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Karnataka.
KARNATAKA, BENGALURU.
ANNEXURE II
Various methods are available for removal of excess proteins, Deproteinization is one such
process. Deproteinization is a process of elimination of organic substances from the enamel
surface before acid etching. It increases the resistance to orthodontic debonding by providing
better adhesion and better acid etching pattern on enamel. According to De-Deus et al. Sodium
hypochlorite (NaOCl) eliminates the organic matter present on the enamel surface by
dissolving it. By eliminating the organic substances from the enamel surface before etching
(deproteinization), orthodontic bond strength can theoretically be increased. .(2)
Enamel demineralization is a significant risk associated with orthodontic treatment when oral
hygiene is poor. Prevention of demineralization during orthodontic treatment is one of the
greatest challenges faced by clinicians despite modern advances in caries prevention.The
development of white spot lesions (WSLs) is attributed to prolonged plaque accumulation
around the brackets. (3)
This study is designed to compare and evaluate the effect of Deproteinization on shear bond
strength of orthodontic brackets in vitro using two different fluoridated adhesives.
REVIEW OF LITERATURE:
6.2
6.3 AIMS AND OBJECTIVES:
The main aim of the study is to evaluate the effect of enamel deproteinization on shear bond
strength and etch pattern.
Group I
37% H3PO4 (15 seconds)
In group I, the enamel surface of each tooth will be cleaned with a nonfluoridated prophylaxis
paste and rubber prophylactic cups for 10 seconds, will be rinsed, dried and etched with 37%
ortho-phosphoric acid (Prime Dental Products, India) for 15 seconds, rinsed with water for 15
seconds and then will be dried with oil-free air for 10 seconds until a frosty white appearance
is obtained.
In group II , the enamel surfaces of the premolars will be cleaned with a nonfluoridated
prophylaxis paste and rubber prophylactic cups for 10 seconds,will be rinsed, dried and
deproteinized with 5.25% NaOCl for 60 seconds using a micro-brush, followed by rinsing,
drying and acid etching with 37% phosphoric acid for 15 seconds. Subsequently, the acid will
be rinsed off, the enamel will be dried.
All samples will be coated with gold electrodepositing, using a sputtering effacoater and
prepared for surface Scanning Electron Microscope (SEM) analysis.The samples will be
subjected to SEM analysis and 5 microphotographs of each sample will be obtained at 500X
magnification and evaluated for the quality of etching pattern of the enamel
B
Other part of the study will be to evaluate the effect of deproteinization on shear bond strength,
60 human maxillary first premolars with no visible enamel defects extracted during routine
orthodontic treatment will be collected after taking consent from the patients. Any soft tissue,
calculus and/or bone remaining on the teeth are to be removed with an ultrasonic dental scaler.
Teeth will be stored in saline solution at 37°C. Each tooth will be polished with pumice and
rinsed with distilled water for 10 seconds
The samples will be divided into 3 groups, and 2 subgroups from each group. 10 samples in
each division.
In group 1, the enamel surface of each tooth will be cleaned with a nonfluoridated prophylaxis
paste and rubber prophylactic cups for 10 seconds, will be rinsed, dried and etched with 37%
ortho-phosphoric acid (Prime Dental Products, India) for 15 seconds, rinsed with water for 15
seconds and then dried with oil-free air for 10 seconds until a frosty white appearance is
obtained. Subsequently, the acid will be rinsed off, the enamel will be dried, a thin layer of
primer will be applied with a micro-brush, and light cured for 20 seconds.
In group 1a, Resin modified GIC will be placed on the bracket mesh covering the entire base of
the bracket, without bubbles or voids, and the bracket will then applied to the tooth using
sufficient force to produce a “flash” of excess adhesive around the bracket to ensure a uniform
thickness of adhesive.
In group 1b, Flouridated adhesive will be used to bond the bracket on to the tooth structure.
In group 2a, the enamel surfaces of the premolars will be cleaned with a nonfluoridated
prophylaxis paste and rubber prophylactic cups for 10 seconds, will be rinsed, dried and
deproteinized with 5.25% NaOCl for 30 seconds using a micro-brush, followed by rinsing,
drying and acid etching with 37% phosphoric acid for 15 seconds. Subsequently, the acid will
be rinsed off, the enamel will be dried, a thin layer of primer will be applied with a micro-
brush, and light cured for 20 seconds. The Resin modified GIC will then be placed on the
bracket for bonding whereas in 2b, Flouridated adhesive will be used for bonding
In group 3a, the enamel surfaces of the premolars will be cleaned with a nonfluoridated
prophylaxis paste and rubber prophylactic cups for 10 seconds, will be rinsed, dried and
deproteinized with 5.25% NaOCl for 30 seconds using a micro-brush, followed by rinsing,
drying and acid etching with 37% phosphoric acid for 15 seconds. Subsequently, the acid will
be rinsed off, the enamel will be dried, a thin layer of primer will be applied with a micro-
brush, and light cured for 20 seconds. The Resin modified GIC will then be placed on the
bracket for bonding whereas in 3b, Flouridated adhesive will be used for bonding.
Each tooth will be vertically mounted on self-cured acrylic blocks so that the crown is exposed
and the specimens will be ready for debonding.
7.3
DEBONDING PROCEDURE:
The embedded specimens would be secured in a jig attached to the base plate of a universal
testing machine (Instron instrument).
A chisel-edge plunger will be mounted in the movable crosshead of the testing machine and
positioned so that the leading edge would be aimed at enamel-adhesive interface. A crosshead
speed of 1 mm/min will be used and the maximum load necessary to debond the bracket is to
be recorded.
The force required to remove the brackets will be measured in Newtons (N) and SBS
(2MPa = 1 N/mm sq.) will be calculated by dividing the force values by the bracket base area.
7.4
FRACTURE ANALYSIS: After debonding procedure, the remnant adhesive on the enamel
surface are to be assessed under a stereomicroscope (SZ-40; Lawrence and Mayo) at 20X
magnification and the Modified Adhesive Remnant Index (ARI) (12) will be quantified.
7.5
STATISTICAL ANALYSIS
The SBS values will be tested with one-way analysis of variance ANOVA, and when the
results found are significant, multiple comparisons will be assessed with Weibull analysis,
Tukey’s Honestly Significant Difference test.
The Chi square will be used to determine significant differences in the ARI scores among the
groups.
7.6 Any other relevant test required during the data analysis time, will be done accordingly.
yes
REFERENCES
1.Pereira T, Jansen W, Pithon M, Souki B, Tanaka O, Oliveira D. Effects of enamel
deproteinization on bracket bonding with conventional and resin-modified glass ionomer
cements. Eur J Orthod. 2012;35(4):442-446.
2. Espinosa R, Valencia R, Uribe M, Ceja I., Saadia M. Enamel deproteinization and its effect
on acid etching: An in vitro Study. J Clin Pediatr Dent. 2008;33(1):13-19.
5. Gorelick L, Geiger A.M, Gwinnett A.J. Incidence of white spot formation after bonding and
banding. Am J Orthod.1982 Feb; 81(2):93-8.
6. Saroglu I., Aras S., Oztas D.,Effect of deproteinization on composite bond strength in
hypocalcified amelogenesis imperfecta. Oral Diseases. 2006;12(3):305-308.
11. Harleen N, Ramakrishna Y, Munshi A. Enamel Deproteinization Before Acid Etching and
its Effect on the Shear Bond Strength – An in vitro Study. J Clin Pediatr Dent. 2011;36(1):19-
24.
12. Bishara S.E, Gordan V .V, VonWald L, Jakobsen J.R. Shear bond strength of Composite,
glass ionomer, and acid primer adhesive. Am J Orthod Dentofacial Orthop 1999; 115:24-28.
9 SIGNATURE OF THE CANDIDATE
10 REMARKS OF GUIDE
11.1 SIGNATURE
11.3 SIGNATURE
11.5 SIGNATURE