osseointegration and mineralised tissue Flashcards

1
Q

what uses are there for implants?

A

BONE DEFECTS

  • Dental Surgery
    • prosthetic implants.
  • Orthopaedic Surgery
    • replacement of worn / diseased joints.
  • Craniofacial reconstruction
    • e.g. tumour surgery.
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2
Q

what is osseointegration?

A

Success & reliability of biomaterials, based on adaptation & interaction of healthy bone to the implant surface

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3
Q

what types of biomaterials are used as dental implants?

A
  • Metals Titanium
    • Pure and alloy
    • Zirconium
    • Stainless steel
    • Cobalt-chromium alloy
  • Hydroxyapatite ceramic materials
  • Hydroxyapatite-coated materials
  • Glass ionomer
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4
Q

what are the mechanisms of osseointegration?

A
  • Forcible insertion of implant
    • Trauma
  • Re-establishment of normal tissue structure and function
    • As other tissues, occurs via multiple overlapping phases
    • Soft tissue repair
    • Additional mineralisation processes also occur
    • Vasoconstriction, haemostasis & inflammation occur as in soft tissues
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5
Q

what occurs after implant insertion?

A
  • Blood vessel injury increases blood release.
  • vasoconstriction
  • protein adsorption
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6
Q

after implant insertion what are the consequences of blood vessel injury?

A
  • increases blood release
  • coagulation - formation of a fibrin clot
    • rich in
      • fibronectin, hyaluronan, vitronectin, thrombospondin.
    • Functions
      • Reservoir of pro-inflammatory cytokines / growth factors.
      • e.g. PDGF, EGF, TNF-a, TGF-b.
      • Provisional matrix for inflammatory cell migration / activation
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7
Q

what occurs during the inflammatory phase after implant insertion?

A
  • Initial cell recruitment to the implant site
  • predominantly neutrophils, monocytes / macrophages.
  • Neutrophil degranulation / phagocytosis.
  • M1 subtype macrophages

release:

  • Proinflammatory cytokines - IL-1, TNF-a.
  • Enzymes (MMPs, myeloperoxidase, lysozyme).
    • Attack bacteria
  • Reactive oxygen species (ROS) :
    • Superoxide radicals -
      • O2
    • Hydrogen peroxide -
      • H2O2.
    • Hydroxyl radicals -
      • .OH.
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8
Q

if the inflammatory phase is an acute response, what occurs after?

A

migration / proliferation of undifferentiated mesenchymal stem cells induced towards implant surface (osteoinduction phase).

  • Aims to increase numbers of undifferentiated mesenchymal stem cells at the implant site
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9
Q

what occurs during the granulation phase after implant insertion?

A
  • inflammatory infiltration ceases
    • replaced with M2 macrophages
    • role in removal of tissue debris
  • fibrin clot changes in composition
    • degraded into granulation tissue
    • rich in hyaluronan
    • Granulation tissue acts as provisional matrix to allow mesenchymal stem cells to differentiate into mature osteoblasts
      • Osteoconduction
  • stem cells and M2 macrophages produce growth factors to regulate the healing process
    • VEGF, bFGF, TGF-ßs, BMPs, PDGF, IGF.
  • angiogenesis takes place
    • Endothelial cell migration, proliferation & differentiation.
    • Formation of vascular loops & capillary network.
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10
Q

what occurs during osteoinduction?

A

Migration / proliferation of bone marrow derived MSCs

  • Enhanced by TGF-ßs, BMPs, PDGF, VEGF
    • Also stimulate stem cells to proliferate at the implant site
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11
Q

what occurs during osteoconduction?

A

Induced by BMPs, TGF-ß, VEGF

  • Also induce differentiation of MSCs into osteoprogenitor cells
    • = Osteoconduction

Inhibited by PDGF & bFGF

  • RUNX2
    • Expression required to form mature osteoblast
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12
Q

what are phenotypic markers of osteoblasts?

A

Alkaline phosphatase

Type I collagen

Osteocalcin

Osteonectin

Osteopontin

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13
Q

what occurs during the tissue remodelling phase after implant insertion?

A
  • mature osteoblasts synthesise ECM - osteoid
    • rich in proteoglycans and hyaluronan
    • lacks type 1 collagen
      • added later
  • matrix mediated mineralisation occurs - HAP formation
  • formation of disorganised trabecular woven bone
    • weak, high porosity
  • matures into lamellar bone
    • more mineralised
  • osteoadaptation occurs
    • bone resorption and remodelling by osteoblastsandclasts
    • due to mechanical loading
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14
Q

how does osteoclast resorption occur?

A
  • Migration to resorption site & attachment to bone.
  • Formation of sealing zone & ruffled border.
  • HAP dissolution.
  • ECM degradation & removal from resorption pit.
  • Apoptosis or return to non-resorbing state.
  • HAP dissolution by HCl secretion through ruffled border to the resorption pit.
  • Carbonic anhydrase II (CAII) activity.
  • Low pH(pH=4)duetoH+ &Cl- pumps.
  • ECM degradation by cysteine proteinases (especially cathepsin K) & MMPs (MMP-9, -14).
  • Also TRAP & ROS.
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15
Q

what is osseointegration?

what occurs

what types are there?

A
  • Mature osteoblasts formed during osteoconduction
    • Begin to form osteoid
      • ECM
    • Can occur adjacent to implant surface/directly attached/towards implant
    • Osteoid fills space between implant and adjacent bone tissue
      • Becomes mineralised by matrix mediated mineralisation later
  • contant osseointegration
  • distance osseointegration
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16
Q

what is distance osseointegration?

what occurs?

A

Distance osseointegration

  • Bone formation from the adjacent tissue
  • Osteoblasts are not attached
    • Form bone towards the implant surface
  • Osteoblasts can then :
    • Undergo apoptosis
    • Become embedded in bone as osteocytes
  • Osteoclasts migrate into site by osteoadaptation
    • Work with osteoblasts to have best fit to bone around implant surface
17
Q

what is contact osseointegration?

what occurs?

A
  • Osteoblasts are attached to the implant
  • osteoid (ECM) is formed adjacent to the implant surface
    • mineralised later by MMM
20
Q

how is soft tissue remodelled after implant insertion?

A
  • restoration of the dental gingival junction
  • fibroblast migration and proliferation
    • growth factors : PDGF, TGF-b, EGF, FGF
  • ECM synthesis
    • collagen type I
    • proteoglycans, hyaluronan, elastin, fibronectin
  • re-epithelialisation
    • de-differentiation
    • migration
    • proliferation
    • differentiation/stratification
    • ecm synthesis
21
Q

what lies between bone and the implant surface

A

Bone NEVER in direct contact with implant surface !!!

Cement line (CL).

22
Q

which material has best osseointegration and mechanical properties?

and why?

A
  • titanium
    • has a narrower cement line
    • allows mineralised layers to be closer to the implant surface

-> increased osseointegration and mechanical properties

23
Q

what are the properties of the cement line?

A

ECM layer identified at bone-implant interface.

  • Rich in CS-decorin, CS-biglycan, hyaluronan.
  • Collagen-free
    • INHIBIT MINERALISATION. - no gap zones
24
Q

what changes are there to the structure of the layers at the bone-implant interface as you move away from the implant surface?

A

As you move from implant surface

  • Increase in type I collagen - more structured
  • therefore more mineralisation
26
Q

why is titanium used as an implant material?

A
  • is good
  • Biocompatible,
  • low corrosion / toxicity,
  • good mechanical properties.
  • cement line is narrower
27
Q

why is the cement line narrower with titanium as the implant material?

A
  • ROS produced by neutrophils and macrophages during the inflammatory phase
    • react with titanium oxide surface
  • Result in formation of titanium peroxy gel (TiOOH)
  • ROS in TiOOH elps degrade ECM components of cement layer
    • proteoglycan and hyaluronan
  • Therefore mineralised tissues are closer to the implant surface
28
Q

why do implants fail?

A
  • Implant failure -
    • insertion (primary),
    • loaded (secondary).
  • Primary factors
    • No single aetiological factor:-
    • Poor surgical technique.
    • Perimplantitis (INFLAMMATION).
      • Poor oral hygiene
    • Impaired healing by host factors.
      • E.g. Smoking, type 2 diabetes
  • Secondary factors
    • Poor bone quality & premature loading.
    • Inadequate bone on implant insertion to withstand stress.
29
Q

how is bone quality classified?

A
  • 4 types of bone described (Brånemark):

Type I

  • Homogeneous cortical bone.

Type II

  • Thick cortical bone with marrow cavity.

Type III

  • Thin cortical bone with dense trabecular bone of good strength.

Type IV

  • Very thin cortical with low density trabecular bone of poor strength.

I, II, III

  • Sufficient cortical bone for initial implant stabilisation and healing.

IV

  • Implant failure.

Higher success rates with mandibular implants than maxillar implants.

  • Maxillar predominantly III and IV.
30
Q

what is the aim of manipulating titanium surfaces for implant use?

A

to modify surface chemistry, composition, topography / roughness

31
Q

what methods are there for manipulation of titanium surfaces for implant use?

A
  • Physical (Mechanical Processing)
    • Machining / Polishing (Blasting).
    • Plasma Treatment (Spraying / Sputtering / Ion Implantation).
    • Laser Treatment.
  • Chemical
    • Acid Etching (HNO3 / HF, HCl / H2SO4).
    • Alkali / Heat Treatment (NaOH, 600-800oC).
    • Anodic Oxidation.
    • Hydrothermal Treatment.
    • Electrochemical Deposition.
    • H2O2 pre-treatment.