首页> 外文期刊>Drug development and industrial pharmacy >Design of high payload PLGA nanoparticles containing melittin/sodium dodecyl sulfate complex by the hydrophobic ion-pairing technique.
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Design of high payload PLGA nanoparticles containing melittin/sodium dodecyl sulfate complex by the hydrophobic ion-pairing technique.

机译:通过疏水离子对技术设计包含蜂毒蛋白/十二烷基硫酸钠复合物的高负载PLGA纳米颗粒。

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摘要

The water-soluble peptide, melittin, was modified with an anionic agent, sodium dodecyl sulfate by hydrophobic ion-pairing. Investigations showed that the formed complex was very soluble in organic solvent, especially, in dimethylsulfoxide and dehydrated alcohol. Furthermore, the physiochemical properties of the complex in the solid state or in an aqueous medium were characterized using octanol/water partition measurement, Fourier transform infrared spectroscopy, and differential scanning calorimetry. The complex was formulated into poly(D,L-lactide-co-glycolide acid) nanoparticles by an emulsion solvent diffusion method. It was found that the nanoparticles of about 130 nm in size can be produced with a high encapsulation efficiency, and the entrapment of nanoparticles prepared with the formed complex increased from about 50% to nearly 100% compared with that for pure melittin. Moreover, the growth inhibitory effects of modified melittin and melittin-loaded nanoparticles in breast cancer MCF-7 cells were not changed comparing with free melittin as determined by (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay.
机译:水溶性肽蜂毒素通过疏水性离子对被阴离子剂十二烷基硫酸钠修饰。研究表明,形成的配合物非常易溶于有机溶剂,特别是二甲基亚砜和脱水醇。此外,使用辛醇/水分配测量,傅里叶变换红外光谱和差示扫描量热法表征了固态或水性介质中复合物的物理化学性质。通过乳液溶剂扩散法将该配合物配制成聚(D,L-丙交酯-乙交酯酸)共聚物纳米粒子。已经发现可以以高的包封效率来生产尺寸为约130nm的纳米颗粒,并且与纯蜂毒肽相比,用形成的复合物制备的纳米颗粒的包封率从约50%增加到近100%。此外,与通过(3-(4,5-二甲基噻唑-2-基)-2,5-确定的游离蜂毒素相比,修饰的蜂毒素和载有蜂毒素的纳米粒子在乳腺癌MCF-7细胞中的生长抑制作用没有改变。二苯基溴化四唑)测定法。

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