Page 333 - Biomedical Engineering and Design Handbook Volume 1, Fundamentals
P. 333

310  BIOMATERIALS

                       Polyurethane is used as a coating for pacemaker leads and for angioplasty balloons. Silicones are
                       used for a variety of catheters, soft contact lenses, and foldable intraocular lenses.
                         This chapter begins with an overview of polymer science topics, including synthesis, structure, and
                       mechanical properties. The remainder of the chapter will discuss individual polymers, including their
                       applications and properties. The polymers are presented in the following order: water-soluble poly-
                       mers, gelling polymers, hydrogels, elastomers, and finally rigid polymers. These five categories are
                       roughly ordered from low to high modulus (i.e., high to low compliance). Water-soluble polymers in
                       solution do not have an elastic modulus since they are fluids, so these are presented first. In fact, most
                       polymers do not have a true elastic modulus since they are viscoelastic and exhibit solid and viscous
                       mechanical behavior, depending on the polymer structure, strain rate, and temperature.
                         Natural tissues are continuously repaired and remodeled to adjust to changes in the physiologic
                       environment. No current synthetic biomaterial or biopolymer can mimic these properties effectively.
                       Consequently, the ideal biomaterial or biopolymer performs the desired function, then eventually
                       disappears and is replaced by natural tissue. Therefore, degradable polymers are of great interest to
                       the biomedical engineering community. Polylactides and their copolymers are currently used as bone
                       screw and sutures since they have good mechanical properties and degrade by hydrolysis so that they
                       can, under optimum conditions, be replaced by natural tissue.
                         In addition to classification as water-soluble polymers, gelling polymers, hydrogels, elastomers,
                       and rigid polymers, polymers can also be classified as bioinert, bioerodable, and biodegradable.
                       Bioinert polymers are nontoxic in vivo and do not degrade significantly even over many years.
                       Polymers can degrade by simple chemical means or under the action of enzymes. For the purposes
                       of this chapter, bioerodable polymers such as polylactide are those that degrade by simple chemical
                       means and biodegradable are those that degrade with the help of enzymes. Most natural polymers
                       (proteins, polysaccharides, and polynucleotides) are biodegradable, while most synthetic degradable
                       polymers are bioerodable. The most common degradation reactions for bioerodable polymers are
                       hydrolysis and oxidation.



           13.2 POLYMER SCIENCE

           13.2.1 Polymer Synthesis and Structure

                       Polymers are frequently classified by their synthesis mechanism as either step or chain polymers.
                       Step polymers are formed by stepwise reactions between functional groups. Linear polymers are
                       formed when each monomer has two functional groups (functionality = 2). The second type of poly-
                       merization is chain polymerization where monomers are added one at a time to the growing polymer
                       chain.
                         Most polymerization techniques yield polymers with a distribution of polymer molecular
                       weights. Polymer molecular weight is of great interest since it affects mechanical, solution, and melt
                       properties of the polymer. Figure 13.1 shows a schematic diagram for a polymer molecular weight
                       distribution. Number of average molecular weight M averages the molecular weight over the num-
                                                             n
                       ber of molecules, while weight of average molecular weight M averages over the weight of each
                                                                     w
                       polymer chain. Equations (13.1) and (13.2) define M and M .
                                                             w     n
                                                          ∑ NM
                                                     M =     i  i                         (13.1)
                                                       n
                                                           ∑ N  i
                                                          ∑  NM  2
                                                     M =     i  i                         (13.2)
                                                       w
                                                          ∑  NM i
                                                             i
                       where N is the number of polymer chains with molecular weight M .
                             i                                          i
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