CaOH Pallavi

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    Cherapunji, Meghalaya.

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    CALCIUM HYDROXIDE

    Presented by:Dr. Pallavi B. Gopeshetti,CODS, Dvg.

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    JOURNEY!!

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    CaCo3 (900-1200c) CaO

    CaO+H2O Ca(OH)2

    Synonyms: calcium hydrate, caustic lime, hydrated lime,lime, limehydrate, slaked lime

    Other uses

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    Amorphous matrix with crystalline fillers

    H H

    O O

    Ca

    Available as 2 paste form1 paste form

    powder liquid form

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    2 paste form

    Base paste:

    *Glycol salicylate-40%, reacts with Ca(OH)2 & ZnO* Tribasic calcium phosphate

    * Calcium tungstate (barium sulphate)- radio opacity*Zinc oxide

    Catalyst paste:

    *Calcium hydroxide-50-60%- Principal reactive ingredient* Zinc oxide

    *Zinc sterate-0.5%- accelerator

    * Ethylene toulene sulfonamide-39.5%, oily compound, acts as carrier

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    2 paste: equal parts of base & catalyst

    Powder form Ca(OH)2 in endodontics messing gun, vertical compaction, injectable formulations,

    lentilospirals, hand file, paper points, Pastinject (specifically designed paste carrier), theMacSpadden compactor, combinations.

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    Mixing equal parts

    Starts acid base reaction

    Results in weakly bonded composite structure

    Chelates of Ca alkyl salicylate & water(the reaction byproduct) forms thecontinuous phase

    & the unreacted ingredient forms the interrupted phase

    Mass is hydrolytically unstable & contains a large % of unreacted Ca(OH)2

    Ca ions & OH ions & salicylate ions are released continuously from the mass

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    Ca(OH)2

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    High alkaline pH

    Modified forms: resins

    Extreme cytotoxicity Buffering actions

    Initial response: necrosis todepth of 1/> mm, coagulatesany hemorragic exudate

    In weeks to months, necroticzone undergoes

    dystrophic calcification whichappears to be stimulus

    for dentine bridge formation

    Neutrophilsinfiltrate into sub necrosis zone

    After 5-8 weeks,only slight inflammation remains

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    Biocompatibility with other restorative materials:

    Setting reactionn properties

    Amalgam &direct restorative mats

    Zinc oxide eugenol

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    chairside prep

    proprietary brands are available

    MAISTO 1975 classified Ca(OH)2 as an alkaline paste

    HOLLAND 1994 classified Ca(OH)2 according to vehicles used

    MAISTO, GOLDBERG, LEONARDO et al told their characteristics.

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    Easiest method: mix Ca(OH)2 wit waterdrawbacks?: no good physiochemical prop.

    Hence, LEONARDO recommended addition of othersubstances

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    CLINICAL IMPORTANCE OF THE VEHICLES

    Velocity of ionic dissociation

    Solubility & resorption rates

    According toFAVA, ideal vehicle shoulda) Allow a gradual & slow Ca+ & OH- ionic release

    b) Allow slow diffusion in the tissues with low solubility in the tissuefluids

    c) Have no adverse effect on the induction of hard tissue deposition

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    Fava, Holland, Lopes et al

    Aqueous (water)

    Viscous Oily (non-water soluble)

    Importance:a) Aqueous: rapid ionic dissociation, high solubility

    appli.disadvantage?

    b) Viscous: slow dissociation of ions over extended periods (due to its mol.wt)

    remains in RCs for 2-4 months

    appli. periodical redressing of RCs

    c) Oily: lowest solubility & diffusion

    TYPES OF VEHICLES & ITS IMPORTANCE

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    AT CHAIRSIDE:

    Water:

    Saline : 9gm NaCl+1000ml water

    Anaesthetic solution :easily available, sterile & easy to handle

    interesting point

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    Ringers solution: NaCl-8.6gmKCl-0.3%

    CaCl-0.33gm

    water-1000ml

    Methylcellulose & Carboxymethlycellulose: 5%-3%2 pastes: Ist: monomer of methlycellulose

    a chemical initiator

    Ca(OH)2particles

    IInd: catalyst

    Ca(OH)2particles

    Methylcellulose monomers polymerize into a porous mesh work matrix & carriesCa(OH)2to P-D organ without involving it in chemical reaction

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    Anionic detergent solutions:reduces surface tension& facilitate substance penetration of Ca(OH)2

    deeper into the tissues

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    AT CHAIRSIDE

    various pharmaceutical preps.

    Adv: a) strong antibacterial action against common microrganisms in RCs

    b) hygroscopic: sustained release of Ca(OH)2

    c) consistency: improved handling properties

    Glycerin:Viscous,colorless,

    characteristicodour, sweetish in

    taste, mol wt.

    92.02, hygroscopic(intracanallubricant)

    Polyethyleneglycol:slightly

    hygroscopic

    Propyleneglycol:itschemically dihydricalcohol with syrupy

    consistency,hygroscopic, nontoxic, mol wt. 76.09

    used in

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    At chairside

    Olive oil: non soluble in water, chemically esters of fatty acids of oleic,linoleic, palmitoleic, estearic & linolenic acids

    promotes low solubility of Ca(OH)2but has improved handling properties

    Fatty acids:New B: P= Ca(OH)2powder 100%L= olive oil 100%

    New B2: P= Ca(OH)265%

    bismuth carbonate 15%

    resin & ZnO 20%

    L= fatty acids 85% & glycol 15%

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    Camphorated parachorophenol: Walkhoff 1891, 33-37% parachorophenol ,63-67% camphor

    disinfection action of parachlorophenol is due to liberation of chlorine in the

    presence of phenol camphor is essential oil wit low solubility in water, hence oily vehicle

    Metacrylacetate: acetic ester metacresol in combination wit benzene Oily liquid wit antibacterial, analgesic & sedative properties

    Less cytotoxic than CMCP

    When mixed with Ca(OH)2= CA cresilate & acetic acid

    Acetic acid suffers an ionic dissociation & gives off H+ which decreases PH

    Eugenol:oil of cloves

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    PROPRIETARY BRANDS

    AQUEOUS:

    Calxyl (oldest by Hermann 1920) Pulpdent & tempcanal

    Cavital

    Reogan

    Calasept

    Calnex

    Hypocal etc

    VISCOUS:

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    VISCOUS:

    Calen

    Calen + camphorated parachlorophenol(0.15ml):Controversies: whyuse cytotoxic CMCP??

    Biocompatib

    le

    Lowliberation of

    P-chlorophenol,not enough

    forcytotoxicity

    P-chlorophenol isreleased, PH ishigh, so protein

    denaturation oftissues, hencephysical barrier

    to deeperpenetration of P-

    chlorophenol

    Extendedantibacte

    rialspectrum

    CMCP+Ca(OH)2

    Ca-P-cholrophenol

    ate, a weaksalt

    Water + salt,takes up H+ &goes back in toP-chlorophenol.gives off OH-

    from water sohigh PH

    maintained

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    OILY VEHICLES

    Endoapex

    L & C Vitapex

    OTHERS

    Flohr (1936)- dentinal chips

    Methylcresilate Collagen gel

    Multical = Ca(OH)2(34%)+barium sulphate 15%+ chloro-timonal(51%)

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    CALCIUM HYDROXIDE & OTHER SUBSTANCES

    RADIOGRAPHIC CONTRAST MEDIA: Why needed?

    Atomic wt.> than Ca Ex.: barium sulphate, bismuth, compounds containing iodine & bromide

    Bismuth salts

    Some degree of toxicity

    Soluble Barium salts

    Extremely toxic material

    Hence, iodine compounds, 3 types

    Soluble iodine organic sub.

    Non soluble organic substance

    Slowly absorbable iodine oils

    Diatrizoate& iothalamate paste

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    Metinyol (prednisolone- sulphacetamide with neomycin) with Ca(OH)2

    Otosporin (polymixin B sulphate + neomycin) with Ca(OH)2

    Ledermix (triamcinolone acetonide & demethylchlorotetracycline Ca)with Ca(OH)2 is very popular

    Metronidazole + CHX + Ca(OH)2

    Metranidazole + ciproflox + polyethyleneglycol 1000 + Ca(OH)2

    CHX is added as vehicle(surfactant)

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    SETTING & NON SETTING CALCIUM HYDROXIDE

    *Dycal (original formula)

    *Reocap

    *Procal

    *Dycal (new formula)

    *Life

    *Renew

    *Reolit

    *MPC*Hydrex

    *Cal-Mer vii

    STRONGEFFECTS

    MEDIUMEFFECTS

    NOEFFECTS

    MATERIAL VEHICLE

    Analar Ca(OH)2 Water

    Pulpdent Methycellulose

    Hypo-Cal Methycellulose

    Reogan Methycellulose

    Setting

    Non-Setting

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    Antimicrobial, tissue dissolving ability, inhibition of tooth resorption, induction of

    hard tissue formation

    Mechanism of antibacterial activity:Related to its release of OH- ions

    OH ions are highly oxidant free radicals

    Shows high reactivity by reacting with biomolecules

    Reactivity is high & indiscriminate hence rarely diffuse away from the siteof application

    a) Damage to bact cytoplasmic membrane:

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    a) Damage to bact. cytoplasmic membrane:

    OH ionsThis removes Peroxide themselves

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    OH ionsinduce lipidperoxidation

    Destruction ofphospholipids,

    structuralcomponents of the

    cellular mem

    OH removes Hatoms from

    unsaturated FAgenerating a free

    lipid radical

    Free lipidic

    radical reactswit O2

    Forms lipidicperoxideradical

    another H+ from2ndFA, generating

    another lipidicperoxide

    act as free radicals,initiating an

    autocatalytic chainreaction

    Further lossof unsaturated

    FA

    Extensive

    mem.damage

    b) Protein denaturation:

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    b) Protein denaturation:

    Loss of

    biologicalactivity of the

    enzyme &disruption of

    cellularmetabolism

    Enzymes haveoptimum activity& stability in anarrow range

    aroundneutrality

    Alkalinizationdue to Ca(OH)2

    Cellularmetabolism is

    highlydependent on

    enzymaticactivity

    Enzymes maintainsits covalent

    structure but thepolypeptide chainis randomlyunraveled

    Inducesbreakdown ofionic bonds that

    maintain thetertiary

    structure of

    proteins

    c) Damage to the DNA

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    c) Damage to the DNA

    OH reacts with bact. DNA

    Induces splitting of the strand

    Genes are lost

    DNA replication is inhibited

    Cellular activity is disarranged

    ROOT CANAL DISINFECTION

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    ROOT CANAL DISINFECTION When in direct contact

    Buffering systems

    Bact. in dentinal tubules

    PH values of Ca(OH)2 decreases in more distinct areas

    12.28-11

    7.4-9.6

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    INEFFICACY OF Ca(OH)2 AGAINST BACT. PRESENT IN DT MAY BE DUE TO

    a) Buffering ability of dentine: protons donors

    b) Arrangement of bact. in the DT

    c) Anatomical variations

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    PHYSICAL BARRIER

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    PHYSICAL BARRIER

    Physiochemical barrier, precludes the proliferation of residual micro

    organisms

    Ist: as it possess antibact prop. acts as chemical barrier

    IInd: physical barrier against bact penetration, withholds substrate orgrowing & by limiting space for its growth

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    BIOCHEMICAL ACTIONS: THERORIES OF MINEALISATION

    EPITACTIC THEORY:Initiators: Chondratin sulphate

    Vit D dependent proteins

    Phosphoproteins

    Phospholipids

    Inhibitor: Pyrophosphate ions.

    Pyrophosphates- Alkaline Phosphates group

    CALCIUM HYDROXIDE INDUCED MINERALISATION

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    CALCIUM HYDROXIDE INDUCED MINERALISATION

    Ca ions + alkaline pH

    'Ca solely from dental pulp,

    Ca acts as initiator ratherthan a substrate for repair

    Local buffering action to inflammatory

    byproducts, alkaline pHneutralizes lactic acid secreted by osteoclasts

    CaOH exerts mitogenic & osteogenic effectsenzymatic pathwaymineralization

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    THE DENTINE BRIDGE

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    THE DENTINE BRIDGE

    High pH materials

    Low pH materials

    PERIAPICAL RESPONSE

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    PERIAPICAL RESPONSE

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    LINERS:

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    BASES

    PULP PROTECTION

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    PULP PROTECTION

    INDIRECT PULP CAPPING

    DIRECT PULP CAPPING

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    Tissue with extensiveinflammatory response

    Basophilic layer

    Necrotic layer

    AFTER PROCEDURE

    Layer

    ofcalcium carbonategranules

    Osteo-odontoblast

    1-2 WEEKS LATER

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    4-5 WEEKS LATER

    Osteodentin

    Odontoblasts

    Dentinebridge

    A FEW MONTHS LATER

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    PULPOTOMY

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    APEXOGENESIS

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    Tooth with immatureroot with vital pulp

    After amputation of

    vital pulp(pulpotomy)

    Apexogenesis

    Dentine bridge

    Ca(OH)2

    Dressing material

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    APEXIFICATION

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    HORIZONTAL ROOT FRACTURES

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    APICAL PLUG

    INTRACANAL MEDICAMENT(ROUTINE & LONG TERM)

    INFECTED ROOT CANALS/PERIAPICAL LESIONS

    WEEPING CANALS

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    ROOT RESORPTIONS (idiopathic/replantation/ transplantation)

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    TREATMENT OF PERFORATIONS

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    ROOT CANAL SEALER

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    DENTINE DESENSITIZOR

    MICROLEAKAGE DETECTOR(Leinfelder et al, 1986)

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    Is it acomplete Resorption

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    Othercapping

    agents??

    completeroot canalmedicamen

    t??

    Resorptionor

    stimulation??

    Is it a truesealer??

    Its physicalproperties??

    Dentinalbridge??

    Is itperfect??

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    Am J of Dent 2002; 15(4) & Am J of Dent 2006; 19(3)

    OOOE 2003

    IEJ 2006

    (systematic review)

    *Leakage freerestorations,

    *Less defectsin bridge

    Composite

    resin

    Ca(OH)2

    More dentinebridging,

    Aged restorationsare not leakageproof,

    biocompatibility

    Composite

    resin

    Ca(OH)2

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    Am J of Dent 2006; 19(3)

    Composite resin > GIC > Ca(OH)2

    *Leakage freerestorations,

    *Less defectsin bridge

    GIC

    Ca(OH)2

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    JOE 1998; 24(4)

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    Othercapping

    agents??

    Will MTArule overCaOH??

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    With MTA

    With Ca(OH)

    Pediatric dent 2006; 28, 399-404

    Ca(OH)2 MTA

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    Solubility Solubility

    Sealing Sealing

    Microleakage Microleakage

    pH pH

    Biocompatibility Biocompatibility

    Compressive strength-7.6,3.8MPa

    Compressivestrength-70MPa

    Dentinal bridge Dentinal bridge

    Contact with blood & moisture Contact with blood & moistureSetting time Setting time

    Appointment Appointment

    Cost Cost

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    ACatholicon??

    Will MTArule overCaOH??

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    IEJ 1999; 32, 361-9

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    , IEJ 1999; 32, 257-82 IEJ 1990; 23, 283-97 J Dent 1991; 19, 3-13 JOE 2009; 35(4), 475-79 J.Appl.oral sci 2003; 11(4)

    Quint. Int 1990; 21(7), 589-97 Pediatric dent 2006; 28, 399-404 IEJ 2002; 36, 225-231 Am J of Dent 2002; 15(4) Am J of Dent 2006; 19(3) OOOE nov 2003 IEJ 2006(systematic review)

    Endodontic practice; Louis Grossman, Seymour Oliet,

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    p yCarlos E Del Rio-11thedition

    Endodontic therapy; Franklin Weine- 6thedition

    Ingles endodontics; Ingle, Bakland, Baumgartner- 6th

    edition Pathways of pulp; Cohen, Hargreaves- 9thedition Operative dentistry;

    Sturdevants art and science of operative dentistry;Roberson , Heymann, Swift- 5thedition Operative dentistry. Modern theory and practice;

    Marzouk, Simonton, Gross- 1stedition

    Seltzer & Benders Dental pulp; Kenneth M Hargreaves,Harold E Goodis Essentials of traumatic injuries to the teeth; J O

    Andreasen & F M Andreasen

    www.google.com

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    Ca(OH)2

    Bacteria

    Tooth

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    M ik L k