Quality Resource Guide
l
Dentifrices and Mouthrinses to Reduce Plaque and Gingivitis 3rd Edition
3
www.metdental.com
Dentifrices
The systematic review
6
reported that seventeen
studies support the antiplaque and antigingivitis
effects of dentifrices containing 0.30 percent
triclosan/2.0
percent
Gantrez
copolymer.
Dentifrices with stannous fluoride had statistically
significant, but marginally clinically significant
evidence of an antiplaque effect; however, they
demonstrated both a statistically and clinically
significant antigingivitis effect. The review focused
on triclosan and stannous fluoride since these
are the two antiseptics that are most often sold in
dentifrices in the United States for the reduction of
plaque and gingivitis.
Triclosan
Triclosan is a broad-spectrum antimicrobial agent
that is marketed for use in oral products. In the
early 1990s, a new dentifrice containing 0.3%
triclosan, 2.0% polyvinylmethyl ether maleic acid
(PVM/MA) copolymer, and 0.243% sodium fluoride
in a silica base was introduced. The addition of the
copolymer to the dentifrice formulation allowed a
greater uptake and retention of triclosan to the
enamel and buccal epithelial cells than when
triclosan was formulated alone. This retention
provided a long-lasting effect that has been well
documented.
7
The product carries the ADA seal
and is approved by the FDA for the reduction of
plaque and gingivitis.
Triclosan/copolymer dentifrice, when
compared
to the placebo dentifrice, demonstrated plaque
reduction of up to 58.9% and gingivitis reduction
of up to 41.9%. No significant adverse effects
(including absence of development of bacterial
resistance) were noted in studies of up to
5 years duration.
8
Triclosan/copolymer dentifrice
also shows
the ability to significantly reduce
supragingival
calculus
formation
(23-57%),
with an average reduction of 37%).
9
Laboratory
studies suggest that, in addition to its antibacterial
activity, this product may also have an anti-
inflammatory effect.
10
Long-term studies suggest
that use of a triclosan/copolymer dentifrice may
be of benefit in stabilizing patients following
periodontal therapy.
8,11,12,13
Studies in humans do not support data from
studies in animals suggesting adverse effects of
triclosan on thyroid and reproductive functions.
It should be noted that doses used in the animal
studies were 10,000-1,000,000 times higher than
those levels found in humans. Further, no clinical
signs of toxicity or changes of various clinical
and biochemical parameters were found in a
study in which subjects brushed twice daily with
a triclosan containing dentifrice. Also, recently,
FDA reaffirmed the inclusion of triclosan in a
toothpaste.
14
A recent 6-months clinical trial
demonstrated the significant reduction of gingival
inflammation when using Colgate Total dentifrice
(triclosan/copolymer/fluoride).
15
Stannous Fluoride
Stannous fluoride was first introduced into the U.S.
market in the 1950s as an additive to dentifrices
aimed at reducing carious lesions. Later, due to
staining and taste issues, it was removed from
dentifrices and replaced by sodium fluoride or
sodium monofluorophosphate as an anti-caries
agent. Stannous fluoride was reformulated in
1997 into a dentifrice additive to reduce plaque
and gingivitis as well as caries activity. However,
the formulation was not successful in the U.S.
marketplace possibly because of problems with
tooth staining.
16
A more recent
formulation
reported
in
the
literature
is
a
dentifrice
containing 0.45% stannous fluoride and sodium
hexametaphosphate. Sodium hexametaphosphate
has been incorporated into the formulation to aid
in the control of calculus and extrinsic tooth
staining via inhibition of pellicle formation and
mineralization.
17
The product carries the ADA Seal
of Acceptance. Studies of this dentifrice have
demonstrated reductions in plaque accumulation
ranging up to 8.5% and reductions in gingivitis
ranging up to 26%. Evaluation of use of this
dentifrice by patients following periodontal therapy
suggests that gingivitis is reduced better than by
a sodium fluoride dentifrice. Tooth staining was
not reported in the most recent studies of this
formulation. Two studies showed that a stannous
fluoride dentifrice inhibited calculus formation
56%
better
than
a
Triclosan/co-polymer/
fluoride dentifrice and also reduced dentinal
hypersensitivity.
18,19
In their systematic review,
Hu
et al.
found that 0.454% stannous fluoride
provided relief from dentin hypersensitivity. The
authors evaluated studies from 2005-2015 that
were 2 to 8 weeks in duration.
20
Most recently
a new form of stannous fluoride stabilized with
zinc phosphate has been introduced into the
U.S. market and has also been found to be
effective in relief of dentin hypersentitivity.
21
Aside from tooth staining (when stannous fluoride
is used without sodium hexametaphosphate)
reported in some studies, no serious adverse
events have been reported following the use
of a stannous fluoride dentifrice. One study
compared a stannous fluoride dentifrice to a
triclosan/copolymer dentifrice and found the
reduction in Gingival Index to be better with
the stannous fluoride product.
22
Another study
compared the two dentifrices for effects on
periodontitis in patients with xerostomia and
found similar beneficial effects.
23
Most recently,
a stannous fluoride dentifrice that is stabilized
with zinc phosphate has been introduced.
24
This
new formulation has been rigorously tested
in
vitro and
through randomized clinical trials for
efficacy pertaining to reduction of oral microbial
flora,
25
control of dental biofilm and gingivitis,
26,27
stain reduction
28
and dentin hypersensitivity.
29
In view of its effect on micro-organisms not only
on biofilm on teeth and gingival tissue, it has also
been demonstrated to be effective against micro-
organisms on other oral surfaces. Therefore it has
been described as a dentifrice for maintenance of
whole mouth health.
24
Table 1
provides information on studies that have
been conducted with triclosan, and with stannous
fluoride.