Among different non-viral gene delivery methods, the technique of co-precipitation of Ca(2+) with DNA in the presence of inorganic anions is an attractive option because of the biocompatibility and biodegradability. In this study, nano-sized CaCO(3)/DNA co-precipitates for gene delivery were prepared. The effect of Ca(2+)/CO(3)(2-) molar ratio on the gene delivery was investigated. The mechanism of the transfection mediated by CaCO(3)/DNA co-precipitates was studied by treatment of the cells with chloroquine, wortmannin and cytochalasin D, respectively. The in vitro gene transfections in different cells were carried out for both solution- based transfection and solid- phase transfection. The gene expression of the calcium carbonate based approach is strongly affected by the Ca(2+)/CO(3)(2-) ratio because the size of CaCO(3)/DNA co-precipitates is mainly determined by the Ca(2+)/CO(3)(2-) ratio. In addition, the encapsulation efficiency of DNA increases with decreasing Ca(2+)/CO(3)(2-) ratio. With a suitable Ca(2+)/CO(3)(2-) ratio, CaCO(3)/DNA co- precipitates could effectively mediate gene transfection with the expression levels higher than that of Lipofectamine 2000 in the presence of serum. The mechanism study shows that CaCO(3)/DNA co-precipitates are internalized via endocytosis of the cells and macropinocytosis is the main route of internalization. Compared with the solution- based transfection, CaCO(3)/DNA co-precipitates in the solid-phase transfection exhibit a lower gene expression level. The calcium carbonate based approach has great potential in gene delivery.
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Univ Coll Dublin, Charles Inst Dermatol, Dublin 4, IrelandUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
Cutlar, Lara
Gao, Yongsheng
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Univ Coll Dublin, Charles Inst Dermatol, Dublin 4, IrelandUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
Gao, Yongsheng
Aied, Ahmed
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Univ Coll Dublin, Charles Inst Dermatol, Dublin 4, IrelandUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
Aied, Ahmed
Greiser, Udo
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Univ Coll Dublin, Charles Inst Dermatol, Dublin 4, IrelandUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
Greiser, Udo
Murauer, Eva Maria
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Paracelsus Med Univ, Div Mol Dermatol, Salzburg, Austria
Paracelsus Med Univ, EB House Austria, Dept Dermatol, Salzburg, AustriaUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
Murauer, Eva Maria
Zhou, Dezhong
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Univ Coll Dublin, Charles Inst Dermatol, Dublin 4, IrelandUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
Zhou, Dezhong
Wang, Wenxin
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Univ Coll Dublin, Charles Inst Dermatol, Dublin 4, IrelandUniv Coll Dublin, Charles Inst Dermatol, Dublin 4, Ireland
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Mashhad Univ Med Sci, Targeted Drug Delivery Res Ctr, Mashhad, Iran
Mashhad Univ Med Sci, Sch Med, Dept Med Biotechnol, Mashhad, IranMashhad Univ Med Sci, Targeted Drug Delivery Res Ctr, Mashhad, Iran
Oskuee, Reza Kazemi
Ramezanpour, Mahdieh
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Mashhad Univ Med Sci, Sch Pharm, POB 91775-1365, Mashhad, IranMashhad Univ Med Sci, Targeted Drug Delivery Res Ctr, Mashhad, Iran
Ramezanpour, Mahdieh
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Gholami, Leila
Malaekeh-Nikouei, Bizhan
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Mashhad Univ Med Sci, Sch Pharm, Nanotechnol Res Ctr, Mashhad, IranMashhad Univ Med Sci, Targeted Drug Delivery Res Ctr, Mashhad, Iran
机构:
Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
Japan Sci & Technol Agcy, CREST, Tokyo, JapanHokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
Moriguchi, Rumiko
Kogure, Kentaro
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Japan Sci & Technol Agcy, CREST, Tokyo, Japan
Kyoto Pharmaceut Univ, Yamashina Ku, Kyoto 6078414, JapanHokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
Kogure, Kentaro
Harashima, Hideyoshi
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Hokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
Japan Sci & Technol Agcy, CREST, Tokyo, JapanHokkaido Univ, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan