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Molecular Nanotechnology
Molecular engineering
DR MEENAL ATHARKAR
ENDODONTIST
2
TECHNOLOGICAL
BREAKTHROUGHS LED TO
3
ADVANCEMENTS
IN MEDICAL AND
DENTAL FIELDS.
MICROSCOPE LED TO DISCOVERY OF
CELL AND MICRO-ORGANISMS
4
BETTER DRUGS, VACCINES, NEWER
ELECTRON MICROSCOPE
INTRODUCED GENETIC MATERIAL
5
MATERIALS AND DIAGNOSTIC METHODS
EMERGENCE OF A NEW TECHNOLOGY
NANOTECHNOLOGY
6
7
Richard P. Feynman (1959)
 Machine tools to make smaller tools - Molecular level
 Nanomachines, Nanorobots & Nanodevices
8
9
 Nano – νανος Dwarf
 Essence of small!
 DEFINITION: Nanotechnology is the engineering DEFINITION: Nanotechnology is the engineering
of functional systems at the molecular scale.
 UPTO 100 nm
 Nanometer(10-9 meter or 1 billionth of a meter)
10
Just to give you an idea
11
The smallest cellular life-forms, the bacteria of the
genus Mycoplasma, are around 200 nm in length
12
Comparative Size Of A Nanometer To A Meter Is The Same As That Of A
Marble To The Size Of The Earth
13
A nanometer is one billionth of a meter; the
head of a pin is about 1 millimeter (mm)
across, equal to 1 million nanometers (nm).across, equal to 1 million nanometers (nm).
14
 AND A LINE OF TEN HYDROGEN ATOMS
IS ONE NM
15
DNA double-helix has aDNA double-helix has a
diameter
around 2 nm
16
 The width of an average hair is 100,000
nanometers.
HISTORY
1959
The late Nobel prize winning physicist Richard P.Feynman
speculated the potential of nanosize devices in his talk “There's
Plenty of Room at the Bottom” on December 29th 1959 at the
annual meeting of the American Physical Society.
17
annual meeting of the American Physical Society.
1974
Taniguchi uses term "nano-technology" in paper on ion-sputter
machining
1977
Drexler originates molecular nanotechnology concept
1981
First technical paper on molecular engineering to build with
atomic precision Scanning Tunneling Microscope invented
1986
AFM invented
1987
First protein engineered
1990
First nanotechnology journal
1991
Carbon nanotube discovered
1997
First design of nanorobotic system
1999
First safety guidelines
2005
Nanoethics meeting
2006
National Academies nanotechnology report calls for
experimentation toward molecular manufacturing.
18
19
 Prof. Kerie Drexler-
Nanotechnology is concerned with materials & systems whose
structures & components exhibit
physical, chemical & biological properties due to their
 New behavior at the nanoscale is not necessarily
predictable from what we know at the macroscale
   Dominance of interfacial phenomena
   Van Der Waals forces, Coulombic forces
20

Manipulating atom by atom - Building blocks
21
(Nanomachines)(Nanomachines)
build
(Nanobots)
manipulate
Mihail (Mike) Roco of the U.S. National
Nanotechnology Initiative has described four
generations of nanotechnology development
The current era, as Roco depicts it, is that of passive
22
GENERATIONS
The current era, as Roco depicts it, is that of passive
nanostructures, materials designed to perform one
task.
NEWER ENZYMES
SYNTHETIC HORMONES
23
 The second phase, which we are just entering,
introduces active nanostructures for
multitasking; for example, actuators, drug
delivery devices, and sensors.delivery devices, and sensors.
PROTEIN MACHINES WILL BE USED TO
MANUFACTURE UNIVERSAL ASSEMBLERS
MADE OF TOUGHER MATERIALS LIKE METAL,
CERAMIC, OR DIAMOND
24
 The third generation is expected to begin
emerging around 2010 and will feature
nanosystems with thousands of interacting
components.components.
25
 A few years after that, the first integrated
nanosystems, functioning (according to Roco) much
like a mammalian cell with hierarchical systems
within systems, are expected to be developed
26
27
Nanotubes
Nanopores
Nanoshells
Dendrimers
Quantum dots
28
Medicine &
Health
Science &
Education
Materials &
Manufacturing
Nanoelectronics
& Computer
technology
Aeronautics &
Space
exploration
Environment &
Energy
Biotechnology
& Agriculture
Problems
29
 Untraceable weapons of mass destruction, networked cameras for use by
the government, and weapons developments fast enough to destabilize
arms races
 Nanotoxicity : Some of the recently developed nanoparticle products may
have unintended consequences. Researchers have discovered that silver
nanoparticles used in socks to reduce foot odor are being released in the
wash with possible negative consequences. Silver nanoparticles, which
are bacteriostatic, may then destroy beneficial bacteria which are
important for breaking down organic matter in waste treatment plants or
farms
30
31
 – AFM
 Scanning tunneling microscopes (STM) and scanning
probe microscopes (SPM)
 - Fluoresce or produce other- Fluoresce or produce other
signals
 - Earlier disease detection
 Improvement of

32
Targeted drug deliveryTargeted drug delivery
Solubility or stability issues
Route of administration
Adverse effects
Antigen/antibody interactionsAntigen/antibody interactions
Binding to membrane-bound receptors
Cancer
Diabetes
Malaria
Hepatitis B
Glaucoma
HIV & STD
33
 Nanorobots /Nanorobots / NanobotsNanobots
 COMPLEX MOLECULAR SYSTEMS-
Seek out a target
Achieve safe cytopenetration
‘Fix’ the target
In pharmaceutical research & clinical diagnosis
Repairing brain damageRepairing brain damage
Improving respiratory capacity
Enabling near instantaneous hemostasis
Mechanically reversing atherosclerosis
Supplementing the immune system
Resolving gross cellular insults
Rewriting or replacing DNA sequences in cells
Gerontological applications
DIAGNOSIS AND TESTING
34
INFECTION CONTROL
35
DELIVER PRECISE DOSES OF DRUGS TO
SPECIFIC CELLS
36
Fate of Nanorobots
 by metabolism & excretion-
Biodegradable or Homing devices
 without need for removal
37
without need for removal
 in the absence of feedback
mechanisms - Physically clog the system -
Negative outcomes
38
Dental
Nanorobotics
BiotechnologyNanomaterials
39
40
 Colloidal suspension
containing millions of
active analgesic dental
nanorobot particles
applied on the patient’s
gingiva
 Nanorobots will pass
through the
tooth/mucosa, proceed
toward the pulp all under

toward the pulp all under
the control of the
onboard nanocomputer,
as directed by the dentist.
 Nanorobots can complete
the journey into the pulp
chamber in
approximately 100
seconds.
 Analgesic Action –
 When the dentist presses the icon for the desired
tooth on the hand-held controller display, the
41
tooth on the hand-held controller display, the
selected tooth immediately numbs (or later, on
command, awakens).
 Nanorobots egress from the tooth via similar
pathways used for ingress; following this, they are
aspirated.
42
No needles -
Greater
patient
comfort &
reduced
anxiety
Greater
selectivity &
controllability
of analgesia
anxiety
Fast &
completely
reversible
action
Avoidance of
most side
effects &
complications
43
 Current methods provide temporary
relief
 Selectively & precisely occlude specific
tubulestubules
 Native biological materials
 Within minutes
 Quick & permanent cure
44
Manipulate the periodontal tissues -
periodontal tissues, includingperiodontal tissues, including gingivagingiva,,
periodontal ligament,periodontal ligament, cementumcementum andand
alveolar bonealveolar bonealveolar bonealveolar bone
Rapid & painless tooth straightening, rotating
& vertical repositioning
Within minutes to hours
45
 Patrol all surfaces
 Delivered by mouthwash / toothpaste



An interesting fact
46
 Heliomolar, microfilled composite resin, a close
Materials
 Heliomolar, microfilled composite resin, a close
examination of this composite suggests that a
form of nanotechnology was in use years ago, yet
never recognized.
47
 Superior esthetics
 Excellent mechanical properties
“Bottom-Up” approach
Building blocks on molecular scale - Assembled into larger
structures

48





49

Non-agglomerated silica - 20 & 75 nm

Zirconia-silica particles
Primary -2 to 20 nm
Agglomerated -0.6 μm
The nanofiller include an aluminosilicate
powder having a mean particle size of about
80nm and a 1:4ratio of alumina to silica.
Nanofillers
Based on particle size
 Megafill
 0.5 - 2 millimeters
 Macrofill
 10 - 100 microns
(canteloupe)
Midifiller
2 m
(beachball)
Minifiller
 Midifill
 1 - 10 microns
 Minifill
 0.1 - 1 microns
 Microfill
 0.01 - 0.1 microns
 Nanofill
 0.005-0.01 microns
(canteloupe)
Nanofiller-
.02 m (pea)
Microfille
r.04 m
(marble)
Nanofill vs. Nanohybrid
 Nanofilled
 nanometer-sized particles
throughout matrix
Microfillers Vs Nanofillers
 Microfiller
 Colloidal particles as
aggregates (0.4 m)
 Nanohybrid
 nanometer-sized particles
combined with more
conventional filler
technology
 Microfillers
 Individual colloidal
particles (0.04 m)
 Nanofiller(s)
 Small particles of size
ranging from 1- 100 nm
53
Resin system used in nano composites
 Bis-Gma,
 Ethoxylated Bis Phenol A Dimethacrylate,
 TEGDMA,
 Photoinitiators And Stabilizers Photoinitiators And Stabilizers
Coupling agent
3-methacryloxypropyltrimethoxysilane or MPTS.
This makes the filler compatible with resin and also
allows chemical bonding of nanomeric particle with
resin matrix while curing
54
Strength &
Fracture Wear rate
Translucency
& Change in
color post- Polish Shrinkage Handling
Strength &
Fracture
resistance
Wear rate &
Opalescent
effect
Change in
color post-
curing
Polish
retention Shrinkage Handling
JADA,Vol. 134, October 2003
55
Transmission electron microscope
56
Results
57
58
Conclusion Of the Study
59
The dental nanocomposite system studied showed
 High Translucency, High Polish And Polish Retention
Similar To Those Of Microfills
 Maintaining Physical Properties And Wear Resistance
Equivalent To Those Of Several Hybrid Composites.
Clinical Implication
60
 The strength and esthetic properties of the resin-
based nanocomposite tested should allow the
clinician to use it for both anterior and posterior
restorations.
ADVANTAGES
61
 When a particle shrinks to a fraction of the wavelength of
visible light (0.4-0.8 μm), then it would not scatter that
particular light, resulting in the human eye’s inability to detect
the particles
 When abraded, filler is lost and voids are very smallWhen abraded, filler is lost and voids are very small
 Small size allows more filler content ( DENSELY PACKED) 69%
by volume and 83.5% byweight
 Properties are similar to liquid – do not thicken the resin
 Increase hardness and wear resistance
 50% reduction in polymerisation shrinkage and less staining
(PPAD Vol. 16, No. 3 220-222)
62
Filtek supreme Filtek supreme flow
The filler’s size, relative amount
(72-78% by weight)
Filtek Z 350
Filtek supreme Filtek supreme flow
63
Synergy compact nanoformulaSynergy duo shade nanoformula
Synergy D6
Barium glass
Amorphous silica
Smallest filler particle size – 20 nm
Average filler particle size – 0.6 m
Filler content – 80% by wt and 65% by vol
Synergy super white and
transparent nanoformula
Synergy flow nanoformula
Nanohybrid composites
Simile universal nanohybrid Artiste nanohybrid flowable Virtuoso Universal
Grandio flow
Particle size - 10 to 50 nm
Aelite Aesthetic Enamel Ice
65
Premise Universal Premise
flowable
Ceram.x
66
Mean glass filler size : 1.1 – 1.5 m
Mean nanofiller size : 10 nm
Mean nanoparticle size : 2.3 nm
67
Tetric evoceram
• Ceramic fillers provide fast and easy polishability, high gloss
and low wear
• Ytterbium trifluoride - exceptionally high level of radiopacity
• Prepolymer (made of ceramic fillers, monomers and
ytterbium fluoride) is responsible for reduction in shrinkage
and shrinkage stress
 Additive - Steady release of Ca & PO4
 Structurally weaken the restoration
68
SpraySpray--drying Techniquedrying Technique - Dicalcium Phosphate
Anhydrous (DCPADCPA) – 50 nm
 Higher Surface:Volume ratio - More efficient -
Less material required
Adhesives
69
 1st dental adhesive using nanotechnology-
 Prime & Bond NT.
 Nanofillers used are of size 7-12 nm
70
5th generation light cure self priming adhesive
Prime & Bond NT Adper Single Bond plus/2
6th generation
Type 1 – Two step self etching adhesive Type 2 – One step self etching adhesive
71
7th generation One step self etching adhesive
G - BondG - Bond Nano Interaction Zone
“Nano Interaction Zone” (NIZ - < 300 nm)
•minimal decalcification and almost no exposure to collagen fibers
•producing an insoluble calcium compound
•better bond less likely to deteriorate from enzymes contained in the
mouth.
72
-10% of 5 nm silica particles
 Nanoparticles dispersed homogeneously
 Nanosize keeps in colloidal suspension
AdvantagesAdvantages
73
 Higher dentin bond strength - better performance
 No shaking of bottle required - stable nanoparticles
 Increase cohesive strength of the adhesive
 Uniform film thickness Uniform film thickness
 Low polymerisation shrinkage and post operative
sensistivity
 Increase the adhesion to both enamel and dentin
 Improve the marginal integrity
74
 World’s first Nano Ionomer by 3 M
-modified glass ionomer material based on bonded
nanofiller technologynanofiller technology
75
 High initial gloss, Smooth final surface


 Quick delivery & right mix every time
 Excellent polish saving time in difficult to polish
situations such as Class V’s,
76

 Better flow
 More hydrophilicMore hydrophilic
 Fewer voids & better pouring
 Enhanced detail precision
77
 Durability & Appearance
 Replacing upper enamel layers

 Nanostructured composite with carbon nanotubes
- More fracture resistant
 20 to 100 times - Hardness & Failure strength of
enamel
 Good biocompatibility
78
79
1. Alter genetics behind tooth loss, gum disease & bone loss
2. Dentition Renaturalization
3. Dentition Replacement
80
 Foresight Institute –

 250,000 Dollars
 First researcher to develop a Nanorobot & a Nanocomputer
 Claimed between from now
 Commercial applications will follow years later
81
Technical (Engineering
obstacles)
FinancialFinancial
Biological
Social & Ethical(Human
Safety)
Environmental Issues
82
 Recycled or disposed of as waste ?
 Ultimately accumulate in the soil, water or
plant life
Worst case scenario : Grey goo Worst case scenario : Grey goo
Governing bodies
83
 Office of Combination Products
 FDA Center
 However, consultations from other Centers
will be sought.will be sought.
Big future for a small invention
84
 U.S. -$118M
 Japan -$120M Japan -$120M
 Europe -$122M
 Others -$65M
85
 8 th December
 2011
 Bangalore
References
86
+ Nanodentistry – Fact or fiction -JADA, Vol. 131, November 2000
+ www.Wikipedia.com
+ Nanodentistry Robert A. Freitas JR., J.D., B.S.- JADA, Vol. 131, November 2000
1559
+ http://research.med.helsinki.fi/corefacilities/proteinchem/
+ Nanorobotics In Dentistry(http://www.dharwadhubli.com)
+ Nanomedicine: destination or journey?(Nanotechnology 13 (2002) R9–R13)
+ Direct Applications Of A Nanocomposite Resin System: Part 2 — Procedures For
Anterior Restorations Douglas A. Terry, DDS*Pract Proced Aesthet Dent 2004;16(9):A-
H
+ www.crn.com
+ Nanotechnology, nanomedicine and nanosurgery IJS(2005)
+ JADA, Vol. 134, October 2003
+ Dental Materials 2 4 ( 2 0 0 8 ) 111–116
87
+Jhaveri HM, Balaji PR , Nanotechnology: the future of dentistry. J Indian Prosthodont
Soc 2005; 5: 15-17.
•Binu NS, Varhease NO. Nanodreams in dentistry-A step ahead the future. JIDA 2002;
173: 299-303.
www.nanoshop.com.
www.Dentsply.com.www.Dentsply.com.
•www.apinanotronics.com/investors/glossory.asp
• www.nano.ir/paper_en.php
• http:// advancednano.blogspot.com/2006_06_01_archive.html
•www.nanotech-now.com/spacetechology.
• http://www.biomed.metu.edu.tr/courses/term_papers/prost-med-apllpolm_sagay.htm.

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Nanotechnology

  • 2. 2
  • 4. MICROSCOPE LED TO DISCOVERY OF CELL AND MICRO-ORGANISMS 4
  • 5. BETTER DRUGS, VACCINES, NEWER ELECTRON MICROSCOPE INTRODUCED GENETIC MATERIAL 5 MATERIALS AND DIAGNOSTIC METHODS
  • 6. EMERGENCE OF A NEW TECHNOLOGY NANOTECHNOLOGY 6
  • 7. 7 Richard P. Feynman (1959)  Machine tools to make smaller tools - Molecular level  Nanomachines, Nanorobots & Nanodevices
  • 8. 8
  • 9. 9  Nano – νανος Dwarf  Essence of small!  DEFINITION: Nanotechnology is the engineering DEFINITION: Nanotechnology is the engineering of functional systems at the molecular scale.  UPTO 100 nm  Nanometer(10-9 meter or 1 billionth of a meter)
  • 10. 10
  • 11. Just to give you an idea 11 The smallest cellular life-forms, the bacteria of the genus Mycoplasma, are around 200 nm in length
  • 12. 12 Comparative Size Of A Nanometer To A Meter Is The Same As That Of A Marble To The Size Of The Earth
  • 13. 13 A nanometer is one billionth of a meter; the head of a pin is about 1 millimeter (mm) across, equal to 1 million nanometers (nm).across, equal to 1 million nanometers (nm).
  • 14. 14  AND A LINE OF TEN HYDROGEN ATOMS IS ONE NM
  • 15. 15 DNA double-helix has aDNA double-helix has a diameter around 2 nm
  • 16. 16  The width of an average hair is 100,000 nanometers.
  • 17. HISTORY 1959 The late Nobel prize winning physicist Richard P.Feynman speculated the potential of nanosize devices in his talk “There's Plenty of Room at the Bottom” on December 29th 1959 at the annual meeting of the American Physical Society. 17 annual meeting of the American Physical Society. 1974 Taniguchi uses term "nano-technology" in paper on ion-sputter machining 1977 Drexler originates molecular nanotechnology concept 1981 First technical paper on molecular engineering to build with atomic precision Scanning Tunneling Microscope invented
  • 18. 1986 AFM invented 1987 First protein engineered 1990 First nanotechnology journal 1991 Carbon nanotube discovered 1997 First design of nanorobotic system 1999 First safety guidelines 2005 Nanoethics meeting 2006 National Academies nanotechnology report calls for experimentation toward molecular manufacturing. 18
  • 19. 19  Prof. Kerie Drexler- Nanotechnology is concerned with materials & systems whose structures & components exhibit physical, chemical & biological properties due to their  New behavior at the nanoscale is not necessarily predictable from what we know at the macroscale    Dominance of interfacial phenomena    Van Der Waals forces, Coulombic forces
  • 20. 20  Manipulating atom by atom - Building blocks
  • 22. Mihail (Mike) Roco of the U.S. National Nanotechnology Initiative has described four generations of nanotechnology development The current era, as Roco depicts it, is that of passive 22 GENERATIONS The current era, as Roco depicts it, is that of passive nanostructures, materials designed to perform one task. NEWER ENZYMES SYNTHETIC HORMONES
  • 23. 23  The second phase, which we are just entering, introduces active nanostructures for multitasking; for example, actuators, drug delivery devices, and sensors.delivery devices, and sensors. PROTEIN MACHINES WILL BE USED TO MANUFACTURE UNIVERSAL ASSEMBLERS MADE OF TOUGHER MATERIALS LIKE METAL, CERAMIC, OR DIAMOND
  • 24. 24  The third generation is expected to begin emerging around 2010 and will feature nanosystems with thousands of interacting components.components.
  • 25. 25  A few years after that, the first integrated nanosystems, functioning (according to Roco) much like a mammalian cell with hierarchical systems within systems, are expected to be developed
  • 26. 26
  • 28. 28 Medicine & Health Science & Education Materials & Manufacturing Nanoelectronics & Computer technology Aeronautics & Space exploration Environment & Energy Biotechnology & Agriculture
  • 29. Problems 29  Untraceable weapons of mass destruction, networked cameras for use by the government, and weapons developments fast enough to destabilize arms races  Nanotoxicity : Some of the recently developed nanoparticle products may have unintended consequences. Researchers have discovered that silver nanoparticles used in socks to reduce foot odor are being released in the wash with possible negative consequences. Silver nanoparticles, which are bacteriostatic, may then destroy beneficial bacteria which are important for breaking down organic matter in waste treatment plants or farms
  • 30. 30
  • 31. 31  – AFM  Scanning tunneling microscopes (STM) and scanning probe microscopes (SPM)  - Fluoresce or produce other- Fluoresce or produce other signals  - Earlier disease detection  Improvement of 
  • 32. 32 Targeted drug deliveryTargeted drug delivery Solubility or stability issues Route of administration Adverse effects Antigen/antibody interactionsAntigen/antibody interactions Binding to membrane-bound receptors Cancer Diabetes Malaria Hepatitis B Glaucoma HIV & STD
  • 33. 33  Nanorobots /Nanorobots / NanobotsNanobots  COMPLEX MOLECULAR SYSTEMS- Seek out a target Achieve safe cytopenetration ‘Fix’ the target In pharmaceutical research & clinical diagnosis Repairing brain damageRepairing brain damage Improving respiratory capacity Enabling near instantaneous hemostasis Mechanically reversing atherosclerosis Supplementing the immune system Resolving gross cellular insults Rewriting or replacing DNA sequences in cells Gerontological applications
  • 36. DELIVER PRECISE DOSES OF DRUGS TO SPECIFIC CELLS 36
  • 37. Fate of Nanorobots  by metabolism & excretion- Biodegradable or Homing devices  without need for removal 37 without need for removal  in the absence of feedback mechanisms - Physically clog the system - Negative outcomes
  • 39. 39
  • 40. 40  Colloidal suspension containing millions of active analgesic dental nanorobot particles applied on the patient’s gingiva  Nanorobots will pass through the tooth/mucosa, proceed toward the pulp all under  toward the pulp all under the control of the onboard nanocomputer, as directed by the dentist.  Nanorobots can complete the journey into the pulp chamber in approximately 100 seconds.
  • 41.  Analgesic Action –  When the dentist presses the icon for the desired tooth on the hand-held controller display, the 41 tooth on the hand-held controller display, the selected tooth immediately numbs (or later, on command, awakens).  Nanorobots egress from the tooth via similar pathways used for ingress; following this, they are aspirated.
  • 42. 42 No needles - Greater patient comfort & reduced anxiety Greater selectivity & controllability of analgesia anxiety Fast & completely reversible action Avoidance of most side effects & complications
  • 43. 43  Current methods provide temporary relief  Selectively & precisely occlude specific tubulestubules  Native biological materials  Within minutes  Quick & permanent cure
  • 44. 44 Manipulate the periodontal tissues - periodontal tissues, includingperiodontal tissues, including gingivagingiva,, periodontal ligament,periodontal ligament, cementumcementum andand alveolar bonealveolar bonealveolar bonealveolar bone Rapid & painless tooth straightening, rotating & vertical repositioning Within minutes to hours
  • 45. 45  Patrol all surfaces  Delivered by mouthwash / toothpaste   
  • 46. An interesting fact 46  Heliomolar, microfilled composite resin, a close Materials  Heliomolar, microfilled composite resin, a close examination of this composite suggests that a form of nanotechnology was in use years ago, yet never recognized.
  • 47. 47  Superior esthetics  Excellent mechanical properties
  • 48. “Bottom-Up” approach Building blocks on molecular scale - Assembled into larger structures  48     
  • 49. 49  Non-agglomerated silica - 20 & 75 nm  Zirconia-silica particles Primary -2 to 20 nm Agglomerated -0.6 μm The nanofiller include an aluminosilicate powder having a mean particle size of about 80nm and a 1:4ratio of alumina to silica.
  • 50. Nanofillers Based on particle size  Megafill  0.5 - 2 millimeters  Macrofill  10 - 100 microns (canteloupe) Midifiller 2 m (beachball) Minifiller  Midifill  1 - 10 microns  Minifill  0.1 - 1 microns  Microfill  0.01 - 0.1 microns  Nanofill  0.005-0.01 microns (canteloupe) Nanofiller- .02 m (pea) Microfille r.04 m (marble)
  • 51. Nanofill vs. Nanohybrid  Nanofilled  nanometer-sized particles throughout matrix Microfillers Vs Nanofillers  Microfiller  Colloidal particles as aggregates (0.4 m)  Nanohybrid  nanometer-sized particles combined with more conventional filler technology  Microfillers  Individual colloidal particles (0.04 m)  Nanofiller(s)  Small particles of size ranging from 1- 100 nm
  • 52.
  • 53. 53 Resin system used in nano composites  Bis-Gma,  Ethoxylated Bis Phenol A Dimethacrylate,  TEGDMA,  Photoinitiators And Stabilizers Photoinitiators And Stabilizers Coupling agent 3-methacryloxypropyltrimethoxysilane or MPTS. This makes the filler compatible with resin and also allows chemical bonding of nanomeric particle with resin matrix while curing
  • 54. 54 Strength & Fracture Wear rate Translucency & Change in color post- Polish Shrinkage Handling Strength & Fracture resistance Wear rate & Opalescent effect Change in color post- curing Polish retention Shrinkage Handling
  • 58. 58
  • 59. Conclusion Of the Study 59 The dental nanocomposite system studied showed  High Translucency, High Polish And Polish Retention Similar To Those Of Microfills  Maintaining Physical Properties And Wear Resistance Equivalent To Those Of Several Hybrid Composites.
  • 60. Clinical Implication 60  The strength and esthetic properties of the resin- based nanocomposite tested should allow the clinician to use it for both anterior and posterior restorations.
  • 61. ADVANTAGES 61  When a particle shrinks to a fraction of the wavelength of visible light (0.4-0.8 μm), then it would not scatter that particular light, resulting in the human eye’s inability to detect the particles  When abraded, filler is lost and voids are very smallWhen abraded, filler is lost and voids are very small  Small size allows more filler content ( DENSELY PACKED) 69% by volume and 83.5% byweight  Properties are similar to liquid – do not thicken the resin  Increase hardness and wear resistance  50% reduction in polymerisation shrinkage and less staining (PPAD Vol. 16, No. 3 220-222)
  • 62. 62 Filtek supreme Filtek supreme flow The filler’s size, relative amount (72-78% by weight) Filtek Z 350 Filtek supreme Filtek supreme flow
  • 63. 63 Synergy compact nanoformulaSynergy duo shade nanoformula Synergy D6 Barium glass Amorphous silica Smallest filler particle size – 20 nm Average filler particle size – 0.6 m Filler content – 80% by wt and 65% by vol Synergy super white and transparent nanoformula Synergy flow nanoformula
  • 64. Nanohybrid composites Simile universal nanohybrid Artiste nanohybrid flowable Virtuoso Universal Grandio flow Particle size - 10 to 50 nm Aelite Aesthetic Enamel Ice
  • 66. Ceram.x 66 Mean glass filler size : 1.1 – 1.5 m Mean nanofiller size : 10 nm Mean nanoparticle size : 2.3 nm
  • 67. 67 Tetric evoceram • Ceramic fillers provide fast and easy polishability, high gloss and low wear • Ytterbium trifluoride - exceptionally high level of radiopacity • Prepolymer (made of ceramic fillers, monomers and ytterbium fluoride) is responsible for reduction in shrinkage and shrinkage stress
  • 68.  Additive - Steady release of Ca & PO4  Structurally weaken the restoration 68 SpraySpray--drying Techniquedrying Technique - Dicalcium Phosphate Anhydrous (DCPADCPA) – 50 nm  Higher Surface:Volume ratio - More efficient - Less material required
  • 69. Adhesives 69  1st dental adhesive using nanotechnology-  Prime & Bond NT.  Nanofillers used are of size 7-12 nm
  • 70. 70 5th generation light cure self priming adhesive Prime & Bond NT Adper Single Bond plus/2 6th generation Type 1 – Two step self etching adhesive Type 2 – One step self etching adhesive
  • 71. 71 7th generation One step self etching adhesive G - BondG - Bond Nano Interaction Zone “Nano Interaction Zone” (NIZ - < 300 nm) •minimal decalcification and almost no exposure to collagen fibers •producing an insoluble calcium compound •better bond less likely to deteriorate from enzymes contained in the mouth.
  • 72. 72 -10% of 5 nm silica particles  Nanoparticles dispersed homogeneously  Nanosize keeps in colloidal suspension
  • 73. AdvantagesAdvantages 73  Higher dentin bond strength - better performance  No shaking of bottle required - stable nanoparticles  Increase cohesive strength of the adhesive  Uniform film thickness Uniform film thickness  Low polymerisation shrinkage and post operative sensistivity  Increase the adhesion to both enamel and dentin  Improve the marginal integrity
  • 74. 74  World’s first Nano Ionomer by 3 M -modified glass ionomer material based on bonded nanofiller technologynanofiller technology
  • 75. 75  High initial gloss, Smooth final surface    Quick delivery & right mix every time  Excellent polish saving time in difficult to polish situations such as Class V’s,
  • 76. 76   Better flow  More hydrophilicMore hydrophilic  Fewer voids & better pouring  Enhanced detail precision
  • 77. 77  Durability & Appearance  Replacing upper enamel layers   Nanostructured composite with carbon nanotubes - More fracture resistant  20 to 100 times - Hardness & Failure strength of enamel  Good biocompatibility
  • 78. 78
  • 79. 79 1. Alter genetics behind tooth loss, gum disease & bone loss 2. Dentition Renaturalization 3. Dentition Replacement
  • 80. 80  Foresight Institute –   250,000 Dollars  First researcher to develop a Nanorobot & a Nanocomputer  Claimed between from now  Commercial applications will follow years later
  • 82. Environmental Issues 82  Recycled or disposed of as waste ?  Ultimately accumulate in the soil, water or plant life Worst case scenario : Grey goo Worst case scenario : Grey goo
  • 83. Governing bodies 83  Office of Combination Products  FDA Center  However, consultations from other Centers will be sought.will be sought.
  • 84. Big future for a small invention 84  U.S. -$118M  Japan -$120M Japan -$120M  Europe -$122M  Others -$65M
  • 85. 85  8 th December  2011  Bangalore
  • 86. References 86 + Nanodentistry – Fact or fiction -JADA, Vol. 131, November 2000 + www.Wikipedia.com + Nanodentistry Robert A. Freitas JR., J.D., B.S.- JADA, Vol. 131, November 2000 1559 + http://research.med.helsinki.fi/corefacilities/proteinchem/ + Nanorobotics In Dentistry(http://www.dharwadhubli.com) + Nanomedicine: destination or journey?(Nanotechnology 13 (2002) R9–R13) + Direct Applications Of A Nanocomposite Resin System: Part 2 — Procedures For Anterior Restorations Douglas A. Terry, DDS*Pract Proced Aesthet Dent 2004;16(9):A- H + www.crn.com + Nanotechnology, nanomedicine and nanosurgery IJS(2005) + JADA, Vol. 134, October 2003 + Dental Materials 2 4 ( 2 0 0 8 ) 111–116
  • 87. 87 +Jhaveri HM, Balaji PR , Nanotechnology: the future of dentistry. J Indian Prosthodont Soc 2005; 5: 15-17. •Binu NS, Varhease NO. Nanodreams in dentistry-A step ahead the future. JIDA 2002; 173: 299-303. www.nanoshop.com. www.Dentsply.com.www.Dentsply.com. •www.apinanotronics.com/investors/glossory.asp • www.nano.ir/paper_en.php • http:// advancednano.blogspot.com/2006_06_01_archive.html •www.nanotech-now.com/spacetechology. • http://www.biomed.metu.edu.tr/courses/term_papers/prost-med-apllpolm_sagay.htm.