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Chapter 7<br />

7.2. Future Prospects<br />

Recent advances <strong>of</strong> the biomedical use <strong>of</strong> polyesters have been paid increasing attention<br />

on dealing with the interaction <strong>and</strong> communication between the materials <strong>and</strong> life systems,<br />

for which the materials are termed as bioactive materials. In order to obtain bioactive<br />

materials, some modifications towards polyesters are usually taken to achieve bioactive<br />

functionalities, including hydrophobicity-hydrophilicity, s<strong>of</strong>tness-hardness, charge-charge<br />

density, stimuli responsiveness, <strong>and</strong> biological functionality. In the past few years, some<br />

efforts have been made by our lab on the functionalization <strong>of</strong> PLA <strong>and</strong> their use in the<br />

biomedical fields. For example, copolymerization <strong>of</strong> lactide monomer with functionalized<br />

cyclic monomers leads to biodegradable polymers with reactive amino or carboxyl groups<br />

which are subsequently used for conjugation with bioactive molecules such as folate, RGD,<br />

sugars, antibody <strong>and</strong> drugs. Then, the use <strong>of</strong> these bio-functionalized materials in, such as<br />

tissue engineering scaffolds or smart drug delivery systems have also been investigated.<br />

Though great efforts have been made, there are still challenges in synthesis <strong>of</strong> biodegradable<br />

polyesters with precise <strong>and</strong> smart properties, such as improved cell adhesions <strong>and</strong><br />

proliferation, precise targeting drug delivery <strong>and</strong> triggered release, promoted cell<br />

internalization <strong>and</strong> so on. Fortunately, by virtue <strong>of</strong> the recent development on the click<br />

chemistry <strong>and</strong> living radical polymerization technique (ATRP, RAFT et al.), it is possible for<br />

us to prepare polyesters with diverse structures <strong>and</strong> architectures, ie. different kinds <strong>of</strong><br />

polymers (natural polymers, synthetic polyesters <strong>and</strong> free radical polymers) can be<br />

conjugated together <strong>and</strong> great amount <strong>of</strong> vinyl monomers can be used to bring additional<br />

properties to the polyesters. Thus, it is possible for us to prepare biomedical polymers with<br />

more pr<strong>of</strong>ound <strong>and</strong> precise functions for specific biomedical use.<br />

A tentative effort has been made in this thesis on the synthesis <strong>of</strong> the biodegradable<br />

copolymers <strong>of</strong> PLA <strong>and</strong> TEMPO-contained PTAm through combination <strong>of</strong> ring-opening<br />

polymerization <strong>and</strong> RAFT living radical polymerization. The biocompatibility <strong>and</strong> potential<br />

biomedical use were also evaluated. However, it is reasonably attractive to make step further<br />

in the application <strong>of</strong> the TEMPO-based radical polymers in biomedical fields based on the<br />

unique electronic, magnetic <strong>and</strong> biological properties <strong>of</strong> the nitroxyl radicals. Tasks are still<br />

remained in the further investigation <strong>of</strong> these materials interaction <strong>and</strong> communication with<br />

cells through electronic transport or nitroxyl radical triggered signal pathway. Materials in the<br />

‐ 132 ‐

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