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首页> 外文期刊>Carbohydrate Polymers: Scientific and Technological Aspects of Industrially Important Polysaccharides >Homogeneous synthesis of quaternized chitin in NaOH/urea aqueous solution as a potential gene vector
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Homogeneous synthesis of quaternized chitin in NaOH/urea aqueous solution as a potential gene vector

机译:NaOH /尿素水溶液中季铵化几丁质的均相合成作为潜在的基因载体

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Water-soluble quaternized chitins (QCs) were homogeneously synthesized by reacting chitin with (3-chloro-2-hydroxypropyl) trimethylammonium chloride (CHPTAC) in 8 wt% NaOH/4 wt% urea aqueous solutions. The chemical structure and solution properties of the quaternized chitins were characterized by H-1 NMR, FT-IR, elemental analysis, dynamic light scattering (DLS) and zeta potential measurements. The results demonstrated that the water-soluble QCs, with a degree of substitution (DS) values of 0.27-0.54, could be obtained by varying the concentration of chitin, the molar ratio of CHPTAC to chitin unit, and the reaction time at room temperature (25 degrees C). Two QCs (DS= 0.36 and 0.54) were selected and studied as gene carriers. Agarose gel retardation assay revealed that both QCs could condense DNA efficiently when N/P ratio >3. The results of particle size and zeta potential indicated that both QCs had a good ability of condensing plasmid DNA into compact nanoparticles with the size of 100-200 nm and zeta potential of +18 to +36 mV. Compared to polyethylenimine (PEI, 25 kDa), the QCs exhibited outstanding low cytotoxicity. Transfection efficiencies of the QCs/DNA complexes were measured using pGL-3 encoding luciferase as the foreign DNA, and the QCs/DNA complexes showed effective transfection efficiencies in 293T cells. These results revealed that the QCs prepared in NaOH/urea aqueous solutions could be used as promising non-viral gene carriers owing to their excellent characteristics. (C) 2016 Published by Elsevier Ltd.
机译:通过使几丁质与(3-氯-2-羟丙基)三甲基氯化铵(CHPTAC)在8 wt%NaOH / 4 wt%尿素水溶液中反应均质合成水溶性季铵化几丁质(QC)。通过H-1 NMR,FT-IR,元素分析,动态光散射(DLS)和Zeta电位测量来表征季铵化几丁质的化学结构和溶液性质。结果表明,通过改变几丁质的浓度,CHPTAC与几丁质单位的摩尔比以及室温下的反应时间,可以获得取代度(DS)值为0.27-0.54的水溶性QCs。 (25摄氏度)。选择两个QC(DS = 0.36和0.54)作为基因载体进行研究。琼脂糖凝胶阻滞试验表明,当N / P比> 3时,两个QC都可以有效地凝结DNA。粒度和ζ电势的结果表明,两个QC均具有良好的能力,可将质粒DNA凝聚成大小为100-200 nm,ζ电势为+18至+36 mV的致密纳米颗粒。与聚乙烯亚胺(PEI,25 kDa)相比,这些QC表现出出色的低细胞毒性。使用编码荧光素酶的pGL-3作为外源DNA来测量QCs / DNA复合物的转染效率,并且QCs / DNA复合物在293T细胞中显示出有效的转染效率。这些结果表明,由于其优异的特性,在NaOH /尿素水溶液中制备的QC可用作有前景的非病毒基因载体。 (C)2016由Elsevier Ltd.出版

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