posted on 2016-06-15, 00:00authored byEmine Guler, Huseyin Akbulut, Caner Geyik, Tulay Yilmaz, Z. Pinar Gumus, F. Baris Barlas, Recep Erdem Ahan, Dilek Odaci Demirkol, Shuhei Yamada, Takeshi Endo, Suna Timur, Yusuf Yagci
Advances
in polymer chemistry resulted in substantial interest
to utilize their diverse intrinsic advantages for biomedical research.
Especially, studies on drug delivery for tumors have increased to
a great extent. In this study, a novel fluorescent graft copolymer
has been modified by a drug and targeting moiety and the resulting
structure has been characterized by alterations in fluorescent intensity.
The polythiophene based hybrid graft copolymer was synthesized by
successive organic reactions and combination of in situ N-carboxy anhydride (NCA) ring opening and Suzuki coupling polymerization
processes. Initially, targeted delivery of the graft copolymer was
investigated by introducing a tumor specific ligand, anti-HER2/neu antibody, on the structure. The functionalized polymer
was able to differentially indicate HER2-expressing A549 human lung
carcinoma cells, whereas no signal was obtained for Vero, monkey kidney
epithelial cells, and HeLa, human cervix adenocarcinoma cells. After
integrating paclitaxel into the structure, cell viability, cell cycle
progression, and radiosensitivity studies demonstrate HER2/neu targeting polymers were most effective to inhibit cell
proliferation. Importantly, the graft copolymer used had no cytotoxic
effects to cells, as evidenced by cell viability and cell cycle analysis.
This work clearly confirms that a specially designed and fabricated
graft copolymer with a highly complex structure is a promising theranostic
agent capable of targeting tumor cells for diagnostic and therapeutic
purposes.