The properties and applications of chlorhexidine in endodontics
The properties and applications of chlorhexidine inendodontics
Z. Mohammadi1,2 & P. V. Abbott31Department of Endodontics, School of Dentistry, Hamedan University of Medical Sciences, Hamedan, Iran; 2Iranian Centre forEndodontic Research (ICER); and 3School of Dentistry, University of Western Australia, Perth, WA, Australia
action of CHX, its antibacterial and antifungal activity,its effect on biofilm, its substantivity (residual antibac-
Mohammadi Z, Abbott PV. The properties and applications
terial activity), its tissue solvent ability, its interaction
of chlorhexidine in endodontics. International Endodontic Jour-
with calcium hydroxide and sodium hypochlorite, its
anticollagenolytic activity, its effect on coronal and
Microorganisms and their by-products are considered
apical leakage of bacteria, its toxicity and allergenicity
to be the major cause of pulp and periradicular
and the modulating effect of dentine and root canal
pathosis. Hence, a major objective in root canal
components on its antimicrobial activity. A Medline
treatment is to disinfect the entire root canal system,
search was performed from 1981 to the end of March
which requires that all contents of the root canal
2008 and was limited to English-language papers. The
system be eliminated as possible sources of infection.
keywords searched on Medline were ‘chlorhexidine
This goal may be accomplished using mechanical
AND endodontics’, ‘chlorhexidine AND root canal
instrumentation and chemical irrigation, in conjunc-
tion with medication of the root canal system between
‘chlorhexidine AND toxicity’. The reference lists of
treatment sessions. To reduce or eliminate bacteria,
each article were manually checked for additional
various irrigation solutions have been advocated.
Chlorhexidine is a cationic molecule, which can be
used during treatment. It has a wide range of antimi-
crobial activity. Its cationic structure provides a uniqueproperty named substantivity. The purpose of this
Received: 1 May 2008; accepted: 18 November 2008
paper is to review the structure and mechanism of
complicated task involving the use of various instru-
mentation techniques, irrigation regimens and intra-
The major causative role of microorganisms in the
canal medicaments. Mechanical instrumentation alone
pathogenesis of pulp and periapical diseases has clearly
does not result in a bacteria-free root canal system and
been demonstrated (Kakehashi et al. 1965, Mo¨ller et al.
when the complex anatomy of the root canal system
1981, Sundqvist 1992). The elimination of microor-
(Hess 1925) is considered, this is not surprising. On the
ganisms from infected root canal systems is a
other hand, ex vivo and clinical evidence has shownthat mechanical instrumentation leaves significantportions of the root canal walls untouched (Peters
Correspondence: Dr Zahed Mohammadi, Department of
et al. 2001) and complete elimination of bacteria by
Endodontics, Hamedan Dental School, Shahid Fahmideh
instrumentation alone is unlikely to occur (Bystro¨m &
Street, Hamedan, Iran (Tel.: +98 918 8729690; fax: +98351 6250344; e-mail: mohammadi_zahed@yahoo.com).
Sundqvist 1981). It is assumed, but not demonstrated,
Chlorhexidine in endodontics Mohammadi & Abbott
that any pulp tissue left in the root canals can serve as
a nutrient source for any remaining microorganisms. Furthermore, tissue remnants also impede the antimi-
Delany et al. (1982) evaluated 0.2% CHX-gluconate in
crobial effects of root canal irrigants and medica-
obtained before, during, immediately after and 24 h
disinfection is necessary to remove residual tissue
after instrumentation, irrigation and medication either
and to kill microorganisms. Chemical treatment of the
with CHX-gluconate or with sterile saline. There was a
root canal can be arbitrarily divided into irrigants,
highly significant reduction in the number of microor-
canal rinses and inter-appointment medicaments.
ganisms in the CHX-treated specimens after instrumen-
Chlorhexidine (CHX) is used widely as an endodontic
tation and irrigation. Basson & Tait (2001) compared
irrigant and medicament, but there has not been an
adequate review of the literature regarding CHX.
[Ca(OH)2], iodine potassium iodide (IKI) and a CHX
Hence, the purpose of this paper is to review different
solution in disinfecting root canal systems that were
aspects of CHX of relevance to endodontics. The
infected with Actinomyces israelii. The root canals were
literature review was performed using a Medline
exposed to either IKI, calcium hydroxide or 2% CHX for
electronic search. The search was performed from
periods of 3, 7 and 60 days. CHX was the only
1981 to the end of March 2008 and was limited to
disinfectant that was able to eliminate A. israelii from
English-language papers. The keywords searched on
all samples at all time periods whilst 25% of the
specimens treated with IKI and 50% of the specimens
‘chlorhexidine AND root canal therapy’, ‘chlorhexi-
treated with Ca(OH)2 still had viable A. israelii after
dine AND substantivity’ and ‘chlorhexidine AND
treatment. Onc¸ag˘ et al. (2003) evaluated the antibac-
toxicity’. The reference lists of each article were
terial properties of 5.25% sodium hypochlorite (NaOCl),
manually checked for additional articles of relevance.
2% CHX and 0.2% CHX plus 0.2% cetrimide [Cetrexidin(GABA Vebas, San Giuliano Milanese, Italy)] after5 min and 48 h in extracted human teeth after the
canals had been infected by Enterococcus faecalis. The
Chlorhexidine is a synthetic cationic bis-guanide that
2% CHX and Cetrexidin were significantly more effec-
consists of two symmetric 4-cholorophenyl rings and
tive against E. faecalis than the 5.25% NaOCl at both
two biguanide groups, connected by a central hexam-
time periods. Two studies (Gomes et al. 2001, Vianna
ethylene chain (Greenstein et al. 1986). CHX is a
et al. 2004) have investigated the ex vivo antimicrobial
positively charged hydrophobic and lipophilic molecule
activity against endodontic pathogens of three concen-
that interacts with phospholipids and lipopolysaccha-
trations (0.2%, 1% and 2%) of two forms of CHX (gel
rides on the cell membrane of bacteria and then enters
and liquid) and compared them with five concentra-
the cell through some type of active or passive
tions of NaOCl (0.5%, 1%, 2.5%, 4% and 5.25%). Both
transport mechanism (Athanassiadis et al. 2007). Its
the 2% gel and 2% liquid formulations of CHX
efficacy is because of the interaction of the positive
eliminated Staphylococcus aureus and Candida albicans
charge of the molecule and the negatively charged
within 15 s, whereas the gel formulation killed
phosphate groups on microbial cell walls (Gomes et al.
E. faecalis within 1 min. All of the tested irrigants
2003a,b), thereby altering the cells’ osmotic equilib-
eliminated Porphyromonas endodontalis, Porphyromonas
rium. This increases the permeability of the cell wall,
gingivalis and Prevotella intermedia within 15 s. The
which allows the CHX molecule to penetrate into the
time required for 1.0% and 2.0% CHX liquid to
bacteria. CHX is a base and is stable as a salt. The most
eliminate all microorganisms was the same as the time
common oral preparation, CHX gluconate, is water-
required for 5.25% NaOCl. These studies confirm that
soluble and at physiologic pH, it readily dissociates and
the antimicrobial action is related to the type, concen-
releases the positively charged CHX component (Green-
tration and presentation form of the irrigants as well as
stein et al. 1986). At low concentration (0.2%), low
the microbial susceptibility to the formulation used.
molecular weight substances, specifically potassium
Zamany et al. (2003) examined the effects of adding
and phosphorous, will leak out of the cell. On the other
a 2% CHX rinse to the conventional treatment protocol.
hand, at higher concentration (2%), CHX is bactericidal
Their results showed that cultivable bacteria were
as precipitation of the cytoplasmic contents occurs,
retrieved at the conclusion of the first visit in one of the
which results in cell death (Gomes et al. 2003a).
CHX cases, whereas seven of the 12 control cases
Mohammadi & Abbott Chlorhexidine in endodontics
without CHX showed growth; this difference was
Another interesting topic is the additive effect of CHX
statistically significant. Siqueira et al. (2007) compared
and hydrogen peroxide. Heling & Chandler (1998)
the effectiveness of 2.5% NaOCl and 0.12% CHX as
studied the antimicrobial effect of irrigant combinations
irrigants in reducing the cultivable bacteria in infected
within dentinal tubules ex vivo against E. faecalis and
root canal systems of teeth with apical periodontitis.
found that a specific combination of 3% hydrogen
They found that the two solutions had comparable
peroxide (H2O2) and CHX was superior in its antibac-
effects in eliminating bacteria and they suggested that
terial activity in dentine compared with other regi-
mens, such as CHX alone and NaOCl. Steinberg et al.
In a randomized clinical trial, Manzur et al. (2007)
(1999) challenged E. faecalis suspensions in trypticase
assessed the antibacterial efficacy of intracanal medi-
soy broth (a culture medium rich in peptides) with
cation with Ca(OH)2, 2% CHX gel and a combination of
various combinations of CHX and H2O2. The experi-
both [Ca(OH)2/CHX] in teeth with chronic apical
ments demonstrated that the combination of the two
periodontitis. Bacteriological samples were obtained
substances totally killed E. faecalis at concentrations
from the operative field and the root canals before and
much lower than that required for each component
after instrumentation in the first treatment session.
alone. According to that study, the bactericidal effect of
Further samples were taken from the canals at the
CHX is derived from its ability to denature the bacterial
commencement of the second appointment 1 week
cell wall whilst forming pores in the membrane,
later. They concluded that the antibacterial efficacies of
whereas H2O2 is effective against intracellular organ-
Ca(OH)2, CHX and a mixture of Ca(OH)2/CHX were
elles, such as DNA. Although the exact synergistic
mechanism of CHX and H2O2 is not known, it can be
Zerella et al. (2005) investigated the effect of a slurry
postulated that the exposure of bacteria to CHX leads to
of Ca(OH)2 mixed in aqueous 2% CHX versus aqueous
a more permeable cell wall that the H2O2 can easily
Ca(OH)2 alone on the disinfection of the root canal
penetrate and hence damage the intracellular organelles
system of root filled teeth that required root canal
(Steinberg et al. 1999). Shabahang et al. (2008) evalu-
re-treatment because the canals had become infected
ated the antibacterial efficacy of the substitution of CHX
again. Twelve (30%) of the 40 samples were positive for
for doxycycline in MTAD against a strain of E. faecalis
bacteria before root filling. The control medication
ex vivo. Findings showed that the presence of doxycycline
disinfected 12 (60%) of 20 teeth including two of four
in the concentration included in the MTAD formulation
teeth that had been originally diagnosed with entero-
was effective in eliminating E. faecalis. Furthermore, the
cocci. The experimental medication resulted in disinfec-
addition of 0.2% CHX did not adversely affect the
tion of 16 of 20 (80%) teeth at the beginning of the
antibacterial action of doxycycline. On the other hand,
third appointment. None of the teeth originally con-
the substitution of 0.2% CHX did not allow the same
taining enterococci showed remaining growth. They
disinfection efficacy on E. faecalis as MTAD.
concluded that a mixture of 2% CHX and a Ca(OH)2
On the whole, although studies comparing the
slurry is as efficacious as aqueous Ca(OH)2 on the
antibacterial effect of CHX and NaOCl have produced
disinfection of infected root filled teeth.
somewhat conflicting results, it seems that when used
Ercan et al. (2004) evaluated the antibacterial activ-
in identical concentrations, their antibacterial effects ex
ity of 2% CHX and 5.25% NaOCl in infected root canals
vivo (in infected dentine) and in vivo (in the root canal
of incisors and premolars. They concluded that both
CHX and NaOCl were effective irrigants for reducingthe number of microorganisms in teeth with a necrotic
Tanomaru et al. (2003) evaluated the effect of
Fungi (or yeasts) constitute a small proportion of the
biomechanical preparation with 5% NaOCl, 2% CHX
usual oral microbiota with Candida species being the
and physiological saline irrigating solutions and
most common of the fungi present in both healthy (30–
Ca(OH)2 dressing in the root canals of dogs’ teeth that
45%) and medically compromised (95%) individuals
contained bacterial endotoxin. They found that biome-
(Siqueira & Sen 2004). Fungi have occasionally been
chanical preparation with the irrigating solutions did
found in infected root canals that have not had any
not inactivate the endotoxin, but the calcium hydrox-
previous endodontic treatment, but they are more
ide intracanal dressing did inactivate the effects
common in filled root canals in teeth that have become
infected some time after treatment or in those that have
Chlorhexidine in endodontics Mohammadi & Abbott
not responded to endodontic treatment (23). Overall,
Infected dentine cylinders were exposed to four different
the occurrence of fungi reported in infected root canals
medications: Ca(OH)2/glycerin; Ca(OH)2/0.12% CHX;
varies between 1% and 17% (Waltimo et al. 2004).
Fungi may be involved in cases of persistent and
erin and 0.12% CHX/zinc oxide. The specimens treated
secondary infections associated with recalcitrant per-
with the Ca(OH)2/camphorated monoparachlorophe-
iradicular lesions and therefore the spectrum of anti-
nol/glycerin paste or with the CHX/zinc oxide paste
microbial activity of endodontic medicaments and
were completely disinfected after 1 h of exposure whilst
irrigants should include these organisms. Thus, med-
the Ca(OH)2/glycerin paste consistently eliminated the
icaments that have antifungal effectiveness may assist
C. albicans after 7 days of exposure. Calcium hydroxide
in the successful management of persistent or second-
mixed with CHX was ineffective in disinfecting dentine
ary endodontic infections caused by fungi (Siqueira &
even after 1 week. In another study, Siqueira et al.
Sen 2004, Waltimo et al. 2004). To try and improve
(2001) investigated the antifungal activity of several
antisepsis in single-appointment endodontic treatment
medicaments against C. albicans, Candida glabrata,
regimes, it has been suggested to irrigate and/or ‘soak’
Candida guilliermondii, Candida parapsilosis and Saccha-
the root canals with either CHX or iodine-IKI solutions
romyces cerevisiae. Calcium hydroxide mixed with
following irrigation with NaOCl. Aqueous CHX solution
CPMC/glycerin as a paste showed the most pronounced
has a wide spectrum of antimicrobial activity at low
antifungal effects. Calcium hydroxide in glycerin,
concentrations and is especially effective against
Ca(OH)2 with CHX and CHX in detergent had less
C. albicans. Furthermore, it binds to surrounding tissues
antifungal activity. Ferguson et al. (2002) sought to
and can then be released again slowly over extended
determine the in vitro susceptibility of C. albicans to
periods of time, a phenomenon known as substantivity.
various irrigants and medicaments. The minimum
Interestingly, it appears that CHX can efficiently inhibit
inhibitory concentrations of NaOCl, hydrogen peroxide,
the initial adherence and perhaps further accumulation
CHX-digluconate and aqueous Ca(OH)2 were deter-
and biofilm formation of fungi and other micro-
mined. Their results revealed that NaOCl, hydrogen
organisms. A recent clinical study has shown that
peroxide and CHX-digluconate were effective against
canals that received a final rinse with a 2% CHX
C. albicans even when significantly diluted. However,
solution were significantly more often free of cultivable
aqueous Ca(OH)2 had no anti-fungal activity. Taken
microorganisms than controls irrigated with NaOCl
together, it can be concluded that CHX is an effective
alone (Siqueira & Sen 2004, Waltimo et al. 2004).
antifungal agent, but its efficacy is significantly less
Sen et al. (1999) evaluated the antifungal properties
of 0.12% CHX, 1% NaOCl and 5% NaOCl againstCandida albicans using a cylindrical dentine tube model.
They reported that C. albicans was more resistant tothese irrigant solutions when the smear layer was
The term biofilm was introduced to designate the thin-
present than when it was absent. When smear layer
layered condensations of microbes that may occur on
was absent, the NaOCl started to display antifungal
various surface structures in nature. Free-floating
activity after 30 min. Waltimo et al. (1999) evaluated
bacteria existing in an aqueous environment, the so-
the susceptibility of seven strains of C. albicans to four
called planktonic form of microorganisms, are a pre-
disinfectants, namely IKI, CHX-acetate (0.5%), NaOCl
requisite for biofilm formation (Bowden & Hamilton
(5% and 0.5%) and Ca(OH)2. Each solution was tested
1998). Biofilms may thus become established on any
individually as well as in pairs using all possible pairs of
organic or inorganic surface substrate where plank-
these four disinfectants. All C. albicans strains tested
tonic microorganisms prevail in a water-based solution.
showed similar susceptibility to these medicaments.
In dental contexts, a well-known and extensively
They were highly resistant to Ca(OH)2, but the NaOCl
studied biofilm structure is established during the
and IKI killed all cells within 30 s and the CHX-acetate
attachment of bacteria to teeth to form dental plaque.
showed complete killing after 5 min. Combinations of
Here, bacteria free in saliva (planktonic organisms)
disinfectants were either equally or less effective than
serve as the primary source of organisms for the
the more effective component of the pair tested.
organization of this specific biofilm (Bowden & Hamil-
Siqueira et al. (2003) evaluated the effectiveness of
ton 1998). In endodontics, the biofilm concept was
four intracanal medications in disinfecting root dentine
initially discussed mainly within the framework of
in bovine teeth experimentally infected with C. albicans.
bacteria on the root tips of teeth with necrotic and
Mohammadi & Abbott Chlorhexidine in endodontics
infected pulps or pulpless and infected root canal
kill was found. The percentage kills of the bacteria
were: 6% NaOCl (>99.99%), 1% NaOCl (99.78%),
thought to be the cause of therapy-resistant apical
Smear ClearÔ (78.06%), 2% CHX (60.49%), REDTA
periodontitis (Tronstad & Sunde 2003). Although not
(26.99%) and BioPureÔ MTADÔ (16.08%). There was
described in as much detail, bacterial condensations
a significant difference between NaOCl (both concen-
(that is, biofilms) on the walls of infected root canals
trations of 1% and 6%) and all other agents. Therefore,
both 1% NaOCl and 6% NaOCl were more efficient in
Antimicrobial agents have often been developed and
eliminating E. faecalis biofilm than the other solutions
optimized for their activity against fast growing,
tested. In another study, Lima et al. (2001) assessed the
dispersed populations containing a single microorgan-
effectiveness of CHX-based or antibiotic-based (clinda-
ism. However, microbial communities grown in bio-
mycin and metronidazole) medications in eliminating
1- and 3-day E. faecalis biofilms. Each biofilm-contain-
antimicrobial agents and microorganisms in mature
ing membrane was thoroughly covered with 1 mL of
biofilms can be notoriously resistant for reasons that
the test medications and incubated for 1 day at 37 °C.
have yet to be adequately explained (Bowden &
The treated biofilms were then aseptically transferred to
Hamilton 1998). There are reports showing that
vials containing a neutralizing agent in saline solution
microorganisms grown in biofilms could be twofold to
and vortexed. Suspensions were diluted 10-fold, seeded
1000-fold more resistant than the corresponding
onto Mitis salivarius agar plates and the colony-forming
planktonic form of the same organisms (Svensater &
units counted after 48 h of incubation. There were
Bergenholtz 2004). Spratt et al. (2001) have evaluated
significant differences between the formulations tested.
the effectiveness of 2.25% NaOCl, 0.2% CHX, 10%
The association of clindamycin with metronidazole
povidone iodine, 5 ppm colloidal silver and phosphate
significantly reduced the number of cells in the 1-day
buffered solution (PBS) as a control against monocul-
biofilms. However, of all medications tested, only 2%
ture biofilms of five root canal isolates including P.
CHX-containing medications were able to thoroughly
intermedia, Peptostreptococcus miros, Streptococcus inter-
eliminate most of both the 1-day and 3-day E. faecalis
medius, Fusobacterium nucleatum and E. faecalis. They
biofilms. On the whole, it seems that although CHX is
reported that NaOCl was the most effective anti-
somewhat effective against bacterial biofilms, NaOCl is
microbial agent followed by the iodine solution. Clegg
the only irrigation solution with the capability of
et al. (2006) evaluated the ex vivo effectiveness against
apical dentine biofilms of three concentrations of NaOCl(6%, 3% and 1%), 2% CHX and a commercially
available mixture of a tetracycline, an acid and adetergent known as BioPure MTAD (Dentsply, Tulsa
Chlorhexidine as well as tetracyclines have a unique
Dental, Tulsa, OK, USA). They reported that the 6%
feature in that dentine medicated with it acquires
NaOCl and 3% NaOCl were capable of disrupting and
antimicrobial substantivity (Khademi et al. 2006). The
removing the biofilm, but the 1% NaOCl and the MTAD
positively charged ions released by CHX can adsorb into
were capable of disrupting the biofilm, but did not
dentine and prevent microbial colonization on the
eliminate the bacteria. The 2% CHX was not capable of
dentine surface for some time beyond the actual the
disrupting the biofilm. Viable bacteria could not be
period of time of application of the medicament
cultured from specimens exposed to 6% NaOCl, 2%
CHX or 1% NaOCl followed by BioPure MTAD. Duna-
The antimicrobial substantivity of CHX has been
vant et al. (2006) evaluated the efficacy of 6% NaOCl,
assessed in several periodontal and endodontic studies.
1% NaOCl, Smear ClearÔ (SybronEndo, Orange, CA,
In an in vivo periodontal study, Stabholz et al. (1993)
USA), 2% CHX, REDTA (Roths International Ltd,
evaluated the substantivity of the human root surface
Chicago, IL, USA) and BioPureÔ MTADÔ against E.
after in situ subgingival irrigation with tetracycline HCL
faecalis biofilms using a novel laboratory testing system.
and CHX. They found that the substantivity of tetracy-
Biofilms grown in a flow cell system were submerged in
cline at 50 mg mL)1 was significantly greater than that
test irrigants for either 1 or 5 min. There was a
of CHX for 12 days and greater than saline for 16 days.
significant relationship between the test agent and the
In a laboratory study, White et al. (1997) evaluated
percentage kill of the bacteria in the biofilm. No
the antimicrobial substantivity of a 2% CHX solution as
significant relationship between time and percentage
an endodontic irrigant. Findings showed that the
Chlorhexidine in endodontics Mohammadi & Abbott
substantivity lasted 72 h. In an in vivo study, Leonardo
years. Haapasalo et al. (2000) introduced a new
et al. (1999) evaluated the antimicrobial substantivity
dentine powder model for studying the inhibitory effect
of 2% CHX used as a root canal irrigating solution in
of dentine on various root canal irrigants and medica-
teeth with pulp necrosis and radiographically visible
ments. They investigated the modulating effect of
chronic periapical lesions. They reported that the CHX
dentine on the antibacterial activity of saturated
prevented microbial activity with residual effects in the
CA(OH)2 solution, 1% NaOCl, 0.5% and 0.05% CHX
root canal system for up to 48 h after application.
acetate and 2/4% and 0.2/0.4% IKI. Dentine powder
However, some other studies have reported that the
had an inhibitory effect on all medicaments tested. The
substantivity of CHX can last for longer periods of time.
effect was dependent on the concentration of the
Khademi et al. (2006) found that 5 min application of
medicament as well as on the length of time the
2% CHX solution induced substantivity for up to
medicament was pre-incubated with the dentine
4 weeks. Rosenthal et al. (2004) evaluated the sub-
powder before adding the bacteria. Similarly, 0.2/
stantivity of 2% CHX solution within the root canal
0.4% IKI lost its effect after pre-incubation for 1 h with
system after 10 min of application and they reported
dentine before adding the bacteria. The effect of 0.05%
that the CHX was retained in the root canal dentine in
CHX and 1% NaOCl on E. faecalis was reduced, but not
antimicrobially effective amounts for up to 12 weeks.
totally eliminated by the presence of dentine. No
Antimicrobial substantivity depends on the number
inhibition could be measured when full strength
of CHX molecules available to interact with the dentine.
solutions of CHX and IKI were used in killing E. faecalis.
Therefore, medicating the canal with a more concen-
Portenier et al. (2001) evaluated the inhibition of the
trated CHX preparation should result in increased
antibacterial effect of saturated Ca(OH)2 solution, CHX-
resistance to microbial colonization. The antibacterial
acetate and IKI by dentine, hydroxylapatite (HA) and
substantivity of three concentrations of CHX solution
bovine serum albumin (BSA). Calcium hydroxide was
(4%, 2% and 0.2%) after 5 min of application has been
totally inactivated by the presence of 28 mg of dentine
powder or BSA. CHX (0.05%) was strongly inhibited by
between the concentration of CHX and its substantivity
BSA and slowed down by dentine. However, HA had
(Mohammadi et al. 2008). On the contrary, Lin et al.
little or no inhibitory effect on CHX. The antibacterial
(2003a) attributed the substantivity of CHX to its ability
effect of 0.2/0.4% IKI on E. faecalis was totally inhibited
to adsorb on to the dentine during the first hour. They
by dentine (28 mg), but was practically unaffected by
stated that it is only after the saturation point is reached
HA or BSA. A stepwise reduction of dentine from 28 to
after the first hour that the antimicrobial capability of
2.8 mg 150 lL)1 was followed by a similar reduction
CHX increases with time. Furthermore, Komorowski
of the inhibition of the antibacterial activity of CHX. IKI
et al. (2000) revealed that 5 min application of CHX did
was not inhibited at all with dentine amounts <28 mg.
not induce substantivity and that the dentine should be
However, the effect of saturated calcium hydroxide
treated with CHX for 7 days. Taken together, it seems
solution was totally eliminated by dentine at all four
that residual antimicrobial activity of CHX in the root
concentrations tested. It could be assumed that inhibi-
canal system remains for up to 12 weeks.
tion by dentine of the antibacterial activity of Ca(OH)2,CHX and IKI occurs by different mechanisms (Portenieret al. 2001). Surprisingly, Ca(OH)
inhibitory effect of all three materials tested. The
The root canal milieu is a complex mixture of a variety
inhibition of Ca(OH)2 by dentine and by the other
of organic and inorganic compounds. Hydroxyapatite,
compounds is, of course, dependent on their quantita-
the main component of dentine, is the major represen-
tive relationships (Portenier et al. 2001). One major
tative of inorganic components present. In addition,
mechanism for resistance of survival of E. faecalis in the
inflammatory exudate, entering the apical root canal in
root canal filled with Ca(OH)2 may be the buffering
purulent infections, is rich in proteins, such as albumin.
effect of dentine against the pH rise. Inorganic HA had
The relative importance of the various organic and
little or no inhibitory activity against CHX as compared
inorganic compounds in the inactivation of root canal
with dentine, whereas BSA was the strongest inhibitor
disinfectants have been studied restrictively (Haapasalo
of CHX, with more than 10% of E. faecalis cells still
et al. 2000). Difficulties in designing experiments that
viable after 24 h of incubation with the medicament.
will give reliable and comparable data have been some
This indicates that periapical inflammatory exudate
of the greatest challenges for researchers for many
entering the root canal is a greater threat to the activity
Mohammadi & Abbott Chlorhexidine in endodontics
of CHX than the dentine walls. Dentine powder totally
the frequency of shaking, the amount of organic matter
eliminated the antibacterial effect of IKI; whereas the
in relation to the amount of irrigant in the system and
major component of dentine, HA did not affect the
the surface area of tissue that was available for contact
antibacterial effect of IKI, nor did BSA. In addition, it is
with the irrigant. Okino et al. (2004) evaluated the
generally known that blood rapidly inactivates the
tissue dissolving ability of 0.5%, 1.0% and 2.5% NaOCl,
antibacterial activity of iodine compounds (Portenier
2% aqueous solution of CHX-digluconate, 2% CHX
et al. 2001). In another study, Portenier et al. (2002)
digluconate gel and distilled water as the control.
assessed the antibacterial activity of CHX and IKI on E.
Bovine pulp fragments were weighed and placed in
faecalis in the presence of dentine, dentine matrix,
contact with 20 mL of each tested substance in a
dentine pre-treated by ethylenediamine tetraacetic acid
centrifuge at 150 rpm until total dissolution. Dissolu-
(EDTA) and citric acid, collagen and heat-killed cells of
tion speed was calculated by dividing the pulp weight
E. faecalis and Candida albicans. Dentine matrix and
by the dissolution time. Distilled water and both
heat-killed microbial cells were the most effective
solutions of CHX did not dissolve the pulp tissue within
inhibitors of CHX, whereas dentine pre-treated by citric
6 h. The mean dissolution speeds for 0.5%, 1.0% and
acid or EDTA showed only slight inhibition. Dentine
and skin collagen showed some inhibition at 1 h, but
0.55 mg min)1, respectively. In another study, Naenni
not after 24 h. IKI was effectively inhibited by dentine,
et al. (2004) assessed the necrotic tissue dissolution
dentine matrix and heat-killed microbial cells. Skin
capacity of 1% (w/v) NaOCl, 10% CHX, 3% and 30%
collagen and dentine pre-treated by EDTA or by citric
hydrogen peroxide, 10% peracetic acid, 5% dichloro-
acid showed little or no inhibitory effect on IKI. The
isocyanurate (NaDCC) and 10% citric acid. Standard-
inhibitory effect of dentine and BSA on the antibacterial
ized necrotic tissue samples obtained from pig palates
activity of CHX and MTAD was assessed in another
were incubated in these solutions and their weight loss
study (Portenier et al. 2006). The presence of dentine
was measured over time. None of the test solutions
or BSA caused a marked delay in the killing of E. faecalis
except NaOCl had any substantial tissue dissolution
by both medicaments. The inhibitory effect of BSA on
capacity. It was concluded that this might be important
the antibacterial activity of CHX and NaOCl has been
when considering the use of irrigants other than
confirmed by Sassone et al. (2008). Taken together, it
NaOCl. On the whole, one of the major disadvantages
seems that dentine, dentine components (HA and
of CHX is that it has no tissue solvent activity.
collagen), killed microorganisms and inflammatoryexudate in the root canal system all reduce or inhibit
the antibacterial activity of medicaments and irrigants.
On the whole, it seems that dentine, dentine compo-
Chlorhexidine is a cationic biguanide whose optimal
nents (HA and collagen), killed microorganisms and
antimicrobial activity is achieved within a pH range of
inflammatory exudates in the root canal system reduce
5.5–7.0 (Athanassiadis et al. 2007). Therefore, it is
likely that alkalinizing the pH by adding Ca(OH)2 toCHX will lead to precipitation of the CHX molecules andthereby decreases its effectiveness. It has been demon-
strated that the alkalinity of Ca(OH)2 when mixed with
Several studies have been conducted in the search for
CHX remained unchanged. Therefore, the usefulness of
an irrigant that meets the four major desirable prop-
mixing Ca(OH)2 with CHX still remains unclear and
erties for root canal irrigants – namely: antimicrobial
controversial (Athanassiadis et al. 2007).
activity, nontoxicity to the periapical tissues, water
When used as an intracanal medicament, CHX was
solubility and the capacity to dissolve organic matter.
more effective than Ca(OH)2 in eliminating E. faecalis
Therefore, an ideal irrigant should dissolve the organic
from inside dentinal tubules (Athanassiadis et al.
matter inside the root canal system. Grossman &
2007). In a study by Almyroudi et al. (2002), all of
Meiman (1941) demonstrated the importance of the
the CHX formulations used, including a CHX/ Ca(OH)2
solvent ability of an endodontic irrigant and empha-
50:50 mix, were efficient in eliminating E. faecalis from
sized that the elimination of pulp tissue from the root
the dentinal tubules with a 1% CHX gel working
canal was important for the ultimate success of root
slightly better than the other preparations. These
canal treatment. Moorer & Wesselink (2003) showed
findings were corroborated by Gomes et al. (2006) in
that tissue dissolution was dependent on three factors:
bovine dentine and Schafer & Bossmann (2005) in
Chlorhexidine in endodontics Mohammadi & Abbott
human dentine where 2% CHX gel had greater activity
canal system of teeth with coronal restorations medi-
against E. faecalis, followed by CHX/ Ca(OH)2 and then
cated with either calcium hydroxide, 2% CHX gel or
with a combination of both. The canals without a
In a study using agar diffusion, Haenni et al. (2003)
coronal restoration, but medicated with CHX, showed
could not demonstrate any additive antibacterial effect
recontamination after an average time of 3.7 days; the
by mixing Ca(OH)2 powder with 0.5% CHX and they
group with Ca(OH)2 after 1.8 days and the group with
showed that the CHX had a reduced antibacterial action.
CHX+Ca(OH)2 after 2.6 days. The canals medicated
However, Ca(OH)2 did not lose its antibacterial proper-
with CHX and restored with IRM showed recontami-
ties in such a mixture. This may be because of the
nation within 13.5 days; the group with Ca(OH)2+IRM
deprotonation of CHX at a pH >10, which reduces its
after 17.2 days and the group with CHX+ Ca(O-
solubility and alters its interaction with bacterial sur-
H)2+IRM after 11.9 days. The group with no medica-
faces as a result of the altered charge of the molecule. In
tion, but restored with IRM, showed recontamination
an in vitro study using human teeth, Ercan et al. (2006)
after an average time of 8.7 days. There were statisti-
showed 2% CHX gel was the most effective agent against
E. faecalis inside dentinal tubules, followed by a Ca(OH)2/
(P < 0.05). All groups without a coronal restoration
2% CHX mix, whilst Ca(OH)2 alone was totally ineffec-
were recontaminated significantly more quickly than
tive, even after 30 days. The 2% CHX gel was also
those restored with IRM, except those teeth that had a
significantly more effective than the Ca(OH)2/2% CHX
restoration, but no medicament. The groups with
mix against C. albicans at 7 days, although there was no
intracanal medication and a coronal restoration were
significant difference at 15 and 30 days. Ca(OH)2 alone
not significantly different from each other.
was completely ineffective against C. albicans. In another
Vivacqua-Gomes et al. (2002) assessed ex vivo coro-
in vivo study using primary teeth, a 1% CHX-gluconate
nal dye penetration of extracted human teeth after root
gel, both with and without Ca(OH)2, was more effective
canal treatment using 1% NaOCl, 1% NaOCl + 17%
against E. faecalis than CH alone over a 48-h period
EDTA, 2% CHX gel, 2% CHX gel + 1% NaOCl and
distilled water. After root canal filling, the teeth were
Schafer & Bossmann (2005) reported that 2% CHX-
incubated at 37 °C for 10 days followed by 10 days
gluconate was significantly more effective against
immersion in human saliva and an additional 10 days
E. faecalis than Ca(OH)2 used alone or a mixture of
in India ink. The teeth were cleared and the maximum
the two. This was also confirmed by Lin et al. (2003b)
depth of dye penetration was determined digitally in
although in a study by Evans et al. (2003) using bovine
millimetres. Results revealed that the least dye pene-
dentine, 2% CHX with Ca(OH)2 was shown to be more
tration occurred with 1% NaOCl + 17% EDTA and 2%
effective than Ca(OH)2 in water. In an animal study,
CHX gel. NaOCl, distilled water and 2% CHX gel + 1%
Lindskog et al. (1998) reported that teeth dressed with
NaOCl had more dye penetration with a significant
CHX for 4 weeks had reduced inflammatory reactions
difference compared with NaOCl + 17% EDTA and 2%
in the periodontium (both apically and marginally) and
CHX gel and compared with one another.
less root resorption. Waltimo et al. (1999) reported that
Other studies have shown that viscous irrigants,
0.5% CHX-acetate was more effective at killing C.
including those containing CHX gluconate, were less
albicans than saturated Ca(OH)2, whilst Ca(OH)2 com-
soluble substances and they can leave residues on the
bined with CHX was more effective than Ca(OH)2 used
root canal surfaces, which may affect the root canal
alone. The high pH of Ca(OH)2 was unaffected when
filling. Lambrianidis et al. (2006) investigated the
combined with CHX in this study. Taken together, it
efficiency of removing Ca(OH)2/CHX gel, Ca(OH)2/
seems that the usefulness of mixing Ca(OH)2 with CHX
CHX solution and Ca(OH)2/saline pastes with the use
of instrumentation and irrigation with NaOCl andEDTA solutions. None of the techniques used in thisstudy removed the inter-appointment root canal med-
icaments effectively (Lambrianidis et al. 2006). Overall,
Because of its antimicrobial substantivity, it seems that
Ca(OH)2/CHX (gel) paste was associated with signifi-
CHX preparations delay entry of bacteria through the
cantly larger amount of residue, whereas the Ca(OH)2/
coronal portion of the tooth into the root canal system.
CHX mixture was associated with less residue than the
In a laboratory study, Gomes et al. (2003b) investi-
other two medicaments. When all these studies are
gated the time required for recontamination of the root
considered it appears as although CHX used as an
Mohammadi & Abbott Chlorhexidine in endodontics
intracanal medicament and/or irrigant may delay
Gomes et al. 2002). The formation of a precipitate could
recontamination of the root canal system via the
be explained by the acid–base reaction that occurs
coronal route because of its substantivity. Overall,
when NaOCl and CHX are mixed together. CHX, a
because of its substantivity, CHX as an intracanal
dicationic acid has the ability to donate protons whilst
medicament/irrigant delays recontamination of the
NaOCl is alkaline and can accept protons from the
root canal system via the coronal route.
dicationic acid. This proton exchange results in theformation of a neutral and insoluble substance, referredto as the ‘precipitate’ (Basrani et al. 2007). Basrani et al.
(2007) evaluated the chemical nature of this precipitate
Marley et al. (2001) assessed the effect of 0.12%
and reported that there was an immediate reaction
CHX-gluconate as an endodontic irrigating solution
when 2% CHX was combined with NaOCl, even at the
on the apical seal of root filled canals using three
low concentration (0.023%). Increasing of the concen-
different cements (Roth’s 801, AH26 and Sealapex).
tration of NaOCl to 0.19% (the sixth dilution in their
At 90 and 180 days after root filling, apical fluid
series) resulted in the formation of a precipitate, which
penetration was measured using the fluid filtration
consisted mainly of para-chloroaniline (PCA). This
method. The results showed no significant differences
occurred through a substitution of the guanidine group
related to the irrigants at both the 90- and 180-day
in the CHX molecule. They found that the amount of
observation periods. Furthermore, the same group
PCA directly increased with the increasing concentra-
reported that at long-term periods (270 and 360
tion of NaOCl. PCA has been shown to be toxic with
days), CHX-gluconate irrigant did not adversely affect
short-term exposure of humans to PCA resulting in
the apical penetration of fluid with the different root
cyanosis, which is a manifestation of methemoglobin
canal cements (Ferguson et al. 2003). Wuerch et al.
formation. In another study, Bui et al. (2008) evaluated
the effect of irrigating root canals with a combination of
Ca(OH)2 on the apical seal of root canal fillings.
NaOCl and CHX on root dentine and dentinal tubules by
They reported that 2% CHX gel and Ca(OH)2 paste
using the environmental scanning electron microscope
did not adversely affect the apical seal. These findings
(FEI Quanta 200, Hillsboro, OR, USA) and a computer
were also confirmed by Engel et al. (2005). Overall, it
program (photoshop cs2, Adobe Systems, San Jose, CA,
seems that medication and/or irrigation with CHX
USA). Their findings indicated that there were no
does not adversely affect the ability of root fillings to
significant differences in the amount of debris remain-
prevent fluid penetration into the root canal system
ing between the negative control group and the
experimental groups although there were significantlyfewer patent tubules in the experimental groups whencompared with the negative control group. They
concluded that the NaOCl/CHX precipitate tends to
A suggested clinical protocol by Zehnder (2006) for
occlude the dentinal tubules and suggested that until
treating the dentine before root canal filling consists of
this precipitate is studied further, caution should be
irrigation with NaOCl to dissolve the organic compo-
exercised when irrigating with both NaOCl and CHX.
nents, irrigation with EDTA to eliminate the smear layer
Taken together, the combination of NaOCl and CHX
and irrigation with CHX to increase the anti-microbial
causes colour changes and formation of a neutral and
spectrum of activity and to impart substantivity.
insoluble precipitate, which may interfere with the seal
Although such a combination of irrigants may enhance
of the root filling. Copious amounts of CHX irrigant
the overall antimicrobial effectiveness (Kuruvilla &
should be administered to prevent discolouring of the
Kamath 1998), the possible chemical interactions
tooth by this precipitate. Alternatively, the canal can be
amongst the irrigants have to be considered. Some
dried using paper points before the final CHX rinse
studies have reported the occurrence of colour change
and precipitation when NaOCl and CHX are combined(Vivacqua-Gomes et al. 2002, Zehnder 2006, Basrani
et al. 2007). Furthermore, concern has been raised that
the colour change may have some clinical relevancebecause of staining and that the precipitate might
During the last two decades, chemical and technical
interfere with the seal of the root filling (Vivacqua-
advances have contributed to increases in resin–dentine
Chlorhexidine in endodontics Mohammadi & Abbott
bond strength. However, the premature loss of bond
concluded that auto-degradation of collagen matrices
strength is one of the problems that still affects adhesive
can occur in resin-infiltrated dentine, but may be
restorations (Mjo¨r et al. 2000) and markedly reduces
prevented by the application of a synthetic protease
their durability (Carrilho et al. 2005b, De Munck et al.
inhibitor, such as CHX (Carrilho et al. 2007b). On the
2005, Frankenberger et al. 2005). The loss of bond
whole, because of its broad-spectrum MMP-inhibitory
strength has been attributed mainly to the degradation
effect, CHX can significantly improve the resin–dentine
of the hybrid layer at the dentine-adhesive interface.
Numerous publications have demonstrated this lack ofbond stability (Wang & Spencer 2003, 2005, Yiu et al.
2004, Carrilho et al. 2005a). The notion that deterio-ration of dentine collagen fibrils contributes to the
Results from a study of the cytotoxic effect of chloreh-
mechanism responsible for bond degradation has been
exidine on canine embryonic fibroblasts and Staphylo-
reported (Hashimoto et al. 2003, Pashley et al. 2004).
coccus aureus showed that bactericidal concentrations
In this context, it has been speculated that a decreasing
of CHX were lethal to canine embryonic fibroblasts
concentration gradient of resin monomer diffusion
whilst noncytotoxic concentrations allowed significant
within the acid-etched dentine and a subsequent resin
bacterial survival (Sanchez et al. 1988). In a study by
elution from hydrolytically unstable polymeric hydro-
Tatnall et al. (1990), the cytotoxic effects of CHX,
gels within the hybrid layers (Wang & Spencer 2003)
hydrogen peroxide and NaOCl were examined on
leaves the collagen fibrils unprotected and vulnerable
cultured human fibroblasts, basal keratinocytes and a
to degradation by endogenous metalloproteinases
transformed keratinocyte line (SVK 14 cells). At con-
(MMPs). The MMPs are a group of 23 mammalian
centrations recommended for wound cleansing, all
enzymes capable of degrading all extracellular matrix
agents produced 100% killing of all cell types. Com-
components. Human dentin contains at least collage-
parison of the ED50 concentration for each agent on all
nase (MMP-8), gelatinases MMP-2 and -9 and enam-
cell types produced a ranking order of toxicity showing
elysin MMP-20 (Martin-De Las Heras et al. 2000,
CHX to be the least toxic antiseptic agent.
Sulkala et al. 2002, 2007, Mazzoni et al. 2006).
Results from a laboratory study on the toxicity of
CHX to human gingival cells showed that the toxic
(Pashley et al. 2004) can be suppressed by protease
potency of CHX is dependent on the length of
inhibitors (Pashley et al. 2004), indicating that MMP
inhibition could be beneficial in the preservation of
medium (Babich et al. 1995). The addition of foetal
hybrid layers. This was demonstrated in an in vivo
study, in which the application of CHX, known to have
Escherichia coli reduced the cytotoxicity of CHX,
a broad-spectrum MMP-inhibitory effect (Gendron et al.
presumably because of the binding of the cationic
1999), significantly improved the integrity of the
CHX to the negatively charged chemical moieties/
hybrid layer in a 6-month clinical trial (Hebling et al.
2005). Carrilho et al. (2007a) evaluated the effect of
1995). These findings suggest that similar reactions
CHX on the resin–dentine bond stability ex vivo. Results
within a root canal may reduce the potential of a
showed that with CHX, significantly better preservation
cytotoxic reaction in the periapical tissues (Boyce
of bond strength was observed after 6 months and
et al. 1995). Boyce et al. (1995) found CHX (0.05%)
protease inhibitors in the storage medium had no effect.
uniformly toxic to both cultured human cells and
Failure analysis showed significantly less failure in the
microorganisms. Agarwal et al. (1997) found that
hybrid layer with CHX, compared with controls after
CHX rapidly disrupts the cell membrane of both
6 months. Furthermore, they evaluated the effect of
crevicular and peripheral blood neutrophils at con-
CHX on the preservation of the hybrid layer in vivo.
centrations above 0.005% within 5 min, indicating
Findings showed that bond strength remained stable in
that its inhibitory effect on neutrophil function is
the CHX-treated specimens, whilst bond strength
mostly because of its lytic properties. Yesilsoy et al.
decreased significantly in control teeth. Resin-infil-
(1995) assessed the short-term toxic effects of CHX in
trated dentine in CHX-treated specimens exhibited
the subcutaneous tissue of guinea pigs and found
normal structural integrity of the collagen network.
moderate inflammation present after 2 days, followed
Conversely, progressive disintegration of the fibrillar
by a foreign-body granuloma formation at 2 weeks.
network was identified in control specimens. They
Mohammadi & Abbott Chlorhexidine in endodontics
(potential damage to DNA) of formocresol, para-
3. The effect of CHX on microbial biofilms is signifi-
against Chinese hamster ovary cells. Results showed
4. CHX has antibacterial substantivity in dentine for
that none of the mentioned agents contributed to
DNA damage. Taken together, in the clinically used
5. Dentine, dentine components (HA and collagen),
concentrations, the biocompatibility of CHX is accept-
killed microorganisms and inflammatory exudate in the
able. The potentially toxic interactions between CHX
root canal system may reduce or inhibit the antibac-
and NaOCl were considered previously.
terial activity of CHX. 6. CHX has little to no ability to dissolve organictissues.
7. Mixing CHX with Ca(OH)2 may enhance its antimi-
Although sensitivity to CHX is rare, contact dermatitis is
a common adverse reaction to CHX (Krautheim et al.
8. Medication and/or irrigation with CHX may delay
2004). Apart from this, CHX may have a number of rare
the contamination of root filled teeth by bacteria
side effects, such as desquamative gingivitis, discolour-
entering through the coronal restoration/tooth inter-
ation of the teeth and tongue or dysgeusia (distorted
taste). Contact with conjunctiva can cause permanent
9. Medication and/or irrigation with CHX will not
damage and accidental contact with the tympanum can
adversely affect the penetration of fluid through the
cause ototoxicity (Dukes 1992). Various allergic reac-
tions to CHX have been described. Contact sensitivity to
10. Combination of NaOCl and CHX causes colour
CHX was first reported by Calnan (1962). Today, CHX is
changes and formation a precipitate, which may
known to elicit allergic contact dermatitis, including
interfere with the seal of the root filling.
connubial contact dermatitis, generally after prolonged
11. CHX can significantly improve the integrity of the
and repeated application (Krautheim et al. 2004). It can
hybrid layer andresin–dentine bond stability.
also cause contact urticaria, photosensitivity, fixed drug
12. The biocompatibility of CHX is acceptable.
eruption and occupational asthma. People at particular
13. In rare cases, CHX may cause allergic reactions.
risk of contact allergy (apart from medical and dentalstaff) are patients with leg ulcers and leg eczema
(Krautheim et al. 2004). Overall, contact sensitivity toCHX seems to be rare as some large studies have shown a
Agarwal S, Piesco NP, Peterson De et al. (1997) Effects of
sensitization rate of about 2% (Osmundsen 1982,
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Bechgaard et al. 1985, Nomura et al. 1989). Even rarer
viability and functions in vitro. Journal of Periodontal Research
are reports of immediate anaphylactic reactions because
of CHX. Ohtoshi et al. (1986) demonstrated IgE antibod-
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intracanal medications: an in vitro study. Journal of Endo-
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risk of using CHX. On the whole, although sensitivity to
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