Design and characterization of PNVCL‐based nanofibers and evaluation of their potential applications as scaffolds for surface drug delivery of hydrophobic drugs

ABSTRACT In this work, nanofiber scaffolds for surface drug delivery applications were obtained by electrospinning poly(N‐vinylcaprolactam) (PNVCL) and its blends with poly(ε‐caprolactone) and poly(N‐vinylcaprolactam)‐b‐poly(ε‐caprolactone). The process parameters to obtain smooth and beadless PNVCL...

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Veröffentlicht in:Journal of applied polymer science 2020-03, Vol.137 (11), p.n/a
Hauptverfasser: Sta, Marwa, Aguiar, Graziele, Forni, Abilio A. J., Medeiros, Simone F., Santos, Amilton M., Demarquette, Nicole R.
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container_issue 11
container_start_page
container_title Journal of applied polymer science
container_volume 137
creator Sta, Marwa
Aguiar, Graziele
Forni, Abilio A. J.
Medeiros, Simone F.
Santos, Amilton M.
Demarquette, Nicole R.
description ABSTRACT In this work, nanofiber scaffolds for surface drug delivery applications were obtained by electrospinning poly(N‐vinylcaprolactam) (PNVCL) and its blends with poly(ε‐caprolactone) and poly(N‐vinylcaprolactam)‐b‐poly(ε‐caprolactone). The process parameters to obtain smooth and beadless PNVCL fibers were optimized. The average fibers diameter was less than 1 μm, and it was determined by scanning electron microscopy analyses. Their affinity toward water was evaluated by measuring the contact angle with water. The ketoprofen release behavior from the fibers was analyzed using independent and model‐dependent approaches. The low values of the release exponent (n
doi_str_mv 10.1002/app.48472
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The low values of the release exponent (n &lt; 0.5) obtained for 20 and 42 °C, indicating a Fickian diffusion mechanism for all formulations. Dissolution efficiencies (DEs) revealed the effect of polymer composition, methodology used in the electrospinning process, and temperature on the release rate of ketoprofen. PNVCL/poly(N‐vinylcaprolactam)‐b‐poly(ε‐caprolactone)‐based nanofibers showed greater ability to control the in vitro release of ketoprofen, in view of reduced kinetic constant and DE, making this material promising system for controlling release of hydrophobic drugs. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. 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The ketoprofen release behavior from the fibers was analyzed using independent and model‐dependent approaches. The low values of the release exponent (n &lt; 0.5) obtained for 20 and 42 °C, indicating a Fickian diffusion mechanism for all formulations. Dissolution efficiencies (DEs) revealed the effect of polymer composition, methodology used in the electrospinning process, and temperature on the release rate of ketoprofen. PNVCL/poly(N‐vinylcaprolactam)‐b‐poly(ε‐caprolactone)‐based nanofibers showed greater ability to control the in vitro release of ketoprofen, in view of reduced kinetic constant and DE, making this material promising system for controlling release of hydrophobic drugs. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. 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Their affinity toward water was evaluated by measuring the contact angle with water. The ketoprofen release behavior from the fibers was analyzed using independent and model‐dependent approaches. The low values of the release exponent (n &lt; 0.5) obtained for 20 and 42 °C, indicating a Fickian diffusion mechanism for all formulations. Dissolution efficiencies (DEs) revealed the effect of polymer composition, methodology used in the electrospinning process, and temperature on the release rate of ketoprofen. PNVCL/poly(N‐vinylcaprolactam)‐b‐poly(ε‐caprolactone)‐based nanofibers showed greater ability to control the in vitro release of ketoprofen, in view of reduced kinetic constant and DE, making this material promising system for controlling release of hydrophobic drugs. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. 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subjects Composition effects
Contact angle
Diameters
Drug delivery systems
Electrospinning
Evaluation
fibers
Hydrophobicity
Ketoprofen
Materials science
Nanofibers
Polymer blends
Polymers
Process parameters
Scaffolds
Stability
stimuli‐sensitive polymers
title Design and characterization of PNVCL‐based nanofibers and evaluation of their potential applications as scaffolds for surface drug delivery of hydrophobic drugs
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