In-vitro cytotoxic activities of poly(2-ethyl-2-oxazoline)-based amphiphilic block copolymers prepared by CuAAC click chemistry
Yazarlar (6)
S. Gulyuz
İstanbul Teknik Üniversitesi, Türkiye
U. U. Ozkose
İstanbul Teknik Üniversitesi, Türkiye
P. Kocak
Yeditepe University, Türkiye
D. Telci
Yeditepe University, Türkiye
O. Yilmaz
Tubıtak Marmara Research Center, Türkiye
Prof. Dr. Mehmet Atilla TAŞDELEN Yalova Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Express Polymer Letters (Q1)
Dergi ISSN 1788-618X Dergi Bilgileri (2018)
Dergi Tarandığı Indeksler SCI
Makale Dili İngilizce Basım Tarihi 01-2018
Kabul Tarihi – Yayınlanma Tarihi 01-01-2018
Cilt / Sayı / Sayfa 12 / 2 / 146–158 DOI 10.3144/expresspolymlett.2018.13
Makale Linki http://www.expresspolymlett.com/letolt.php?file=EPL-0008460mi=c
UAK Araştırma Alanları
Polimer Bilimi
Özet
Synthesis and characterization of well-defined amphiphilic block copolymers containing poly (2-ethyl-2-oxazoline) as hydrophilic block and poly (ε-caprolactone) or poly (L-lactide) as hydrophobic block is achieved by copper-catalyzed azide-alkyne cycloaddition (CuAAC) click chemistry. The clickable precursors, α-alkyne-functionalized poly (ε-caprolactone) and poly (L-lactide) and ω-azido-functionalized poly (2-ethyl-2-oxazoline) are simply prepared and joined using copper sulfate/ascorbic acid catalyst system at room temperature. The structures of precursors and amphiphilic block copolymers are characterized by spectroscopic, chromatographic and thermal analyses. The cytotoxic activities of resulting amphiphilic block copolymers and their precursors are investigated in the prostate epithelial and cancer cells under in-vitro conditions. The treatment of the healthy prostate epithelial cell line PNT1A reveals that no significant cytotoxicity, whereas some significant toxic effects on the prostate cancer cell lines are observed.
Anahtar Kelimeler
Amphiphilic block copolymers | Copper-catalyzed azide-alkyne cycloaddition click chemistry | In-vitro cytotoxic activity | Molecular engineering | Polymer synthesis | Polyoxazolines