Effects of polyvinylpyrrolidone and ethyl cellulose in polyurethane electrospun nanofibers on morphology and drug release characteristics Elektro-eğirme yöntemi ile üretilen poliüretan nanoliflerin morfolojileri ve ilaç salım özellikleri üzerinde polivinilpirolidon ve etil selülozun etkileri


Gençtürk A., Kahraman E., GÜNGÖR S., Özsoy Y., Saraç A. S.

Turkish Journal of Pharmaceutical Sciences, cilt.17, sa.6, ss.638-644, 2020 (ESCI) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 17 Sayı: 6
  • Basım Tarihi: 2020
  • Doi Numarası: 10.4274/tjps.galenos.2019.87094
  • Dergi Adı: Turkish Journal of Pharmaceutical Sciences
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), Scopus, Academic Search Premier, EMBASE, International Pharmaceutical Abstracts, Directory of Open Access Journals, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.638-644
  • Anahtar Kelimeler: Electrospun nanofibers, drug release, polyurethane, polyvinylpyrrolidone, ethyl cellulose, DELIVERY, MATS, DISSOLUTION
  • İstanbul Üniversitesi Adresli: Evet

Özet

© Turk J Pharm Sci, Published by Galenos Publishing House.Objectives: Polyurethanes (PUs) are a popular choice for composing nanofibers due to their spinnability, biocompatibility, high chemical stability, and good mechanical and elasticity properties. The desired release behaviors are also achieved by using combinations of PUs and various polymers. In this study, we investigated effects of polyvinylpyrrolidone (PVP) and ethyl cellulose (EC) on PU electrospun nanofibers in terms of morphological structures and drug release characteristics. Materials and Methods: Nanofibers were prepared using blends of PU with either EC or PVP in different ratios by electrospinning. The effects of PVP or EC on the morphology and diameter of the prepared nanofibers were examined with scanning electron microscope (SEM). The compatibility of the components used in the formulations of nanofibers was determined by attenuated total reflection (ATR)-fourier-transform infrared (FTIR). Donepezil hydrochloride (DNP), a water soluble compound, was selected as a model drug to examine its release characteristics from both PU/PVP and PU/EC electrospun nanofibers. In vitro drug release studies from electrospun nanofibers were performed according to the method defined in the monograph as the “paddle over disk method” of United States Pharmacopeia 38. Results: The SEM images showed that addition of EC or PVP to PU solutions did not affect the generation of nanofibers, and those formed had a smooth surface without beads in nanoscale. The ATR-FTIR spectra disclosed that EC and PVP were separately incorporated into the PU matrix. The in vitro release data indicated that the presence of EC or PVP in PU nanofibers dramatically changed the release behavior of DNP. PU/EC nanofibers (F4) provided sustained drug release with the Korsmeyer-Peppas drug release kinetic mechanism, in which the release rate was controlled by diffusion of the drug, while all of the PU/PVP nanofibers exhibited fast drug release. Conclusion: Overall, these characteristics of PU/EC (10/8) electrospun nanofibers has suggested their potential use as a drug carrier from which water-soluble drug release may occur in a sustained fashion.