González-Larraza Pamela G, López-Goerne Tessy M, Padilla-Godínez Francisco J, González-López Marco A, Hamdan-Partida Aida, Gómez Esteban
Department of Health Care, Autonomous Metropolitan University Xochimilco, Coyoacan, Mexico City 04960, Mexico.
Department of Mathematics and Physics, Western Institute of Technology and Higher Education, San Pedro Tlaquepaque, Jalisco 45604, Mexico.
ACS Omega. 2020 Sep 23;5(39):25381-25389. doi: 10.1021/acsomega.0c03759. eCollection 2020 Oct 6.
Cancer is a major public health problem being one of the main causes of morbidity and mortality today. Recent advances in catalytic nanomedicine have offered new cancer therapies based on the administration of nanoparticles (NPs) of platinum (Pt) dispersed in catalytic mesoporous nanomaterials (titania, TiO) with highly selective cytotoxic properties and no adverse effects. A half maximal inhibitory concentration (IC) study was carried out in cancerous cell lines (HeLa, DU-145, and fibroblasts) to evaluate the cytotoxic effect of different nanomaterials [Pt/TiO, TiO, and Pt(acac)] synthesized by the sol-gel method at concentrations 0-1000 μg/mL. The assays showed that IC values for Pt in functionalized TiO (NPt) in HeLa (53.74 ± 2.95 μg/mL) and DU-145 (75.07 ± 5.48 μg/mL) were lower than those of pure TiO (74.29 ± 8.95 and 82.02 ± 6.03 μg/mL, respectively). Pt(acac) exhibited no cytotoxicity. Normal cells (fibroblasts) treated with NPt exhibited no significant growth inhibition, suggesting the high selectivity of the compound for cancerous cells only. TiO and NPt were identified as antineoplastic compounds . Pt(acac) is not recommendable because of the low cytotoxicity observed.
癌症是一个重大的公共卫生问题,是当今发病和死亡的主要原因之一。催化纳米医学的最新进展提供了基于分散在具有高选择性细胞毒性特性且无不良影响的催化介孔纳米材料(二氧化钛,TiO)中的铂(Pt)纳米颗粒(NP)给药的新型癌症疗法。在癌细胞系(HeLa、DU-145和成纤维细胞)中进行了半数最大抑制浓度(IC)研究,以评估通过溶胶-凝胶法在0-1000μg/mL浓度下合成的不同纳米材料[Pt/TiO、TiO和Pt(acac)]的细胞毒性作用。试验表明,HeLa(53.74±2.95μg/mL)和DU-145(75.07±5.48μg/mL)中功能化TiO(NPt)中Pt的IC值低于纯TiO(分别为74.29±8.95和82.02±6.03μg/mL)。Pt(acac)没有表现出细胞毒性。用NPt处理的正常细胞(成纤维细胞)没有表现出明显的生长抑制,表明该化合物仅对癌细胞具有高选择性。TiO和NPt被鉴定为抗肿瘤化合物。由于观察到的低细胞毒性,不推荐使用Pt(acac)。