2011 Lecture 13

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Transcript of 2011 Lecture 13

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    Biomaterials

    BME 551 / 551EPE

    Tissue Engineering

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    Objectives1. Understand how the definitions for biomaterial and biocompatibility

    have evolved with time.

    2. Discuss how surface chemistry affects cell adhesion and proteinadsorption. Know how these events are important to biomaterialsdevelopment.

    3. Compare and contrast bulk degradation and surface degradation.

    4. Know the factors that play a role in determining a materialsbiocompatibility.

    5. Discuss the advantages/disadvantages of in vitro and in vivobiocompatibility testing.

    6. Describe the general methods by which biomaterials are beingdesigned to be biomimetic.

    7. Discuss current strategies for tailoring biomaterials for specifictissue-engineering applications (e.g., modularization,

    micropatterning, stimuli responsiveness, peptide grafting, etc.)

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    Biomaterials:

    Evolution of definition.

    Synthetic material used to replace part of a living system or to function

    in intimate contact with living tissue A systemically and pharmacologically inert substance designed for

    implantation within or incorporation with living systems

    A nonviable material used in a medical device intended to interact with

    biological systems Materials of synthetic as well as natural origin in contact with tissue,

    blood, and biological fluids and intended for use for prosthetic,diagnostic, therapeutic, and storage applications without adversely

    affect the living organism and its components Any substance (other than drugs) or combination of substances

    synthetic or natural in origin which can be used for any period of time,as a whole or as a part of a system, which treats, augments, or replaces

    any tissue organ or function of the body

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    Biomaterials and Medical DevicesLimitations

    Poor tissue integration No growth or adaptation

    Adverse reaction (fibrosis) withsurrounding tissue

    Loss of mechanical integrity with time

    Increased risk of infection

    Lack of biologically relevant instructive

    properties

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    Traditional Biomaterials and

    Medical DevicesPreformance Criteria

    Biologically inert

    Biocompatible

    Non-viable

    Mechanical strength and function

    Amenability to engineering design, manufacturing, andsterilization

    .not found naturally within the body

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    Next Generation Biomaterials

    and Medical DevicesRevised Preformance Criteria

    Biologically inert

    Biocompatible

    Non-viable

    Mechanical strength and function Amenability to engineering design, manufacturing, and sterilization

    Biodegradable

    Induces cell and tissue integration

    Smart (i.e., physiologically-responsive)

    Instructional (i.e., controls cell fate)

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    Types of Biomaterials

    Synthetic (metals, polymers, ceramics,

    composites) Nature-derived (e.g., plant-derived)

    Naturally-derived (e.g., tissue-derived) Semi-synthetic or hybrid

    What are the major factors that contribute to

    specific biomaterial choices?

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    Materials and their Medical Uses

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    Question:

    What are the important design criteria when

    identifying a biomaterial to incorporate as partof tissue engineering design solutions?

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    Tailoring Biomaterials

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    Biomaterials: Surface Chemistry

    Adhesion properties of cells and proteins is

    dependent upon surface chemistry (general:

    hydrophobic, electrostatic, van der Waals, hydrogenbonding, or specific receptor-ligand)

    Cell Adhesion

    Protein Adsorption

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    Cell-Surface Interface

    Specific Interactions receptor-ligand

    Non-specific Interactions

    hydrophobicity/hydrophilicity Surface topology/architecture

    Physical

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    Protein Adsorption

    There are three main mechanisms by which surfaceproperties can modify the cell response throughprotein adsorption:

    Differential affinity of proteins for differentsurfaces

    Modulation of the biological activity of the

    adsorbed adhesion protein due to conformationalchanges

    Substrate activation of a cellular adhesion protein

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    Immobilization via Adsorption

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    Covalent Bonding and Graft

    Polymerization

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    Self-Assembled Monolayers

    Substrate (glass coverslip or silicon wafer)

    pretreated with a thin layer of titanium (1-5

    nm); followed by a thin layer of gold (10-200 nm)

    Adsorption of alkane thiol (R-SH) solutionor vapors to gold surface

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    Self-Assembled Monolayers

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    Microcontact Printing

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    Biomaterial Processing

    Micromachining

    Fiber bonding

    Solvent casting and particulate leaching Membrane lamination

    Melt molding

    Electrospinning

    Extrusion

    Three-dimensional printing Gas foaming

    Freeze-drying

    Polymer/ceramic composite foams

    In situ polymerization; self-assembly

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    Electrospinning Process

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    Electrospinning Collection Schemes

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