1Atatürk University Faculty of Science, Department of Molecular Biology and Genetics, Erzurum, Turkey.
2Ege University Faculty of Science, Department of Biology, Izmir, Turkey.
Arh Hig Rada Toksikol. 2023 Sep 30;74(3):207-217. doi: 10.2478/aiht-2023-74-3768. eCollection 2023 Sep 1.
The aim of this safety study in mice was to determine toxicity and biodistribution potential of a single and multiple doses of L-glutamic acid-g-p(HEMA) polymeric nanoparticles as a drug delivery system. The single dose did not cause any lethal effect, and its acute oral LD was >2.000 mg/kg body weight (bw). Multiple doses (25, 50, or 100 mg/kg bw) given over 28 days resulted in no significant differences in body and relative organ weights compared to control. These results are supported by biochemical and histological findings. Moreover, nanoparticle exposure did not result in statistically significant differences in micronucleus counts in bone marrow cells compared to control. Nanoparticle distribution was time-dependent, and they reached the organs and even bone marrow by hour 6, as established by imaging with the IVIS spectrum imaging system. In conclusion, L-glutamic acid-g-p(HEMA) polymeric nanoparticles appear biocompatible and have a potential use as a drug delivery system.
这项在小鼠体内进行的安全性研究旨在确定 L-谷氨酸-g-p(HEMA) 聚合物纳米粒作为药物递送系统的单次和多次剂量的毒性和生物分布潜力。单次剂量未引起任何致死作用,其急性口服 LD 大于 2000mg/kg 体重(bw)。在 28 天内给予多次剂量(25、50 或 100mg/kg bw)与对照组相比,体重和相对器官重量无显著差异。这些结果得到了生化和组织学发现的支持。此外,与对照组相比,骨髓细胞中的微核计数没有因纳米颗粒暴露而出现统计学上的显著差异。纳米颗粒的分布具有时间依赖性,通过 IVIS 光谱成像系统进行的成像显示,它们在 6 小时内即可到达器官,甚至骨髓。总之,L-谷氨酸-g-p(HEMA)聚合物纳米粒具有生物相容性,有望作为药物递送系统使用。