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Influence of pressure on mandibular angiosomes: What implications for decellularization?
Corentin Serra1, Romain Monchaux2, Benjamin Salmon3
1Laboratory of Mechanics and Interfaces, ENSTA, Institut Polytechnique de Paris, 91120, Palaiseau, France; Faculté de Santé, Université Paris Cité, 75005, Paris, France; Maxillofacial and Plastic Surgery, Necker Children Hospital, APHP, 75015, Paris, France.
This study reveals how blood flow territories in the human mandible change with pressure, crucial for improving bone grafting techniques and decellularization protocols.
Area of Science:
- Biomedical Engineering
- Anatomy
- Regenerative Medicine
Background:
- Bone vascularization is poorly understood, hindering reconstructive surgery and bone graft viability.
- Current anatomical methods struggle to map complex, pressure-dependent blood flow in bone.
Purpose of the Study:
- To develop and validate a novel method for analyzing pressure-dependent vascular territories in the human mandible.
- To optimize decellularization by perfusion protocols for bone allografts.
Main Methods:
- Integrated pressure-controlled perfusion with 3D imaging (contrast-enhanced cone beam computed tomography) on human cadaveric mandibles.
- Utilized a custom segmentation pipeline to create pressure maps of mandibular vascular distribution.
- Systematically increased perfusion pressure to observe territory expansion and resistance patterns.
Main Results:
- Identified a low-pressure anastomosis between maxillary, facial, and mental arteries, indicating shared intraosseous territories.
- Observed a radial perfusion pattern from the inferior alveolar artery with increasing resistance towards cortical bone.
- Determined perfusion saturation around 100-125 hPa, aligning with physiological pressures, and noted higher thresholds for cortical bone.
Conclusions:
- Pressure-driven perfusion analysis offers critical insights into bone vascularization dynamics.
- Optimizing pressure parameters can enhance decellularization efficiency for bone allografts, improving integration and viability.
- Findings challenge static angiosoma models, emphasizing the need for pressure-controlled anatomical studies in bone vascularization research.
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