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in tissue engineering manipulates matter at the nanoscale, mimicking natural structures to enhance cell-material interactions. This approach improves scaffold properties, enabling precise control over the cellular microenvironment and offering new possibilities for tissue regeneration.

Various nanomaterials, including , , and carbon-based structures, are used to create advanced scaffolds. These materials improve cell adhesion, drug delivery, and tissue formation while raising important safety and regulatory considerations in medical applications.

Fundamentals of Nanotechnology in Tissue Engineering

Definition of nanotechnology

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  • Nanotechnology manipulates matter at nanoscale (1-100 nm) blending engineering, physics, chemistry, and biology
  • Relevance to cell and tissue engineering mimics natural extracellular matrix (ECM) structures enhancing cell-material interactions
  • Improves scaffold properties enabling precise control over cellular microenvironment (pore size, stiffness)

Types of nanomaterials for scaffolds

  • Nanofibers created through polymers offer high surface area-to-volume ratio mimicking ECM structure
  • Nanoparticles including metallic (gold, silver), polymeric, and ceramic feature tunable size and surface properties
  • Carbon-based nanomaterials (carbon nanotubes, graphene) provide high mechanical strength and electrical conductivity
  • combine different nanomaterials for tailored mechanical and biological properties (strength, )

Applications and Considerations

Nanotechnology in tissue engineering

  • Cell-material interactions improved through increased surface roughness enhancing protein adsorption and cell adhesion
  • use nanoparticles for controlled release kinetics and targeted delivery to specific tissues
  • Tissue regeneration enhanced by nanoscale topography guiding cell growth and incorporating growth factors
  • improved through nanomaterial-induced angiogenesis promoting tissue formation

Safety and regulation of nanomaterials

  • Safety concerns include potential toxicity, long-term effects on cells, and biodegradation in the body
  • Regulatory bodies (FDA, EMA) provide guidelines for nanomaterial-based medical devices
  • Risk assessment protocols involve in vitro and in vivo testing evaluating and immunogenicity
  • Ethical considerations balance innovation with patient safety requiring transparency in reporting nanomaterial properties
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© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.

© 2024 Fiveable Inc. All rights reserved.
AP® and SAT® are trademarks registered by the College Board, which is not affiliated with, and does not endorse this website.
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