2011
DOI: 10.1002/jps.22310
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A Three-Dimensional Polycaprolactone Scaffold Combined with a Drug Delivery System Consisting of Electrospun Nanofibers

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Cited by 55 publications
(13 citation statements)
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“…Many other studies have also shown that ECM-like nanofibers with tailored nanofiber architecture (diameter, aligned or random orientation, pore size, porosity), controlled degradability, and immobilized soluble signal can provide desired cell stimulatory cues to promote cell adhesion, orientation, proliferation, differentiation, and tissue formation [5,6]. Exploiting these advantages, electrospun nanofibers have been tested for engineering bone tissue [7,8], wound dressing [9,10], artificial vessel formation [11], neural tissue regeneration [12,13], and vehicles for drug delivery [14,15] and biomolecular transport [16]. …”
Section: Introductionmentioning
confidence: 99%
“…Many other studies have also shown that ECM-like nanofibers with tailored nanofiber architecture (diameter, aligned or random orientation, pore size, porosity), controlled degradability, and immobilized soluble signal can provide desired cell stimulatory cues to promote cell adhesion, orientation, proliferation, differentiation, and tissue formation [5,6]. Exploiting these advantages, electrospun nanofibers have been tested for engineering bone tissue [7,8], wound dressing [9,10], artificial vessel formation [11], neural tissue regeneration [12,13], and vehicles for drug delivery [14,15] and biomolecular transport [16]. …”
Section: Introductionmentioning
confidence: 99%
“…The 15-mer peptide was encapsulated in the PEO layer with variation in the thickness of the PCL layers [48]. They continue their work on PCL and PEO monitoring the release of Rhodamine B [50], earlier this year reporting ways to overcome edge-effects in layer-bylayer electrospun micro/nanofibrous mats of PCL and PEO with the ultimate goals of soft and hard tissue regeneration [51].…”
mentioning
confidence: 99%
“…Using the core-shell spinning technique, matrices can also be used as drug delivery systems (DDS) in order to release incorporated drugs in a controlled manner. Yoon et al used a core-shell laminated, structured, electrospun mat of hydrophobic PCL and hydrophilic poly(ethylene oxide) (PEO)/rhodamine-B fibers in a normal PCL matrix [28] . Rhodamine was released from the scaffold by the drug delivery system, which was controlled by the thickness of the PCL layer.…”
Section: Muscle Tissue Engineeringmentioning
confidence: 99%