By- Dr.Prathamesh Fulsundar
 Used as adjunct to mechanical plaque control.
 Many vehicles may be used to deliver anti plaque
agents such as:
 MOUTH RINSES,
 TOOTHPASTES,
 SPRAY,
 IRRIGATORS,
 CHEWING GUM,
 VARNISHES.
Approaches to chemical supragingival plaque
control:
1. ANTIADHESIVE: Prevention of attachment of
bacterial biofilm.
2. ANTIMICROBIAL : by inhibition of bacterial
proliferation and as bactericidal.
3. PLAQUE REMOVAL
4. ANTIPATHOGENIC
1. Should eliminate only the pathogenic
bacteria.
2. Prevent development of resistant bacteria.
3. Exhibit substantivity i.e. ability of an agent
to bind to tissue surfaces and to be released
over time to deliver an adequate dose of
active principal ingredient the agent
carries. (CHX gets adsorbed to oral tissues).
4. Safe to oral tissues at
concentrations and dosages
recommended.
5. Significantly reduce and gingivitis
and prevent colonization of
microorganisms.
6. Should not stain the teeth or alter
taste.
Depending on the antimicrobial efficiency and
relative substantitivity.
1st generation: decreases plaque scores by 20-
50%, but efficacy is decreased by poor
retention in the mouth. E.g. antibiotics ,
phenols etc.
2nd generation : 70-90%
more effectively retained by oral tissues
and release slowly. E.g. Bisbiguanides
CHEMICAL PLAQUE CONTROL AGENTS
FIRST GENERATION
Eg: antibiotics, phenol,quarternary ammonium compounds & sanguinarine
SECOND GENERATION
Eg: Bisbiguanides,(chlorhexidine)
THIRD GENERATION
Eg: delmopinol
1. Antibiotics: penicillin,
vancomycin
2. Enzymes: proteases, lipase,
dextranase
3. Bisbiguanide: chlorhexidine,
alexidine
4. Quaternary ammonium
compounds: cetylpyridinium
chloride, benzalkonium chloride
5. Phenols and essential oils:
thymol, triclosan
6. Natural products: sanguinarine
7. Fluorides: sodium fluoride,
stannous F
8. Metal salts: tin, zinc, copper
9. Oxygenating agents: Hydrogen
peroxide
10. Detergents: sodium lauryl sulfate
11. Amine alcohols: octapinol,
delmopinol
 Phenol derivative
 Is synthetic and ionic
 Used as a topical antimicrobial
agent
 Broad spectrum of action
including both gram positive
and gram negative bacterias
 It also includes mycobacterium
spores and Candida species
TRICLOSAN
ACT ON CYTOPLASMIC MEMBRANE
INDUCE LEAKAGE OF CELLULAR CONSTITUENTS
BACTERIOLYSIS
Triclosan is included in tooth paste to
reduce plaque formation
Used along with Zinc citrate or co-
polymer Gantrez to enhance its
retention within the oral cavity
Triclosan delay plaque formation
It inhibits formation of prostaglandins
& leukotrienes there by reduces the
chance of inflammation
eg: Zn & Cu ions
MECHANISM OF ACTION
 It reduces the glycolytic activity in bacteria
&delays bacterial growth
 Cationic antiseptics & surface active agents
 Effective against gram positive organisms
MECHANISM OF ACTION
 Positively charged molecule reacts with
negatively charged cell membrane phosphates and
thereby disrupts the bacterial cell wall structure
Eg: Benzanthonium chloride, Benzalleonium
chloride and cetylpyredinium
 It is a benzophenanthredine alkaloid
 It is most effective against gram –ve organisms
 Used in mouth rinse
 Vancomycin,erythromycin,Niddamycin and
Kanamycin
 Due to bacterial resistance problems the use of
antibiotics has been reduced
Considered to most effective
antiplaque agents.
Second generation agents
exhibiting substantivity and broad
antimicrobial properties.
 It is a cationic
bisbiguanide
 Effective against gram
+ve, gram –ve organisms,
fungi, yeasts and viruses
 Exhibit antiplaque &
antibacterial properties
CHX due to its dicationic nature,
binds to enamel pellicle or tooth
surface and salivary proteins. This
adsorbed CHX is released of a period
of time.
Mode of delivery of CHX: mouth rinse,
gels, tooth paste, dental floss, and
tooth picks.
Antimicrobial action and antiplaque action
1. ANTIMICROBIAL:
a. at low concentration is bacteriostatic -
positively charged chlorhexidine molecule
will adhere to negatively charged bacterial
cell surface. Integrity of cell membrane
disrupted causing leakage of intracellular
components.
b. at high concentration is bactericidal –
causes precipitation of bacterial cytoplasm
so cell death.
Antibacterial action of chlorhexidine
It shows two actions
1. Bacteriostatic at low concentrations
Bacterial cell wall(-ve charge)
Reacts with +ve charged chlorhexidine molecule
Integrity of cell membrane altered
CHX binds to inner membrane phospholipids & increase
permeability
Vital elements leak out & this effect is reversible
2. Bacteriocidal action
increased concentration of chlorhexidine
Progressive greater damage to membrane
Larger molecular weight compounds lost
Coagulation and precipitation of cytoplasm
Free CHX molecule enter the cell & coagulates proteins
Vital cell activity ceases
cell death
ANTIPLAQUE ACTION:
 Prevents formation of acquired pellicle.
Blocks the acidic group of salivary
glycoproteins which reduces their adsorption
to hydroxyapetite.
 Reduces the ability of bacteria to bind to
tooth surface. Adsorption of CHX to bacterial
capsule or glycocalyx and prevents them
binding on to tooth surface.
 CHX competes for Ca ions which are required
for agglutination of plaque.
ADVERSE EFFECTS OF CHLORHEXIDINE
1. Brownish staining of tooth or restorations
2. Loss of taste sensation
3. Rarely hypersensitivity to chlorhexidine has been
reported
4. Stenosis of parotid duct has also been reported
 Enzymes has been used as active agents in
antiplaque preparations
 It is due to the fact that enzymes would be able
to breakdown already formed matrix some
plaques and calculus
 Some are proteolytic and have bactericidal
action
eg:Mucinase, mutanase, dextranase etc
 Inhibits plaque growth and reduces
gingivitis
Mechanism of action
 Interfere with plaque matrix formation &
also reduces bacterial adherence
 It causes weak binding of plaque to
tooth, thus aiding in easy removal of
plaque by mechanical procedures
 It is therefore indicated as a pre brushing
mouth rinse
Adverse effect of delmopinol
1. Staining of tooth & tongue
2. Taste disturbances
3. Mucosal soreness & erosion
 A disclosing agent is a
preparation in liquid, tablet
or lozenge from which
contains a dye or other
coloring agents
 A disclosing agent is used
for identifying bacterial
plaque
 When applied to the teeth,
the agents imparts its colour
to soft deposits but can be
rinsed easily from clean
tooth surface
IDEAL PROPERTIES
 Intensity of colour
 Duration of intensity
 Taste
 Irritation to mucous membrane
 Diffusibility
 Astringent and antiseptic property
Agents used for disclosing plaque
a. Iodine preparations
 Skinners iodine solution
 Diluted tincture of iodine
b. Mercurochrome preparations
 Mercurochrome soln 5
 Flavored mercurochrome disclosing solution
c. Bismark brown
d. Mebromin
e. Erythrosine
f. Fast green
g. Fluoresin
h. Two tone solutions
i. Basic fuschin
Chemical plaque control

Chemical plaque control

  • 1.
  • 2.
     Used asadjunct to mechanical plaque control.  Many vehicles may be used to deliver anti plaque agents such as:  MOUTH RINSES,  TOOTHPASTES,  SPRAY,  IRRIGATORS,  CHEWING GUM,  VARNISHES.
  • 3.
    Approaches to chemicalsupragingival plaque control: 1. ANTIADHESIVE: Prevention of attachment of bacterial biofilm. 2. ANTIMICROBIAL : by inhibition of bacterial proliferation and as bactericidal. 3. PLAQUE REMOVAL 4. ANTIPATHOGENIC
  • 4.
    1. Should eliminateonly the pathogenic bacteria. 2. Prevent development of resistant bacteria. 3. Exhibit substantivity i.e. ability of an agent to bind to tissue surfaces and to be released over time to deliver an adequate dose of active principal ingredient the agent carries. (CHX gets adsorbed to oral tissues).
  • 5.
    4. Safe tooral tissues at concentrations and dosages recommended. 5. Significantly reduce and gingivitis and prevent colonization of microorganisms. 6. Should not stain the teeth or alter taste.
  • 6.
    Depending on theantimicrobial efficiency and relative substantitivity. 1st generation: decreases plaque scores by 20- 50%, but efficacy is decreased by poor retention in the mouth. E.g. antibiotics , phenols etc. 2nd generation : 70-90% more effectively retained by oral tissues and release slowly. E.g. Bisbiguanides
  • 7.
    CHEMICAL PLAQUE CONTROLAGENTS FIRST GENERATION Eg: antibiotics, phenol,quarternary ammonium compounds & sanguinarine SECOND GENERATION Eg: Bisbiguanides,(chlorhexidine) THIRD GENERATION Eg: delmopinol
  • 8.
    1. Antibiotics: penicillin, vancomycin 2.Enzymes: proteases, lipase, dextranase 3. Bisbiguanide: chlorhexidine, alexidine 4. Quaternary ammonium compounds: cetylpyridinium chloride, benzalkonium chloride 5. Phenols and essential oils: thymol, triclosan
  • 9.
    6. Natural products:sanguinarine 7. Fluorides: sodium fluoride, stannous F 8. Metal salts: tin, zinc, copper 9. Oxygenating agents: Hydrogen peroxide 10. Detergents: sodium lauryl sulfate 11. Amine alcohols: octapinol, delmopinol
  • 10.
     Phenol derivative Is synthetic and ionic  Used as a topical antimicrobial agent  Broad spectrum of action including both gram positive and gram negative bacterias  It also includes mycobacterium spores and Candida species
  • 11.
    TRICLOSAN ACT ON CYTOPLASMICMEMBRANE INDUCE LEAKAGE OF CELLULAR CONSTITUENTS BACTERIOLYSIS
  • 12.
    Triclosan is includedin tooth paste to reduce plaque formation Used along with Zinc citrate or co- polymer Gantrez to enhance its retention within the oral cavity Triclosan delay plaque formation It inhibits formation of prostaglandins & leukotrienes there by reduces the chance of inflammation
  • 13.
    eg: Zn &Cu ions MECHANISM OF ACTION  It reduces the glycolytic activity in bacteria &delays bacterial growth
  • 14.
     Cationic antiseptics& surface active agents  Effective against gram positive organisms
  • 15.
    MECHANISM OF ACTION Positively charged molecule reacts with negatively charged cell membrane phosphates and thereby disrupts the bacterial cell wall structure Eg: Benzanthonium chloride, Benzalleonium chloride and cetylpyredinium
  • 16.
     It isa benzophenanthredine alkaloid  It is most effective against gram –ve organisms  Used in mouth rinse
  • 17.
     Vancomycin,erythromycin,Niddamycin and Kanamycin Due to bacterial resistance problems the use of antibiotics has been reduced
  • 18.
    Considered to mosteffective antiplaque agents. Second generation agents exhibiting substantivity and broad antimicrobial properties.
  • 19.
     It isa cationic bisbiguanide  Effective against gram +ve, gram –ve organisms, fungi, yeasts and viruses  Exhibit antiplaque & antibacterial properties
  • 20.
    CHX due toits dicationic nature, binds to enamel pellicle or tooth surface and salivary proteins. This adsorbed CHX is released of a period of time. Mode of delivery of CHX: mouth rinse, gels, tooth paste, dental floss, and tooth picks.
  • 21.
    Antimicrobial action andantiplaque action 1. ANTIMICROBIAL: a. at low concentration is bacteriostatic - positively charged chlorhexidine molecule will adhere to negatively charged bacterial cell surface. Integrity of cell membrane disrupted causing leakage of intracellular components. b. at high concentration is bactericidal – causes precipitation of bacterial cytoplasm so cell death.
  • 22.
    Antibacterial action ofchlorhexidine It shows two actions 1. Bacteriostatic at low concentrations Bacterial cell wall(-ve charge) Reacts with +ve charged chlorhexidine molecule Integrity of cell membrane altered CHX binds to inner membrane phospholipids & increase permeability Vital elements leak out & this effect is reversible
  • 23.
    2. Bacteriocidal action increasedconcentration of chlorhexidine Progressive greater damage to membrane Larger molecular weight compounds lost Coagulation and precipitation of cytoplasm Free CHX molecule enter the cell & coagulates proteins Vital cell activity ceases cell death
  • 24.
    ANTIPLAQUE ACTION:  Preventsformation of acquired pellicle. Blocks the acidic group of salivary glycoproteins which reduces their adsorption to hydroxyapetite.  Reduces the ability of bacteria to bind to tooth surface. Adsorption of CHX to bacterial capsule or glycocalyx and prevents them binding on to tooth surface.  CHX competes for Ca ions which are required for agglutination of plaque.
  • 25.
    ADVERSE EFFECTS OFCHLORHEXIDINE 1. Brownish staining of tooth or restorations 2. Loss of taste sensation 3. Rarely hypersensitivity to chlorhexidine has been reported 4. Stenosis of parotid duct has also been reported
  • 26.
     Enzymes hasbeen used as active agents in antiplaque preparations  It is due to the fact that enzymes would be able to breakdown already formed matrix some plaques and calculus  Some are proteolytic and have bactericidal action eg:Mucinase, mutanase, dextranase etc
  • 27.
     Inhibits plaquegrowth and reduces gingivitis Mechanism of action  Interfere with plaque matrix formation & also reduces bacterial adherence  It causes weak binding of plaque to tooth, thus aiding in easy removal of plaque by mechanical procedures  It is therefore indicated as a pre brushing mouth rinse
  • 28.
    Adverse effect ofdelmopinol 1. Staining of tooth & tongue 2. Taste disturbances 3. Mucosal soreness & erosion
  • 29.
     A disclosingagent is a preparation in liquid, tablet or lozenge from which contains a dye or other coloring agents  A disclosing agent is used for identifying bacterial plaque  When applied to the teeth, the agents imparts its colour to soft deposits but can be rinsed easily from clean tooth surface
  • 30.
    IDEAL PROPERTIES  Intensityof colour  Duration of intensity  Taste  Irritation to mucous membrane  Diffusibility  Astringent and antiseptic property
  • 31.
    Agents used fordisclosing plaque a. Iodine preparations  Skinners iodine solution  Diluted tincture of iodine b. Mercurochrome preparations  Mercurochrome soln 5  Flavored mercurochrome disclosing solution c. Bismark brown d. Mebromin e. Erythrosine f. Fast green g. Fluoresin h. Two tone solutions i. Basic fuschin