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Synthesis and evaluation of some novel thiomers as mucoadhesive ...

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Rajesh J. Oswal et al Der Pharma Chemica, 2012, 4 (4):1385-1396<br />

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Fig.2 Comparative IR spectra <strong>of</strong> Starch <strong>and</strong> CMS-C<br />

Fig.3 Comparative IR spectra <strong>of</strong> Guar gum <strong>and</strong> CMG-C<br />

The formation <strong>of</strong> CMS-C <strong>and</strong> CMG-C w<strong>as</strong> confirmed by the FT-IR spectrum (Fig. 2 <strong>and</strong> 3) <strong>of</strong> the derivative.<br />

Comparison <strong>of</strong> the FT-IR spectra <strong>of</strong> native starch with CMS-C indicated the introduction <strong>of</strong> substituent groups -C=O<br />

absorption around 1750-1754 cm -1 . As the thiolation reaction continued there w<strong>as</strong> an increment in the absorption<br />

due to carbon–sulphur stretching (C-S) at 1365 cm -1 .Also stretching due to nitrogen-hydrogen (N-H) at 3276 cm -1.<br />

Similarly Comparison <strong>of</strong> the FT-IR spectra <strong>of</strong> Guar gum with CMG-C indicated the introduction <strong>of</strong> substituent<br />

groups -C=O absorption around 1700–1711 cm -1 . As the thiolation reaction continued there w<strong>as</strong> an increment in the<br />

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