Superparamagnetic anisotropic nano-assemblies with longer blood circulation in vivo: a highly efficient drug delivery carrier for leukemia therapy

体内 各向同性 白血病 药物输送 药代动力学 材料科学 纳米- 药品 分布(数学) 长春新碱 药理学 生物医学工程 医学 纳米技术 免疫学 外科 化疗 环磷酰胺 生物 复合材料 数学 生物技术 数学分析 物理 量子力学
作者
Fei Xiong,Jilai Tian,Ke Hu,Xiawen Zheng,Jianfei Sun,Caiyun Yan,Yao Juan,Lina Song,Yu Zhang,Ning Gu
出处
期刊:Nanoscale [The Royal Society of Chemistry]
卷期号:8 (39): 17085-17089 被引量:26
标识
DOI:10.1039/c6nr05781k
摘要

Leukemia, unlike solid tumors, has no definite shape and spreads throughout the whole circulatory system, therefore the therapy of leukemia requires medication to stay longer in the circulatory system. Anisotropic nanoparticles, showing longer blood circulating life than that of isotropic nanoparticles reported in previous research, meet the demands of leukemia therapy. Based on this strategy, superparamagnetic anisotropic nano-assemblies (SANs) were fabricated and loaded with vincristine (VCR) to form VCR-SANs. When compared to the same dose of VCR-loaded isotropic nano-assemblies (SINs), the decrease in the leukocytes count and the positive expression ratio of CD13 in the VCR-SANs group were 19.38% and 16.4%, respectively, which indicated the improved anti-leukemia activity of the VCR-SANs. From the results of the pharmacokinetics study, the VCR-SANs remarkably held the amount of drug removed from the whole body per unit time half of the isotropic group and the concentration of drug in blood plasma against time was 2.1 times the isotropic group, demonstrating the rapid and sustained release behavior and longer blood circulation when combined with the results of in vivo tissue distribution studies. In summary, anisotropic nano-assemblies were found to be more promising than isotropic nano-assemblies via our in vivo and in vitro examinations.
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