Title | Core-sheath nanofibers as drug delivery system for thermoresponsive controlled release |
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Authors | Lv, Y., Pan, Q., Bligh, S.W.A., Li, H., Wu, H, Sang, Qingqing and Zhu, Li-Min |
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Abstract | In this work, a smart drug delivery system of core–sheath nanofiber is reported. The core-sheath nanofibers were prepared with thermoresponsive poly-(N-isopropylacrylamide) (PNIPAAm) (as core) and hydrophobic ethylcellulose (EC) (as sheath) by coaxial electrospinning. Analogous medicated fibers were prepared by loading with a model drug ketoprofen (KET). The fibers were cylindrical without phase separation and have visible core-sheath structure as shown by scanning and transmission electron microscopy. X-ray diffraction patterns demonstrated the drug with the amorphous physical form was present in the fiber matrix. Fourier transform infrared spectroscopy analysis was conducted, finding that there were significant intermolecular interactions between KET and the polymers. Water contact angle measurements proved that the core-sheath fibers from hydrophobic transformed into hydrophobic when the temperature reached the lower critical solution temperature. In vitro drug-release study of nanofibers with KET displayed that the coaxial nanofibers were able to synergistically combine the characteristics of the two polymers producing a temperature-sensitive drug delivery system with sustained release properties. In addition, they were established to be non-toxic and suitable for cell growth. These findings show that the core–sheath nanofiber is a potential candidate for controlling drug delivery system. |
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Keywords | poly(N-isopropylacrylamide); ethylcellulose; ketoprofen; coaxial electrospinning; controlled drug release |
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Journal | Journal of Pharmaceutical Sciences |
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Journal citation | 106 (5), pp. 1258-1265 |
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ISSN | 0022-3549 |
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Year | 2017 |
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Publisher | Elsevier |
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Accepted author manuscript | |
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Digital Object Identifier (DOI) | https://doi.org/10.1016/j.xphs.2016.12.031 |
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Publication dates |
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Published online | 26 Jan 2017 |
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Published | 26 Jan 2017 |
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Published in print | May 2017 |
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