Wang Zhou, Jiang Yibei, Tian Guangjian, Zhu Chuyu, Zhang Yi
Department of Inorganic Materials, School of Minerals Processing and Bioengineering, Central South University, Changsha 410083, China.
J Funct Biomater. 2024 Mar 20;15(3):75. doi: 10.3390/jfb15030075.
Montmorillonite has been refined to overcome uncertainties originating from different sources, which offers opportunities for addressing various health issues, e.g., cosmetics, wound dressings, and antidiarrheal medicines. Herein, three commercial montmorillonite samples were obtained from different sources and labeled M1, M2, and M3 for Ca-montmorillonite, magnesium-enriched Ca-montmorillonite, and silicon-enriched Na-montmorillonite, respectively. Commercial montmorillonite was refined via ultrasonic scission-differential centrifugation and labeled S, M, or L according to the particle sizes (small, medium, or large, respectively). The size distribution decreased from 2000 nm to 250 nm with increasing centrifugation rates from 3000 rpm to 12,000 rpm. Toxicological evaluations with human colon-associated cells and human skin-associated cells indicated that side effects were correlated with excess dosages and silica sand. These side effects were more obvious with human colon-associated cells. The microscopic interactions between micro/nanosized montmorillonite and human colon-associated cells or human skin-associated cells indicated that those interactions were correlated with the size distributions. The interactions of the M1 series with the human cells were attributed to size effects because montmorillonite with a broad size distribution was stored in the M1 series. The M2 series interactions with human cells did not seem to be correlated with size effects because large montmorillonite particles were retained after refining. The M3 series interactions with human cells were attributed to size effects because small montmorillonite particles were retained after refining. This illustrates that toxicological evaluations with refined montmorillonite must be performed in accordance with clinical medical practices.
蒙脱石已被提纯以克服源自不同来源的不确定性,这为解决各种健康问题提供了机会,例如化妆品、伤口敷料和止泻药。在此,从不同来源获得了三种商业蒙脱石样品,并分别标记为M1、M2和M3,分别代表钙蒙脱石、富镁钙蒙脱石和富硅钠蒙脱石。商业蒙脱石通过超声裂解-差速离心法进行提纯,并根据粒径(分别为小、中或大)标记为S、M或L。随着离心速率从3000转/分钟增加到12000转/分钟,粒径分布从2000纳米降至250纳米。对人结肠相关细胞和人皮肤相关细胞的毒理学评估表明,副作用与过量剂量和硅砂有关。这些副作用在人结肠相关细胞中更为明显。微米/纳米级蒙脱石与人结肠相关细胞或人皮肤相关细胞之间的微观相互作用表明,这些相互作用与粒径分布有关。M1系列与人细胞的相互作用归因于尺寸效应,因为M1系列中储存了粒径分布较宽的蒙脱石。M2系列与人细胞的相互作用似乎与尺寸效应无关,因为提纯后保留了大的蒙脱石颗粒。M3系列与人细胞的相互作用归因于尺寸效应,因为提纯后保留了小的蒙脱石颗粒。这表明,对提纯蒙脱石的毒理学评估必须按照临床医学实践进行。