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Manganese Oxide Nanoparticles Inhibit the Growth of Subcutaneous U-87MG Glioblastoma Xenografts in Immunodeficient Mouse

机译:氧化锰纳米颗粒抑制免疫缺陷小鼠皮下U-87MG胶质母细胞瘤异种移植物的生长

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摘要

Our previous study demonstrated that manganese oxide nanoparticles (MnO NP) selectively destroyed U-87MG and U251 human glioblastoma cells in vitro. MnO NP were synthesized and studied by electron microscopy. Their antitumor properties were studied in vivo on the model of immunodeficient SCID mice with subcutaneous xenografts of U-87MG human glioblastoma. The mice were injected subcutaneously with MnO NP in doses of 0.96 and 1.92 mg/kg (calculated for Mn) 3 days a week over 3 weeks. In was shown that MnO NP in these doses significantly suppressed the growth of U-87MG glioblastoma xenografts: on day 21 from the start of the treatment, the tumor growth inhibition index was 61.1 and 99.22, respectively. These results indicate the necessity of the further studies of MnO NP as a potential oncolytic agent for the therapy of human glioblastomas.
机译:我们之前的研究表明,氧化锰纳米颗粒(MnO NP)在体外选择性地破坏了U-87MG和U251人胶质母细胞瘤细胞。合成了MnO NP,并通过电子显微镜进行了研究。在免疫缺陷SCID小鼠的体内模型上研究了它们的抗肿瘤特性,该模型具有U-87MG人胶质母细胞瘤的皮下异种移植物。小鼠皮下注射MnO NP,剂量为0.96和1.92mg / kg(以Mn计算),每周3天,持续3周。结果表明,这些剂量的MnO NP显著抑制了U-87MG胶质母细胞瘤异种移植物的生长:在治疗开始后的第21天,肿瘤生长抑制指数分别为61.1%和99.22%。这些结果表明有必要进一步研究MnO NP作为治疗人胶质母细胞瘤的潜在溶瘤剂。

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