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M A X I L L O FA C I A L R E G I O N
BONE BIOLOGY &
HEALING
M O D E R A T O R –
D R . R A J A S E K H A R G .
P R E S E N T E D B Y -
D R . S H E E T A L K A P S E
CONTENTS
• Introduction
• Embryology and development
• Structure
• Chemical composition
• Mechanical properties
• Biomechanics of craniomaxillofacial skeleton
• Fracture and role of blood supply
• Biological reaction and healing of bone
• Complications of bone healing
• Metals, surfaces and tissue interactions
INTRODUCTION
• WHAT IS BONE ?
• FUNCTION ?
• NUMBERS
EMBRYOLOGY AND DEVELOPMENT
MEMBRANOUS
OSSIFICATION
Frontal
Parietal
Nasal bones
Maxilla
Zygoma
Mandible
ENDOCHONDRAL
OSSIFICATION
Skull base
Occipital bone
Nasal septum
Internal
components of the nose
STRUCTURE
CHEMICAL COMPOSITION
INORGANIC
1. Hydroxyapatite
[Ca10(PO4)6(OH)2]
2. Magnesium
3. Potassium
4. Chlorine
5. Iron
6. Carbonate
ORGANIC
1. 90% collagen, primarily type I
2. 10% Non-collagenous proteins
and lipids
a. 23% osteonectin
b. 15% osteocalcin
c. 9% sialoprotein,
d. 9% phosphoproteins
e. 5% α2-HS-glycoproteins
f. 4% proteoglycans
g. 3% albumin
MECHANICAL PROPERTIES
Collagen fibers Mineral phase
Specific
orientation
Specific length
Shear forces
Tensile forces Compressive forces
• Elongation of 2%
• Strength about 1Mpa
• Tensile strength = 2/3rd
compressive strength
BIOMECHANICS OF
CRANIOMAXILLOFACIAL SKELETON
Maximum bite forces in an average population
200 to 300 N - incisor area
300 to 500 N - premolar region
500 to 700 - molar area
R. C. W. Wong, H. Tideman, L. Kin, M. A. W. Merkx:
Biomechanics of mandibular reconstruction: a review. Int. J. Oral
Maxillofac. Surg. 2010; 39: 313–319.
FRACTURE AND ROLE OF
BLOOD SUPPLY
INJURY
INTRAVASCULAR CLOTTING CONGESTION
DECREASED BLOOD SUPPLY
NECROSIS
OSTEOBLASTIC ACTIVITY
OSTEOCLASTIC ACTIVITY
BONY BRIDGING
VASCULAR INVASION
BIOLOGICAL REACTION AND
HEALING OF BONE
• Dependent on the biological and biomechanical environment, three basic
scenarios can be differentiated:
1. Primary bone healing (contact or gap healing)
2. Secondary bone healing via callus formation
Sufficient blood supply
Presence of specific cells
Adequate mechanical conditions
Undisturbed
fracture healing
1. PRIMARY BONE HEALING
(CONTACT OR GAP HEALING)
• In cases where inter-fragmentary motion can be completely avoided, a healing
pattern results which is characterized by an increased amount of intracortical
remodelling, inside and in between the fragment ends.
• As long as there is no destruction of bone in the contact areas, the motion in the
gap is small enough to keep inter-fragmentary strain below 2%.
• The pattern of direct healing per se is not a goal to strive for, but the absence of
this pattern, ie, the formation of periosteal callus under conditions of plate
fixation is an indicator that complete immobilization was not achieved.
a Functionally stable
fixation of a mandibular
fracture with excellent
repositioning as a precondition
for primary bone healing.
b Enlarged section of (a):
primary bone healing contact
area, direct bony bridging
showing osteons crossing the
fracture area.
a Stable fixation, load
sharing with contact area
superiorly and gap area
inferiorly.
b Enlarged section of (a):
primary healing gap area:
complete filling of the fracture
gap with lamellar bone in a
direction parallel to the
fracture surface.
2. SECONDARY BONE HEALING
VIA CALLUS FORMATION
• In cases when no fracture fixation or just loose adaptation fixation is done,
macromotion between the fragment ends occurs.
• The strain in between the fragments exceeds what bone can tolerate, and
new bone developing between the fracture ends would be destroyed before
it is formed.
Endosteal callus
Periosteal callus
In between the fracture ends a tissue differentiation cascade
takes place, during which stiffness and strength increases and
strain tolerance gradually decreases.
Hematoma
Granulation tissue
Connective tissue
Fibrocartilage
Mineralized cartilage
Woven bone
Compact bone
Secondary bone healing,
phase 1: hematoma filling the fracture gap.
Secondary bone healing,
phase 2: granulation tissue and connective tissue replacing the
hematoma in the fracture gap.
• The elongation to
rupture is found to
be between 5% and
17%.
• Fibrous tissue is
found in areas where
tensile forces act,
• Cartilage is formed
in zones of
hydrostatic pressure
Secondary bone healing,
phase 3: fibrocartilage replacing the connective tissue in the
fracture gap.
Secondary bone healing,
phase 4: woven bone replaced by lamellar bone through Haversian
remodelling.
COMPLICATIONS OF BONE HEALING
1. Non-union
2. Delayed union
3. Malunion
FACTORS
PATIENT ASSOCIATED
OPERATOR ASSOCIATED
HARDWARE ASSOCIATED
LOCAL
SYSTEMIC
METALS, SURFACES AND TISSUE
INTERACTIONS
 62.5% iron
 18% chromium
 14% nickel
 2.5% molybdenum
 minor elemental
316 L iron-base alloy
Allergic reactions to nickel 3–15%
Titanium alloys
 Ti grades 1–4
 Ti-6Al-7Nb alloy
 Ti-15Mo alloy
(α & β)
FIXATION DEVICE BLOOD
BLOOD PROTEINS COVERING
THE FIXATION DEVICE
(matrix for platelets and other cells)
PLATELET
DEGRANULATION
INFLAMMATION
(cytokines & growth factors)
HEMATOMA
FORMATION
Proliferation
Remodelling
BIODEGRADABLE MATERIALS
Water and CO2
In the future, maxillofacial
fracture fixation may utilize
biodegradable bone adhesives
and composites in lieu of the
traditional titanium plate/screw
systems. The adhesives
currently under study are in the
cyanoacrylate polymer family,
namely, butyl-2-cyanoacrylate.
REFERENCE
1. Fonseca Raymond J, Walker Robert V, Barber H Dexter, Powers, Michael P,
Frost David E. oral and maxillofacial trauma. China: Saunders; 2013.
2. Hom, Hebda, Gosain, Friedman. Essential tissue healing of the face and neck.
India. Peoples medical publishing house.
3. AOCMF principles of internal fixations of craniomaxillofacial skeleton, trauma
& orthognathic surgery.
4. Rowe NL, William JL. Maxillofacial injuries. 1st ed. India ISBN 978-81-312-
1840—2 2009.
THANK YOU

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Bone biology and bone healing

  • 1. M A X I L L O FA C I A L R E G I O N BONE BIOLOGY & HEALING M O D E R A T O R – D R . R A J A S E K H A R G . P R E S E N T E D B Y - D R . S H E E T A L K A P S E
  • 2. CONTENTS • Introduction • Embryology and development • Structure • Chemical composition • Mechanical properties • Biomechanics of craniomaxillofacial skeleton • Fracture and role of blood supply • Biological reaction and healing of bone • Complications of bone healing • Metals, surfaces and tissue interactions
  • 3. INTRODUCTION • WHAT IS BONE ? • FUNCTION ? • NUMBERS
  • 4. EMBRYOLOGY AND DEVELOPMENT MEMBRANOUS OSSIFICATION Frontal Parietal Nasal bones Maxilla Zygoma Mandible ENDOCHONDRAL OSSIFICATION Skull base Occipital bone Nasal septum Internal components of the nose
  • 6. CHEMICAL COMPOSITION INORGANIC 1. Hydroxyapatite [Ca10(PO4)6(OH)2] 2. Magnesium 3. Potassium 4. Chlorine 5. Iron 6. Carbonate ORGANIC 1. 90% collagen, primarily type I 2. 10% Non-collagenous proteins and lipids a. 23% osteonectin b. 15% osteocalcin c. 9% sialoprotein, d. 9% phosphoproteins e. 5% α2-HS-glycoproteins f. 4% proteoglycans g. 3% albumin
  • 7. MECHANICAL PROPERTIES Collagen fibers Mineral phase Specific orientation Specific length Shear forces Tensile forces Compressive forces • Elongation of 2% • Strength about 1Mpa • Tensile strength = 2/3rd compressive strength
  • 9.
  • 10.
  • 11. Maximum bite forces in an average population 200 to 300 N - incisor area 300 to 500 N - premolar region 500 to 700 - molar area
  • 12. R. C. W. Wong, H. Tideman, L. Kin, M. A. W. Merkx: Biomechanics of mandibular reconstruction: a review. Int. J. Oral Maxillofac. Surg. 2010; 39: 313–319.
  • 13. FRACTURE AND ROLE OF BLOOD SUPPLY INJURY INTRAVASCULAR CLOTTING CONGESTION DECREASED BLOOD SUPPLY NECROSIS OSTEOBLASTIC ACTIVITY OSTEOCLASTIC ACTIVITY BONY BRIDGING VASCULAR INVASION
  • 14. BIOLOGICAL REACTION AND HEALING OF BONE • Dependent on the biological and biomechanical environment, three basic scenarios can be differentiated: 1. Primary bone healing (contact or gap healing) 2. Secondary bone healing via callus formation Sufficient blood supply Presence of specific cells Adequate mechanical conditions Undisturbed fracture healing
  • 15. 1. PRIMARY BONE HEALING (CONTACT OR GAP HEALING) • In cases where inter-fragmentary motion can be completely avoided, a healing pattern results which is characterized by an increased amount of intracortical remodelling, inside and in between the fragment ends. • As long as there is no destruction of bone in the contact areas, the motion in the gap is small enough to keep inter-fragmentary strain below 2%. • The pattern of direct healing per se is not a goal to strive for, but the absence of this pattern, ie, the formation of periosteal callus under conditions of plate fixation is an indicator that complete immobilization was not achieved.
  • 16. a Functionally stable fixation of a mandibular fracture with excellent repositioning as a precondition for primary bone healing. b Enlarged section of (a): primary bone healing contact area, direct bony bridging showing osteons crossing the fracture area. a Stable fixation, load sharing with contact area superiorly and gap area inferiorly. b Enlarged section of (a): primary healing gap area: complete filling of the fracture gap with lamellar bone in a direction parallel to the fracture surface.
  • 17. 2. SECONDARY BONE HEALING VIA CALLUS FORMATION • In cases when no fracture fixation or just loose adaptation fixation is done, macromotion between the fragment ends occurs. • The strain in between the fragments exceeds what bone can tolerate, and new bone developing between the fracture ends would be destroyed before it is formed. Endosteal callus Periosteal callus
  • 18. In between the fracture ends a tissue differentiation cascade takes place, during which stiffness and strength increases and strain tolerance gradually decreases. Hematoma Granulation tissue Connective tissue Fibrocartilage Mineralized cartilage Woven bone Compact bone
  • 19. Secondary bone healing, phase 1: hematoma filling the fracture gap.
  • 20. Secondary bone healing, phase 2: granulation tissue and connective tissue replacing the hematoma in the fracture gap. • The elongation to rupture is found to be between 5% and 17%. • Fibrous tissue is found in areas where tensile forces act, • Cartilage is formed in zones of hydrostatic pressure
  • 21. Secondary bone healing, phase 3: fibrocartilage replacing the connective tissue in the fracture gap.
  • 22. Secondary bone healing, phase 4: woven bone replaced by lamellar bone through Haversian remodelling.
  • 23. COMPLICATIONS OF BONE HEALING 1. Non-union 2. Delayed union 3. Malunion FACTORS PATIENT ASSOCIATED OPERATOR ASSOCIATED HARDWARE ASSOCIATED LOCAL SYSTEMIC
  • 24. METALS, SURFACES AND TISSUE INTERACTIONS  62.5% iron  18% chromium  14% nickel  2.5% molybdenum  minor elemental 316 L iron-base alloy Allergic reactions to nickel 3–15% Titanium alloys  Ti grades 1–4  Ti-6Al-7Nb alloy  Ti-15Mo alloy (α & β)
  • 25. FIXATION DEVICE BLOOD BLOOD PROTEINS COVERING THE FIXATION DEVICE (matrix for platelets and other cells) PLATELET DEGRANULATION INFLAMMATION (cytokines & growth factors) HEMATOMA FORMATION Proliferation Remodelling
  • 26. BIODEGRADABLE MATERIALS Water and CO2 In the future, maxillofacial fracture fixation may utilize biodegradable bone adhesives and composites in lieu of the traditional titanium plate/screw systems. The adhesives currently under study are in the cyanoacrylate polymer family, namely, butyl-2-cyanoacrylate.
  • 27. REFERENCE 1. Fonseca Raymond J, Walker Robert V, Barber H Dexter, Powers, Michael P, Frost David E. oral and maxillofacial trauma. China: Saunders; 2013. 2. Hom, Hebda, Gosain, Friedman. Essential tissue healing of the face and neck. India. Peoples medical publishing house. 3. AOCMF principles of internal fixations of craniomaxillofacial skeleton, trauma & orthognathic surgery. 4. Rowe NL, William JL. Maxillofacial injuries. 1st ed. India ISBN 978-81-312- 1840—2 2009.

Notas del editor

  1. Pic of tensile forces and compressive forces
  2. This process is called primary or direct bone healing, since it does not proceed through the entire tissue differentiation cascade
  3. During the course of secondary healing, periosteal and is formed. In between the fracture ends a tissue differentiation cascade takes place, during which stiffness and strength increases and strain tolerance gradually
  4. During the course of secondary healing, periosteal and endosteal callus is formed. In between the fracture ends a tissue differentiation cascade takes place, during which stiffness and strength increases and strain tolerance gradually decreases. The differentiation cascade starts with a, thereafter develops which proceeds through connective tissue, fibrocartilage, and mineralized cartilage to woven and finally to compact bone.
  5. Initially a hematoma is found between the fragment ends (Fig 1.3.3-3a–b). The function of the hematoma in the course of fracture healing is still controversial. There is some evidence that the leukocytes within the blood may transform into fibroblasts and other cells of the supporting tissue system. The hematoma might as well act as a guiding structure, which, as a spacer, determines the size and shape of the callus. Then fibroblasts occur within the hematoma.
  6. This creates an inflammatory environment that recruits mesenchymal stem cells (MSCs) to the site of healing, followed by expansion of these cells and their differentiation into either osteoblasts or chondrocytes. Via intramembranous ossification, the osteoblast cells form new bone on the existing bone surface, flanking the fracture site, generating the hard callus. In the center, over the site of fracture, which is a more hypoxic environment and one that is less mechanically sound, chondrocytes form a cartilaginous or soft callus via endochondral ossification.
  7. Initially a hematoma is found between the fragment ends (Fig 1.3.3-3a–b). The function of the hematoma in the course of fracture healing is still controversial. There is some evidence that the leukocytes within the blood may transform into fibroblasts and other cells of the supporting tissue system. The hematoma might as well act as a guiding structure, which, as a spacer, determines the size and shape of the callus. Then fibroblasts occur within the hematoma.
  8. Ti for CMF applications because removal is not suggested. The driving force behind this change is primarily related to the superior corrosion resistance, lower stiffness, and enhanced diagnostic imaging compatibility associated with Ti and its alloys