Fundamentals of scaffolds for tissue engineering Flashcards

1
Q

motivation of te

A
  • regeneration of damaged tissues and organs by combining: cells, biomaterials and signals
  • development of in vitro models to provide the perfect scenario in which study the principles of tissue growth and structure
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2
Q

what are the two main paths of te

A
  1. cell-seeded scaffolds are either cultured in vitro to synthesize tissues which can be implanted into an injured site
  2. Implanted directly into the injured site, using the body’s own systems, where regeneration of tissues or organs is induced in vivo
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3
Q

requirements and challenges for scaffolds

A
  • biocompatibility
  • biodegradability
  • biometic
  • fabrication
  • special requirements
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4
Q

what are the different materials used for scaffold fabrication

A
  • polymers: ductile, tough, flexible, malleable (complex shapes), but not very high strength
  • ceramics: rigid, hard, compressive strength, osteoconductive
  • composites: advantages of both
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5
Q

elasticity

A

small reversible changes in the interatomic spacing and streching of interatomic bonds

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6
Q

plasticity

A

breaking of existing bonds and reforming bonds with neighboring atoms

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7
Q

brittle

A

lack of ductility; don’t exhibit substantial elastic or plastic deformation before fracture

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8
Q

pros and cons of natural polymers

A

pros:
- similar composition to native ecm: promotes cell adhesion, porliferation, differentiation, migration
- enzymatic degradation and metabolic absorption

cons:
- variable enzymatic disgestion from different patients: hard to control degradation rate
- natural variation in structure & composition: variable mechanical properties
- potential immune rejection

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9
Q

pros and cons of synthetic polymers

A

pros:
- can be designed with tailored properties for specific applications
- control of: mechanical properties, degradation rate and type, size, shape, etc.

cons:
- biocompatibility: high concentration of degradation product affecting potential pH balance, can provoke inflammation or even fibrosis

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10
Q

fabrication techniques

A
  • solvent casting/particulate leaching
  • melt molding
  • freeze-drying
  • phase separation
  • gas foaming
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11
Q

solvent casting & particle leaching

A

porogens are added to a solution and mixed then a solution transfer to a mold in which we introduce the pixture polymers and wait for gleation/polymerization which gives us a nanoporous scaffold and after pore leaching we have macroporous scaffold
while more porogens more holes and the smaller the porogens the smaller the holes

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12
Q

emulsion freeze-drying

A
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13
Q

sintering

A

compacting to form a solid mass of material by pressure or heat without reaching the melting point

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14
Q

3D stereolithography

A
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15
Q

selective laser sintering

A

selectivly sinterise the shape we want through the laser, having programmed beforehand that desired shape

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16
Q

3D bioprinting

A
17
Q

electrospinning

A

a unique approach using electrostatic forces to produce fine fibers from polymer solutions or melts and the fibers thus produced have a thinner diameter and a larger surface area than those obtained from conventional spinning processes
around 800nm and 1.4um

18
Q

mechanical characterization of scaffolds

A
  • bulk properites
  • tensile/compression test
  • flexural test
  • torison test
  • creep test
  • micro-nano indentation
19
Q

polymer characteristics

A

molecular weight, variation f(t)
thermal properties and crystallinity
hydrophobicity/hydrophillicity
porosity

20
Q

surface treatment and sterilization methods

A
  • surface tratment - adsp
  • sterilization methods
  • interaction between material and cells (in vitro vs. in vivo)
21
Q

surface treatment

A
  • chemical etching: NaOH or KOH, solvent immersion
  • plasma activation (
    reactive with oxygen)
  • coating: immersion or ALD and other deposition methods
22
Q

sterilization methods

A
  • radiation uv light, gamma radiation
  • heat: autoclave, dry heat
  • chemical: 70% etanol, ethylene oxyde gas
23
Q

interactions

A
  • adhesion
  • infiltration(migration)
  • phenotype
  • FBR
  • encapsulation
  • degradation