Topic 2 Flashcards

(46 cards)

1
Q

What are nano- and microfabrication technologies?

A

used to create scaffolds with controlled surface topography
- study cell material interaction and cell biomechanics
- investigate cellular processes, such as adhesion, migration and differentiation
- enhance cell-material interaction without changing chemical composition

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2
Q

What is photolithography?

A

light is used to generate structures on plantar surfaces. Resolution depends on the wavelength of the light used.

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3
Q

Process of photolithography

A
  1. Substrate preparation:
    The substrate is prepared and cleaned to ensure a suitable surface for the photoresist.
  2. Photoresist application:
    A thin layer of photoresist is applied to the substrate, typically using a spinning technique to create a uniform coating.
  3. Mask alignment and exposure:
    The mask is aligned with the photoresist-coated substrate, and light is shone through the mask, exposing the photoresist in specific areas according to the pattern on the mask.
  4. Development:
    The exposed photoresist is developed, meaning that the exposed portions are selectively removed or altered based on the type of photoresist used (positive or negative).
  5. Etching or deposition:
    The patterned photoresist acts as a mask for subsequent processes, such as etching away unwanted material or depositing a new material in the desired pattern.
  6. Photoresist removal:
    Finally, the remaining photoresist is removed, leaving behind the patterned substrate.
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4
Q

Why is titanium used for photolithography

A

with a top coat of caalcium phosphate, promote bone cell growth

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5
Q

Why micro patterning?

A

helps to enhance biocompatibility and control cell morphology

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6
Q

What is thermal nano-printing lithography (NIL)?

A

mechanical embossing technique for large area patterns with resolution of 5-10nm.

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7
Q

Process of thermal nano-printing lithography

A

solid polymer between a hard stamp and substrate
temp raises to about Tg making the polymer now viscous and the stamp ad substrate compress it (keep temperature and pressure stable)
Temp is lower again so now a solid polymer with the compress new shape

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8
Q

Basic process steps for NIL

A

1 - begin heating
2 - begin embossing
3 - begin cooling
4 - remoulding at elevated T
5 - demolding at ambient

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9
Q

What is soft lithography?

A

use of elastomeric materials. method for generating atterns onto a surface with nanometric resolution.
includes replica moulding, micro contact printing, microtranfer moulding etc

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10
Q

What is the most common type of silicon?

A

polydimethylsiloxane
- two methyl side groups for each silicon atom

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11
Q

Properties of polydimethylsiloxane

A
  • low youngs modulus
  • glass transition temp.= 120
  • optically transparent for wavelengths from the near UV to the near IR (300-800nm)
  • chemically inert
  • biocompatible
  • stable at temperatures required for biological processes (37-95)
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12
Q

Process of Replica Moulding

A

1 - fabrication of the intial pattern by photolithhography
2 - mixing of PDMS base with curing agent (10:1)
3 - pouring the PDMS liquid solution in the master surface
4 - thermal curing of PDMS (typically 80 for 30 minutes)
5 - PDMS replica peeling off

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13
Q

What is the collapse of PDMS microstructures?

A

collapse caused by adhesion force to the ground
if groups are too close or pillars too high

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14
Q

When won’t PDMS collapse?

A
  • the height of the posts is lower than hc (critical height)
  • the spacing between the posts is higher than wc (critical spacing)
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15
Q

What is particulate leaching?

A

a leaching agent (porogen) such as polymer microspheres, salt crystals, sugar crystals, is mixed with a polymeric solution
the dispersion is moulded in the desired shape. After the solvent evaporation, pores are created by treating the material with porogen-soluble solvent.

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16
Q

Advantages of particulate leaching

A
  • the pore size can be controlled by size and amount of particulate particles used
  • the pore density can be controlled by changing the concentration of leaching agent
  • simple and low cost
  • the porosity of scaffolds obtained from this method is reported to be around 50-90%
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17
Q

Limitations of particulate leaching

A
  • the pore shape of the scaffold produced cannot be controlled
  • non compatible with polymers that are soluble in the solvent of the porogen
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18
Q

What is freeze-drying?

A

(or lyophilisation) is a drying process in which the solvent and/r the suspension medium is crytallised at low temperatures and thereafter sublimed from the solid state directly into the vapour state
- can prepare 3D porous scaffolds with porosity beyond 90% and a pore disameter range of 20-400um

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19
Q

Process of freeze drying

A

1 - the polymer solution is poured into the mould
2 - the temperature of the mould is decreased to solidify the whole system (below freezing point -20, -80)
3 - the frozen product is dried under vaccum resulting in the sublimation of solvent crystals

20
Q

Advantages of freeze drying

A
  • high porosity
  • pore interconnectivity
  • control of pore size
  • compatible with bioactive materials
21
Q

Limitations of feeeze drying

A
  • irregularity in pore sizes
  • use of cytotoxic solvents
  • time consuming process
  • high energy consumption
22
Q

What is electrospinning?

A

the process of using electrostatic forces to form polymer fibres known as electrospinning

23
Q

What are the 3 phases of electrospinning?

A

1 - jet initiation
2 - bending instability
3 - solidification of fibres

24
Q

Process of electrospinning

A

1 - stress induced on the charged solution by the electric field and formation of the taylor cone
2 - at high potentials, the electric force overcomes the surface tension and a thin jet emerges at the tip of the cone
3 - chaotic motion of the filament due to electrically driven bending instability, stretching of the jet and solvent evaporation
4 - collection of non woven fibres on the collector

25
What are the solution properties of electrospinning?
- if the solution is too dilute, the polymer fibre will break up into droplet before reaching the collector - if the solution is too concentrate, the fibres cannot be formed due to the high viscosity
26
Parameters of electrospinning
working distance - decrease the distance beyond critical point = thicker fibres and morphological defects increase distance - thinner fibres, may lead to instability voltage - must exceed critical voltage to overcome surface tension of the polymer and maintain a jet flow rate - increased flow rate = low stretching, large pore size and fibre diameter above critical flow rate
27
What are the fibre properties?
- biometric structure - high exposed surface area - porosity
28
What is an additive manufacturing process?
a structure is fabricated using a layer by layer deposition
29
Advanatages of layer by layer
- the 3D printing technique can create defined scaffolds with controlled pore size and interconnectivity and ability to support cell growth and tissue formation
30
limitations of layer by layer
- the availability of biomaterials with the stability and desired properties for 3D printing of scaffolds is restricted depending on the printing nanotechnology used - the production time needed to fabricate scaffolds dramatically increases as the scaffold design becomes more precise and intricate.
31
What are some 3D printing technologies?
- direct 3D printing - bioplotter printing - fused deposition modelling - selective laser sintering - stereolithography
32
What is fused deposition modelling (FDM)?
a 3D printing technique that uses thermoplastic polymers
33
The process of FDM
1 - a coiled thermoplastic polymer filament extruded through a heated nozzle onto a fabrication platform 2 - upon contact with the base/platform, the polymer hardens ad sets 3 - after a layer has been deposited, the process repeats itself in a layer by layer process until the CAD structure has been completed
34
Advantages of FDM
- high porosity with no solvent - good control over the mechanical strength of scaffolds obtained
35
Disadvantages of FDM
- requires size consistency in preformed filaments - limited applicability to biodegradable polymers, excluding PCL and PLA - high processing temperature - suitable for thermoplastics polymers/composites
36
What is stereolithography (SLA)?
uses UV curable materials
37
What are the 4 main components of SLA?
1 - a tank containing photo-sensitive liquid resin 2 - a dynamic mirror system 3 - mobile-built platforms 4 - UV laser for irradiating the resin
38
Process of SLA
- platform is used for the deposition of a layer of photosensitive lquid which is photocured using the UV laser - once the resin solidifies, the platform gets lowered and the first layer is covered with the second one - this is repeated - the uncured resin is washed off
39
Advantages of SLA
- construction of a scaffold structure having a sophisticated design - high resolution
40
Disadvantages of SLA
- use of photosensitive resins which can cause cytotoxicity - more expensive than other approaches - requires post-processing to remove the uncured resin
41
What is 3D bioprinting?
consists of printing and depositing living cells on a substrate or tissue through an automated dispensing system
42
What is bioink?
referred to as cell-laden fluid materials that may have additional containing maxtrix components, and they are loaded into the 3D printer for fabrication tissue-like constructs
43
Collagen as a bioink material
+ - high biological revelance - - soluble in acid
44
Hyaluric acid as a bioink material
+ - cell proliferation, capable of gelatine - - poor in structure stability
45
Gelatin as a bioink material
+ - high solubility in water, biocompatible, thermal reversile gelatin - - low rigidity, poor shape stability
46
Chitosan as a bioink material
+ - biocompatible, antibacterial features - - low gelatin rate