Open AccessFabrication and characterization of forcespun polycaprolactone microfiber scaffolds
Author(s) -
Deepa Kodali,
Farooq Syed,
Shaik Jeelani,
Vijaya K. Rangari
Publication year - 2020
Publication title -
materials research express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.383
H-Index - 35
ISSN - 2053-1591
DOI - 10.1088/2053-1591/abcac1
Subject(s) - polycaprolactone , microfiber , electrospinning , materials science , composite material , fiber , nanofiber , differential scanning calorimetry , crystallinity , scanning electron microscope , ultimate tensile strength , tissue engineering , rotational speed , dynamic mechanical analysis , biomedical engineering , polymer , medicine , physics , quantum mechanics , thermodynamics
Forcespinning technique was used to fabricate sub-micron size polycaprolactone (PCL) fibers. Forcespinning method uses centrifugal forces for the generation of fibers unlike the electrospinning method which uses electrostatic force. PCL has been extensively used as scaffolds for cell regeneration, substrates for tissue engineering and in drug delivery systems. The aim of this study is to qualitatively analyze the force spun fiber mats and investigate the effect of the spinneret rotational speed on the fiber morphology, thermal and mechanical properties. The extracted fibers were characterized by scanning electron microscopy differential scanning calorimetry, tensile testing and dynamic mechanical analysis. The results showed that higher rotational speeds produced uniform fibers with less number of beads. The crystallinity of the fibers decreased with increase in rotational speeds. The Young’s modulus of the forcespun fibers was found to be in the range of 3.5 to 6 MPa. Storage and loss moduli decreased with the increase in the fiber diameter. The fibers collected at farther distance from spinneret exhibited optimal mechanical properties compared to the fibers collected at shorter distances. This study will aid in extracting fibers with uniform geometries and lower beads to achieve the desired nanofiber drug release properties.