Synthesis of L-DOPA conjugated doxorubicin-polyethylenimine nanocarrier and evaluation of its cytotoxicity on A۳۷۵ and HepG۲ cell lines

Objective(s): Polyethylenimine (PEI) is one of the most-extensively investigated cationic polymers for gene and drug delivery. Recently, great attention has been directed to design of carriers for co-delivery of nucleic acids and small molecules. These delivery systems are able to overcome the limitations of gene or drug delivery alone. The aim of this study is to prepare a targeted nano-carrier for co-delivery of doxorubicin (Dox) and gene using polyethylenimine. Materials and Methods: In order to prepare the ligand-containing polymer conjugates, succinic anhydride was conjugated onto the hydroxyl group of Dox through an ester bond following the protection of Dox amines by Fmoc. Drug-polymer conjugates were then coupled with L-DOPA in order to prepare the targeted nanocarriers to the cells through Large Amino Acid Transporter-۱ (LAT-۱). The PEI derivatives were characterized using ۱H-NMR. The toxicity of conjugated polymer, Dox and PEI was assessed on HepG۲ and A۳۷۵ cell lines with different expression level of LAT-۱ transporters using MTT assay. Results: The chemical structure of PEI conjugate was confirmed by ۱H-NMR. The cytotoxicity measurement demonstrated a cell line-dependent toxicity profile at the concentrations tested in this study. It was shown that there was no significant difference in cell-induced toxicity between conjugated polymer and its parent form in A۳۷۵ cell line while the cytotoxicity of conjugated polymer was significantly lower than the parent PEI in HepG۲ cells.Conclusion: These results provide promising evidence for further evaluation of PEI conjugate for co-delivery of drug and gene via LAT-۱ transporters.

کلیدواژه ها:

Cytotoxicity ، Doxorubicin ، L-DOPA ، Polyethylenimine