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
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
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
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
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.
This
process is called primary or direct bone healing, since it does
not proceed through the entire tissue differentiation cascade
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
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.
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.
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.
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.
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