Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan.
Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan; Frontier Research Center on Fundamental and Applied Sciences of Matters, National Tsing Hua University, Hsinchu 30013, Taiwan.
J Colloid Interface Sci. 2020 Jan 15;558:137-144. doi: 10.1016/j.jcis.2019.09.114. Epub 2019 Sep 30.
Platinum oxide (PtO) nanoparticles (NPs) have been shown to possess anticancer activity by releasing ionic Pt species under biological conditions. However, the dissolution kinetics and the changes in the chemical state of Pt during PtO dissolution have not yet been studied. To fill this gap, we prepared a composite (designated as PtO@MMT-2) containing PtO NPs on hollow mesoporous silica nanospheres and studied the dissolution of the material in different biorelevant media. We found that the release of Pt was retarded due to the adsorption of biomolecules on PtO NPs during the degradation of host silica. The biomolecules adsorption also lowered the accessibility of PtO NPs, resulting in the reduced catalase-like activity of the NPs. In line with the results, the cytotoxicity of PtO@MMT-2, which was positively correlated to the amount of Pt uptake, was reduced by biomolecules adsorption. Our findings should be applicable to other metal (oxide) NPs under biological conditions and may provide implications for the design of nanomaterials for practical therapeutic applications.
氧化铂(PtO)纳米颗粒(NPs)已被证明在生物条件下通过释放离子 Pt 物种具有抗癌活性。然而,PtO 溶解过程中的溶解动力学和 Pt 的化学状态变化尚未得到研究。为了填补这一空白,我们制备了一种包含 PtO NPs 的复合材料(命名为 PtO@MMT-2),负载在中空介孔硅纳米球上,并研究了该材料在不同生物相关介质中的溶解情况。我们发现,由于宿主硅的降解过程中生物分子吸附在 PtO NPs 上,Pt 的释放受到了阻碍。生物分子的吸附也降低了 PtO NPs 的可及性,导致 NPs 的类过氧化氢酶活性降低。结果表明,PtO@MMT-2 的细胞毒性与 Pt 的摄取量呈正相关,而生物分子的吸附降低了其毒性。我们的发现应该适用于生物条件下的其他金属(氧化物)NPs,并可能为实际治疗应用的纳米材料设计提供启示。