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In general way, results demonstrated that three chemicals (fluoxetine, vitamins B2 and B12)
are transferred to microenvironment generated by weakly acidic solution of chitosan but in
different proportions, due to the structural feature and solubility of each. Table 1 describes
the relative increase of the fluorescence and absorption intensities of the chemicals when
chitosan concentration ranges from zero to 1.0 g.L
-1
.
Both vitamins belong to the class of hydro soluble vitamins (Sun et al., 2007), while the
fluoxetine drug is slightly soluble in water (Darwish, 2005).
The low solubility promotes
some molecules of fluoxetine to migrate from aqueous environment to the more rigid
environment generated by chitosan (the higher the concentration) causing a proportionately
greater increase of absorbance and fluorescence intensities. However, the fluorescence
intensities of vitamin B12 also increase in the same proportion and the absorbance
intensities in proportion even higher, despite the hydro soluble nature of this vitamin.
Figure 2.
Absorption spectra and chemical structures of vitamin B12 (A), vitamin B2 (B)
and fluoxetine (C).
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Study of Interactions with Drug and Nutritional Substances 609
These results demonstrate that the transfer process of chemicals from aqueous environment
to the chitosan aggregates is influenced by solubility of the molecules in water and/or by the
molecular structure. Particularly, the structure molecular of vitamin B12 seems to have an
interesting effect in this case. Vitamin B12 belong to the cobalamins, a class of octahedral
Co(III) complexes which contain a planar framework called a corrin, with the metal center
coordinated in the equatorial position by the four corrin nitrogens. Her energies of excited
states are sensitive to the nature of the ligands of center coordinated and are influenced by
water content of the surrounding environment (Solheim et al., 2011). These characteristics
may be the reason for the more significant increase of the spectral properties of the vitamin
B12, with increasing concentration of chitosan (lower water content), compared with the
vitamin B2.
In fact, some molecules of fluoxetine or vitamins B2 or B12, are transferred to
microenvironment generated by weakly acidic solution of chitosan. Among the three, the
vitamin B2 is transferred in a smaller proportion. However, for all of them is expected that
its loss in the diet, caused by administration of chitosan, is not so significant.
From our observations, possible risks to the patient should be considered when prolonged
treatment with chitosan is prescribed and perhaps extra care should be taken when
chitosan and fluoxetine are prescribed together in slimming diets. In the case of vitamins,
essential for many physiological functions, there must be some precautions to minimize
the impacts generated by this therapeutic, as the replacement of nutrients in the diet of
patient.
Figure 3.
Fluorescence spectra of fluoxetine in acid aqueous solution of chitosan.
Chitosan concentrations: 0.00; 0.050; 0.60 and 1.0 (from the base to the top).
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610
Figure 4.
Fluorescence spectra of vitamin B12 in acid aqueous solution of chitosan. Chitosan
concentrations: 0.00; 0.050; 0.60 and 1.0 (from the base to the top).
Figure 5.
Fluorescence spectra of vitamin B2 in acid aqueous solution of chitosan. Chitosan
concentrations: 0.00; 0.050; 0.60 and 1.0 (from the base to the top).
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Study of Interactions with Drug and Nutritional Substances 611
Figure 6.
Behavior of absorption intensities of fluoxetine, vitamin B12 and B2.
Chemicals
I
ABS
Vitamin B12
107 %
80 %
Vitamin B2
30 %
14 %
fluoxetine
109 %
40 %
Table 1.
Relative increase on the fluorescence (I) and absorption (ABS) intensities of the fluoxetine,
vitamins B2 and B12 when chitosan concentration ranges from zero to 1.0 g.L
-1
.
This paper seeks to warn to possible problems connected with the excessive loss of vitamins
and other nutrients by the body during prolonged treatment with chitosan, as well as due
the concomitant use of chitosan and fluoxetine.
4. Conclusions
Innumerous studies have described the formation of aggregates in naturals (Kim et al., 2000;
Pelletier et al., 2000; Zhbankov et al., 2003), as chitosan ((Rodrigues, 2005; Hennen, 2005;
Rodrigues et al., 2008) and synthetic (Kalyanasundaram, 1987; Neumann & Rodrigues, 1994;
Neumann et al., 1995; Gomes et al., 2006; Gomes et al., 2007; Sur, 2010) polymers solutions
and these molecular structures occur due to intra- and intermolecular interactions.
Chitosan is a polysaccharide precursor of materials suitable to release and/or dissolve drugs
into the human body (Hennen, 2005), among other uses. However, the study of spectral
properties of chemicals, fluoxetine, vitamins B2 and B12, demonstrated that the
microenvironment generated by weakly acidic solution of chitosan also is able to sequester
some B2, B12 and fluoxetine molecules, despite the hydro soluble nature of vitamins.