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Toxicity, pharmacokinetics, and in vivo efficacy of biotinylated chitosan surface-modified PLGA nanoparticles for tumor therapy

机译:生物素化壳聚糖表面修饰的PLGA纳米粒子在肿瘤治疗中的毒性,药代动力学和体内功效

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Abstract Based on our previous work on the PLGA nanoparticles modified with biotinylated chitosan (Bio-CS-PLGA NPs), we further studied the stability, toxicity, pharmacokinetics, and in vivo efficacy. The safety of NPs was studied through single-dose toxicity test in mice, and the result showed that NPs were well tolerated at the dose of 300?mg/kg. Compared with the free EPB group, the NPs group exhibited higher plasma drug concentration, longer half-life time. EPB-loaded NPs significantly inhibited the tumor growth compared to free EPB. All results suggested that Bio-CS-PLGA NPs were stable, safe, and showed a promising potential on targeted drug delivery.
机译:摘要基于我们先前对生物素化壳聚糖修饰的PLGA纳米颗粒(Bio-CS-PLGA NPs)的研究,我们进一步研究了其稳定性,毒性,药代动力学和体内功效。通过小鼠单剂量毒性试验研究了NP的安全性,结果表明,在300?mg / kg的剂量下,NP的耐受性良好。与游离EPB组相比,NPs组血浆药物浓度更高,半衰期更长。与游离EPB相比,加载EPB的NPs显着抑制了肿瘤的生长。所有结果表明,Bio-CS-PLGA NP稳定,安全,并且在靶向药物递送方面显示出广阔的前景。

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