodiumhypochloriteusedasthecontrol[Table1].Thedecontaminatingefficacywas
thenassessedbytheoccurrenceofturbidityinthethioglycolatebroth.TheGPconeswhichwerenot
decontaminatedanddirectlyplacedinthebrothdevelopedturbidity.TheconesdecontaminatedwithAloeveraand
thenplacedinthebrothremainedclearevenafter24hours,indicatingtheabsenceofthemicrobialcontaminants.
Table1
Zonesofinhibitioninmillimeters(mm)obtainedagainstthetestorganisms
DISCUSSION

Goto:

TheimportanceofGPdecontaminationtopreventanybacterialcontaminationoftherootcanalduringthe
obturationprocedureisnowwidelyrecognizedinendodonticpractice.Thus,itisimperativetoemployarapid,
reliable,inexpensiveandeffectivedecontaminant.Glutaraldehydehasbeeneffectivelyusedasachemosterilizeror
ahighleveldisinfectant.Aqueoussolutionsof2%glutaraldehydehaveabroadspectrumofactionandthus
effectiveagainstmostofthemicroorganisms,andhasbeenusedeffectivelyfordecontaminatingendodonticfiles
priortosterilizationinaglassbeadsterilizerHowever,BoucherfoundthatBacillussubtilissporesareresistantto
treatmentwithGlutaraldehyde.[911]70%concentratedEthanoliswidelyusedindentistry.However,studies
indicatethatitprovidesanintermediatelevelofdisinfection,andthesurfacerequiringdecontaminationrequiresto
besubmergedatleastfor10minutes.[12]2%Chlorhexidinekillsbacteriabydisruptionofthecellmembranesand
byinducingprecipitationofthecytoplasm.IthashoweverbeenreportedbySequeiraetal.thatitisineffectiveeven
after10minutesofsurfaceexposureandrequiresmuchlongerdurationsofcontact.[1315]
Sodiumhypochloritehasastrongantibacterialandsporicidaleffect,andactsbyamechanisminvolvingthe
liberationofactivechlorine,(apowerfuloxidizingagent)whichinturninactivatesthebacterialenzymes.Sodium
hypochlorite5.25%hasbeenfoundtobeeffectiveindecontaminatingGPcones.However,itisimperativethat
afterdisinfection,theGPconeshouldberinsedinethylalcoholtoremovecrystallizedsodiumhypochloritebefore
obturationasthecrystalsmayimpairthehermeticseal.Aloeverahasbeenusedfromtimeimmemorialforthe
treatmentofamultitudeofailmentsrangingfrompepticulcerstoitsuseincosmetics.Ithasawellestablished
antimicrobialactivityascribedtocompoundsthatarenowspecificallyidentifiedaspcoumaricacid,ascorbicacid,
pyrocatecholandcinnamicacid.[15]AnothermajoradvantageisthatAloeveragelhasbeenfoundtobeeffective
indecontaminatingGPconeswithinoneminute.Tosubstantiatetheseresults,furtherindepthstudiesincorporating
moreisolatesfromclinicalsamplesarerequired.
CONCLUSION

Goto:

Withinthelimitsofthisstudy,itcanbeconcludedthatAloeveragelcanbeusedeffectivelyfordecontaminating
GPconeswithinashortduration,andholdsapromisingfutureasamediumforstorageofGPpoints.
Footnotes
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410334/

Goto:
3/4

7/7/2015

EvaluationofantimicrobialefficacyofAloeveraanditseffectivenessindecontaminatingguttaperchacones

SourceofSupport:Nil
ConflictofInterest:Nonedeclared.

REFERENCES

Goto:

1.CruseWP,BelliziR.Ahistoricreviewofendodontics16891963,PartI.JEndod.19806:4959.[PubMed]
2.JyotiBB.Phytotherapeuticsinconservativedentistryandendodonticsareview.JConservDent.20058:319.
3.CardosoCL,KotakaCR,RedmerskiR,GuilhermettiM,QueirozAF.Rapiddecontaminationofguttapercha
coneswithsodiumhypochlorite.JEndod.200925:498501.[PubMed]
4.RamasubramanianTS,SivakumarVT,ThirumalaiAV.AntimicrobialactivityofAloevera(L.)Burm.f.against
pathogenicmicroorganisms.JBioSciRes.20104:2518.
5.ArunkumarS,MuthuselvamM.AnalysisofphytochemicalconstituentsandantimicrobialactivitiesofAloevera
L.againstclinicalpathogens.WorldJAgricSci.20095(5):5726.
6.AgarryOO,OlaleyeMT,BelloMichaelCO.ComparativeantimicrobialactivitiesofAloeveragelandleaf.Afr
JBiotechnol.20054:14134.
7.ReynoldsT,DweckAC.Aloeveraleafgel:Areviewupdate.JEthnoPharmacol.199968:337.[PubMed]
8.GomesBP,ViannaME,MatsumotoCU,RossiVdeP,ZaiaAA,FerrazCC,etal.Disinfectionofguttapercha
coneswithchlorhexidineandsodiumhypochlorite.OralSurgOralMedOralPatholOralRadiolEndod.
2005100:5127.[PubMed]
9.AttinT,ZirkelC,PelzK.Antibacterialpropertiesofelectronbeamsterilizedguttaperchacones.JEndod.
200127:1724.[PubMed]
10.Subbiah,SubbaRaoCV,BalajiRG.Effectofdisinfectantsandglassbeadsizeonefficacyofglassbead
sterlizer.JConservDent.20058:2331.
11.GnauHL,GoodellGG,ImamuraGM.Rapidchairsidesterilizationofendodonticfilesusing6%Sodium
hypochlorite.JEndod.200935:12534.[PubMed]
12.deSouzaRE,deSouzaEA,SousaNetoMD,PietroRC.Invitroevaluationofdifferentchemicalagentsfor
thedecontaminationofguttaperchacones.PesquiOdontolBras.200317:757.[PubMed]
13.RedmerskiR,BullaJR,MorenoT,GarciaLB,CardosoCL.Disinfectionofguttaperchaconeswith
chlorhexidine.BrazJMicrobiol.200738:64955.
14.SiqueiraJF,Jr,daSilvaCH,CerqueiraM,dasD,LopesHP,deUzedaM.Effectivenessoffourchemical
solutionsineliminatingBacillussubtilissporesonguttaperchacones.EndodDentTraumatol.199814:1246.
[PubMed]
15.LawrenceR,TripathiP,JayakumarE.IsolationPurificationandEvaluationofantibacterialagentsfromAloe
vera.BrazJMicrobiol.200940:90615.[PMCfreearticle][PubMed]
ArticlesfromJournalofConservativeDentistry:JCDareprovidedherecourtesyofMedknowPublications

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410334/

4/4

Potrebbero piacerti anche