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International Journal of Bioprinting                                     Stability of 3D-printed PEO tablets







































            Figure 2. Differential scanning calorimetry (DSC) traces of physical mixture (PM), hot-melt extrudate (HME), and printed samples of formulation F .
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            Since all formulations displayed similar patterns, only DSC traces of F  are presented to avoid repetition.
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            Table 2. Melting point (T ) of polyethylene oxide (PEO) after each process.
                              m
             Formulation                                           T , mean ± SD (°)
                                                                    m
                                               PM                      HME                    Printed
             F                              72.11 ± 0.15             67.06 ± 0.82            64.42 ± 0.32
             1
             F                              71.18 ± 0.37             65.61 ± 0.51            65.13 ± 1.22
             2
             F                              71.87 ± 0.25             67.06 ± 1.51            65.41 ± 1.33
             3
             F                              71.24 ± 0.28             66.3 ± 1.43             64.86 ± 2.30
             4
            Note: SD is calculated from the mean of triplicates. Abbreviations: PM: Physical mixture; HME: Hot-melt extrudates.

            (Figures 3 and  4). Theophylline is a crystalline material   be observed in the peak position, shape, and width in
            whose diffractogram displays numerous sharp peaks, with   thermally processed samples compared to non-thermally
            the highest peak at a 2θ of 12.6°. EC and HPC exhibited   processed samples. Since all formulations displayed similar
            a halo-shape diffractogram due to their amorphous   diffractograms, only the diffractogram for F  is presented
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            structures. The diffractogram of PEO, a semi-crystalline   (Figure 4) to avoid repetition.
            polymer, exhibited characteristic crystalline peaks at   Changes  in  crystal  structure  and  lattice  strain  can
            2θ of 18.8° and 23°. Since both M  of PEO have similar   result  in peak split,  a  phenomenon noticed in  PEO
                                                                                32
                                        w
            characteristics according to previous studies  and proved   peaks, especially in formulations F  and F  containing PEO
                                               11
            similar in DSC tests, only PEO 7 M was studied for   7 M (Figure 4). Moreover, there was a broadening in all
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            crystallinity in this work.
                                                               crystalline peaks of HME and printed samples compared
               Meanwhile,  in  the  diffractograms  of  formulations,   to PM samples, reflecting a change in crystal size or lattice
            the characteristic peaks of theophylline and PEO were   also reported in other studies.  Overall, based on peak
                                                                                        3,6
            detected, indicating the presence of both materials in the   broadening and deformation, as well as the findings of
            crystalline state. However, some noticeable changes can   other studies, PEO appears to have exhibited a change in
            Volume 10 Issue 5 (2024)                       412                                doi: 10.36922/ijb.4055
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