Thermosensitive folic acid-targeted poly (ethylene-co-vinyl alcohol) hemisuccinate polymeric nanoparticles for delivery of epirubicin to breast cancer cells

被引:9
作者
Hassanzadeh, Farshid [1 ,2 ]
Maaleki, Sahar [2 ]
Varshosaz, Jaleh [1 ,3 ]
Khodarahmi, Ghadam Ali [2 ]
Farzan, Maryam [2 ]
Rostami, Mahboubeh [1 ,2 ]
机构
[1] Isfahan Univ Med Sci, Novel Drug Delivery Syst Res Ctr, Esfahan 8174673461, Iran
[2] Isfahan Univ Med Sci, Dept Med Chem, Sch Pharm, Esfahan 8174673461, Iran
[3] Isfahan Univ Med Sci, Dept Pharmaceut, Sch Pharm, Esfahan, Iran
关键词
Targeted polymeric nanoparticles; Thermosensitive; EVOH; Epirubicin (EPI); Breast cancer; DRUG-DELIVERY; IN-VITRO; SYSTEMS; RELEASE; DOXORUBICIN; THERAPY; VIVO; COMBINATION; RESISTANCE; LIPOSOMES;
D O I
10.1007/s13726-016-0483-z
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A novel thermosensitive folic acid (FA)-targeted succinylated poly (ethylene-co-vinyl alcohol) (EVOH) (EVOHS-FA) nanocarrier was synthesized for the specific delivery of epirubicin (EPI) to MCF-7 breast cancer cell line. Three different ratios of synthesized EVOH-Suc were reacted with FA. The structure of the desired products (EVOHS40-FA, EVOHS60-FA and EVOHS80-FA) was confirmed by H-1 NMR and FTIR techniques. Nanoparticles were obtained by nano-precipitation procedure using DMSO/H2O as solvent/anti-solvent. The particle size, zeta potential, entrapment efficacy and in vitro release profile of the final formulations in different temperatures were measured. The optimized nanoparticles had the particle size of 214 +/- 8.5 nm, zeta potential of -29.6 mV, PDI of 0.198 +/- 0.04, and a high encapsulation efficiency that released the drug efficiently within 450 h at the temperature of 40 degrees C compared to 37 degrees C. The morphology of nanoparticles was studied by scanning electron microscopy. The in vitro cytotoxicity was evaluated using the MTT assay on MCF-7 cell lines in response to temperatures of 37 and 40 degrees C. The MTT assay indicated that the targeted nanoparticles carrying EPI were significantly more cytotoxic than the non-targeted nanoparticles and the free drug at 40 degrees C.
引用
收藏
页码:967 / 976
页数:10
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