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CHARACTERIZATION AND DEGRADATION BEHAVIOUR OF<br />

TRIBLOCK COPOLYMER<br />

Ing. Ludmila Nová<br />

Supervisor: Pr<strong>of</strong>. RNDr. Milada Vávrová, CSc.<br />

Consultant: Ing. Lucy Vojtová, PhD.<br />

Institute <strong>of</strong> Chemistry and Technology <strong>of</strong> Environmental Protection, Faculty <strong>of</strong> Chemistry,<br />

Brno University <strong>of</strong> Technology, Purkyňova 118, 612 00 Brno<br />

E-mail:nova@fch.vutbr.cz<br />

ABSTRACT<br />

This work is focused on the study<strong>in</strong>g <strong>of</strong> the thermoreversible behaviors <strong>of</strong> two copolymers,<br />

PLGA-PEG-PLGA and the same but modified with itaconic acid (ITA-PLGA-PEG-<br />

PLGA-ITA). The critical gel concentrations (CGC) and the critical gel temperatures (CGT)<br />

were determ<strong>in</strong>ed. As for PLGA-PEG-PLGA the CGC and CGT equal to 19,2 w% and 34,5<br />

°C, respectively, was observed. Second polymer <strong>of</strong> ITA-PLGA-PEG-PLGA <strong>in</strong>dicated the<br />

shift <strong>of</strong> the sol-gel transition curve down to the lower values <strong>of</strong> both CGC (15,3 w%) and<br />

CGT (25 °C). The degradation behaviors <strong>of</strong> PLGA-PEG-PLGA <strong>in</strong> a phosphate buffer (pH<br />

7.4) at 37 °C were <strong>in</strong>vestigated. A significant decrease <strong>in</strong> the molecular weight and <strong>in</strong>crease <strong>in</strong><br />

the polydispersity with<strong>in</strong> 10 days (until the samples have dissolved) was observed.<br />

INTRODUCTION<br />

Poly(lactic acid) and poly(glycolic acid) have been under extensive study s<strong>in</strong>ce they were<br />

<strong>in</strong>troduced as biodegradable polymers hav<strong>in</strong>g hydrolytically unstable backbones. Therefore,<br />

these biopolymers can be used for a certa<strong>in</strong> type <strong>of</strong> biomedical application such as <strong>in</strong>jectable<br />

polymer drug delivery systems, tissue implants or resorbable bone adhesives. The prevail<strong>in</strong>g<br />

mechanism for the biopolymer degradation is a simple random chemical hydrolysis [1]. The<br />

most common explanation for this heterogeneous degradation process comes from the<br />

absorption <strong>of</strong> water, followed by a hydrolytic cleavage <strong>of</strong> ester bonds, which generates cha<strong>in</strong><br />

fragments with the acidic groups (Fig. 1). This process is characterized by a decrease <strong>in</strong><br />

molecular weight, an <strong>in</strong>crease <strong>in</strong> polydispersity (PD = Mw/Mn) and polymer mass loss<br />

accompanied by an <strong>in</strong>crease <strong>in</strong> low molecular cha<strong>in</strong> compound concentration <strong>in</strong> the<br />

surround<strong>in</strong>g medium [2 – 7].<br />

H<br />

CH 3<br />

O<br />

O<br />

CH 3<br />

O<br />

O<br />

x<br />

O<br />

poly(lactic-co-glycolic acid)<br />

O<br />

O<br />

y<br />

OH<br />

CH<br />

H 3<br />

OH<br />

HO<br />

O<br />

lactic acid<br />

Fig. 1: Scheme <strong>of</strong> the PLGA degradation.<br />

+<br />

2x 2y<br />

H<br />

HO<br />

H<br />

O<br />

OH<br />

glycolic acid<br />

The <strong>in</strong>jectable biodegradable thermosensitive ABA triblock copolymers consist<strong>in</strong>g <strong>of</strong><br />

hydrophobic biodegradable copolymer <strong>of</strong> poly(lactic acid-co-glycolic acid) (PLGA) and<br />

hydrophilic poly(ethylene glycol) (PEG) act<strong>in</strong>g as A and B block, respectively, were<br />

synthesized via r<strong>in</strong>g-open<strong>in</strong>g polymerization method <strong>in</strong> a bulk at 155 °C. The ABA<br />

Sborník soutěže Studentské tvůrčí č<strong>in</strong>nosti Student 2006 a doktorské soutěže O cenu děkana 2005 a 2006<br />

Sekce DSP 2006, strana 218

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