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首页> 外文期刊>Journal of Microencapsulation: Microcapsules Liposomes Nanoparticles Microcells Microspheres >Metal ion-assisted drug-loading model for novel delivery system of cisplatin solid lipid nanoparticles with improving loading efficiency and sustained release
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Metal ion-assisted drug-loading model for novel delivery system of cisplatin solid lipid nanoparticles with improving loading efficiency and sustained release

机译:金属离子辅助载药模型用于提高载药效率和缓释的顺铂固体脂质纳米粒新型传递系统

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摘要

Metal ion-assisted drug loading model, in which metal ion was used to modify the microstructure of lipid layer, has been developed to improve drug loading efficiency of solid lipid nanoparticles (SLNs). The microstructure and properties of metal ion-assisted cisplatin-loading SLNs were investigated by infra-red spectroscopy, fluorescence spectroscopy and zetasizer. The reactions of hydrogenated soybean lecithin with Zn2+, Cu2+, Mn(2+)and Mg(2+)have been detected; the mechanism for higher drug encapsulation efficiency (EE) has been investigated. In metal ion introduction SLNs, the compact degree of the lipid molecules was increased due to the electrostatic interaction between metal ions and phospholipid acyl and choline polarity groups, which result in increasing of drug EE. Meanwhile, these electrostatic interactions slowed the releasing rate of encapsulated drug. The study of cytotoxic activity in vitro indicated that the cell cytotoxicity of metal ions introduction SLNs depended on both cell uptake of SLNs and drug releasing from SLNs.
机译:已经开发了金属离子辅助药物加载模型,其中使用金属离子修饰脂质层的微观结构,以提高固体脂质纳米颗粒(SLNs)的药物加载效率。通过红外光谱,荧光光谱和zetasizer技术研究了负载金属离子的顺铂SLNs的微观结构和性能。已检测到氢化大豆卵磷脂与Zn2 +,Cu2 +,Mn(2+)和Mg(2+)的反应;已经研究了提高药物封装效率(EE)的机制。在金属离子引入SLN中,由于金属离子与磷脂酰基和胆碱极性基团之间的静电相互作用,脂质分子的致密度增加,这导致药物EE增加。同时,这些静电相互作用减慢了包封药物的释放速率。体外细胞毒性活性的研究表明,引入金属离子的SLNs的细胞毒性取决于SLNs的细胞摄取和从SLNs释放的药物。

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