Figure 4 shows FT-IR spectra of PVA, SA, and the blend monolith (PVA/SA-3), Copanlisib which clearly implies that the blend monolith consists of both polymers. In
the spectrum of SA, peaks at 1,600 and 1,410/cm are ascribed to asymmetric and symmetric carboxylate stretching vibrations of SA, respectively. These two vibrations are also observed in all the spectra of the blend monoliths and shift to a higher frequency range. These data clearly suggest the strong interaction between PVA and SA in the blend monolith [14]; the hydrogen bond between the carboxyl group of SA and hydroxyl group of PVA is formed. This interaction may be related to the specific solvent of the phase separation for the combination of PVA and SA. Figure 4 FT-IR spectra of PVA, SA, and the PVA/SA monolith (PVA/SA-3). The pH-sensitive property of the PVA/SA blend monolith with different mixed ratios is shown in Figure 5. At first, the dried blend monolith is placed in an acidic solution (pH 1.0). The monolith is gradually swollen. After 9 h, the sample is transferred into in a neutral solution (pH 7.4). Under the acidic condition, the swelling ratio decreases with increasing the SA content; while the swelling ratio significantly increases as the SA content increases under the neutral condition. This behavior can be
explained by the acidic form of the carboxylate group of SA in pH 1.0 and the neutralized form in pH 7.4; the electrostatic repulsion of the carboxylate group increases, leading to the increase Lumacaftor supplier of the swelling ratio [18–20]. Figure 5 Effect of pH on swelling behaviors of PVA/SA blend monoliths. Conclusions The PVA/SA blend monolith with nanoscale porous structure and pH-responsive property is successfully fabricated via TINIPS without any templates. We have first achieved the fabrication of a monolith containing SA by the appropriate selection of
the solvent for the phase separation. PVA and SA are widely used as biomaterials due to their good biocompatibility. A combination of this 17-DMAG (Alvespimycin) HCl feature and nanoscale structural characteristics of the present blend monolith offers promising prospects for the applications in bio-related and environmental fields. SA provides the pH-sensitive property in the blend monolith, which may be potentially useful for controlled drug delivery systems. Moreover, the present study is highly significant to suggest the possibility to fabricate blend monoliths consisting of bioactive polymers which can not form monolithic structure solely. Further studies on the fabrication of blend monoliths of functional polymers and their bio-related applications are under way in our laboratory. Acknowledgements This study is financially supported by the Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (No.