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Tese_Tânia Vieira.pdf - Ubi Thesis

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Chapter III – Results and Discussion<br />

of chitosan (Anitha et al. 2009; Delair 2011; Potara et al. 2011). One peak at 1585.68 cm -1 was<br />

observed and corresponds to the deformation in the chitosan (Delair 2011).<br />

In dextran spectrum was verified a peak at 2950.07 cm -1 that corresponds to a C–H<br />

stretching (Kumar et al. 2012). The peak at 1636.30 cm -1 was also observed and corresponds to<br />

the sulfate asymmetric stretching (Delair 2011). Another peak was found at 1220.72 cm -1 that<br />

belongs to S=O vibrations (Delair 2011).<br />

When examining FT-IR spectrum of chitosan/dextran nanoparticles, changes in the amine<br />

and sulfate absorption bands were detected (figure 10 red). These spectral changes were<br />

attributed to the electrostatic interaction between the chitosan amine and dextran sulfate<br />

groups (Anitha et al. 2011). The formation of the chitosan/dextran nanoparticles was noticed by<br />

the appearance of a specific band at 1531.68 cm -1 that was also observed by Delair and<br />

coworkers (Delair 2011). The band at 1220.72 cm -1 in the dextran spectrum, broadened and was<br />

separated into two peaks along with the complexation process, as already observed by Delair and<br />

coworkers (Delair 2011). Tyaboonchai and collegues reported that the complex formation by a<br />

shift of the N-H bending adsorption at 1652 cm -1 and 1599 cm -1 for chitosan, to 1623 cm -1 in the<br />

chitosan/dextran nanoparticles was consistent with the presence of electrostatic interaction<br />

(Tiyaboonchai et al. 2007; Delair 2011). Such phenomenon was also herein observed, the<br />

appearance of a band at 1633.41 cm -1 in the chitosan/dextran nanoparticles spectrum.<br />

36

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