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A COMPARISON OF THE ENAMEL DEMINERALIZATION INHIBITION AND SHEAR BOND STRENGTH OF TWO ORTHODONTIC RESINS by JAMES HENRY ALLEN JOHN O. BURGESS, COMMITTEE CHAIR ANDRE’ FERREIRA P. LIONEL SADOWSKY A THESIS Submitted to the graduate faculty of the University of Alabama at Birmingham, in partial fulfillment of the requirements for the degree of Master of Science BIRMINGHAM, ALABAMA 2009

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A COMPARISON OF THE ENAMEL DEMINERALIZATION INHIBITION AND SHEAR BOND STRENGTH OF TWO ORTHODONTIC RESINS

by

JAMES HENRY ALLEN

JOHN O. BURGESS, COMMITTEE CHAIR ANDRE’ FERREIRA

P. LIONEL SADOWSKY

A THESIS

Submitted to the graduate faculty of the University of Alabama at Birmingham, in partial fulfillment of the requirements for the degree of

Master of Science

BIRMINGHAM, ALABAMA

2009

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A COMPARISON OF THE ENAMEL DEMINERALIZATION INHIBITION AND SHEAR BOND STRENGTH OF TWO ORTHODONTIC RESINS

JAMES HENRY ALLEN

DENTISTRY

ABSTRACT

White spot lesions (WSLs) left on the teeth after orthodontic treatment are a huge

compromise to the esthetic outcome of a treated case. Patient compliance with oral

hygiene instruction is often low and thus WSLs occur in a large proportion of finished

cases. Amorphous calcium phosphate (ACP) has recently emerged as a viable alternative

to fluoride therapy in preventing enamel demineralization by promoting remineralization.

ACP has been added as filler in an orthodontic bracket adhesive with the expectation of

preventing WSLs in poorly compliant patients. The purpose of this study was to compare

the enamel demineralization inhibition and shear bond strength of an ACP filled

orthodontic bracket adhesive and a conventional adhesive.

Ninety previously extracted human 3rd molar teeth were divided into three groups

of thirty. Within each group, half the teeth were bonded with brackets using the ACP

filled adhesive and the other half were bonded with brackets using the conventional

adhesive. After creating a 2mm window around the bracket, Group 1 was submerged in

an acidic gel for ten days. Demineralization depth and shear bond strength were

recorded. Groups 2 and 3 were stored in distilled water for ten days and 24 hours

respectively after which the brackets were fractured and the shear bond strengths were

recorded. The study found that teeth bonded with the ACP filled adhesive had a 29.8%

reduction in demineralization depth when compared to the conventional adhesive. The

average shear bond strength of the ACP filled adhesive (5.5 MPa) was significantly less

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than the conventional adhesive (18.5 MPa) in all three treatment groups. In conclusion,

there was significantly less demineralization with the ACP filled adhesive but the low

bond strengths greatly increase the risk of clinical bond failures.

Keywords: WHITE SPOT LESIONS, AMORPHOUS CALCIUM PHOSPHATE, ORTHODONTICS, SHEAR BOND STRENGTH, ESTHETICS

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ACKNOWLEDGMENTS

I would like to thank Dr. John Burgess, Dr. Lionel Sadowsky, Dr. Andre Ferreira,

and Ms. Sandre McNeal for their guidance during the thesis process. I would like to

thank 3M Unitek for supplying the brackets and Bosworth Company for providing the

Aegis Ortho used in the study. A special thanks to Dr. Deniz Cakir, Preston Beck, and

Ian Mugisa for all their help in the lab during the project. Finally, I would like to thank

my fellow 3rd year residents for all of your support and friendship. Although I am

looking forward to graduating, I will miss our time together immensely.

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TABLE OF CONTENTS

Page

ABSTRACT ........................................................................................................................ ii

ACKNOWLEDGMENTS ................................................................................................. iv

LIST OF TABLES ............................................................................................................. vi

LITERATURE REVIEW ....................................................................................................1

White Spot Lesions and Orthodontics .......................................................................1 Compliance Dependant Modalities for White Spot Lesion Prevention ....................4 Manual Products ............................................................................................4 Fluoride Products ...........................................................................................5 ADA Foundation Amorphous Calcium Phosphate (ACP) ............................6 CPP-ACP (Recaldent) ....................................................................................7 Non-Compliant Modalities for White Spot Lesion Prevention ................................8 Fluoride Products ...........................................................................................8 Development of ACP Filled Composites .....................................................11 Aegis Ortho Studies ...............................................................................................12 Present Study .........................................................................................................14 A COMPARISON OF THE ENAMEL DEMINERALIZATION INHIBITION AND SHEAR BOND STRENGTH OF TWO ORTHODONTIC RESINS ......................15 GENERAL CONCLUSIONS ............................................................................................38 GENERAL LIST OF REFERENCES ...............................................................................39

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LIST OF TABLES

Table Page 1 Study Design ..........................................................................................................23

2 Mean Lesion Depths (µm) .....................................................................................26 3 Shear Bond Strengths (MPa) .................................................................................27 4 Mode of Failure......................................................................................................28

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LITERATURE REVIEW

White Spot Lesions and Orthodontics

The traditional goals of orthodontic treatment have always been function,

esthetics, stability and longevity, but not necessarily in that order. In our society, great

emphasis is placed on appearance. Orthodontists play a significant role in assisting

patients in achieving their esthetic goals. An attractive appearance gives individuals an

advantage in life.1 This is important in our ever increasing competitive world where first

impressions are all important. Tooth shape, tooth proportionality, gingival heights,

incisal edge relationships, smile arc and buccal corridors are some of the smile

components that create optimal esthetics.2 Discolorations on the tooth surface known as

“white spot lesions” detract from the optimal esthetic goals of treatment outcomes.

White spot lesions have a white frosty appearance that often appear in the shape of a ring

circling the position the bracket occupied on the tooth during orthodontic treatment. As

the demineralization producing these lesions occurs slowly, white spots lesions are often

not noticed by the patient until the orthodontic appliances have been removed from their

teeth. These white marks left behind on the teeth compromise the esthetic expectations

of both the orthodontist and more importantly the patient.

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White spot lesions (WSLs) have been defined as a subsurface enamel porosity

from carious demineralization that presents as a milky white opacity when located on

smooth surfaces.3 Since enamel translucency is directly related to its mineral content, the

optical properties of demineralized enamel are different from adjacent sound enamel.

The porous enamel scatters light differently and clinically results in a frosty white

appearance. White spot lesions occur frequently and can be found in 50% to 96% of

orthodontic patients compared to 11% to 24% of untreated controls.3,4,5 WSLs are more

often seen on maxillary lateral, mandibular canine and premolar, and fist molar teeth and

are often found on the gingival aspect of the bracket and under loose fitting bands where

oral hygiene is more difficult.6,7 In a scanning microscope study, Gwinnett and Ceen 8

showed that bacterial accumulation was greatest at the resin/enamel interface and the

most important factor in plaque accumulation was the surface area of composite resin

exposed. Gwinnett and Ceen stated that normal wear of the resin matrix constantly

exposes filler particles which contribute to a persistently roughened surface, and this

predisposes the resin surface to a rapid attachment and growth of oral microorganisms.

Lim et al. 9 studied bacterial adhesion to various orthodontic raw materials and reported

that bacteria adhered most to orthodontic adhesives because the roughened surface

provides protective niches for bacterial colonization. Another scanning microscope study

revealed that bacterial accumulation was constantly detected in a ten micrometer gap at

the resin enamel interface due to the polymerztion shrinkage of the composite.10

Auxiliaries such as Class II correctors, power chains, underlaces, o-ties and intrusion

arches can also increase the number of potential plaque harboring areas. Studies have

shown that fixed orthodontic appliances not only induce a rapid increase in the volume of

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dental plaque, but such plaque has a lower pH than that in non-orthodontic patients.8,11

There is a rapid shift in the composition of the bacterial flora of the plaque following the

introduction of orthodontic appliances with an increase in the amount of Streptococci

mutans.12 A rigorous oral hygiene regimen is needed to overcome this new environment

challenge. Most orthodontic offices take great care in instructing the patient on proper

oral hygiene home care. This usually consists of proper brushing and flossing techniques

and frequencies along with the use of a fluoride toothpaste and mouth rinse. Often an

anti-cariogenic diet is recommended to reduce the intake of fermentable carbohydrates.

Despite these efforts, patient compliance remains an issue. Weinstein et al.13 studied 70

dental patients with a high plaque index and instructed them in proper oral hygiene

procedures. At 24 weeks only 13 percent had reduced plaque levels compared to their

starting values. If patient compliance is poor, the accumulation of plaque soon triggers

the demineralization process which ultimately results in WSLs.

Enamel is the most highly mineralized and hardest substance in the body. The

primary mineral component is hydroxyapatite (HAP) which is a crystalline calcium

phosphate with the formula Ca10(PO4)6(OH)2. Naturally, enamel is in a constant flux of

demineralization and remineralization depending on the pH of the oral environment.

Bacterial plaque accumulating around orthodontic appliances metabolize fermentable

carbohydrates and produce lactic acid that lowers the pH of the local environment.

Arneberg and coworkers 14 showed that the plaque pH in orthodontic patients following a

sucrose challenge could fall as low as 4 in the upper incisor region. When the pH dips

below the critical pH (5.5) of the enamel, calcium and phosphate ions dissolve out the

enamel and flow into the plaque fluid and saliva. This demineralization occurs until the

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plaque fluid becomes saturated with respect to calcium and phosphate. If this frequently

occurs, the demineralization/remineralization balance is interrupted and net

demineralization is seen. Demineralization can occur and become clinically evident

within four weeks after appliance placement which is typically the length of time

between orthodontic appointments.15 White spot lesions development is considered an

iatrogenic effect of fixed orthodontic treatment and can be subject to litigation.

Recognizing and documenting poor oral hygiene before irreversible changes occur and

instituting an effective remedy, which may very well result in termination of treatment, is

the orthodontists responsibility. Continuing treatment under unfavorable conditions, such

as poor oral hygiene, can leave oneself open to charges of supervised neglect.16

Orthodontists, therefore, must monitor and take the responsibility of WSL prevention.

Compliance Dependant Based Modalities for White Spot Lesion Prevention

Manual Products

Proper patient education is the first step in preventing enamel demineralization.

The patient must understand that daily plaque removal is required to control WSLs. The

easiest and least expensive method of plaque removal is mechanical debridment with

toothbrushes and dental floss. Patients must be trained in proper brushing and flossing

techniques. Patients may be spending adequate time, yet still achieving unsatisfactory

results with poor oral hygiene technique. Electric toothbrushes can be utilized and have

been shown to help patients become more proficient at removing plaque.17 Sharma and

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Barnes have shown that water jets are an effective adjunct to toothbrushes and result in

better plaque removal in orthodontic patients.18,19

Fluoride Products

In addition to mechanical plaque removal, there are products available which

require patient compliance that can be recommended for home use such as fluoride

dentifrice and fluoride mouthwash. Fluoride is effective in preventing dental caries.

Addition of fluoride to the public water system was one of the great public health

successes of the 20th century and is considered the single most effective public health

measure for preventing tooth decay. Fluoride incorporates into the surface enamel to

form fluoroapatite which makes the enamel less soluble and more resistant to acid attack.

Sodium fluoride, sodium monofluorophosphate, stannous fluoride, amine fluoride or

acidulated phosphate fluoride are the different forms of fluoride that are incorporated into

the topical fluoride products. It is not recommended that the fluoride concentration be

below 0.1% for orthodontic patients.20 Antiplaque fluoridated dentifrice has been shown

to be more effective than fluoride only dentifrice at preventing demineralization around

appliances bonded with composite material.21 O’Rielly and Featherstone 22 found that

fluoride dentifrices alone were not able to stop enamel demineralization in non-compliant

orthodontic patients. Arneberg et al. 14 discovered that the plaque pH and plaque

fluoride levels are proportional in orthodontic patients with the fluoride reservoir quickly

becoming depleted at low pH. Thus the fluoride effect is limited when the pH drops

below 4.5 and the solubility product of fluoroapatite is exceeded. A systematic review of

the literature by Chadwick 6 concluded that the use of topical fluorides in addition to

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fluoride toothpaste should reduce the incidence of decalcification in orthodontic patients.

Another systematic review of the literature from the Cochrane Clinical Trials Register

(Jan 2004), MEDLINE (1966 to December 2004), and EMBASE (1974 to December

2004) concluded that there is little evidence as to which method or combination of

methods is most effective to deliver fluoride and recommended the best practice for

orthodontic patients is daily rinsing with 0.05% sodium fluoride mouth rinse.23

However, Geiger and coworkers 24 showed that less than 15% of patients rinsed with

fluoride mouth rinse as they were instructed.

ADA Foundation Amorphous Calcium Phosphate (ACP)

Although fluoride has been the mainstay in caries prevention, calcium phosphates

provide an alternate approach to preventing enamel demineralization by promoting

remineralization. Calcium phosphates have a significant medical and dental history since

they are components of normal hard tissues such as enamel, dentin and bone and are

therefore very biocompatible. In 1920 Albee reported that a ‘triple calcium phosphate’

compound used in a bony defect promoted new bone formation. In 1963, Posner was

credited with first discovering a precipitate that formed an amorphous pattern in his

laboratory when trying to make apatite. A year later, investigators under the direction of

Posner first reported amorphous calcium phosphate (ACP) as a component of human hard

tissues.25 ACP is one of many calcium phosphates and has gained attention in dental

research. ACP, because of its high solubility and rapid conversion to HAP in aqueous

environments, possesses characteristics suitable for enamel remineralization. The

American Dental Association Foundation’s Paffenbarger Research Center (PRC) is

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leading many research efforts in developing ACP and licensing it for commercial use.

The PRC’s formulation of ACP has demonstrated remineralized enamel lesions.26 The

first product on the market utilizing this technology was Enamelon toothpaste which was

introduced in 1999. It consisted of a dual compartment container where calcium and

phosphate were kept separated until squeezed out of the tube at which time they reacted

to form ACP which precipitated onto the tooth surface. Currently this technology has

been added to several products such as toothpastes and whitening agents. Unfortunately

these products require patient compliance. Since the PRC’s ACP is highly soluble, it

quickly washes away and must be frequently reapplied to provide benefit. This low

substantivity has lead to the development of other technologies with the aim of providing

a delivery vehicle that will provide a sustained release of ACP to the tooth.

CPP-ACP (Recaldent)

Recaldent (Bonlac Bioscience International Pty Ltd, Melbourne, Australia) is a

technology that uses casein phosphopeptides (CPP), a milk protein, to stabilize ACP in

solution. The multiple phosphoseryl residues of CPP bind to forming nanoclusters of

ACP, preventing growth to the critical size requiring phase transformations to HAP.

Casein phosphopeptide-amorphous calcium phosphate (CPP-ACP) is incorporated into

supragingival dental plaque by binding onto the surfaces of bacteria cells and the

intercellular plaque matrix causing significant increases in plaque levels of calcium and

phosphate. This increased level of calcium and phosphate helps maintain a

supersaturated enamel interphase with the tooth surface depressing enamel

demineralization and enhancing enamel remineralization.27 CPP-ACP solutions, when

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applied to molar teeth of rats, reduced caries by 55% compared to controls.28 In a

human in situ enamel demineralization study, a 1.0% CPP-ACP solution used twice daily

produced a 51% reduction in enamel mineral loss.29 The addition CPP-ACP to sugar

free chewing gums, resulted in a dose related increase in enamel remineralization. At the

high end, 56.4mg of CPP-ACP produced a 152% increase in enamel remineralization

relative to the control gum.30 A chewing gum and mouthrinse study demonstrated that

CPP-ACP increased plaque levels of calcium and phosphate and that significant levels

remained 3 hours after application.31 Although CPP-ACP has demonstrated

substantivity and positive results with respect to enamel remineralization, patient

compliance remains an issue in the success of these products.

Non-Compliant Modalities for White Spot Lesion Prevention

Fluoride Products

There are several modalities available to help protect the patient from white spot

lesions that require much less patient compliance. These products come in the form of

topical applications applied by the dental professional or adhesive materials used to bond

orthodontic appliances. Fluoride varnish can be applied by the orthodontist and results

in prolonged contact and subsequent release of fluoride to the tooth structure. Ogaard et

al. 32 showed a 48% reduction in the depth of naturally occuring enamel lesions treated

with the fluoride varnish Duraphat (Colgate Oral Pharmaceuticals Inc., Canton, MA).

Todd et al. 7 reported 50% less enamel demineralization with a single application of

Duraflor (Pharmascience Inc., Montreal Canada) to teeth bonded with orthodontic

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appliances. Demito 33 showed that two applications of Duraflor promoted a 38%

reduction in the mean lesion depth adjacent to orthodontic brackets. Although varnishes

are effective in reducing demineralization, they require repeated applications and discolor

teeth which is often objectionable to the patient. A prospective trial comparing a fluoride

releasing sealant (Reliance M5 Protection Plus) with a control showed no significant

difference in the amount of enamel demineralizaton.34 Another fluoride releasing sealant

(ProSeal; Reliance Orthodontic Products, Itasca, IL) released fluoride ions for 17 weeks

in an in vitro study. In addition, it had the ability to be recharged with topical

applications of acidulated phosphate fluoride.35 An in-vitro study conducted by Hu and

Featherstone 36 demonstrated that enamel demineralization was significantly less in teeth

treated with ProSeal than in teeth treated with fluoride varnish or unfilled sealants. A

more recent study showed that ProSeal reduced enamel demineralizaiton by 92% over

untreated controls and provided significantly more protection than a fluoride varnish or

unfilled sealant.37 Although ProSeal has been shown to protect against WSLs, the resin

has to be removed with a bur when orthodontic appliances are removed and resin tags

remain in the enamel which can cause unesthetic staining and compromise future

whitening results.

Glass ionomer cements (GIC) release fluoride and have been used as orthodontic

adhesives for their demineralizaiton preventative affects.38 Although GICs provide a

fluoride reservior capable of sustained release with the ability to be recharged with

fluoride, their lower bond strength compared to composite resins produced more clinical

debonds which limited their polularity.39,40,41 To improve the physical characteristics of

GICs, light-activated resins were incorporated into the mix to give it added strength.

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Resin-modified glass ionomer cements (RMGI) have improved bond strengths while

providing the fluoride release of GICs, and thus are more widely used as orthodontic

adhesives.42,43,44 Gorton et al. 45conducted an in vivo study comparing the

demineralization around orthodontic brackets bonded with a RMGI with the

demineralization around brackets bonded with a conventional composite resin. Subjects

in the study also used a fluoridated toothpaste. The conclusion reached after a 4 week

period was that the RMGI significantly reduced the prevalance and severity of enamel

demineralization. Sudjalim et al. 46 bonded twenty extracted human 3rd molar teeth with a

RMGI and twenty extracted human 3rd molar teeth with a light-cured resin control. Each

group was subjected to topical applications of either CPP-ACP (TM with Recaldent),

NaF 9000 ppm gel, or a combination of CPP-ACP and NaF gel. The test specimens were

immersed in a demineralizing solution for 96 hours and removed for additional topical

treatments every 4 hours. Sudjalim concluded that the use of RMGI would significantly

reduce the development of enamel demineralizaton. Further, he found that the topical

application of both the CPP-ACP and NaF in combination with the RMGIC provided the

most protection against enamel demineralization and recommended this protocol for at

risk orthodontic patients.

Fluoride releasing composite resins and compomers, a hybrid of glass ionomer

and composite resin, have the ability to prevent enamel decalcification. In a in-vivo

study, Millet et al. 47 reported that 20% of fluoride releasing compomer bonded teeth

were affected by decalcification while 26% of control teeth were affected. Sonis et al. 48

demonstrated in a prospective clinical trial no decalcifacation on teeth bonded with a

fluoride releasing composite resin while the 12.6% of the control teeth experienced

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decalcifications. Similarly, Underwood et al. 49 following a split mouth clinical study

concluded that an experimental fluoride-exchanging resin held promise as a clinically

useful orthodontic adhesive as it demonstrated significantly less demineralization

compared with a control. Conversely, a systematic review by Derks et al. 50 reported that

fluoride-releasing bonding materials have no significant effect in the preventing WSL

demineralizations.

Development of ACP Filled Composites

Amorphous calcium phosphate has been incorporated as fillers into dental

resin-based resorative materials to take advantage of its ability to remineralize dental hard

tissues. ACP has been marketed as a “smart” material because it has been shown to

release higher levels of calcium and phosphate under acidic conditions.51,52 However,

ACPs high solubility weakens the resin in which it is filled due to the voids left behind

after the ACP leaches out of the polymer matrix.53 Mechanical properties were improved

by introducing glass-forming elements during the preparation of the ACP filler which

permitted a stronger interaction with the surrounding resin matrix. These modified ACP

fillers not only improved the mechanical properties, they also produced a more sustained

release of calcium and phosphate at levels required for HAP formation.54,55 Artificial

lesions created on bovine incisors recovered 38% of lost mineral when covered with an

ACP-containing composite.26 Langhorst et al. 56 created artificial enamel lesions by

submersing teeth for 72 hours in a 4 pH demineralizing solution at 37 ۫C. The teeth were

then cycled through a demineralization and remineralization scheme for 1 month.

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Quantitative digital image analysis of matched areas from contact microradiographs taken

before and after treatment indicated higher mineral recovery with ACP composites

compared to a commercial orthodontic F-releasing cement (14.4% vs. 4.3%,

respectively), while the control specimens showed an average of 55.4% further

demineralization. Park et al. 57 demonstrated similar mechanical improvements with

glass modified ACP and suggested its use as a base and liner material under dental

restorations. Skrtic et al. 58 studied the effect of combinations of seven different resin

matrices and three types of ACP fillers on the release rates of calcium and phosphate.

Skrtic concluded that UDMA, a urethane di-methacrylate resin, appears to have

advantages over Bis-GMA and highly carboxylated monomer systems such as

PMGDMA in producing higher ion release rates. UDMA also has reduced water sorption

and polymerization shrinkage thus enhancing the strength of the resin matrix.59 With the

systematic improvements in mechanical and ion release properties, Skrtic advocated

ACP-filled composite resins for use as orthodontic bracket adhesives. Now the

orthodontic profession had a potential non-compliant WSL prevention product that

offered an alternative to fluoride therapy.

Aegis Ortho Studies

In March 2004, Aegis Ortho became the first available ACP-containing

orthodontic adhesive to receive Food and Drug Aministration approval. The proprietary

formula of Aegis Ortho utilizes a UDMA resin base along with a mix of various fillers

including ACP. To date, no published studies on the ability of Aegis Ortho to prevent

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enamel demineralization. The studies involving Aegis Ortho have been more concerned

with its mechanical properties in order to establish its validity as an orthodontic adhesive.

Using 30 freshly extracted human third molars, Dunn et al. 60 compared the shear bond

strength (SBS) of Aegis Ortho and a conventional resin-based composite adhesive

(Transbond XT, 3M Unitek). Each tooth was bonded with two brackets - one bonded

with Transbond XT and the other bonded with Aegis Otho. After bonding, the specimens

were stored in water at 37 degrees C for 24 hours and then tested for shear bond strength.

The results showed that Aegis Ortho failed at significantly weaker SBS values than did

Transbond XT, 1.2 MPa and 10 MPa respectively. Foster et al. 61 compared the SBS of

Aegis Ortho with a conventional composite resin (Transbond XT, 3M Unitek) and a

resin-modified glass ionomer cement (Fuji Ortho LC, GC America Inc, Alsip, III). Each

adhesive was used according to manufacturers’ instructions to bond brackets on 20

premolars. The teeth were mounted in acrylic and stored at 370 C for 40 hours prior to

debonding. Foster’s results showed that there was a statistically significant difference in

SBS values between Aegis Ortho and Transbond XT, 6.6 MPa and 15.2 MPa

respectively. There was no statistical difference between Aegis Ortho and Fuji Ortho LC

although Aegis Ortho values were lower, 6.6 MPa and 8.3 MPa respectively. Uysal et al.

62 tested the shear bond strength of lingual retainers bonded with Aegis Ortho and a

conventional lingual retainer composite (Transbond-LR, 3M Unitek). Uysal concluded

that Aegis Ortho had a significantly reduced bond strength when compared to

conventional composite resin cements. Although the shear bond strengths were

significantly lower than the composite resin controls, they were in the range of what has

been reported as being clinically acceptable.63,64,60 Tavas et al. 63 reported that shear/peel

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strengths of orthodontic brackets should be 5.9 MPa within 24 hours. In another study

Reynolds 64 determined that the clinically acceptable minimum bond strength values for

direct orthodontic bonding systems are 5.9-7.8 MPa.

Present Study

Bosworth Company’s bonding protocol for previous studies 60,61,62 did not include

the use of a primer. Bosworth Company has since changed the bonding protocol for

Aegis Ortho to include their self-etching primer, Aqua Bond. The present study was

designed to test the SBS of orthodontic brackets bonded with Bosworth Company’s new

bonding protocol for Aegis Ortho and compare the values to the SBS values of the

industry standard, Transbond XT. Due to the “smart” characteristics of the ACP

containing products, the bond strength after submersion in a low pH demineralizing

solution was also tested to determine if an acidic environment deteriorated the bond

strength. Since there have been no published studies of the demineralizing inhibition

capabilities of Aegis Ortho, this study compared enamel lesion depth adjacent to

orthodontic brackets bonded with Aegis Ortho and Transbond XT after a demineralizing

treatment. The intensions of this study were to test the bond strength and

demineralization prevention capability of a relatively new product that has the potential

to be a tool for combating white spot lesions in non-compliant patients.

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A COMPARISON OF THE ENAMEL DEMINERALIZATION INHIBITION AND SHEAR BOND STRENGTH OF TWO ORTHODONTIC RESINS

by

JAMES HENRY ALLEN

In preparation for The Angle Orthodontist

Format adapted for thesis

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ABSTRACT

White spot lesions (WSLs) left on the teeth after orthodontic treatment are a huge

compromise to the esthetic outcome of a treated case. Patient compliance with oral

hygiene instruction is often low and thus WSLs occur in a large proportion of finished

cases. Amorphous calcium phosphate (ACP) has recently emerged as a viable alternative

to fluoride therapy in preventing enamel demineralization by promoting remineralization.

ACP has been added as filler in an orthodontic bracket adhesive with the expectation of

preventing WSLs in poorly compliant patients. The purpose of this study was to compare

the enamel demineralization inhibition and shear bond strength of an ACP filled

orthodontic bracket adhesive and a conventional adhesive.

Ninety previously extracted human 3rd molar teeth were divided into three groups

of thirty. Within each group, half the teeth were bonded with brackets using the ACP

filled adhesive and the other half were bonded with brackets using the conventional

adhesive. After creating a 2mm window around the bracket, Group 1 was submerged in

an acidic gel for ten days. Demineralization depth and shear bond strength were

recorded. Groups 2 and 3 were stored in distilled water for ten days and 24 hours

respectively after which the brackets were fractured and the shear bond strengths were

recorded. The study found that teeth bonded with the ACP filled adhesive had a 29.8%

reduction in demineralization depth when compared to the conventional adhesive. The

average shear bond strength of the ACP filled adhesive (5.5 MPa) was significantly less

than the conventional adhesive (18.5 MPa) in all three treatment groups. In conclusion,

there was significantly less demineralization with the ACP filled adhesive but the low

bond strengths greatly increase the risk of clinical bond failures.

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INTRODUCTION

In today’s society, esthetics is probably the most important reason patients seek

orthodontic treatment. Much emphasis has been placed on identifying esthetic smile

components to aid the orthodontist in delivering a beautiful smile. Sarver et al. 1

advocates identifying and recording the positive attributes of a patient’s smile during the

initial exam so that treatment planning will not negatively affect those attributes. The

natural translucency of the patient’s enamel is a characteristic that should not worsen

with orthodontic treatment. However, white spot lesions (WSLs) often develop around

orthodontic appliances during the treatment period resulting in un-esthetic opacities that

lead to patient dissatisfaction. WSLs have been defined as a subsurface enamel porosity

from carious demineralization that presents as a milky white opacity when located on

smooth surfaces.2 Since enamel translucency is directly related to its mineral content, the

optical properties of demineralized enamel are different from adjacent sound enamel.

The porous enamel scatters light differently and clinically results in a frosty white

appearance. It has been reported that anywhere from 50% to 96% of orthodontic patients

get WSLs during treatment.2,3,4 WSLs are more often seen on maxillary lateral,

mandibular canine and premolar, and first molar teeth.5,6 They are often found on the

gingival aspect of the bracket and under loose fitting bands where oral hygiene is more

difficult. Studies have shown that there is a rapid shift in the composition of the bacterial

flora of plaque following the introduction of orthodontic appliances resulting in an

increase in the amount of acidogenic Streptococci mutans which are strongly associated

with enamel demineralization.7 It has also been demonstrated that there is a rapid

increase in the volume of dental plaque after the placement of fixed orthodontic

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appliances and this plaque has a lower pH than plaque found in non-orthodontic

patients.8,9 Naturally, enamel is in a constant flux of demineralization and

remineralization depending on the balance of the oral environment. Net demineralization

results when poor oral hygiene efforts fail to remove the plaque that has accumulated

around the orthodontic appliances. Each time fermentable carbohydrates are consumed,

the acidogenic plaque around the appliances produce lactic acid that causes a dip in pH

below the solubility threshold of enamel. When this occurs, calcium and phosphate

diffuse out of the enamel disrupting the ordered arrangement of enamel crystals which

produce enamel translucency. This process can occur with WSLs becoming clinically

evident within four weeks, a typical orthodontic appointment interval.10

Patient compliance with proper oral hygiene and a low cariogenic diet is crucial in

preventing white spot lesions. It is the responsibility of the orthodontist to teach the

patient how to effectively clean around the appliances and to monitor the patient’s oral

hygiene at each office visit. Fluoride therapy has been the predominant treatment utilized

in caries prevention and is incorporated in many products such as toothpastes, gels and

mouth rinses designed for at home use by the patient. Fluoride incorporates into the

surface enamel to form fluoroapatite which makes enamel less soluble and more resistant

to acid attack. The recommended fluoride concentration is above 0.1% for orthodontic

patients and the best daily practice for preventing enamel demineralization is using a

fluoride dentifrice along with a fluoride mouth rinse.5,10,11 However, Geiger and

coworkers 12 showed that less than 15% of patients rinsed with fluoride mouth rinse as

they were instructed. O’Rielly and Featherstone 13 concluded that fluoride dentifrices

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alone were not able to stop enamel demineralization in non-compliant orthodontic

patients.

In-office applications of fluoride releasing products have been utilized in an

attempt to reduce the effects of poor patient compliance. These products include

elastomerics, varnishes, sealants, resin modified glass ionomer cements and adhesives

that are applied to or adjacent to the enamel and have shown the ability to reduce enamel

demineralization.6,14,15,16,17,18,19,20,21,22 These products are designed to provide a constant

source of fluoride to the tooth; however, Arneberg et al. 23 reported that plaque pH and

plaque fluoride levels are proportional in orthodontic patients with the fluoride reservoir

quickly becoming depleted at low pH. Arneberg showed that the plaque pH in

orthodontic patients following a sucrose challenge could fall as low as 4 in the upper

incisor region. The fluoride effect becomes limited when the pH drops below 4.5 and the

solubility of fluoroapatite is exceeded.24

Amorphous calcium phosphate (ACP) provides an alternative to fluoride in

regards to preventing enamel demineralization and has gained much attention in the

dental research community over the past decade. ACP is an important intermediate in the

formation of the main mineral component of enamel, hydroxyapatite (HAP). ACP

possesses characteristics suitable for enamel remineralization because of its high

solubility and rapid conversion to hydroxyapatite in aqueous environments.25 ACP has

been incorporated in many desensitizing and whitening products with the unofficial claim

of reducing enamel demineralization. To increase ACP’s substantivity it has been

packaged with casein phosphopeptides (CPP) which are milk proteins that stabilizes ACP

in solution by slowing its conversion to HAP. This CPP-ACP combination is marketed

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as Recaldent (Bonlac Bioscience International Pty Ltd, Melbourne, Australia). CPP-ACP

is incorporated into supragingival dental plaque by binding to the surfaces of bacteria and

various components of the intercellular plaque matrix causing significant increases in

plaque levels of calcium and phosphate. This increased level of calcium and phosphate

helps to maintain a state of supersaturation with respect to enamel mineral, thereby

depressing enamel demineralization and enhancing enamel remineralization.26,27,28,29,30

Although CPP-ACP has a clinical history of success when used frequently, patient

compliance is still an integral part of its clinical effectiveness.

Amorphous calcium phosphate has been incorporated as a filler in dental resin-

based resorative materials to take advantage of its ability to remineralize dental hard

tissues.31,32 ACP has also been marketed as a “smart” material because it releases higher

levels of calcium and phosphate ions under acidic conditions.33,34 This property, in

theory, makes an ACP filled resin a great choice in dental applications where poor oral

hygiene persists. However, ACPs high solubility results in voids in the resin after the

ACP dissolves out of the polymer matrix leading to weakening of the resin.35 Initially,

ACP filled resins were advocated in non-stess bearing conditions such as bases or liners

under dental restorations.36 ACP filled resins were recommended for use as orthodontic

adhesives to prevent enamel demineralization adjacent to orthodontic brackets after

improvements in mechanical properties were made.25,37,38

In March 2004, Aegis Ortho (Harry J. Bosworth Co., Skokie, Ill) became the first

available ACP-containing orthodontic adhesive to receive Food and Drug Aministration

approval. The proprietary formula of Aegis Ortho utilizes a UDMA resin base along

with a mix of various fillers including ACP. To date, there have been no published

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studies on the ability of Aegis Ortho to prevent enamel demineralization. The studies

involving Aegis Ortho have been more concerned with its mechanical properties in order

to establish its validity as an orthodontic adhesive. Dunn et al. 39 compared the shear

bond strength (SBS) of Aegis Ortho and a conventional resin-based composite adhesive

(Transbond XT, 3M Unitek). They reported that Aegis Ortho had significantly lower

shear bond strength than did Transbond XT, 1.2 MPa and 10 MPa respectively. Dunn

concluded that Aegis Ortho did not have suitable mechanical strength for use as an

orthodontic bracket adhesive. Foster et al. 40 compared the SBS of Aegis Ortho with a

conventional composite resin (Transbond XT, 3M Unitek) and a resin-modified glass

ionomer cement (Fuji Ortho LC, GC America Inc, Alsip, III). Foster’s results concluded

that Transbond XT with a 15.2 MPa bracket bond strength was statistically greater than

the 6.6 MPa produced by Aegis Ortho. There was no statistical difference between

Aegis Ortho and Fuji Ortho LC although Aegis Ortho values were lower, 6.6 MPa and

8.3 MPa respectively. Although the shear bond strengths of Aegis Ortho were

significantly lower than the composite resin controls, they were in the range (5.9-7.8

MPa) of bonds that are clinically acceptable.39,41,42 The original bonding protocol for

Aegis Ortho did not call for the use of a priming agent. After low SBS were reported for

Aegis Ortho, the Bosworth Company changed the bonding protocol for Aegis Ortho by

adding their self etching primer, Aqua Bond.

Patient compliance remains a hinderance to the effectiveness of proven techniques

and products in preventing white spot lesions. The present in vitro study is designed to

evaluate a new orthodontic product intended to prevent white spot lesions with little or no

patient compliance. For the purposes of the present study, the null hypotheses assumed

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that there were no statistically significant differences in (1) the depth of demineralization

adjacent to orthodontic brackets bonded with Aegis Ortho and Transbond XT and 2) the

mean shear bond strengths of orthodontic brackets bonded with Aegis Ortho and

Transbond XT under various treatment conditions. Therefore, the specific aims of the

present in vitro study were 1) to bond brackets following manufacturer’s instructions to

human third molar teeth using either an ACP-filled resin (Aegis Ortho) or a traditional

composite (Transbond™ XT), fracturing them at 24 hours and 10 days to compare

bracket shear bond strengths and modes of failure, 2) to demineralize enamel in a 2 mm

unprotected window around the bracket for 10 days and measure the lesion depth at

0.5mm from the bracket base, comparing Aegis Ortho and Transbond™ XT, and 3) to

determine if the increased release of ACP-filler at low pH decreases bond strength.

MATERIALS AND METHODS

Study Design

Ninety extracted human third molar teeth were collected. The teeth were

inspected under 10x magnification and were free of visible opacities, decalcifications,

fractures, or peculiar morphology. The teeth were stored in 10% sodium hypochlorite for

approximately two months prior to the study. Three groups of thirty teeth were

established based on the treatment conditions under which the teeth were to be tested.

The three groups were further randomly assigned to two groups of fifteen teeth each

depending on the bonding adhesive to be used for adhering the brackets (.018-in MBT

Victory Series, 3M Unitek, Monrovia, CA) (Table 1).

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Table 1

Study design

Treatment Condition Groups Aegis Ortho Transbond XT

Group 1: 10 Day Demineralization (n = 30)

n = 15 n = 15

Group 2: 10 Day H2O Storage (n = 30)

n = 14 n = 15

Group 3: 24 Hour H2O Storage (n = 30)

n = 15 n = 15

In group 1, the thirty teeth were cleaned and the mesiobuccal cusp of each tooth was

pumiced with fluoride free flour pumice for 10 seconds, rinsed with sterile water, and

dried with oil/moisture free air. A two millimeter by seven millimeter piece of protective

barrier tape was placed on the tooth at the approximate occlusal aspect of the bracket

position. The purpose of the tape was to eliminate any variables due to the different

bonding protocols that might affect the demineralization study. In the order of random

assignment, the brackets were bonded to the extracted teeth according to manufacturer’s

instructions. The teeth bonded with Transbond XT were conditioned with 37%

phosphoric acid for 30 seconds, rinsed with sterile water for 10 seconds, and dried with

oil/moisture free air until the enamel had a frosty appearance. A thin coat of Transbond

XT primer (3M Unitek) was applied and photopolymerized for 10 seconds. Transbond

XT light-cured adhesive paste (3M Unitek) was then applied to the base of the bracket

and the bracket was placed on the mesiobuccal cusp parallel to the long axis of the tooth.

Under magnification, the bracket was placed on the tooth adjacent to the barrier tape and

excess bonding material was removed with an explorer. The adhesive was

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photopolymerized for 20 seconds on the mesial aspect of the bracket and 20 seconds on

the distal aspect of the bracket using an Ortholux™ LED curing light (3M Unitek) with a

power density of 1000 mW/cm. The teeth bonded with Aegis Ortho were conditioned

with 35% phosphoric acid (Harry J. Bosworth Co., Skokie, Ill) for 30 seconds, rinsed

with sterile water for 10 seconds, and dried with oil/moisture free air. A self-etching

primer, Aqua Bond (Harry J. Bosworth Co.), was then rubbed onto the enamel surface for

15 seconds. The teeth were rinsed with sterile water for 10 seconds and dried with

oil/moisture free air. Aegis Ortho light-cured adhesive paste (Harry J. Bosworth Co.,

Skokie, Ill) was applied to the base of the bracket and the bracket was placed on the

mesiobuccal cusp parallel to the long axis of the tooth. Under magnification, the bracket

was placed adjacent to the barrier tape and excess bonding material was removed with an

explorer. The adhesive was photopolymerized for 20 seconds on the mesial aspect of the

bracket and 20 seconds on the distal aspect of the bracket using an Ortholux™ LED

curing light (3M Unitek) with a power density of 1000 mW/cm2. The tape was removed

from all 30 teeth in group 1 and any residual adhesive residue removed with alcohol. The

teeth were coated with a clear acid resistant nail varnish (Revlon, New York, NY) leaving

a 2 millimeter circumferential window of unprotected enamel adjacent to the bracket.

The demineralizing solution was prepared by buffering a 1M solution of 85% lactic acid

with a 1M solution of sodium hydroxide to make a stock solution of pH 4.5. A calibrated

sensION2 pH/ISE meter (Hach Company, Loveland, CO) was used to measure the pH.

Thirty grams of medium viscosity Carboxymethyl Cellulose (Sigma-Aldrich Co., St.

Louis, MO) were added to 500 mls of stock solution and stirred with a kitchen mixer

until a gel like consistency was attained. A final pH of 4.5 was confirmed with the pH

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meter. The bracketed teeth were completely submerged in the demineralizing solution

and stored at 37 ۫ C for 10 days. In groups 2 and 3, the teeth were bonded in random

order similarly to group 1 with the omission of the two millimeter by seven millimeter

piece of protective barrier tape since these groups were not to undergo demineralization

treatment. Group 2 was stored in distilled water at 37 ۫ C for 10 days. Group 3 was stored

in distilled water at 37 ۫ C for 24 hours.

At the conclusion of the respective treatment times, the teeth in all three groups

were mounted in acrylic cylinders and positioned in the Instron testing machine. A shear

force was applied at the bracket/tooth interface using a sharp chisel-shaped rod attached

to the upper platen of the universal testing machine (Model 5565, Instron, Norwood, MA)

at a crosshead speed of 0.5mm per minute until bracket failure. The bracket bond

strengths (N) were recorded for all teeth and after dividing by the cross-sectional area of

the bracket base, the bond strength in MPa was calculated. Each tooth was then

inspected under magnification and the mode of failure recorded.

The teeth in group 1 were then removed from the acrylic cylinders and sectioned

buccolingually through the bonding sites using an Isomet low speed saw (Model 1180,

Buehler, Lake Bluff, IL). The sections were stained with methylene blue dye so that the

enamel lesions could be accurately observed and measured at 300x using a digital

microscope (Keyence, VHX-600 series, Woodcliff Lake, NJ). At a distance of 0.5 mm

from the occlusal aspect of where the bracket was bonded, the depth of each enamel

lesion was measured in µm.

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Statistical Analysis

A two-way ANOVA analysis was used to compare the shear bond strengths of the

resin groups and treatment groups. A one factor ANOVA analysis was also used to

compare the demineralization depth between the two resin groups. The modes of failure

were analyzed using a Chi-square test. Statistical significance for all tests was

determined at p<.05. All analysis was done using SAS version 9.1 (Cary, NC).

RESULTS

The mean enamel lesion depths from group 1 are listed in Table 2. The mean

lesion depth of enamel bonded with Aegis Ortho at a distance of .5mm from the bracket

base was statistically less than the mean lesion depth of enamel bonded with Transbond

XT (p < .0006). Due to enamel fracture during the shearing of brackets in the Transbond

XT group, five samples were unable to be sectioned and lesion depth accurately

measured.

Table 2

Mean lesion depths (µm)

   Resin Group 

  

Mean Lesion Depth (ìm) 

Std Dev.

Aegis Ortho (n=15)  51.80 ±13.88 P < .0006Transbond XT (n=10)  73.25 ±12.23

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There was a statistically significant difference in the mean shear bond strengths

between brackets bonded with Aegis Ortho and brackets bonded with Transbond XT

(Table 3). The Aegis Ortho bonds failed at statistically lower SBS values in every

treatment group than the Transbond XT bonds.

Table 3 Shear Bond Strengths (MPa)   Resin Group 

Tx Group 1:  10 Day Demineralization (MPa ± Std Dev) 

Tx Group 2:  10 Day H2O Storage 

(MPa ± Std Dev)  

Tx Group 3:  24 Hour H2O Storage 

(MPa ± Std Dev) 

Aegis Ortho  5.26  ± 3.61 4.64 ± 2.21 6.52  ± 1.68

Transbond XT  17.09  ± 6.05 21.21 ± 7.32 17.28  ± 5.63P‐value  < .001 < .001 < .001 There were no statistically significant differences in the bracket SBS values

between the treatment groups in teeth bonded with Aegis Ortho. There was a statistically

significant difference in bracket SBS values between the treatment groups in teeth

bonded with Transbond XT with treatment group 2 SBS producing statistically higher

values than treatment groups 1 or 3 (p-values <.024 and <.031 respectively).

There was a statistically significant difference in the mode of failure between the

two resin groups (p < .0001). The Aegis Ortho group failed 93.18% at the resin/enamel

interface with zero enamel fractures. The Transbond XT group failed 33.33% at the

resin/enamel interface, 31.11% at the resin/bracket interface, and 35.56% within the

enamel.

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Table 4

Mode of Failure

  % failure at resin/enamel 

% failure at resin/bracket

% failure within enamel

Aegis Ortho  93.18  6.82 0Transbond XT  33.33  31.11 35.56

DISCUSSION

White spot lesions adjacent to orthodontic brackets are a major concern to the

orthodontist and the patient. These lesions can progress to frank cavitations requiring

dental restorations if left untreated. WSLs naturally regress in size after orthodontic

appliances are removed, but the enamel will never recover its original translucency.43

Therefore, it is most important to prevent WSLs rather than attempt to treat them after

they occur. Unfortunately most currently available methods of preventing WSLs require

patient compliance. Patients with WSLs have proven to be non-compliant and are

unlikely to comply with further preventive methods. Orthodontists therefore seek

methods of preventing WSLs that do not require patient compliance.

Amorphous calcium phosphate (ACP) has recently been incorporated as a filler

into a composite resin matrix. This product is marketed as the orthodontic adhesive

Aegis Ortho (Harry J. Bosworth Co., Skokie, Ill). There have been no referred

publications reporting the effectiveness of Aegis Ortho in preventing enamel

demineralization adjacent to orthodontic brackets. However previous studies have

shown that ACP filled composite resins have the ability to remineralize artificially

created enamel lesions. Skrtic et al. 31 created artificial enamel lesions and covered them

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with an experimental ACP composite. After cycling them through a

demineralization/remineralization sequence, measurements showed that 38% of lost

mineral was regained in lesions under the ACP composite. Langhorst et al. 32 created

artificial enamel lesions and covered them with an ACP composite. The teeth were then

cycled through a demineralizaiton/remineralization protocol for 1 month. Quantitative

digital image analysis of matched areas from contact microradiographs taken before and

after treatment indicated higher mineral recovery with ACP composites compared to a

commercial orthodontic F-releasing cement (14.4% vs. 4.3%, respectively), while control

specimens showed an average of 55.4% further demineralization. While these studies

showed positive results, they measure mineral recovery of previously created enamel

lesions that are covered with an ACP composite. This is not what happens in an

orthodontic clinical scenario where the demineralization occurs adjacent to the composite

and the starting point is sound enamel. Clinically the ACP first leaches out of the

composite matrix into the plaque biofilm where it then diffuses into the tooth to form

HAP. In my study, sound enamel adjacent to orthodontic brackets was subjected to 240

continuous hours of demineralization solution at pH 4.5 with no cycling protocol. The

lesion depth was measured 0.5mm from the composite pad which is clinically where most

WSLs occur. The results showed that human molar teeth bonded with Aegis Ortho had a

29.82% reduction in demineralization depth compared to teeth bonded with Transbond

XT (p = .0006). The mean lesion depth of enamel bonded with Aegis Ortho was

51.80µm while the mean lesion depth of enamel bonded with Transbond XT was

73.25µm. This study was not designed to mimic the oral environment, but to detect if

Aegis Ortho could reduce demineralization on adjacent enamel under continuous acid

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attack. Therefore, the clinical effect of Aegis Ortho in the present study could be

underestimated due to the conditions of the study.

Glass fillers are added to composite resins to increase strength, decrease

polymerization shrinkage, add esthetic properties, and provide a coefficient of thermal

expansion similar to tooth structure. A silane coupling agent is used to chemically bond

the organic resin and the inorganic filler. Poor or no bonding of the filler to the resin

matrix causes the filler to act as porosity in the composite and lowers fracture toughness

and flexural strength of the composite resin.44 The primary purpose of the ACP filler in

Aegis Ortho is to leach out of the polymer matrix so it can provide calcium and

phosphate for enamel remineralization. This makes an ACP filled composite inherently

weaker than conventional glass filled composites. Although many improvements have

been made in the mechanical properties of ACP filled composites leading to the

introduction of Aegis Ortho, initial bond studies of Aegis Ortho showed unfavorable

results compared to conventional composites.39,40 The bonding protocol for Aegis Ortho

during these studies did not include the use of a primer. A self etching primer (SEP),

Aqua Bond (Harry J. Bosworth Co., Skokie, Ill), was added to the bonding protocol of

Aegis Ortho since these study results were published. Unpublished data from Bosworth

Company reported an average bracket shear bond strength value after a two hour water

storage at 37 ۫C that was statistically similar to Transbond XT (3M Unitek) (9.8 MPa vs

10.2 MPa; p>0.05). These results were not confirmed by the results of the present study.

The mean SBS values of Aegis Ortho in all treatment groups were significantly lower

than the mean SBS values of Transbond XT (Table 3). Group 3 (24 hour water storage)

exhibited the most similar test conditions to the previous studies by Dunn and Foster.

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The 24 hour mean SBS for Aegis Ortho in the present study was 6.5 MPa which was

greater than Dunn’s 1.2 MPa for Aegis Ortho implying that the Aqua Bond primer in the

present study improved the bond numbers. This conflicts with the mean bracket SBS

reported by Foster with Aegis Ortho of 6.6 MPa which implies no additional benefit from

the Aqua Bond. Erickson et al (2008) stated that the acidic monomers in self-etching

primers (SEP) can remove some of the etched enamel structure created by the

conventional etch, and the scrubbing action can also damage the etched enamel rods

resulting in shallower resin tags and weaker bond strengths. SEM images taken at 3000x

of the different etched surfaces in the present study show a more ordered arrangement of

enamel rods in the conventionally etched enamel, whereas the enamel rods appear to be

less orderly in the pre-etch, SEP enamel. This could account for some of the reduced

bond strength of Aegis Ortho. Perhaps Bosworth Company should use a conventional

priming agent as an alternative to the SEP. SEM images taken at 50x and 500x show

cracks in the composite surface of polished Aegis Ortho discs where the filler particles

disrupt the polymer matrix. This results in less available bonding surface and provides

diffusion channels for deeper penetration of water and bacterial enzymes that are known

to degrade the polymeric chain integrity.45 The reduced bonding area available, diffusion

channels for greater water sorption, and etch pattern all contribute to the low SBS values

and the mode of bond failure being 93.2% at the resin/enamel interface.

ACP has been marketed as a “smart” material because it produced increased

levels of calcium and phosphate ions at lower pH levels.33,34 In the present study, there

was no statistical difference in the mean SBS values of Aegis Ortho submerged in

demineralization solution at pH 4.5 for 10 days (group 1) compared to Aegis Ortho stored

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in water for 10 days (group 2). This suggests that the increased release of ACP filler at

lower pH has no effect on the bond strength of the material. This could be due to the

small amount of exposed surface area of composite around the perimeter of an

orthodontic bracket compared to the surface area of composite under a bracket bonded to

the enamel surface. Perhaps more time is needed see the effects of lost filler on bond

strengths.

Clinical bond failures of orthodontic brackets result in emergency office visits,

extend the overall treatment time, and add to the expense of the orthodontic treatment.

Tavas et al. 41 reported that shear/peel strengths of direct bonded adhesives should

develop 5.9 MPa within 24 hours. Reynolds 42 determined that the minimum bond

strength values in direct orthodontic bonding systems that are clinically acceptable are

5.9-7.8 MPa. While the mean SBS of the Aegis Ortho in groups 1 and 2 were slightly

below these numbers, the group 3 values of Aegis Ortho were within the minimally

acceptable range. Linklater et al. 46 studied patterns of bond failures in vivo and

determined that maxillary anterior teeth had the least amount of bond failures at around

2%. Since the maxillary anterior teeth comprise the esthetic zone where WSLs have the

largest negative esthetic impact, orthodontists should consider using Aegis Ortho in the

maxillary anterior region despite its lower shear bond strengths especially in higher caries

risk patients.

CONCLUSIONS

Under the conditions of the present study, the following conclusions are made:

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1. Aegis Ortho reduces enamel lesion depth by 29.82% compared to a traditional

composite resin bracket adhesive when subjected to an acid challenge.

2. The mean shear bond strength associated with Aegis Ortho was significantly

lower than the traditional composite resin control.

3. The increased release of ACP-filler at low pH does not significantly reduce the

mean shear bond strength of the material.

4. Orthodontists should consider bonding maxillary anterior teeth with Aegis Ortho

for increased WSL protection on at risk patients where compliance issues are

anticipated.

REFERENCES

1. Sarver, D., & Ackerman, M. (2003). Dynamic smile visualization and quantification. American Journal of Orthodontics and Dentofacial Orthopedics , 124, 4-12.

2. Summitt, J. B., Robbins, J. W., Schwartz, R. S. (2006). Fundamentals of Operative Dentistry: A Contemporary Approach (3rd edition). 2-4.

3. Gorelick, L., Geiger, A. M., & Gwinnett, A. J. (1982). Incidence of white spot formation after bonding and banding. American Journal of Orthodontics and Dentoficial Orthopedics , 81 (2), 93-98. 4. Boersma, J. G., van der Veen, M. H., Lagerweij, M. D., Bokhout, B., & Prahl-Andersen, B. (2005). Caries prevalence measured with QLF after treatment with fixed orthodontic appliances: influencing factors. Caries Research , 39 (1), 41-47. 5. Chadwick, B. L., Roy, J., Knox, J., & Treasure, E. T. (2005). The effect of topical fluorides on decalcification in patients with fixed orthodontic appliances: A systematic review. American Journal of Orthodontics and Dentofacial Orthopedics , 128 (5), 601-606.

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6. Todd, M. A., Staley, R.N., Kanellis, M.J., Donly, K.J., & Wefel, J.S. (1999). Effect of a fluoride varnish on demineralization adjacent to orthodontic brackets. American Journal of Orthodontics and Dentofacial Orthopedics , 116 (2), 159-167. 7. Scheie, A., Arneberg, P., & Krogstad, O. (1984). Effect of orthodontic treatment on prevalance of Streptococcus mutans in plaque and saliva. Scand Journal of Dental Research , 92, 211-217. 8. Gwinnett, A., & Ceen, R. (1979). Plaque distribution on bonded brackets: A scanning microscope study. American Journal of Orthodontics and Dentofacial Orthopedics , 75 (6), 667-677. 9. Bishara, S., & Ostby, A. (2008). White Spot Lesions: Formation, Prevention, and Treatment. Seminars in Orthodontics , 14 (3), 174-182. 10. Ogaard, B., Rolla, G., & Arends, J. (1988). Orthodontic appliances and enamel demineralization. Part 1. Lesion development. American Journal of Orthodontics and Dentofacial Orthopedics , 94, 68-73. 11. Benson, P. E., Shah, A. A., Millett, D. T., Dyer, F., Parkin, N., & Vine, R. S. (2005). Fluorides, orthodontics and demineralizatiion: a systematic review. Journal of Orthodontics , 32, 102-114. 12. Geiger, A. M., Gorelick, L., Gwinnett, A. J., & Benson, B. J. (1992). Reducing white spot lesions in orthodontic populations with fluoride rinsing. American Journal of Orthodontics and Dentofacial Orthopedics , 101 (5), 403-407. 13. O'Reilly, M., & Featherstone, J. (1987). Demineralization and remineralization around orthodontic appliances: an in vivo study. American Journal of Orthodontics and Dentofacial Orthopedics , 92, 33-40. 14. Banks, P. A., Chadwick, S. M., Asher-McDade, C., & Wright, J. L. (2000). Fluoride-releasing elastomerics - a prospective controlled clinical trial. European Orthodontic Society , 22, 401-407. 15. Ogaard, B. (1996). Microradiography and confocal laser scanning microscopy applied to enamel lesions formed in vivo with and without fluoride varnish treatment. European Journal of Oral Science , 378-383. 16. Demito, C., Vivaldi-Rodrigues, G., Ramos, A.L., & Bowman, S.J. (2004). The efficacy of a fluoride varnish in reducing enamel demineralization adjacent to orthodontic brackets: an in vitro study. Orthodontic Craniofacial Research, 7, 205-210.

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17. Hu, W., & Featherstone, J. (2005). Prevention of enamel demineralization: An in-vitro study using light-cured filled sealant. American Journal of Orthodontics and Dentofacial Orthopedics , 128 (5), 592-600. 18. Soliman, M., Bishara, S. E., Wefel, J., Heilman, J., Warren, J. (2006). Fluoride release from an orthodontic sealant and its clinical implication. Angle Orthodontist , 76 (2), 282-288. 19. Buren, J. L., Staley, R. N., Wefel, J., & Qian, F. (2008). Inhibition of enamel demineralization by an enamel sealant, Pro Seal: An in-vitro study. American Journal of Orthodontics and Dentofacial Orthopedics , 133 (4), S88-S94. 20. Gorton, J., Featherstone, J. (2003). In vivo inhibition of demineralization around orthodontic brackets. American Journal of Orthodontics and Dentofacial Orthopedics , 123 (1), 10-14. 21. Sudjalim, T. R., Woods, M. G., Manton, D. J., & Reynolds, E. C. (2007). Prevention of demineralization around orthodontic brackets in vitro. American Journal of Orthodontics and Dentofacial Orthopedics , 131 (6), 705e1-705e9. 22. Underwood, M. L., Rawis, H. R., Zimmerman, B. F. (1989). Clinical evaluation of a fluoride-exchanging resin as an orthodontic adhesive. American Journal of Orthodontics and Dentofacial Orthopedics , 96 (2), 93-99. 23. Arneberg, P., Giertsen, E., & Emberland, H. (1997). Intra-oral variations in total plaque fluoride related to plaque pH. A study in orthodontic patients. Caries Research , 31, 451-456. 24. Ogaard, B. (2008). White Spot Lesions During Orthodontic Treatment: Mechanisms and Fluoride Preventice Aspects. Seminars in Orthodontics , 14 (3), 183-193. 25. Skrtic, D., Antonucci, J. M., & Eanes, E. D. (2003). Amorphous Calcium Phosphate-Based Bioactive Polymeric Composites for Mineralized Tissue Regeneration. Journal of Research of the National Institute of Standards and Technology , 108 (3), 167-182. 26. Reynolds, E., Cain, C., Webber, E., Black, C., Riley, P., Johnson, I., et al. (1995). Anticariogenicity of Calcium Phosphate Complexes of Tryptic Casein Phosphopeptides in the Rat. Journal of Dental Research , 74, 1272-1279. 27. Reynolds, E. (1997). Remineralizaiton of Enamel Subsurface Lesions by Casein Phosphopeptide-stabilized Calcium Phosphate Solutions. Journal of Dental Research , 76 (9), 1587-1595. 28. Reynolds, E. (1998). Anticariogenic complexes of amorphous calcium phosphate stabilized by casein phosphopeptides. A review. Spec Care Dentist , 18 (1), 8-16.

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29. Shen, P., Cai, F., Nowicki, A., Vincent, J., & Reynolds, E. (2001). Remineralization of Enamel Subsurface Lesions by Sugar-free Chewing Gum Containing Casein Phosphopeptide-Amorphous Calcium Phospate. Journal of Dental Research , 80 (12), 2066-2070. 30. Reynolds, E., Cai, F., Shen, P., & Walker, G. (2003). Retention in Plaque and Remineralization of Enamel Lesions by Various Forms of Calcium in a Mouthrinse or Sugar-free Chewing Gum. Journal of Dental Research , 82 (3), 206-211. 31. Skrtic, D., Hailer, A., Takagi, S., Antonucci, J., & Eanes, E. (1996). Quantitative Assessment of the Efficacy of Amorphous Calcium Phosphate/Methacrylate Composites in Remineralizing Caries-like Lesions Artificially Produced in Bovine Enamel. Journal of Dental Research , 75 (9), 1679-1686. 32. Langhorst, S., O'Donnell, J., & Skrtic, D. (2009). In vitro remineralization of enamel by polymeric amorphous calcium phosphate composite: Quantitative microradiographic study. Dental Materials , 25 (7), 884-891. 33. Xu, H. H., Weir, M. D., & Sun, L. (2008). Calcium and phosphate ion releasing composite: Effect of pH on release and mechanical properties. Dental Materials , doi:10.1016/j.dental.2008.10.009. 34. Regnault, W. F., Icenogle, T. B., Antonucci, J. M., & Skrtic, D. (2007). Amorphous calcium phosphate/urethane methacrylate resin composites. Journal of Materials Science: Materials in Medicine , doi:10.1007/s10856-007-3178-3. 35. Skrtic, D., & Antonucci, J. (2007). Dental Composites Based on Amorphous Calcium Phosphate - Resin Composition/Physiochemical Properties Study. J Biomater Appl , 21 (4), 375-393. 36. Park, M. S., Eanes, E. D., Antonucci, J. M., & Skrtic, D. (1998). Mechanical properties of bioactive amorphous calcium phosphate/methacrylate composites. Dental Materials , 14, 137-141. 37. Skrtic, D., Antonucci, J. M., & Eanes, E. D. (1996). Improved properties of amorphous calcium phosphate fillers in remineralizing resin composites. Dental Materials , 12 (5), 295-301. 38. Skrtic, D., Antonucci, J. M., Eanes, E. D., Eichmiller, F. C., & Schumacher, G. E. (2000). Physiochemical Evaluation of Bioactive Polymeric Composites Based on Hybrid Amorphous Calcium Phosphates. J. Biomed. Mat. Res., Applied Biomaterials , 53 (4), 381-391. 39. Dunn, W. (2007). Shear bond strength of an amorphous calcium-phosphate-containing orthodontic resin cement. American Journal of Orthodontics and Dentofacial Orthopedics , 131 (2), 243-247.

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40. Foster, J. A., Berzins, D. W., & Bradley, T. G. (2008). Bond Strength of an Amorphous Calcium Phosphate-Containing Orthodontic Adhesive. The Angle Orthodontist , 78 (2), 339-344. 41. Tavas, M. A., & Watts, D. C. (1984). A visible light activated direct bonding material: an in vitro comparative study. British Journal of Orthodontics , 11, 33-37. 42. Reynolds, I. R. (1975). A review of direct orthodontic bonding. British Journal of Orthodontics , 2, 171-178. 43. Willmot, D. (2008). White Spot Lesions After Orthodontic Treatment. Seminars in Orthodontics , 14 (3), 209-219. 44. Van Noort, R. (2002). Resin Composites and Polyacid-Modified Resin Composites. In Introduction to Dental Materials (2 ed., pp. 96-106). Elsevier Health Sciences. 45. Brantley, W., & Eliades, T. (2001). Orthodontic Materials. New York: Thieme Stuttgart. 46. Linklater, R., & Gordon, P. (2003). Bond failure patterns in vivo. American Journal of Orthodontics and Dentofacial Orthopedics , 123 (5), 534-539.

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GENERAL CONCLUSIONS

The aim of the present study was to evaluate the shear bond strength of an

ACP filled composite resin designed to provide protection against

demineralization around orthodontic brackets. The study also measured the depth

of enamel demineralization around an orthodontic bracket when subjected to a

continuous acid assault. The results showed that the enamel lesion depth adjacent

to the ACP filled resin was reduced by 29.82% over the lesion depth adjacent to a

traditional composite resin bracket adhesive. The mean shear bond strength

associated with Aegis Ortho was significantly lower than the traditional

composite resin control. The increased release of ACP-filler at low pH does not

significantly reduce the mean shear bond strength of the material. Since bond

failure rates are typically low in the anterior, orthodontists may consider bonding

maxillary anterior teeth with an ACP filled composite resin for increased WSL

protection on at risk patients where compliance issues are anticipated.

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GENERAL LIST OF REFERENCES 1. Shaw, W. C., Rees, G., Dawe, M., & Charles, C. R. (1985). The influence of dentofacial appearance on the social attractiveness of young adults. American Journal of Orthodontics and Dentofacial Orthopedics , 87 (1), 21-26. 2. Sarver, D., & Ackerman, M. (2003). Dynamic smile visualization and quantification. American Journal of Orthodontics and Dentofacial Orthopedics , 124, 4-12. 3. Summitt, J. B., Robbins, J. W., Schwartz, R. S. (2006). Fundamentals of Operative Dentistry: A Contemporary Approach (3rd edition). 2-4. 4. Gorelick, L., Geiger, A. M., & Gwinnett, A. J. (1982). Incidence of white spot formation after bonding and banding. American Journal of Orthodontics and Dentoficial Orthopedics , 81 (2), 93-98. 5. Boersma, J. G., van der Veen, M. H., Lagerweij, M. D., Bokhout, B., & Prahl-Andersen, B. (2005). Caries prevalence measured with QLF after treatment with fixed orthodontic appliances: influencing factors. Caries Research , 39 (1), 41-47. 6. Chadwick, B. L., Roy, J., Knox, J., & Treasure, E. T. (2005). The effect of topical fluorides on decalcification in patients with fixed orthodontic appliances: A systematic review. American Journal of Orthodontics and Dentofacial Orthopedics , 128 (5), 601-606. 7. Todd, M. A., Staley, R.N., Kanellis, M.J., Donly, K.J., & Wefel, J.S. (1999). Effect of a fluoride varnish on demineralization adjacent to orthodontic brackets. American Journal of Orthodontics and Dentofacial Orthopedics , 116 (2), 159-167. 8. Gwinnett, A., & Ceen, R. (1979). Plaque distribution on bonded brackets: A scanning microscope study. American Journal of Orthodontics and Dentofacial Orthopedics , 75 (6), 667-677. 9. Lim, B. S., Lee, S. J., Lee, J. W., Ahn, S. J. (2008). Quantitative analysis of adhesion of cariogenic streptococci to orthodontic raw materials. American Journal or Orthodontics and Dentofacial Orthopedics , 133 (6), 882-888. 10. Sukontapatipark, W., El-Agroudi, M. A., Selliseth, N. J., Thunold, K., & Selvig, K. A. (2001). Bacterial colonization associated with fixed orthodontic applances. A scanning electron microscope study. European Journal of Orthodontics , 23, 475-484. 11. Bishara, S., & Ostby, A. (2008). White Spot Lesions: Formation, Prevention, and Treatment. Seminars in Orthodontics , 14 (3), 174-182.

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12. Scheie, A., Arneberg, P., & Krogstad, O. (1984). Effect of orthodontic treatment on prevalance of Streptococcus mutans in plaque and saliva. Scand Journal of Dental Research , 92, 211-217. 13. Weinstein, P., Milgram, P., Melnich, S., Beach, B., & Spadofora, A. (1989). How effective is oral hygeine instruction? Results after 6 and 4 weeks. Journal of Public Health Dentistry , 49 (1), 32-38. 14. Arneberg, P., Giertsen, E., & Emberland, H. (1997). Intra-oral variations in total plaque fluoride related to plaque pH. A study in orthodontic patients. Caries Research , 31, 451-456. 15. Ogaard, B., Rolla, G., & Arends, J. (1988). Orthodontic appliances and enamel demineralization. Part 1. Lesion development. American Journal of Orthodontics and Dentofacial Orthopedics , 94, 68-73. 16. Machen, D. (1989). Legal Aspects of Orthodontic Practice: Risk Management Concepts. American Journal Orthodontics and Dentofacial Orthopedics , 96 (2), 173-175. 17. Weijden, G. A., Timmerman, M. R., Reijerse, E., Danser, M. M., Mantel, M. S., & Velden, N. U. (2005). The long-term effect of an oscillating/rotating electric toothbrush on gingivitis An 8-month clinical study. Journal of Clinical Periodontology , 21 (2), 139-145. 18. Barnes, C.M., Russell, C. M., Reinhardt, R. A., Payne, J. B., Lyle, D. M. (2005). Comparison of Irrigation to Floss as an Adjunct to Toothbrushing: Effect of Bleeding, Gingivitis, and Supragingival Plaque. Journal of Clinical Dentistry , 16, 71-77. 19. Sharma, N. C., Lyle, D. M., Qaqish, J. G., Galustians, J. & Schuller, R. (2008). Effect of a dental water jet with orthodontic tip on plaque and bleeding in adolescent patients with fixed orthodontic appliances. American Journal of Orthodontics and Dentofacial Orthopedics , 133 (4), 565-571. 20. Ogaard, B. (2008). White Spot Lesions During Orthodontic Treatment: Mechanisms and Fluoride Preventice Aspects. Seminars in Orthodontics , 14 (3), 183-193. 21. Moura, M. S., de Melo Simplicio, A. H., & Cury, J. A. (2006). In-vivo effects of fluoridated antiplaque dentifrice and bonding material on enamel demineralization adjacent to orthodontic appliances. American Journal of Orthodontics and Dentofacial Orthopedics , 130 (3), 357-363. 22. O'Reilly, M., & Featherstone, J. (1987). Demineralization and remineralization around orthodontic appliances: an in vivo study. American Journal of Orthodontics and Dentofacial Orthopedics , 92, 33-40.

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23. Benson, P. E., Shah, A. A., Millett, D. T., Dyer, F., Parkin, N., & Vine, R. S. (2005). Fluorides, orthodontics and demineralizatiion: a systematic review. Journal of Orthodontics , 32, 102-114. 24. Geiger, A. M., Gorelick, L., Gwinnett, A. J., & Benson, B. J. (1992). Reducing white spot lesions in orthodontic populations with fluoride rinsing. American Journal of Orthodontics and Dentofacial Orthopedics , 101 (5), 403-407. 25. Boskey, A. L. (1997). Amorphous Calcium Phosphate: The Contention of Bone. Journal of Dental Research , 76, 1433-1436. 26. Skrtic, D., Hailer, A., Takagi, S., Antonucci, J., & Eanes, E. (1996). Quantitative Assessment of the Efficacy of Amorphous Calcium Phosphate/Methacrylate Composites in Remineralizing Caries-like Lesions Artificially Produced in Bovine Enamel. Journal of Dental Research , 75 (9), 1679-1686. 27. Reynolds, E. (1997). Remineralizaiton of Enamel Subsurface Lesions by Casein Phosphopeptide-stabilized Calcium Phosphate Solutions. Journal of Dental Research , 76 (9), 1587-1595. 28. Reynolds, E., Cain, C., Webber, E., Black, C., Riley, P., Johnson, I., et al. (1995). Anticariogenicity of Calcium Phosphate Complexes of Tryptic Casein Phosphopeptides in the Rat. Journal of Dental Research , 74, 1272-1279. 29. Reynolds, E. (1998). Anticariogenic complexes of amorphous calcium phosphate stabilized by casein phosphopeptides. A review. Spec Care Dentist , 18 (1), 8-16. 30. Shen, P., Cai, F., Nowicki, A., Vincent, J., & Reynolds, E. (2001). Remineralization of Enamel Subsurface Lesions by Sugar-free Chewing Gum Containing Casein Phosphopeptide-Amorphous Calcium Phospate. Journal of Dental Research , 80 (12), 2066-2070. 31. Reynolds, E., Cai, F., Shen, P., & Walker, G. (2003). Retention in Plaque and Remineralization of Enamel Lesions by Various Forms of Calcium in a Mouthrinse or Sugar-free Chewing Gum. Journal of Dental Research , 82 (3), 206-211. 32. Ogaard, B. (1996). Microradiography and confocal laser scanning microscopy applied to enamel lesions formed in vivo with and without fluoride varnish treatment. European Journal of Oral Science , 378-383. 33. Demito, C., Vivaldi-Rodrigues, G., Ramos, A.L., & Bowman, S.J. (2004). The efficacy of a fluoride varnish in reducing enamel demineralization adjacent to orthodontic brackets: an in vitro study. Orthodontic Craniofacial Research, 7, 205-210.

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34. Winderoth, C. J., Weinstein, M., & Borislow, A. J. (1999). Effectiveness of a fluoride releasing sealant in reducing decalcification during orthodontic treatment. American Journal of Orthodontics and Dentofacial Orthopedics , 116 (6), 629-634. 35. Soliman, M., Bishara, S. E., Wefel, J., Heilman, J., Warren, J. (2006). Fluoride release from an orthodontic sealant and its clinical implication. Angle Orthodontist , 76 (2), 282-288. 36. Hu, W., & Featherstone, J. (2005). Prevention of enamel demineralization: An in-vitro study using light-cured filled sealant. American Journal of Orthodontics and Dentofacial Orthopedics , 128 (5), 592-600. 37. Buren, J. L., Staley, R. N., Wefel, J., & Qian, F. (2008). Inhibition of enamel demineralization by an enamel sealant, Pro Seal: An in-vitro study. American Journal of Orthodontics and Dentofacial Orthopedics , 133 (4), S88-S94. 38. Millet, D. T., Nunn, J. H., Welbury, R. R., & Gordon, P. H. (1999). Decalcification in relation to brackets bonded with glass ionomer cement or a resin adhesive. Angle Orthodontist , 69 (1), 65-70. 39. Miller, J. R., Mancl, L., Arbuckle, G., Baldwin, J., & Phillips, R. W. (1996). A three-year clinical trial using a glass ionomer cement for the bonding of orthodontic brackets. Angle Orthodontist , 66 (4), 309-312. 40. Miguel, J. A., Almeida, M. A., & Chevitarese, O. (1995). Clinical comparison between a glass ionomer cement and a composite for direct bonding of orthodontic brackets. American Journal of Orthodontics and Dentofacial Orthopedics , 107 (5), 484-487. 41. Klockowski, R., Davis, E. L., Joynt, R. B., Wiezkowski, G., & MacDonald, A. (1989). Bond strength and durability of glass ionomer cements used as bonding agents in the placement of orthodontic brackets. American Journal of Orthodontics and Dentofacial Orthopedics , 96 (1), 60-64. 42. Cacciafesta, V., Sfondrini, M. F., Barina, E., Scribante, A., Garino, F., Klersy, C. (1998). Effects of saliva and water contamination on the enamel shear bond strength of a light cured glass ionomer cement. American Journal of Orthodontics and Dentofacial Orthopedics , 113 (4), 402-407. 43. Coupes-Smith, K. S., Rossouw, P. E., Titley, K. C., & Paedo, D. (2003). Glass ionomer cements as luting agents for orthodontic brackets. Angle Orthodontist , 73 (4), 436-444. 44. McCourt, J. W., Cooley, R. L., & Barnwell, S. (1991). Bond strength of light-cured fluoride-releasing base-liners as orthodontic bracket adhesives. American Journal of Orthodontics and Dentofacial Orthopedics , 100 (1), 47-52.

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45. Gorton, J., Featherstone, J. (2003). In vivo inhibition of demineralization around orthodontic brackets. American Journal of Orthodontics and Dentofacial Orthopedics , 123 (1), 10-14. 46. Sudjalim, T. R., Woods, M. G., Manton, D. J., & Reynolds, E. C. (2007). Prevention of demineralization around orthodontic brackets in vitro. American Journal of Orthodontics and Dentofacial Orthopedics , 131 (6), 705e1-705e9. 47. Millett, D. T., McCluskey, L. A., McAuley, F., Creanor, S. L., Newell, J., & Love, J. (2000). A Comparative Clinical Trial of a Compomer and a Resin Adhesive for Orthodontic Bonding. Angle Orthodontist , 70 (3), 233-240. 48. Sonis, A. L., & Snell, W. (1989). An evaluation of a fluoride-releasing, visible light-activated bonding system for orthodontic bracket placement. American Journal of Orthodontics and Dentofacial Orthopedics , 95 (4), 306-311. 49. Underwood, M. L., Rawis, H. R., Zimmerman, B. F. (1989). Clinical evaluation of a fluoride-exchanging resin as an orthodontic adhesive. American Journal of Orthodontics and Dentofacial Orthopedics , 96 (2), 93-99. 50. Derks, A., Katsaros, C., Frencken, J.E., van’t Hof, M.A., & Kuijpers-Jagtman, A.M. (2004). Caries-Inhibiting Effect of Preventive Measures during Orthodontic Treatment with Fixed Appliances. Caries Research , 38, 413-420. 51. Xu, H. H., Weir, M. D., & Sun, L. (2008). Calcium and phosphate ion releasing composite: Effect of pH on release and mechanical properties. Dental Materials , doi:10.1016/j.dental.2008.10.009. 52. Regnault, W. F., Icenogle, T. B., Antonucci, J. M., & Skrtic, D. (2007). Amorphous calcium phosphate/urethane methacrylate resin composites. Journal of Materials Science: Materials in Medicine , doi:10.1007/s10856-007-3178-3. 53. Skrtic, D., & Antonucci, J. (2007). Dental Composites Based on Amorphous Calcium Phosphate - Resin Composition/Physiochemical Properties Study. J Biomater Appl , 21 (4), 375-393. 54. Skrtic, D., Antonucci, J. M., & Eanes, E. D. (1996). Improved properties of amorphous calcium phosphate fillers in remineralizing resin composites. Dental Materials , 12 (5), 295-301. 55. Skrtic, D., Antonucci, J. M., Eanes, E. D., Eichmiller, F. C., & Schumacher, G. E. (2000). Physiochemical Evaluation of Bioactive Polymeric Composites Based on Hybrid Amorphous Calcium Phosphates. J. Biomed. Mat. Res., Applied Biomaterials , 53 (4), 381-391.

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56. Langhorst, S., O'Donnell, J., & Skrtic, D. (2009). In vitro remineralization of enamel by polymeric amorphous calcium phosphate composite: Quantitative microradiographic study. Dental Materials , 25 (7), 884-891. 57. Park, M. S., Eanes, E. D., Antonucci, J. M., & Skrtic, D. (1998). Mechanical properties of bioactive amorphous calcium phosphate/methacrylate composites. Dental Materials , 14, 137-141. 58. Skrtic, D., Antonucci, J. M., & Eanes, E. D. (2001). Effect of the Monomer and Filler Systems on the Remineralizing Potential of Bioactive Dental Composites Base on Amorphous Calcium Phosphate. Polymers for Advanced Technologies , 12, 369-379. 59. Skrtic, D., Antonucci, J. M., & Eanes, E. D. (2003). Amorphous Calcium Phosphate-Based Bioactive Polymeric Composites for Mineralized Tissue Regeneration. Journal of Research of the National Institute of Standards and Technology , 108 (3), 167-182. 60. Dunn, W. (2007). Shear bond strength of an amorphous calcium-phosphate-containing orthodontic resin cement. American Journal of Orthodontics and Dentofacial Orthopedics , 131 (2), 243-247. 61. Foster, J. A., Berzins, D. W., & Bradley, T. G. (2008). Bond Strength of an Amorphous Calcium Phosphate-Containing Orthodontic Adhesive. The Angle Orthodontist , 78 (2), 339-344. 62. Uysal, T., Ulker, M., Akdogan, G., Ramoglu, S.I., & Yilmaz, E. (2008). Bond Strength of Amorphous Calcium Phosphate-Containing Orthodontic Composite Used as a Lingual Retainer Adhesive. The Angle Orthodontist , 79 (1), 117-121. 63. Tavas, M. A., & Watts, D. C. (1984). A visible light activated direct bonding material: an in vitro comparative study. British Journal of Orthodontics , 11, 33-37. 64. Reynolds, I. R. (1975). A review of direct orthodontic bonding. British Journal of Orthodontics , 2 (3), 171-178.