Designing Double-layered Nanofibrous Membranes as a Wound Dressing Material


TIĞLI AYDIN R. S., Eroglu A. N., KARAKEÇİLİ A., Calimli A.

FIBERS AND POLYMERS, cilt.17, sa.11, ss.1765-1775, 2016 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 17 Sayı: 11
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1007/s12221-016-6668-4
  • Dergi Adı: FIBERS AND POLYMERS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1765-1775
  • Anahtar Kelimeler: Poly(2-hydroxylethyl methacrylate), Nanofiber, Double-layered, Wound dressing, Antimicrobial, ELECTROSPUN NANOFIBERS, SCAFFOLDS, AMPICILLIN, COMPOSITE, RELEASE, PCL, METHACRYLATE), PROTEINS, SURFACES, ACETATE
  • Ankara Üniversitesi Adresli: Evet

Özet

New generation wound dressings require the criteria that both bioactive and conventional wound dressing materials can recompense the fundamental properties like defense of wound from microbial invasion, dehydration during the wound care duration and mimic the healing process. In this study, functional double-layered nanofibrous composite membranes were fabricated via electrospinning method. The matrices consist of a sheet of ampicillin loaded poly(2-hydroxylethyl methacrylate/polyacrylic acid (pHEMA/pAA) nanofibers on the upper side (first layer: pH sensitive antibacterial barrier) and a sheet of poly(epsilon-caprolactone) (PCL)/gelatin nanofibers (second layer: bioactive part). Ampicillin was successfully incorporated to double-layered matrices which greatly changed the mechanical properties, biodegradability and water uptake ratios (up to 4 fold higher values). The success of the antimicrobial activity of ampicillin on Staphylococcus aureus and Escherichia coli was indicated by the inhibition zone test. pH sensitivity was confirmed by the swelling and ampicillin release studies by shifting pH value to basic environment. Thus, double-layered pHEMA-pAA nanofibers suggest as a potential wound dressing material for its pH sensitive drug delivery ability and its bioactive part.