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Influence of the Processes Parameters on the Properties of The ...

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Chapter 2.<br />

<str<strong>on</strong>g>Processes</str<strong>on</strong>g> to Manufacture Foams and to Functi<strong>on</strong>alize <str<strong>on</strong>g>the</str<strong>on</strong>g> Surface<br />

(f)<br />

(g)<br />

(h)<br />

(i)<br />

Scaffolds are processed to fabricate a tubular or sheet-types.<br />

After evaporati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> solvent, <str<strong>on</strong>g>the</str<strong>on</strong>g> salt particles in <str<strong>on</strong>g>the</str<strong>on</strong>g> c<strong>on</strong>struct are leached out to make an openpore<br />

structure.<br />

Scaffolds are freeze-dried for a desired time under low temperature.<br />

Scaffolds are obtained by finally under <str<strong>on</strong>g>the</str<strong>on</strong>g> return to <str<strong>on</strong>g>the</str<strong>on</strong>g> room temperature.<br />

Polymer soluti<strong>on</strong><br />

Salt (NaCl)<br />

(a) Mixing (b) Polymer soluti<strong>on</strong> (c) Evaporati<strong>on</strong> (d) Moulding (e) Gel pressing<br />

(f) Shaping (g) Salt leaching (h) Freeze-drying (i) Scaffolds<br />

Figure 2.4: Procedure <str<strong>on</strong>g>of</str<strong>on</strong>g> scaffolds by gel-pressing method.<br />

[Kim, 2007]<br />

2.5 PLGA Microspheres for Tissue-Engineered Scaffold<br />

PLGA-based microspheres are biodegradable particulate delivery systems providing both drug<br />

protecti<strong>on</strong>, encapsulated inside a polymeric matrix, and its release at a slow and c<strong>on</strong>tinuous rate.<br />

Microsphere manufacturing usually involves (1) <str<strong>on</strong>g>the</str<strong>on</strong>g> c<strong>on</strong>trolling <str<strong>on</strong>g>of</str<strong>on</strong>g> a disintegrated polymer, (2) cell toxicity,<br />

and (3) a suitable envir<strong>on</strong>ment for cell culture. <strong>The</strong> size and degradable pr<str<strong>on</strong>g>of</str<strong>on</strong>g>ile can be easily managed by<br />

c<strong>on</strong>trolling <str<strong>on</strong>g>the</str<strong>on</strong>g> molecular weight <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> polymer and <str<strong>on</strong>g>the</str<strong>on</strong>g> process <str<strong>on</strong>g>of</str<strong>on</strong>g> fabricati<strong>on</strong>.<br />

PLGA microspheres are particularly attractive for tissue regenerati<strong>on</strong> approaches ei<str<strong>on</strong>g>the</str<strong>on</strong>g>r as an<br />

injectable system or as <str<strong>on</strong>g>the</str<strong>on</strong>g> integral part <str<strong>on</strong>g>of</str<strong>on</strong>g> a replacement clinical c<strong>on</strong>struct. <strong>The</strong> small, spherical nature <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

<str<strong>on</strong>g>the</str<strong>on</strong>g>se polymers enables <str<strong>on</strong>g>the</str<strong>on</strong>g> encapsulati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> growth factors or o<str<strong>on</strong>g>the</str<strong>on</strong>g>r drugs, and <str<strong>on</strong>g>the</str<strong>on</strong>g>ir subsequent delivery to a<br />

specific and designated area. C<strong>on</strong>trolled release <str<strong>on</strong>g>of</str<strong>on</strong>g> bioactive molecules, such as cytokines and growth<br />

factors, has become an important aspect <str<strong>on</strong>g>of</str<strong>on</strong>g> tissue engineering because it allows modulati<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> cellular<br />

functi<strong>on</strong> and tissue formati<strong>on</strong> at <str<strong>on</strong>g>the</str<strong>on</strong>g> afflicted site. Cell cultures using microspheres have an advantage <str<strong>on</strong>g>of</str<strong>on</strong>g><br />

passage abbreviati<strong>on</strong> to improve cell activity. <strong>The</strong> PLGA microspheres regulate many aspects <str<strong>on</strong>g>of</str<strong>on</strong>g> cellular<br />

activity, including cell proliferati<strong>on</strong>, cell differentiati<strong>on</strong>, and extracellular matrix metabolism, in a time- and<br />

c<strong>on</strong>centrati<strong>on</strong>-dependent fashi<strong>on</strong>. <strong>The</strong> procedure to prepare PLGA microsphere scaffolds is presented in<br />

Figure 2.5.<br />

(a)<br />

(b)<br />

(c)<br />

(d)<br />

(e)<br />

<strong>The</strong> polymer is dissolved in a solvent, and is ready to add to a soluti<strong>on</strong> in surfactant.<br />

<strong>The</strong> polymer soluti<strong>on</strong> is dropped into an aqueous soluti<strong>on</strong> in surfactant by a pipette.<br />

This soluti<strong>on</strong> is stirred at 400 rpm for 7 h using a mechanical stirrer.<br />

<strong>The</strong> fabricated microspheres are collected from <str<strong>on</strong>g>the</str<strong>on</strong>g> bottom by a centrifugal separator.<br />

<strong>The</strong> hardened microspheres are centrifuged, washed with dei<strong>on</strong>ised water.<br />

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