共 46 条
Synthesis, characterisation and preliminary investigation of the haemocompatibility of polyethyleneimine-grafted carboxymethyl chitosan for gene delivery
被引:43
作者:
Liu, Xuan
[1
]
Mo, Yunfei
[1
,2
]
Liu, Xiaoyu
[1
,2
]
Guo, Rui
[1
,2
]
Zhang, Yi
[1
,2
]
Xue, Wei
[1
,2
]
Zhang, Yuanming
[3
]
Wang, Changyong
[4
,5
]
Ramakrishna, Seeram
[6
]
机构:
[1] Jinan Univ, Key Lab Biomat, Guangdong Higher Educ Inst, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Dept Biomed Engn, Guangzhou 510632, Guangdong, Peoples R China
[3] Jinan Univ, Dept Chem, Guangzhou 510632, Guangdong, Peoples R China
[4] Acad Mil Med Sci, Inst Basic Med Sci, Dept Adv Interdisciplinary Studies, Beijing 100850, Peoples R China
[5] Acad Mil Med Sci, Tissue Engn Res Ctr, Beijing 100850, Peoples R China
[6] Jinan Univ, GHMICR, Guangzhou 510632, Guangdong, Peoples R China
来源:
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
|
2016年
/
62卷
关键词:
Biocompatibility;
Chitosan;
Gene carrier;
Haemocompatibility;
Polyethyleneimine;
TRANSFECTION EFFICIENCY;
NONVIRAL VECTORS;
PROTEIN CORONA;
IN-VITRO;
NANOPARTICLES;
CELLS;
DNA;
CONJUGATION;
COMPLEXES;
COPOLYMER;
D O I:
10.1016/j.msec.2016.01.050
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
The development of safe and efficient gene carriers is the key to the clinical success of gene therapy. In the present study, carboxymethyl chitosan (CMCS) was prepared by chitosan (CS) alkalisation and carboxymethylation reactions. Then polyethyleneimine (PEI) was grafted to the backbone of CMCS by an amidation reaction. The CMCS-PEI copolymer showed strong complexation capability with DNA to form nanoparticles, and achieved lower cytotoxicity and higher transfection efficiency compared with PEI (25 kDa) towards 293T and 3T3 cells. Moreover, the haemocompatibility of the CMCS-PEI copolymer was investigated through the aggregation, morphology and lysis of human red blood cells (RBCs), along with the impact on the clotting function with activated partial thromboplastin time (APTT), prothrombin time (PT) and thromboelastographic (TEG) assays. The results demonstrated that the CMCS-PEI copolymer with a concentration lower than 0.05 mg/mL had little impact on the aggregation, morphology or lysis of RBCs, or on blood coagulation. Therefore, the copolymer may be a strong alternative candidate as an effective and safe non-viral vector. (C) 2016 Elsevier B.V. All rights reserved.
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页码:173 / 182
页数:10
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