Thermoresponsive and bioactive poly(vinyl ether)-based hydrogels synthesized by radiation copolymerization and photochemical immobilization


Karakecili A., Satriano C., Gumuederelioglu M., Marletta G.

RADIATION PHYSICS AND CHEMISTRY, cilt.77, sa.2, ss.154-161, 2008 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 77 Sayı: 2
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1016/j.radphyschem.2007.04.014
  • Dergi Adı: RADIATION PHYSICS AND CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.154-161
  • Anahtar Kelimeler: thermoresponsive hydrogel, biomodification, photochemical immobilization, cell culture, cell detachment, HUMAN ENDOTHELIAL-CELLS, EXTRACELLULAR-MATRIX, POLYMER SURFACES, ETHYLENE-GLYCOL, VINYL ETHER, RGD, ENHANCEMENT, ADHESION, INSULIN, GROWTH
  • Ankara Üniversitesi Adresli: Hayır

Özet

A thermoresponsive hydrogel was synthesized by radiation copolymerization of ethylene glycol vinyl ether (EGVE) and butyl vinyl ether (BVE) in the presence of cross-linking agent diethylene glycol divinyl ether. The gel was modified by a cell adhesion factor RGD by photochemical immobilization technique. While the unmodified hydrogel shows fully hydrated form at low temperatures (+4 degrees C) and it extensively dehydrates at 37 degrees C, the biomodified hydrogel still kept its thermo responsive character after immobilization. The effectiveness of immobilization was checked with FTIR-ATR and XPS. The use of bioactive thermoresponsive hydrogels in cell culture applications was investieated. For this purpose, cell culture experiments were realized by L929 mouse fibroblasts. Cell attachment experiments revealed the effect of immobilized RGD with higher values of cell attachment (similar to 85%), which were obtained especially in the absence of serum. The thermoresponsive character of the hydrogel was useful for the application of low-temperature treatment in order to recover the attached viable cells from the surface of the hydrogel without using trypsin. When the culture temperature was decreased from 37 to 10 degrees C for 30 min similar to 80% of the cells were detached from the hydrogel surface. (c) 2007 Elsevier Ltd. All rights reserved.