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首页> 外文期刊>Journal of nanotechnology >Drug-Carrying Magnetic Nanocomposite Particles for Potential Drug Delivery Systems
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Drug-Carrying Magnetic Nanocomposite Particles for Potential Drug Delivery Systems

机译:用于潜在药物输送系统的载药磁性纳米复合颗粒

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Drug-carrying magnetic nanocomposite spheres were synthesized using magnetitenanoparticles and poly (D,L-lactide-co-glycolide) (PLGA) for the purpose of magnetic targeted drug delivery. Magnetic nanoparticles (∼13 nm on average) of magnetite were prepared by a chemical coprecipitation of ferric and ferrous chloride salts in the presence of a strong basic solution (ammonium hydroxide). An oil-in-oil emulsion/solvent evaporation technique was conducted at 7000 rpm and 1.5–2 hours agitation for the synthesis of nanocomposite spheres. Specifically, PLGA and drug were first dissolved in acetonitrile (oily phase I) and combined with magnetic nanoparticles, then added dropwise into viscous paraffin oil combined with Span 80 (oily phase II). With different contents (0%, 10%, 20%, and 25%) of magnetite, the nanocomposite spheres were evaluated in terms of particle size, morphology, and magnetic properties by using dynamic laser light scattering (DLLS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and a superconducting quantum interference device (SQUID). The results indicate that nanocomposite spheres (200 nm to 1.1 μm in diameter) are superparamagnetic above the blocking temperature near 40 K and their magnetization saturates above 5 000 Oe at room temperature.
机译:为了磁性靶向药物递送的目的,使用磁性纳米颗粒和聚(D,L-丙交酯-乙交酯-乙交酯)(PLGA)合成了载药磁性纳米复合球。在强碱性溶液(氢氧化铵)存在下,通过铁和氯化亚铁盐的化学共沉淀制备磁铁矿的磁性纳米粒子(平均约13 nm)。在7000 rpm和1.5–2小时的搅拌下进行了油包油乳液/溶剂蒸发技术,以合成纳米复合球。具体而言,首先将PLGA和药物溶解在乙腈中(油相I),并与磁性纳米颗粒混合,然后滴加到与Span 80混合的粘性石蜡油中(油相II)。通过使用不同含量(0%,10%,20%和25%)的磁铁矿,通过使用动态激光散射(DLLS),扫描电子显微镜对纳米复合球的粒径,形态和磁性进行了评估( SEM),透射电子显微镜(TEM)和超导量子干涉仪(SQUID)。结果表明,纳米复合球(直径200 nm至1.1μm)在40 blockingK附近的阻断温度以上具有超顺磁性,并且在室温下其磁化强度在5 000 Oe以上达到饱和。

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