2019
DOI: 10.1007/s00396-019-04568-5
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Electrospun PCL-based polyurethane/HA microfibers as drug carrier of dexamethasone with enhanced biodegradability and shape memory performances

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Cited by 25 publications
(14 citation statements)
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“…PCL based PU electrospun microfiber with apatite nanoparticles were prepared to enhance the biological characteristic and shape memory properties. This composite nanofibers showed controlled drug delivery [ 86 ]. The addition of apatite with various ratio to determine the shape memory features and 3 wt% of HA showed excellent recovery with short recovery time.…”
Section: Other Biopolymer Coatingsmentioning
confidence: 99%
“…PCL based PU electrospun microfiber with apatite nanoparticles were prepared to enhance the biological characteristic and shape memory properties. This composite nanofibers showed controlled drug delivery [ 86 ]. The addition of apatite with various ratio to determine the shape memory features and 3 wt% of HA showed excellent recovery with short recovery time.…”
Section: Other Biopolymer Coatingsmentioning
confidence: 99%
“…Polymeric electrospun mats are very versatile materials and they can be used for the production of monolayer and multilayer films and/or sandwich type composites [ 6 , 7 , 8 , 9 ]. Moreover, the electrospun mats can be easily modified by reinforcing the fibers with organic [ 10 , 11 ] and inorganic nanofillers [ 12 , 13 , 14 ] and metallic nanoparticles [ 15 , 16 ]. Therefore, the electrospun mats have gained interest in the industrial sector since they can be easily processed as multifunctional materials and can be applied in different industrial fields such as controlled release of drugs [ 13 ], antioxidants [ 10 , 17 ] and/or antimicrobial [ 17 ] agents; in addition they have piezoelectric properties [ 18 ] and shape memory performance [ 19 , 20 ].…”
Section: Introductionmentioning
confidence: 99%
“…For areas where degradation should be tunable like drug delivery, PUs are usually developed in forms of electrospun networks [ 160 , 161 ], hydrogels [ 162 , 163 ], membranes [ 164 ] or nanocarriers like micelles [ 165 ] when quick drug release is needed. As PUs degradation process is mainly determined by the SS, degradation rates for tailored drug release time are obtained by varying the type and amount of polyols undergoing hydrolytic and enzymatic degradations such as polyesters-based polyols, to hydrophilic polyols undergoing water uptake and oxidative degradation like polyether-based polyols [ 166 , 167 ].…”
Section: Conventional (Fossil-based) Pu For Biomedical Applicationsmentioning
confidence: 99%