Blood compatible N-maleyl chitosan-graft-PAMAM copolymer for enhanced gene transfection

被引:23
作者
Sarkar, Kishor [1 ]
Chatterjee, Abhisek [2 ,3 ]
Chakraborti, Gopal [2 ,3 ]
Kundu, Patit P. [1 ]
机构
[1] Univ Calcutta, Dept Polymer Sci & Technol, Kolkata 700009, W Bengal, India
[2] Univ Calcutta, Dept Biotechnol, Kolkata 700019, W Bengal, India
[3] Univ Calcutta, Dr BC Guha Ctr Genet Engn, Kolkata 700019, W Bengal, India
关键词
Chitosan; PAMAM dendrimer; Self-assembled; Nanoparticle; Hemolysis; In vitro transfection; IN-VIVO; MOLECULAR-WEIGHT; DELIVERY; DNA; DENDRIMERS; POLYETHYLENIMINE; VECTORS; NANOPARTICLES; CYTOTOXICITY; CARRIER;
D O I
10.1016/j.carbpol.2013.06.035
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
To improve transfection efficiency, we prepared N-maleyl chitosan-graft-polyamidoamine (NMCTS-graft-PAMAM) copolymer. Self-assembled NMCTS-graft-PAMAM/pDNA complexes were prepared by complex coacervation method at different N/P (nitrogen to phosphate ratio) ratios. The copolymer effectively formed complexes with pDNA at lower N/P ratio (N/P ratio 1.0) than that of unmodified chitosan (N/P ratio 2.0) and the complexes were spherical with particle size of 100-150 nm. The copolymer showed significant protection of DNA from nuclease attack with lower toxicity against HeLa cell. The copolymer also showed no noticeable hemolytic effects up to 10 mg/mL indicating no detectable disturbance of the red blood cell membranes. The transfection efficiency of the copolymer was increased significantly compared to that of chitosan and reached up to 36 +/- 2% at N/P ratio 7.0 which was higher than that of PEI (30 +/- 3% at N/P ratio 10). Therefore, the copolymer may be a strong alternative candidate as effective nonviral vector. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:596 / 606
页数:11
相关论文
共 57 条
[1]   Nonviral approaches for neuronal delivery of nucleic acids [J].
Bergen, Jamie M. ;
Park, In-Kyu ;
Horner, Philip J. ;
Pun, Suzie H. .
PHARMACEUTICAL RESEARCH, 2008, 25 (05) :983-998
[2]   Dendrimers in drug research [J].
Boas, U ;
Heegaard, PMH .
CHEMICAL SOCIETY REVIEWS, 2004, 33 (01) :43-63
[3]   Poly-L-glutamic acid derivatives as vectors for gene therapy [J].
Dekie, L ;
Toncheva, V ;
Dubruel, P ;
Schacht, EH ;
Barrett, L ;
Seymour, LW .
JOURNAL OF CONTROLLED RELEASE, 2000, 65 (1-2) :187-202
[4]   Dendrimers in gene delivery [J].
Dufès, C ;
Uchegbu, IF ;
Schätzlein, AG .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (15) :2177-2202
[5]   CARBAMYLATION DECREASES THE CYTOTOXICITY BUT NOT THE DRUG-CARRIER PROPERTIES OF POLYLYSINES [J].
EKRAMI, HM ;
SHEN, WC .
JOURNAL OF DRUG TARGETING, 1995, 2 (06) :469-475
[6]   Synthesis of 6-N,N,N-Trimethyltriazole Chitosan via "Click Chemistry" and Evaluation for Gene Delivery [J].
Gao, Yu ;
Zhang, Zhiwen ;
Chen, Lingli ;
Gu, Wangwen ;
Li, Yaping .
BIOMACROMOLECULES, 2009, 10 (08) :2175-2182
[7]   Dendritic vectors for gene transfection [J].
Guillot-Nieckowski, Marine ;
Eisler, Sara ;
Diederich, Francois .
NEW JOURNAL OF CHEMISTRY, 2007, 31 (07) :1111-1127
[8]   Synthesis and properties of a novel biodegradable poly(ester amine) copolymer based on poly(L-lactide) and low molecular weight polyethylenimine for gene delivery [J].
Guo, Qing Fa ;
Liu, Ting Ting ;
Yan, Xi ;
Wang, Xiu Hong ;
Shi, Shuai ;
Luo, Feng ;
Qian, Zhi Yong .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2011, 6 :1641-1649
[9]   DELIVERY OF DNA INTO MAMMALIAN-CELLS BY RECEPTOR-MEDIATED ENDOCYTOSIS AND GENE-THERAPY [J].
GUY, J ;
DRABEK, D ;
ANTONIOU, M .
MOLECULAR BIOTECHNOLOGY, 1995, 3 (03) :237-248
[10]   Developmental toxicity of low generation PAMAM dendrimers in zebrafish [J].
Heiden, Tisha C. King ;
Dengler, Emelyne ;
Kao, Weiyuan John ;
Heideman, Warren ;
Peterson, Richard E. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 225 (01) :70-79