Week 9 - Tissue Compatibility Flashcards

1
Q

Is there a completely inert biomaterial?

A

No - all elicit a non specific inflammatory response around foreign matter

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2
Q

How long after implantation does cellular invasion occur?

A

24 hours - layer of tissue is formed

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3
Q

What is the difference between implant response and regular wounds?

A
  • An implant never gets better

- No matter how hard the body tries, it cannot heal the implant

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4
Q

What actions does the body take to remove the implant?

A

When it cannot be digested, the body tries to extrude the object or surround it with a dense fibrous sheath

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5
Q

If the object is not chemically and physically inert, what cells are primary involved in the implant response?

A

Macrophages and giant cells

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6
Q

What is the generalised response to metal implants?

A
  • Most pure metals tend to evoke very strong immune response

- Certain antibodies are produced to help destroy

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7
Q

Are there any exceptions to the metal implant response?

A

Gold and platinum

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8
Q

What happens to metals in the body with regard to oxidation?

A
  • The body corrodes and forms oxides
  • Dense oxide layer may passivate the metal
  • Ti the best because of this
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9
Q

What happens when metal ions are leached from the implant and why does it happen?

A

What: they can further leach into the blood and cause toxicity
Why: not specifically antigens but they form metalloprotein complexes which are antigens

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10
Q

Are ceramics antigens within the body?

A

No - the only biomaterial to not be recognised as antigens, meaning the body loves them

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11
Q

Are ceramics bioinert/bioactive?

A

At the very least bioinert, at the best bioactive

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12
Q

What types of ceramics are mostly used?

A

Oxides - often in their highest oxidation state

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13
Q

Why are bioglass based and calcium phosphates used?

A

They are both bioactive and can either bond to bone directly or enhance bone formation (bioglass even bond to soft tissues)

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14
Q

What are the systemic effects of implants?

A

Immune diseases, cancer, changes in blood pressure, particles being transported, wear particles and toxic buildup

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15
Q

What are the requirements for blood compatibility of biomaterials?

A
  • Cannot allow blood coagulation
  • Must not cause hemolysis
  • Should be smooth
  • Should be compatible with endothelial cells
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16
Q

What are the factors affecting blood compatibility?

A

Surface roughness, surface wettability, electrical properties and chemical properties

17
Q

Why surface roughness for blood compatibility?

A

The rougher the surface, the higher the contact surfaces area available for clotting

18
Q

Why surface wettability for blood compatibility?

A

Hydrophobic was thought to be better but not strong correlation

19
Q

Why electrical properties for blood compatibility?

A

Relates to the amount of potential built up by blood flow over the surface - a negatively charged surface tends to reduce clotting

20
Q

Why chemical properties for blood compatibility?

A

Related to electrical properties but highly reactive chemical elements = bad blood compatibility

21
Q

What are carcinogens?

A

Substances causing the onset of cancerous disease

22
Q

Why is the form of the implant important for carcinogenicity?

A

Physical form is often important but so is surface chemistry - e.g. when polymers are in sheet form they create cancer but less in fibre form

23
Q

What are some examples of known or suspected carcinogens?

A

Nickel and cobalt

24
Q

What are examples of systemic and host responses to implants?

A

Hypertension, blood composition changes, metabolic or enzymatic changes due to metal ion content and metal allergy causing loosening of implants

25
What factors affect the risk to patients following implantation?
Increasing periods of implantation and increased surface area
26
Why synthetic biomaterials?
Immune responses are caused between autografts, allografts and xenografts
27
What is the relevance of protein adsorption?
Protein adsorbed on the surface of the biomaterial is what is seen by cells - makes it the key determinant to controlling bioreaction to implants