Amino acid functionalized macroporous gelatin cryogels: Characterization and effects on cell proliferation

Bayrak G., PERÇİN DEMİRÇELİK I., KILIÇ SÜLOĞLU A., DENİZLİ A.

PROCESS BIOCHEMISTRY, cilt.110, ss.100-109, 2021 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 110
  • Basım Tarihi: 2021
  • Doi Numarası: 10.1016/j.procbio.2021.08.002
  • Dergi Adı: PROCESS BIOCHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Aqualine, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Communication Abstracts, Compendex, Food Science & Technology Abstracts, INSPEC, Metadex, Pollution Abstracts, Veterinary Science Database, Civil Engineering Abstracts
  • Sayfa Sayıları: ss.100-109
  • Anahtar Kelimeler: Cell proliferation, Histidine, Gelatin, PHEMA, MAH, TISSUE, SCAFFOLDS, HYDROGELS, METHACRYLATE)
  • Hacettepe Üniversitesi Adresli: Evet

Özet

Gelatin and N-methacryloyl-(L)-histidine methyl ester [MAH] containing poly(2-hydroxyethyl methacrylate) [PHEMA] based cryogels were prepared to aid in enhancing cell proliferation. In order to evaluate effects of MAH comonomer and gelatin, cryogels were prepared containing different amounts of gelatin and MAH. Accordingly, four different groups of cryogels which were PHEMA, poly(2-hydroxyethyl methacrylate)-gelatin [PHEMA/GEL], poly(2-hydroxyethyl methacrylate-N-methacryloyl-(L)-histidine methyl ester) [PHEMAH] and poly(2hydroxyethyl methacrylate-N-methacryloyl-(L)-histidine methyl ester)-gelatin [PHEMAH/GEL] were prepared and a total of eight cryogel groups were obtained depending on the varying gelatin ratios. Swelling tests, scanning electron microscope (SEM), microcomputed tomography (Micro-CT) and Fourier transform infrared spectroscopy- Attenuated Total Reflectance (FTIR-ATR) were performed for characterization studies. FTIR-ATR studies confirmed that gelatin and MAH were incorporated into the cryogel structures. Average pore size of cryogels was in the range of 18-198 mu m confirmed by Micro-CT and SEM analysis. Then, cryogels were evaluated for cell proliferation abilities by MTT analysis for 24 h and 48 h for cell viability in L929 mouse fibroblast cells. Cell viability of PHEMAH/0.2GEL cryogels reached 209 %. Interaction and proliferation of fibroblast cells on cryogels demonstrated by SEM examination.