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International Journal of Bioprinting               DEX-Loaded PLGA microspheres enhance cartilage regeneration






















































            Figure 2. Characterization and analysis of PLGA-dex60, PLGA-dex30, PLGA-dex15, and PLGA-dex0 microspheres: SEM, pore size, FTIR, XRD, TGA,
            DTG, and DSC results. (A–D) Scanning electron microscopy (SEM) images of the structures of PLGA-dex60 MPs (A), PLGA-dex30 MPs (B), PLGA-dex15
            MPs (C), and PLGA-dex0 MPs (D). (E) Distributions of pore sizes and average pore sizes of various groups of PLGA MPs. (F) Fourier transform infrared
            spectroscopy (FTIR) results of various groups of PLGA MPs. (G) X-ray diffraction (XRD) pattern of various groups of PLGA MPs. (H) Thermogravimetric
            analysis (TGA) results of various groups of PLGA MPs. (I) Derivative thermogravimetric analysis (DTG) results of various groups of PLGA MPs. (J)
            Differential scanning calorimeter (DSC) curves and (K) distribution of weight average molecular weight changes.


            of  PLGA  was observed  between 1750  and  1755  cm ,   X-ray crystallographic (XRD) analysis was conducted to
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            while that of DEX appeared between 1650 and 1660 cm .   investigate potential alterations in the crystalline structure
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            Given the potential overlap of DEX’s carbonyl peak with   of the drug, thereby exploring the crystalline properties of
            PLGA’s C=O peak, the intensity of PLGA’s C=O stretching   DEX within the MPs. As illustrated in Figure 2G, the XRD
            vibration peak may decrease with increasing DEX loading.   spectra of the four groups of PLGA MPs displayed broad
            After physical mixing of PLGA with DEX, the C=O    and diffuse non-crystalline diffraction peaks, indicating
            stretching  vibration peak of  DEX  remained  discernible,   the presence of characteristic peaks of the drug DEX in the
            and its intensity increased proportionally with the rise in   XRD spectra of drug-loaded MPs. This suggests that DEX
            drug loading. This intensity augmentation correlated with   in the MPs adopts an amorphous structure or lacks a long-
            the concentration of DEX in the MPs, almost disappearing   range periodic arrangement, predominantly existing in
            relative to blank MPs.                             an amorphous state. Notably, no significant characteristic


            Volume 10 Issue 5 (2024)                       389                                doi: 10.36922/ijb.3396
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