Adhesives Flashcards

1
Q

Adhesive

A
  • general term
  • in specific contexts can be replaced by designations like cement, glue, paste, fixative, and bonding agent
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2
Q

Bonding/groutin

A
  • creating durable interfacial bond between the material and the host tissue while space-filling (bone cement)
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3
Q

Sealing

A
  • prevention of ingress of moisture, air, biological fluids, bacteria, and other species through the bonded zone
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4
Q

Abhesion

A
  • prevention of adhesion (non-fouling surfaces)
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5
Q

Adherend

A
  • surface to which an adhesive adheres
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6
Q

Basics of Adhesives

A
  • generally presented as fluid agents that have a means of converting into a solid form
  • utility is based on context (hard or soft tissue, timescale, and strength/durability needed)
  • primarily used in wound closure and surgical adhesives
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7
Q

Logic of Adhesion

A
  • effective intimate contact area between surfaces becomes too minimal for adhesion due to IMFs
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8
Q

Requirements

A
  • wet both adherend surfaces (may require etchant or primer on surface, or roughening, to increase porosity, etc.)
  • create a fluid-solid interface resistant to tensile load through nanoscale primary (covalent, ionic, and metallic) or secondary bonds (hydrogen, VdW), micro-mechanical bonds or interlocking (can be disrupted by air voids, weak boundaries, etc)
  • solidifies so the interface becomes resistant to shear forces
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9
Q

Means of solidification

A
  • phase transformation
  • solvent evaporation
  • polymerization of monomers or oligomers (widely used but susceptible to polymerization shrinkage phenomena!)
  • acid/base reactions
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10
Q

Bone/Tooth Cements

A
  • PMMA/MMA cement is used to fix acetabular and femoral components in a THA
  • solidifies through benzyol peroxide initiator, free radical reaction, or using an amine activator (exothermic reaction, so avoid too high temperatures otherwise bubbles occur… 5-13 min to set)
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11
Q

Bonding of PMMA, Polymerization Shrinkage

A
  • bonding occurs through microscale interlocking, polymer penetrated interstices of cancellous bone (adapts to surface of stem)
  • shrinkage can create unwanted porosity at interface between metal implant and bone cement (this is a weak link, and can lead to micro-cracks)
  • heating the implant surface will induce pore formation AWAY from prothesis surface
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12
Q

Alternative Bone/Tooth Cement list

A
  • inorganic calcium phosphate systems
  • zinc phosphate
  • poly (carboxylic acid) cements
  • zinc polyacrylate cements
  • glass-ionomer cements (GIC)
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13
Q

Inorganic calcium phosphate systems

A
  • e.g. hydroxyapatite and tricalcium phosphate
  • bond through intermolecular adhesion to calcified tissue, micro-mechanical interlocking
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14
Q

Zinc phosphate

A
  • traditional cement formed of zinc oxide powder and phosphoric acid solution
  • effective in vivo for 10-20 years (dental)
  • bonding is micro-mechanical interlocking through surface roughness
  • opaque upon hardening
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15
Q

Glass-ionomer cements (GIC)

A
  • based on poly (acrylic acids), use aluminosilicate glass powder instead of zinc
  • crosslinking through calcium and aluminum ions and silica gel formations
  • forms translucent, rigid cement with similar adhesive properties to zinc
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16
Q

Acid-Etching enamel and dentin

A
  • dentin is hydrated with a “smear layer” of denatured collagen, so hard to bind
  • three stages: 1) acid etchant for about 10 sec to remove outer layer, demineralizing, leaving residual type 1 collagen fibrils and proteoglycans
    2) hydrophilic monomer primer rehydrates for porosity
    3) bonding agent added to permeate and seal (forms IPN region, hybrid interphase zone, about 4 microns thick)
17
Q

Soft Tissue adhesive requirements

A
  • temporary with unique properties
  • spread easily on wound surfaces that are wet
  • provide adequate work time before solidifying
  • develop/maintain adhesion
  • provide hemostasis, facilitate wound healing, be biocompatible
  • cyanoacrylate esters and fibrin tissue adhesives used widely
18
Q

Cyanoacrylate esters

A
  • methyl cyanoacrylate
  • polymerize quickly in the presence of weak bases
  • more hydrophobic (n-butyl) spread faster
  • can be brittle and dislodge
  • cytotoxicity concerns
19
Q

Fibrin sealants

A
  • creating synthetic clot, mixing fibrinogen/factor XIII (Solution A) and thrombin/CaCl2 for stability (Solution B)
  • isolate fibrinogen from pooled donor plasma
  • provides hemostasis, minimal inflammation but lower strength
  • widely used
20
Q

Catecholic bioadhesives

A
  • designed based on adhesive protein from mussels
  • 4-arm dopamine-terminated PEG (cPEG)
  • adhesive hydrogels formed in 30 seconds
  • great biocompatibility and durability
21
Q

Hydrogel sealants

A
  • based on PEG block photopolymerized with biodegradable oligomers (PLA)