Polyionic complex of single-walled carbon nanotubes and PEG-grafted-hyperbranched polyethyleneimine (PEG-PEI-SWNT) for an improved doxorubicin loading and delivery: development and in vitro characterization

被引:24
作者
Farvadi, Fakhrossadat [1 ]
Tamaddon, AliMohammad [2 ,3 ]
Sobhani, Zahra [4 ]
Abolmaali, Samira Sadat [1 ]
机构
[1] Shiraz Univ Med Sci, Dept Pharmaceut Nanotechnol, Shiraz, Iran
[2] Shiraz Univ Med Sci, Ctr Nanotechnol Drug Delivery, Shiraz, Iran
[3] Shiraz Univ Med Sci, Sch Pharm, Dept Pharmaceut Nanotechnol, Shiraz, Iran
[4] Shiraz Univ Med Sci, Sch Pharm, Dept Pharmaceut, Shiraz, Iran
关键词
Cancer therapy; carbon nanotube; doxorubicin; PEG-grafted polyethyleneimine; polyionic complexation; DRUG-DELIVERY; TARGETED DELIVERY; GENE DELIVERY; CANCER-CELLS; DNA; TRANSFECTION; RESISTANT; COPOLYMER; GLYCOL);
D O I
10.1080/21691401.2016.1181642
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To take advantages of single-walled carbon nanotubes (SWNTs) for cellular delivery of chemotherapeutic agents (e.g. doxorubicin) in order to decrease general toxicities of doxorubicin (DOX) and to promote the efficacy, we aimed to develop a novel approach to stabilize SWNTs through consequent steps of oxidation and PEG-g-PEI polyionic complexation (PEG-PEI-SWNT). The DOX loading capacity of modified SWNTs was about 900%. Moreover, it showed an enhanced dispersibility in physiologic-stimulated medium. DOX release was prolonged, independent of dilution, and exhibited an acidic pH-stimulated release. Therefore, PEG-PEI-SWNT could be used for cancer chemotherapy in vivo.
引用
收藏
页码:855 / 863
页数:9
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