TY - JOUR
T1 - Blends of paclitaxel with POSS-based biodegradable polyurethanes
T2 - Morphology, miscibility, and specific interactions
AU - Guo, Qiongyu
AU - Knight, Pamela T.
AU - Wu, Jian
AU - Mather, Patrick T.
PY - 2010/6/8
Y1 - 2010/6/8
N2 - The morphology, miscibility, and specific interactions of paclitaxel (PTx) with a family of polyhedral oligosilsesquioxane (POSS)-based biodegradable thermoplastic polyurethanes (POSS TPUs) were investigated systematically using wide-angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). These POSS TPUs incorporate an alternating multiblock structure formed by POSS hard segments and the soft segments composed of polylactide/caprolactone copolymer (P(DLLA-co-CL)). They feature variable poly(ethylene glycol) (PEG) content from 0 to 14 wt % through adjusting the poly(ethylene glycol) (PEG) molecular weight in P(DLLA-co-CL) soft segments of fixed molar mass of M̄n = 12 kg/mol and further to 52 wt % utilizing pure PEG M̄n = 1 kg/mol in the soft segments. Using WAXD, it was found that PTx is amorphous in all proportions in the PTx/POSS TPU blends prepared using a solution-casting method. Interestingly, the PTx not only exhibits excellent miscibility in all of these PTx/POSS TPU blends over the whole range of the drug concentration, but also serves as an antiplasticizer by increasing the blend Tg gradually from the polymer Tg up to the Tg of amorphous PTx. The T g-composition dependences in these blends were well fitted by the Gordon-Taylor equation. The glass transition breadth of the blends increases significantly only for drug concentrations higher than 50 wt % for most of the POSS TPUs, suggesting some spatial heterogeneity at these high drug concentrations. On the other hand, the slight increment of the blend melting temperature, Tm, and latent heat, H, indicates enhanced phase separation between the POSS hard segments and the TPU soft segments upon drug incorporation. Gordon-Taylor analysis and FTIR results confirm that the PEG incorporated in the POSS TPUs exhibits strong H-bonding interactions with the PTx. Although PEG can promote the favorable interactions in the PTx/POSS TPU blends, we showed that the more hydrophobic LA/CL repeat units are still required in the soft segments in order to achieve molecular-level miscibility. This systematic investigation of the PTx/POSS TPU systems may be of great value to design plasticizer/antiplasticizer for new polymer materials with controlled and tailored properties, especially for those PLA- or PCL-based biodegradable polymer systems.
AB - The morphology, miscibility, and specific interactions of paclitaxel (PTx) with a family of polyhedral oligosilsesquioxane (POSS)-based biodegradable thermoplastic polyurethanes (POSS TPUs) were investigated systematically using wide-angle X-ray diffraction (WAXD), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). These POSS TPUs incorporate an alternating multiblock structure formed by POSS hard segments and the soft segments composed of polylactide/caprolactone copolymer (P(DLLA-co-CL)). They feature variable poly(ethylene glycol) (PEG) content from 0 to 14 wt % through adjusting the poly(ethylene glycol) (PEG) molecular weight in P(DLLA-co-CL) soft segments of fixed molar mass of M̄n = 12 kg/mol and further to 52 wt % utilizing pure PEG M̄n = 1 kg/mol in the soft segments. Using WAXD, it was found that PTx is amorphous in all proportions in the PTx/POSS TPU blends prepared using a solution-casting method. Interestingly, the PTx not only exhibits excellent miscibility in all of these PTx/POSS TPU blends over the whole range of the drug concentration, but also serves as an antiplasticizer by increasing the blend Tg gradually from the polymer Tg up to the Tg of amorphous PTx. The T g-composition dependences in these blends were well fitted by the Gordon-Taylor equation. The glass transition breadth of the blends increases significantly only for drug concentrations higher than 50 wt % for most of the POSS TPUs, suggesting some spatial heterogeneity at these high drug concentrations. On the other hand, the slight increment of the blend melting temperature, Tm, and latent heat, H, indicates enhanced phase separation between the POSS hard segments and the TPU soft segments upon drug incorporation. Gordon-Taylor analysis and FTIR results confirm that the PEG incorporated in the POSS TPUs exhibits strong H-bonding interactions with the PTx. Although PEG can promote the favorable interactions in the PTx/POSS TPU blends, we showed that the more hydrophobic LA/CL repeat units are still required in the soft segments in order to achieve molecular-level miscibility. This systematic investigation of the PTx/POSS TPU systems may be of great value to design plasticizer/antiplasticizer for new polymer materials with controlled and tailored properties, especially for those PLA- or PCL-based biodegradable polymer systems.
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U2 - 10.1021/ma100662x
DO - 10.1021/ma100662x
M3 - Article
AN - SCOPUS:77953141186
SN - 0024-9297
VL - 43
SP - 4991
EP - 4999
JO - Macromolecules
JF - Macromolecules
IS - 11
ER -