Dipartimento di Scienza e Tecnologia del Farmaco, Università degli Studi di Torino, Torino, Italy.
Centro Ricerche di Neurobiooncologia, Policlinico di Monza Foundation, Vercelli, Italy.
Nanomedicine (Lond). 2017 Mar;12(6):639-656. doi: 10.2217/nnm-2016-0380. Epub 2017 Feb 10.
Methotrexate-loaded biocompatible nanoparticles were tested for preliminary efficacy in glioma treatment.
MATERIALS & METHODS: Behenic acid nanoparticles, prepared by the coacervation method, were loaded with the ester prodrug didodecylmethotrexate, which was previously tested in vitro against glioblastoma human primary cultures. Nanoparticle conjugation with an ApoE mimicking chimera peptide was performed to obtain active targeting to the brain.
RESULTS & CONCLUSION: Biodistribution studies in healthy rats assessed the superiority of ApoE-conjugated formulation, which was tested on an F98/Fischer glioma model. Differences were observed in tumor growth rate (measured by MRI) between control and treated rats. In vitro tests on F98 cultured cells assessed their susceptibility to treatment, with consequent apoptosis, and allowed us to explain the apoptosis observed in glioma models.
载甲氨蝶呤的生物相容性纳米颗粒在神经胶质瘤治疗中的初步疗效进行了测试。
采用凝聚法制备了硬脂酸纳米颗粒,并用前体药物双十二烷基甲氨蝶呤进行负载,该前体药物已在体外针对神经母细胞瘤原代培养物进行了测试。通过与载脂蛋白 E 模拟嵌合体肽偶联来实现对大脑的主动靶向。
在健康大鼠中的生物分布研究评估了载脂蛋白 E 偶联制剂的优势,该制剂在 F98/Fischer 神经胶质瘤模型中进行了测试。在 MRI 测量的肿瘤生长速率方面,对照组和治疗组之间存在差异。对体外培养的 F98 细胞进行的体外测试评估了它们对治疗的敏感性,包括随后的细胞凋亡,并解释了在神经胶质瘤模型中观察到的细胞凋亡。