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Size characterization of drug-loaded polymeric core/shell nanoparticles using asymmetrical flow field-flow fractionation

机译:使用不对称流场-流分馏法表征载药聚合物核/壳纳米粒子的尺寸

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Asymmetrical flow field-flow fractionation (AsFlFFF) was used to determine the size distribution of drug-loaded core/shell nanoparticles which have a lipid core of lecithin and a polymeric shell of a Pluronic. AsFlFFF provided separation of the drug-loaded core/shell nanoparticles from smaller coreless polymeric micelles, thus allowing accurate size analysis of the drug-loaded nanoparticles without interference by the coreless micelles. It was found from AsFlFFF that the drug-loaded nanoparticles have broad size distributions ranging from 100 to 600 nm in diameter. It was also found that, after the nanoparticles had been stored for 70 days, they disappeared as a result of self-degradation. Being a separation technique, AsFlFFF seems to be more useful than transmission electron microscopy or dynamic light scattering for size analysis of core/shell nanoparticles, which have broad and bimodal size distributions.
机译:使用不对称流场流分馏法(AsFlFFF)确定载有卵磷脂脂质核和Pluronic聚合物壳的载药核/壳纳米颗粒的尺寸分布。 AsFlFFF提供了从较小的无核聚合物胶束中分离出载药的核/壳纳米颗粒的方法,从而可以对载药的纳米颗粒进行准确的尺寸分析,而不受无核胶束的干扰。从AsFlFFF发现,载有药物的纳米颗粒具有直径范围为100至600nm的宽尺寸分布。还发现,将纳米颗粒储存70天后,它们由于自降解而消失。作为一种分离技术,AsFlFFF似乎比透射电子显微镜或动态光散射对核/壳纳米粒子的尺寸分析更有用,这些粒子具有宽的和双峰的尺寸分布。

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