Structuring of biodegradable polymers Flashcards

1
Q

What are the 4 different structuring methods for biodegradable polymers?

A
  • Construction of random structures
  • Fibres
  • Construction of ordered structures
  • More controlled (random) structure
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2
Q

What are the importance of scaffold dimensions ?

A
  • The pore size is dependent of the tissue/cell type
  • The pore structure needs to be known
  • Pores need to be interconnected
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3
Q

What about pore structure determines whether the tissue carries out certain functions

SPECIFIC EXAMPLES

A
  • Vascularisation needs a pore size of at least 250micro meters
  • Fibroblast in-growth requires a scaffold pore size between 5 and 15 micro meters
  • Hapatocytes (liver cells) need a pore size of 20micrometers
  • Osteoid cells require a pore size between 40-100micrometers
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4
Q

What is the construction of random structures method and how to we carry it out

A

This is similar to the technique we would use to introduce porosity into metals
It makes micrometer scale pores
It can be done by
- Effervescent salt
- High pressure CO2 gas
- Freeze drying
- Solvent casting and particulate leaching (Salt/ Sugar Particles)

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5
Q

How do we use effervescent salts to create random porous structures in bidegradable polymers
This is a type of gas foaming

A
  • These create foams
    Gas is used as a porogan via the use of effervescent salt
    COME BACK
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6
Q

What is the meaning of the word porogen

A

Any of a mass of particles, of a specified shape and size, used to make pores in moulded structures used for tissue engineering (they are dissolved away after the structure has set)

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7
Q

How do we use solvent casting and particulate leaching to create porous biomaterials ?
What controlled the porosity and connectivity of the biomaterial?
Salt/ sugar particles

A

The polymer is mixed with solvent (e.g. PLA) and a salt
It is then cast and vacuum dried
The salt is then washed out
The overall porosity is controlled by the salt size
The ratio or polymer to salt particulates controlled the connectivity

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8
Q

In creating random porous biomaterials what is one thing all the methods have in common

A

They all carryout a combination of 2 immiscible( the materials in these different phases do not mix) phases

solid-liquid-gas

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9
Q

What is Gas Foaming and how do we carry it out

A

Gas (normally CO2) or effervescent salts are mixed with a polymer to create a polymer matrix

The equipment for this is expensive but once paid for the CO2 is cheap

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10
Q

Freeze drying. What is it and how do we carry it out?

A

Method of Random porous material manufacturing
A solvent polymer mixture which phase separates at low temperatures
The solvent then sublimes (transitioning from solid- gas state without passing through the liquid state) , leaving spaces(pores) in the freeze dries material where it once was
This method is time consuming. Takes about 4 days per sample

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11
Q

What are some of the advantages of randoms porous materials

A
  • Experimentally easy technique

- Can make interconnected porous structures

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12
Q

What are some of the disadvantages of random porous materials

A
  • They don’t have good structural stability
  • The porosity and morphology are hard to control independently
  • Poor mechanical integrity
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13
Q

How do we make polymer fibres by spinning

A

A polymer solution is filtered and then passed through a spinnerette. The fibre created is then stretched, washed and a fibre finish is applied.
Once dries this long stretch of fibres is either packaged up or cut into usable lengths.
There are different variations to this method
- Wet spinning in a chemical bath
- Dry spinning using solvent evaporation
- Melt spinning using solidification
Industrially the fibres range from 10-100 micro meters in diameter
This is used for Silk-PLA-PCL

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14
Q

How are polymer fibres treated once made. What is this particularly useful for

A

Knitting and Weaving

This is often used for vascular implants

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15
Q

What is electrospinning

A

Electrospinning uses an electrical charge to form a mat of fine fibres. When the electrical force at the surface of a polymer solution or polymer melt over comes the surface tension, a charge jet is ejected

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16
Q

Additive manufacturing techniques , what are they?

Example

A

Family of fabrication processes that were developed to make engineering prototypes in minimum lead time based on CAD models.
In May 2013 a 3D bioresorbable splint was printed to keep a new born babies airways open

17
Q

What are some of the advantages and disadvantages of additive manufacturing techniques

A
  • Reduced lead time to produce prototype component or to manufacture parts
  • Increased ability to compute manifacturing properties or components and assemblies
  • Manufacturing of bespoke parts
  • This might help develope a distributed economy so people/ hospitals can print their own parts.
18
Q

What are the two main types of additive manufacturing techniques

A

Printing techniques- 3D printing and wax printing
Laser based techniques- STereolithography and selected laser sintering
Fused deposition modelling

19
Q

How does 3D printing work?

A
  1. A layer of powder is spread on a platform
  2. Inkjet printer head deposits drops of binder of selected parts of the cross section
  3. The binder dissolves and joins the adjacent powder particles
  4. The table is then lowered by a layer thickness
  5. New layer of powder is deposited and the system repeats over and over again until the finished shape is created
  6. The shape is then shaken to remove powder and get part

This can currently be carried out with the material being printed directly

20
Q

What are some of the advantages and disadvantaged of 3D printing

A
\+ Easy process 
\+ Patient specific 
- The binder can be toxic 
- The pore size is limited by the size of the powder 
- Not great mechanical strength
21
Q

Laser based techniques

A

Laser based machines that either photo-polymerise (polymer changes properties when exposed to light) liquid monomers or sinter(the process of compacting and forming a solid mass of material by heat or pressure without melting it to the point of liquefaction) powdered material

22
Q

Stereolithography is an example of a laser based technique how is it carried out

A
  1. A photocurable monomer is used
  2. Layer by layer this is hit by a laser beam, with the table moving a layer lower each new layer. This UV laser solidifies part of the cross section.
  3. Once the shape is completed it is removed and the supporting structure is broken off and the part is cured in an oven.
23
Q

Give examples of where Stereolithography (SL) scaffold have been used

A

They have been used in bone tissue engineering

They have also been used to create nerve guide conduits- Here the structure of the nerve/ axon schwann cells are mimicked using PEG, PLA and PCL. The contact guidance is created through the use of grooves with a depth of about 20micrometers

24
Q

Selective laser sintering is another example of a laser based technique

A

A moving laser beam sinters heat fusible powders in areas corresponding to the CAD design layer at a time. After each layer is completed, the table moved downwards one layer and a new layer of powder is spread. The areas not sintered, the powder is shaken loose and removed

25
Q

What are some advantages and disadvantages of stereolithography

A

+These are the highest resolution techniques available, pore size can be down to 10micrometers

  • The monomers themselves can be costly
  • Limited by the development of photopolymerisable liquid monomer materials
26
Q

What are some advantages and disadvantages of selective laser sintering

A
\+ Good compressive strength 
\+ Wide range of materials 
\+ Solvent free
- High processing temperatures
- Pore size is dependent on the powder particulate size
27
Q

What is fused deposition modelling

A

This is a type of 3D Bioprinting practice

  • The material is either thermally or chemically treated as it passes through a nozzle
  • The nozzle moved to extrude a fibre of polymeric material from which the physical model is built layer by layer by lowering the table upon which the model sits
  • The nozzle also creates a support structure to support overhanging or unconnected features which are manually removed post processing
28
Q

What examples have there been of fused deposition modelling

A

It has been used in osteochondral tissue engineering to grow cartilage and bone together
It has also been used to help fix vascular networks by using a sacraficial structure that can easily be dissolved in water. Within the 3D scaffold prototype vasculature is incorperated
Hydrogels have also been used as tracks for vasculature

29
Q

What are the positives and negatives of fused deposition modelling

A

+ This method can easily be used to make different morphologies and densities which can then be layered for different tissue growth
+ Good compressive strength
+ Solvent Free
- High Processing temperatures
- Limited material range
- Inconsistent pore openings
- Requires support structure for irregular shapes

30
Q

How do we carry out bioprinting

also known as Organ Printing

A

Similar process to fused deposition modelling and inkjet printing
Thermo responsive Gels are printed and then cells are sprayed onto the solidifying thin layer of polymer solution. However in the process of spraying the cells may be damaged or cell aggregation could occur within the droplets. Tissue spheroids can be used as building blocks for the organs

  • The material choices for this method are limited
31
Q

Why would we used additive manufacturing over other options

A

Foams are normally much softer thane either soft or hard tissue. This can be over come by additive manufacturing because we can design precise mechanical properties,
More controllable materials also mean better tissue growth

32
Q

Electrospinning 3D objects

The combination of what?

A

Occurs when we we combine additive manufacturing with electrospinning
Gives us the opportunity to create 3D manufactured electrospun objects
You electrospin on a construct and replicate the underlying pattern by changing the height of the collectors
Field lines curve towards objects that stick out so this can be used in the process
This process enables electrospun mats- within these electrospun mats stem cell niches can be replicated. Microfibrous mats with added relief cam be replicated easily

33
Q

PolyHIPEs

High Internal Phase Emulsions

A

Water droplets are surrounded by a very thin film of polymer. Said polymer is then cured and the remainder is dried forming polyHIPE
Porosity and connectivity can be tuned and structured by combining them with stereo-lithography

34
Q

Define Hydrogel

A

Insoluble network of polymer chains that swell in aqueous solutions

35
Q

Hydrogels undergo swelling in analogy to…

A

… dilution of free polymer chains in solution

This swelling depends on temperature and pH

36
Q

What are hydrogel responses to temperature and pH

A
  • They impct the swelling behaviour
  • We often use hydrogels that collapse at body temp
  • Ionic hydrogels with acidic side groups collapse at a low pH
37
Q

What use could a pH sensitive hydrogel have

A

Could be used for glucose sensing

  • Boronic acid binds to glucose
  • Quencher releases fluorescent tag in the hydrogel