CHAPTER

55BiomaterialDegradation

5.1 Introduction: Degradation in the Biological Environment

Biomaterial degradation: uncontrolled vs. controlled degradation Mild environment within body: neutral pH, temp, ions, specific reactions

in vivo testing

5.2 Corrosion/Degradation of Metals and Ceramics Metal degradation: corrosion --- metal durability within body / biocompatibility

5.2.1. Fundamentals of Corrosion

(1) Oxidation-reduction reactions corrosion: electrochemical process & electron transfer

Anode: oxidation reactionCathode: reduction reactions 1) in acidic milieu 2) oxygen in acidic solution 3) oxygen in neutral or basic solution

Battery: electrochemical (galvanic) cell two metal strips salt bridge wire connection with voltmeter

(2) Half-cell potentials standard reduction potential (electron affinity)

with standard hydrogen electrode (H2 gas through 1M HCl with platinum)

actual reduction potential: Nernst equation galvanic series

metals towards the bottom of Table 5-3 : easy oxidation (unstable, degradation)

(3) Nernst equation temp & conc. of metal ions (4) Galvanic corrosion two different types of metals in the body connected via physiological fluid

more active metal (oxidation, anodic) complex corrosion process

oxidation rate = reduction rateslow overall corrosion (passivation)

5.2.2. Pourbaix Diagrams and Passivation Pourbaix diagram: regions of corrosion and non-corrosion

as a function of cell potential and pH 1) corrosion2) immune: cathode protection3) passivation: surface oxidation

--- stable solid film (oxide or hydroxide)

no rate prediction

rate = current flow / surface area other factors involved

5.2.3. Contribution of Processing Parameters enhanced corrosion in vivo microstructure w/in implant ---- change in localized ion conc. ---- corrosion rate

(1) Crevice corrosionat a narrow, deep crack O2 depletion anodic reaction in the creviceO2 reduction (pH increase) Cl- influxinsoluble hydroxide & H+ liberationpH decrease

(2) Pitting corrosion flaw or disrupted passivation filmsmall anode and large cathode 1) inequality in surface area2) rates of the redox reactions

dissolution of anodic regions

(3) Intergranular corrosion

grain boundaries --- high energy --- more active region[intergranular attack]

5.2.4. Contribution of the Mechanical Environment location of implants --- corrosion rate

(1) Stress & Galvanic corrosion bending ---- tensile side (anodic) & compressed side[galvanic corrosion]

(2) Stress corrosion cracking metals under both tension and corrosive environment small cracks ---- crack propagation and brittle fracture

(3) Fatigue corrosion continuous loading --- disruption of passivating film --- surface exposure

[corrosion] fatigue cycle, corrosion fatigue, premature device failure

(4) Fretting corrosionmotion near the implant (not by loading) removal of the metal’s passivating layer [nick on the surface]

5.2.5. Contribution of the Biological Environment biological milieu ---- corrosion rate in vivo (1) inflammatory cells

pH and strong oxidizing agents growth of the passive layer

(2) proteins 1) protein binding to metal surface 2) proteins as electron carriers3) metal binding proteins [equilibrium favoring metal dissolution]

(3) bacteriadevice infectionby-products H2 consumption and anodic dissolution

5.2.6. Means of Corrosion Control

(1) devices with few stress raisers (2) combination of metals (located close in galvanic series) (3) non-reactive metals and metals with passive oxide coating (4) heat-treated stainless steel (5) nitric acid pre-treatment (6) surface coating

5.2.7. Ceramic Degradation passivating layer 형성 more stable in physiological environment (ionic character) inert / resorbable / controlled surface reactivity

ceramic degradation under mechanical environmentstress induced degradation ceramic porosity [stress raiser & surface area 증가 ]

5.3. Degradation of Polymers polymer degradation in the body rate of polymer degradation 5.3.1. Primary Means of Polymer Degradation (1) swelling/dissolution [plasticizer]

1) ductility 2) crystallinity3) mechanical & thermal properties (Tg) 4) complete dissolution in aqueous environment

(2) chain scission bond rupture ---- molecular weight 감소 hydrolysis / oxidation

5.3.2. Chain Scission by Hydrolysis Hydrolysis

1) reactivity of groups of the polymer backbone2) extent of interchain bonding 3) amount of media (water)

Susceptibility to hydrolysis 1) a large number of cleavable groups2) hydrophilic domains for water influx3) low initial mol. wt. and low X-link density 4) low or no crystallinity 5) Tg < body temp6) high surface area to volume ratio

5.3.3. Chain Scission by Oxidation (1) Oxidation via highly reactive species

homolysis vs. heterolysisextent of oxidative degradation

1) number of susceptible chemical domains 2) lower mol wt polymers3) less tight X-linking

(2) Metal-catalyzed oxidation metal corrosion ---- strong oxidizing agents ---- attack polymer coating

5.3.4. Other Means of Degradation (1) Environmental stress cracking

(stress corrosion cracking in metals)polymer ---- tensile stress ---- deep crack on the exterior ---- fracture

(2) Enzyme-catalyzed degradation enzymes --- affinity for certain chemical groups in polymer ---- catalysts

hydrolytic or oxidative degradation

5.3.5. Effects of Porosity pores --- stress raiser (mechanically induced degradation)

--- surface area (more space for cleavage)

5.4. Biodegradable Materials controlled biomaterial degradation

temporally nature of the material (tissue engineering, drug delivery) biodegradation / bioerosion

5.4.1. Biodegradable ceramics calcium phosphate --- calcium hydroxyapatite & tricalcium phosphate (hydrated calcium sulfate or bioactive glasses)

(1) Erosion mechanisms solubility, local pH, dissolution of grain boundaries

(2) Factors that influence degradation rate 1) chemical susceptibility of the material 2) crystallinity 3) amount of media (water) 4) surface area / volume ratio5) high mechanical stress 6) pH drop

5.4.2. Biodegradable Polymers (1) Introduction to biodegradable polymers and definitions

Hydrolytic degradation of polymers 1) bulk degradation

water penetration rate > polymer degradation rate [cracks and fissures] 2) surface degradation

water penetration rate < polymer degradation rate [implant thickness 감소 , with mechanical integrity maintained] no good integration with the surrounding tissue in vivo

(2) Degradation mechanism 1) breaking X-linked bonds between water-soluble polymer chains 2) cleavage of hydrophobic side chains to reveal hydrophilic groups 3) cleavage of polymer backbone

(3) Factors that influence degradation rate enzyme degradation 1) amount of enzyme

2) number of cleavable moieties hydrolytic degradation

1) reactivity of chem groups2) bonding between chains3) amount of media4) surface area

5.5 Techniques: Assays for Extent of Degradation in vitro and in vivo testing signs of degradation

1) mass loss2) different physical and chemical properties3) visual inspection --- color and crack formation 4) material surface with light and electron microscopy

corrosion test for metallic implants in vitro 1) electrochemical testing

IV-curve 분석