Ion release and in vitro enamel fluoride uptake associated
with pit
and fissure sealants containing microencapsulated remineralizing agents
Brant D. Burbank, bs, msob, Ryan L.
Cooper, bs, msob, Alyssa Kava, bs, Jennifer M. Hartjes, bs,
William A. McHale, bs, Mark A. Latta, bs, ms, dmd & Stephen
M. Gross, phd
Abstract: Purpose: To determine if pit-and-fissure
sealants with microencapsulated remineralizing agents
with sustained release of fluoride, calcium and phosphate ions could promote
enamel fluoride uptake by demineralized tooth structure. Methods: Sealants that contained 5 w/w% microcapsules with aqueous solutions of 5M Ca(NO3)2 or 0.8M NaF or 6.0M K2HPO4 or a mixture of all three were prepared.
Ion release profiles were measured as a function of time. Enamel fluoride
uptake by demineralized tooth structure was
determined. Results: Sustained
release of fluoride, calcium and phosphate ions from a sealant was
demonstrated. Fluoride uptake by demineralized enamel
was significantly increased compared to a control sealant manufactured without
microcapsules (P< 0.01). Bovine enamel that contained 2.2±2.1 μg F/g of enamel prior to exposure to a sealant
without microcapsules had 2.3±0.5 after 90 days. Enamel exposed to sealant with
5w/w% NaF microcapsules went from 3.5±3.5 μg F/g of enamel prior to exposure to 148±76 after 90
days. Enamel exposed to sealant with 2 w/w% NaF, 2
w/w% Ca(NO3)2 and 1 w/w% K2HPO4 microcapsules went from 1.7±0.7 μg F/g of enamel
prior to exposure to 190±137 after 90 days. (Am J Dent 2017;30:59-64).
Clinical significance: Sealants with encapsulated remineralizing agents were capable of releasing
biologically available fluoride, calcium, and phosphate ions. Incorporation of
these microcapsules in pit and fissure sealants is a promising method for remineralization determined by enamel fluoride uptake
measurements.
Mail: Dr.
Stephen Gross, School of Dentistry, Creighton University, 2500 California
Plaza, Omaha, NE 68178, USA. E-mail: stephengross@creighton.edu
Light energy transmission and Vickers hardness ratio
of bulk-fill resin
based composites at different thicknesses cured by a dual-wave or a
single-wave light curing unit
Ario Santini, md, bds, dds, phd, Reem Khalil Naaman, bds, mclindent & Mohammed Saeed Aldossary, bds, mclindent
Abstract: Purpose: To quantify light energy
transmission through two bulk-fill resin-based composites and to measure the
top to bottom surface Vickers hardness ratio (VHratio)
of samples of various incremental thicknesses, using either a single-wave or
dual-wave light curing unit (LCU). Methods: Tetric EvoCeram Bulk
Fill (TECBF) and SonicFill (SF) were studied. Using
MARC-RC, the irradiance delivered to the top surface of the samples 2, 3, 4 and
5 mm thick (n= 5 for each thickness) was adjusted to 800 mW/cm2 for 20 seconds (16 J/cm2) using either a single-wave, Bluephase or a dual-wave, Bluephase G2 LCUs. Light energy transmission through to the bottom surface of the
specimens was measured at real time using MARC-RC. The Vickers hardness (VH)
was determined using Vickers micro hardness tester and the VHratio was calculated. Data were analyzed using a general linear model in Minitab 16;
ɑ= 0.05. Results: TECBF was
more translucent than SF (P< 0.05). The mean VHratio was higher than 80% in 2, 3 and 4 mm increment thickness for both materials
(except for 4 mm TECBF when cured with the dual-wave Bluephase G2). SF showed significantly higher VH ratio than TECBF at all different
thickness levels (P< 0.05), except at the 2 mm level (P> 0.05). TECBF
showed significantly greater VH ratio when cured with the single-wave Bluephase than when using the dual-wave Bluephase G2 (P< 0.05). (Am J Dent 2017;30:65-70).
Clinical significance: The transmission of light energy
through to the bottom surface and the VHratio are
material dependent. Although TECBF is more translucent than SF, it showed lower VHratio compared to SF when cured with dual-wave Bluephase G2.
Mail: Dr. Mohammed Saeed
Aldossary, P.O.Box 13743 Riyadh 11414, Saudi Arabia.
E-*: msfd99@hotmail.com
Effect of oxygen inhibition in universal adhesives
on dentin bond durability
and interfacial characteristics
Akimasa Tsujimoto, dds, phd, Wayne W. Barkmeier, dds, ms, Toshiki Takamizawa, dds, phd,
Mark A. Latta, dmd, ms & Masashi Miyazaki, dds, phd
Abstract: Purpose: To evaluate the effects of
oxygen inhibition of universal adhesive on dentin bond durability and
interfacial characteristics. Methods: The
three universal adhesives used were Scotchbond Universal Adhesive, Prime & Bond Elect, and G-Premio Bond. Shear bond strength (SBS) and shear fatigue strength (SFS) of resin
composite bonded to adhesive with and without an oxygen inhibited layer (OIL)
on dentin using total-etch and self-etch modes were determined. Surface free
energy (SFE) and SFE parameters of cured adhesive with and without an OIL on dentin using total-etch and self-etch modes were
also measured by the sessile drop method. Results: The presence of an OIL in universal adhesives promoted higher SBS and SFS
regardless of etching mode. In addition, regardless of adhesive type and
etching modes, the specimens with an OIL showed a
higher ratio of SFS/SBS than those without an OIL. Further, the SFEs,
especially total SFE, polarity force and hydrogen bonding force, of cured
adhesives with an OIL were significantly higher than
those without an OIL. (Am J Dent 2017;30:71-76).
Clinical significance: The present findings indicated
that the oxygen inhibition of universal adhesive did not impair the dentin bond
durability and interfacial characteristics of the adhesive.
Mail: Dr. A. Tsujimoto,
1-8-13 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-8310, Japan; E-mail:
tsujimoto.akimasa@nihon-u.ac.jp
A global approach to assess the economic benefits of
increased consumption
of sugar-free chewing gum
Reinhard Rychlik, md, phd, phd, Fabian Kreimendahl, msc, Cornelia
Blaich, dmd, Hanny Calache, phd, mdsc,
Franklin Garcia-Godoy, dds, ms, phd, phd, Elizabeth Kay, bds,
mph, phd, Yan Si, phd, David Zilberman, phd
& Stefan Zimmer, dds, mphd, phd
Abstract: Purpose: To analyze the influence of increasing the average
consumption of sugar-free gum (SFG) in 25 industrialized countries on dental
expenditures due to caries by the national health care systems. It was assumed
that large cost savings were possible, because the regular consumption of SFG
significantly reduces the relative risk of caries and therefore, improves
dental health, which reduces expenditures on dental treatments. Methods: A budget impact analysis (BIA)
was performed to model the decrease in the relative risk of caries and the
subsequent cost savings for dental care. Annual consumption of SFG, dental
expenditures due to caries, chewing frequencies by age groups and the relative
risk reduction for caries due to the consumption of SFG were identified and
used as model parameters. Three different scenarios for the increase in the
number of SFG were calculated. Besides overall results for all countries
together, analyses were conducted for countries grouped by regions and the
Human Development Index (HDI). Results:
For the entity of all 25 analyzed countries together, possible annual cost
savings range from US$805.77 M in the scenario with the lowest increase of SFG
consumption up to US$18,248 billion in the scenario with the biggest increase
of SFG consumption. Europe and the USA show potential cost savings of US$1,061
billion and US$2,071 billion per year, respectively, if all chewers increase
their consumption of SFG by 1 piece per day. The analysis showed the potential
cost savings in dental expenditures due to caries that can be achieved by only
slightly increasing the consumption of SFG. The regular consumption of SFG
cannot replace good dental hygiene like tooth brushing, but can have a significant
impact on dental health, which can lead to increased cost savings for health
care systems worldwide. (Am J Dent 2017;30:77-83).
Clinical significance: Based on
the fact that a regular consumption of sugar-free chewing gum has the
beneficial effect of reducing caries prevalence, an increased consumption may
not only lead to improved dental health but significant cost savings in
expenditures for dental treatment worldwide.
Mail: Dr. Reinhard Rychlik, Institute of
Empirical Health Economics, Am Ziegelfeld 28, D-51399 Burscheid, Germany. E-mail: reinhard.rychlik@ifeg.de
Effects of desensitizing agents for cervical dentin
hypersensitivity:
A randomized clinical trial
Kyeong-Hwan Han, dmd, msc, Ju-Hee Hong, dh, msc, Joo-Hee Shin, dds, msc, phd, Jeong-Yol Lee, dmd, msc, phd
& Sang Wan Shin, dds, mph, phd, msc
Abstract: Purpose: To evaluate the clinical efficacy of five commercially
available desensitizing agents with different mechanisms applied to
hypersensitive teeth. Methods: A
randomized clinical trial was conducted on subjects suffering dentin
hypersensitivity in Korea University Guro Hospital
from October 2013 to April 2015. A total of 64 subjects met the selection
criteria and were randomly assigned to five commercially available
desensitizing agents, and applied according to the manufacturers’ instructions.
Before and after application of desensitizing agents, subjects were evaluated
with the Visual Analogue Scale (VAS) at baseline, 1 week, 1 month and 3 months.
The difference between the degree of reduction of
hypersensitivity in relation to time were evaluated with the repeated-measures
ANOVA (P< 0.05). Results: Practitioner and subject-measured VAS values at 1 week, 1 month and 3 months
showed a significant difference in all products compared with the first visit.
On the other hand, no statistically significant differences
between the products was shown. Desensitizing agents used in this
clinical trial relieved dentin hypersensitivity up to 3 months. (Am J Dent 2017;30:84-88).
Clinical significance: The five
tested desensitizing agents with different mechanisms were clinically effective
in relieving dentin hypersensitivity up to 3 months and showed statistically
significant pain reduction when compared to baseline scores.
Mail: Dr.
Sang Wan Shin, Department of Prosthodontics,
Institute for Clinical Dental Research, Korea University Medical Center, Korea
University, 97, Guro-Dong, Guro-Ku,
Seoul, Korea, 152-703. E-mail: swshin@korea.ac.kr
Antibiotic prophylaxis for
preventing dental implant failure and postoperative infection: A
systematic review of randomized controlled trials
Zhuogeng Chen, dds, msc, Donghui Chen, dds, msc, Shangwei Zhang, dds, msc, Li
Tang, dds, phd & Qiuying Li, dds, msc
Abstract: Purpose: To investigate whether
prophylactic antibiotics are beneficial on patients undergoing routine dental
implant placement procedures and to investigate which administration regimen is
the most effective. Methods: The
primary outcome was implant failure; the secondary outcome was postoperative
infection. In the fixed-effects model, the Mantel-Haenszel method was used to calculate pooled relative risks (RRs) at 95% confidence
intervals (CIs). To determine the outcomes, the quality of available evidence
was assessed using the Grading of Recommendations Assessment, Development, and
Evaluation (GRADE). Results: Prophylactic
antibiotics significantly decreased the incidence of implant failure (RR, 0.29;
95% CI, 0.15-0.55; P= 0.0002; I2= 0%)
but did not decrease infection. There was no statistically significant
difference between single preoperative antibiotics (SPA) and preoperative and
postoperative antibiotics (PPA) while treating patients with dental implant
failure (RR, 1.07; 95% CI, 0.31-3.62; P= 0.92). No statistically significant
difference was observed between SPA and PPA when prescribed to treat infection
postoperatively (RR, 1.05; 95% CI, 0.29-3.85; P= 0.94; I2= 0%). (Am J Dent 2017;30:89-95).
Clinical significance: The administration of
prophylactic antibiotics significantly reduced the failure of dental implants
under ordinary conditions. Furthermore, single preoperative antibiotics and
preoperative and postoperative antibiotics had similar effects on dental
implant failures and infections.
Mail: Dr. Li Tang, Department of
Implant Dentistry, Stomatology Hospital, Guangxi Medical
University, 10 Shuangyong Road, Nanning, Guangxi
530021, China. E-mail: gxtangli@163.com
Effect of different concentrations and application
times
of proanthocyanidin gels on dentin erosion
Ana Paula Boteon, dds, Anuradha Prakki, dds, ms, phd, Marília Afonso Rabelo Buzalaf, dds, ms, phd,
Daniela Rios, dds, ms, phd & Heitor
Marques Honório, dds, ms, phd
Abstract: Purpose: To analyze the effect of different concentrations and application times
of proanthocyanidin gels on dentin before an erosive
challenge in order to evaluate if there is a dose-response or application
time-response relationship in the use of these gels for erosion prevention. Methods: 80 bovine root dentin blocks
were randomly and equally divided into 10 groups and treated according to the
two factors under study (purified grape seed proanthocyanidin gel concentration and time of application): 0.05P1: 0.05% proanthocyanidin gel during 1 minute; 0.05P5: 0.05% proanthocyanidin gel during 5 minutes; 1P1: 1% proanthocyanidin gel
during 1 minute; 1P5: 1% proanthocyanidin gel during
5 minutes; 5P1: 5% proanthocyanidin gel during 1
minute; 5P5: 5% proantho-cyanidin gel during 5
minutes; 10P1: 10% proanthocyanidin gel during 1
minute; 10P5: 10% proanthocyanidin gel during 5
minutes; Control 1: placebo gel during 1 minute; and Control 5: placebo gel
during 5 minutes. The gels were applied over dentin blocks once before the
first erosive challenge. After that, the blocks were subjected to three erosive
cycles per day, during 5 days. Profilometry was used
to quantify the dentin loss (µm). Data were analyzed by two-way ANOVA and
Fisher's test (P< 0.05). Results: Statistical analysis showed that there was no significant difference between
the application times. The different concentrations of proanthocianidin gels presented similar results (P> 0.05). All tested gels resulted in
significantly less wear when compared to the placebo gel. (Am J Dent 2017;30:96-100).
Clinical significance: Grape seed proanthocyanidin gels could be considered as a promising therapy to diminish erosive dentin wear
because it may interact with the exposed collagen, enhancing the demineralized organic matrix stabilization, which acts as a
barrier against the diffusion of the acids from erosion.
Mail: Prof. Heitor Marques
Honório, Department of Pediatric Dentistry, Orthodontics and Public Health,
Bauru School of Dentistry, University of São Paulo (FOB-USP), Alameda Octávio Pinheiro Brisola, 9-75, Vila Universitária,
17012-901, Bauru, SP, Brazil. E-mail: heitorhonorio@usp.br
Antimicrobial action and long-term effect of
overnight denture cleansers
Amanda Peracini, dds, msc, phd, Ingrid
Machado Andrade, dds, msc, phd, Viviane Cristina Oliveira, msc,
Ana Paula Macedo, msc, phd, Claudia
Helena Silva-Lovato, dds, msc, phd, Valéria Oliveira Pagnano, dds, msc, phd, Evandro Watanabe, msc, phd & Helena de Freitas Oliveira Paranhos, dds, msc, phd,
Abstract: Purpose: To evaluate two denture
cleansers for overnight soaking (0.5% sodium hypochlorite and peroxide
alkaline) regarding efficacy against Candida spp. biofilms (randomized clinical trial) and their
effects on the physical properties of a denture base acrylic resin simulating a
period of 5 years of use (laboratory study). The Candida spp. were identified and their
resistance to main antifungal agents was evaluated. Methods: 32 complete denture wearers were instructed to brush their
dentures three times a day and to soak them (≥ 8 hours) in: control –
water (C); alkaline peroxide (AP); or 0.5% sodium hypochlorite (SH). According to a randomized sequence, each
solution was used for three alternate periods of 7 days. The antimicrobial
action was performed by counting the colony forming units (CFU) of Candida spp. For collection of the
biofilm, each upper complete denture was placed in a Petri dish, the internal
surface was brushed (Tek brush) with saline solution
for 2 minutes and the suspension was transferred to a test tube. After
dilutions (100 to 10-3), aliquots of 50 µL were seeded
inside Petri dishes containing Candida Chromagar.
After incubation, the colonies were counted and the values of CFU/mL calculated. Data were transformed in log10 (CFU
+1) and analyzed by the Friedman test (α= 0.05) followed by Wilcoxon and Bonferroni tests
(α= 0.05). Each of the different species identified perfunctorily has been
confirmed through the identification of yeasts kit. The resistance to
antifungal agents (amphotericin B, nystatin, flucytosine, econazole, ketoconazole, miconazole and fluconazole) was
also evaluated. Adverse effects were estimated on heat-polymerized resin
specimens, simulating a 5-year period of overnight use. Acrylic resin specimens
were randomly distributed into three groups: C: Control (distilled water), AP:
alkaline peroxide; and SH: 0.5% sodium hypochlorite. Color change, surface
roughness and flexural strength were evaluated at baseline and after immersion
procedures. Data were compared by Kruskall-Wallis
followed by Dunn’s test (color change and surface roughness) and one-way ANOVA
(flexural strength) (α= 0.05). Results: There was a reduction of Candida spp.
counts after using both solutions (AP and SH). The Candida spp. most often isolated was C. albicans, followed by the C. glabrata.
Only 24.7% of isolate strains were resistant to at least one of the tested antifungals, highlighting azole compounds. Immersion in AP [5.73 (5.45-5.91)] caused significantly higher color
change, with lower ΔE values for C [1.12 (1.15-1.37)] followed by SH [3.70
(3.51-3.98)]. The NBS values were classified as “slight” for C (1.12) group and
“considerable” for AP (5.27) and SH (3.40). No solution altered surface
roughness significantly. Flexural strength (in MPa)
was significantly lower for C (64.59), AP (63.96 ± 12.98) and SH (62.84 ± 8.62)
when compared to a group without any immersion (109.12 ± 8.37). (Am J Dent 2017:30:101-108).
Clinical significance: Both solutions tested presented
antimicrobial action against Candida spp. and may be useful for denture biofilm control, but should be used with
caution as an overnight immersion solution since they may damage denture bases
in the long-term. Candida was most
frequently isolated at baseline and after using the products. Only 24.7% of
isolate strains were resistant to at least one of the tested antifungals, especially with azole compounds.
Mail: Dr.
Helena de Freitas Oliveira Paranhos, Department of Dental Materials and
Prosthodontics, Ribeirão Preto Dental School, University of São Paulo, Avenida
do Café S/N, Ribeirão Preto, SP, CEP: 14040-904, Brazil. E-mail: helenpar@forp.usp.br
Comparison of nanofluoridated hydroxyapatite of varying fluoride content
for dentin tubule occlusion
Qinghua Yu, ms, Hongyan Liu, phd, Zhiguo Liu, phd, Yan Peng, PhD, Xiaoning Cheng,
ms, Ke Ma, ms & Yakun Ji, ms
Abstract: Purpose: To evaluate the viability of a series of nano-fluoridated hydroxyapatite (nano-FHA) formulations of varying fluoride content for the
occlusion of exposed dentin tubules, in comparison to nano-hydroxyapatite (nano-HA). Methods: Nano-FHA powders with varying levels of fluoride
ion were synthesized to substitute hydroxyl ions (–OH) present in hydroxyapatite (HA). Nano-FHA
were defined as 2nFHA,4nFHA,6nFHA, 8nFHA and 10nFHA,
with the molar ratio of F- to Ca2+ of
0.002,0.004,0.006,0.008 and 0.01, respectively. The powders were synthesized
using a wet chemistry route, and characterized by transmission electron
microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The methylthiazol tetrazolium (MTT) assay was used to assess cell viability toward nano-FHA.
According to the content of F-, the nano-nFHA and nano-HA powders were divided into six groups,
with the artificial saliva as control. They were spread over the dentin surface
for 1 minute and repeated three times per day for 7 consecutive days. After
washing and brushing with distilled water for an additional 7 days, scanning
electron microscopy was used to evaluate the in vitro plugging rate of the
tubules and penetrating depth. Results: The
2nFHA, 4nFHA, 6nFHA, 8nFHA and 10nFHA powders were prepared and characterized.
The 8nFHA had less crystallinity compared to 2nFHA,4nFHA, and 6nFHA.The MTT assay (from 12 to 120 hours)
showed that the cell viability of the L-929 fibroblasts in the 2nFHA, 4nFHA,
6nFHA, 8nFHA, 10nFHA, and nano-HA groups ranged from
80.54 ± 3.35% to 112.9 ± 4.8%. Most of the nano-FHA
powders successfully occluded dentin tubules. The plugging rate of 8nFHA was
significantly higher than that of the 2nFHA, 4nFHA, 6nFHA and nano-HA groups. The penetrating depth of the 8nFHA group
into the tubules was also significantly higher than that of the other nano-FHA and nano-HA group. (Am J Dent 2017;30:109-115).
Clinical significance: The nano-FHA
formulation 8nFHA showed higher plugging rate and penetrating depth into the
tubules. It has the potential to be used as a desensitizing agent in treating
dentin hypersensitivity with better long-term durability and efficacy of dentin
tubule occlusion.
Mail: Prof. Qinghua Yu, Department of Operative Dentistry and Endodontics, Guanghua School of Stomatology,
Sun Yat-sen University, Guangzhou 510055, P. R. China.
E-mail: yuqinghua1966@126.com