Riedle Sebastian, Wills John W, Miniter Michelle, Otter Don E, Singh Harjinder, Brown Andy P, Micklethwaite Stuart, Rees Paul, Jugdaohsingh Ravin, Roy Nicole C, Hewitt Rachel E, Powell Jonathan J
Food Nutrition & Health Team, Food & Bio-based Products Group, AgResearch, Grasslands Research Centre, Tennent Drive, Private Bag 11008, Palmerston North, 4442, New Zealand.
Riddet Institute, Massey University, Private Bag 11222, Palmerston North, 4442, New Zealand.
Small. 2020 May;16(21):e2000486. doi: 10.1002/smll.202000486. Epub 2020 May 4.
Human exposure to persistent, nonbiological nanoparticles and microparticles via the oral route is continuous and large scale (10 -10 particles per day per adult in Europe). Whether this matters or not is unknown but confirmed health risks with airborne particle exposure warns against complacency. Murine models of oral exposure will help to identify risk but, to date, lack validation or relevance to humans. This work addresses that gap. It reports i) on a murine diet, modified with differing concentrations of the common dietary particle, food grade titanium dioxide (fgTiO ), an additive of polydisperse form that contains micro- and nano-particles, ii) that these diets deliver particles to basal cells of intestinal lymphoid follicles, exactly as is reported as a "normal occurrence" in humans, iii) that confocal reflectance microscopy is the method of analytical choice to determine this, and iv) that food intake, weight gain, and Peyer's patch immune cell profiles, up to 18 weeks of feeding, do not differ between fgTiO -fed groups or controls. These findings afford a human-relevant and validated oral dosing protocol for fgTiO risk assessment as well as provide a generalized platform for application to oral exposure studies with nano- and micro-particles.
人类通过口服途径接触持久性非生物纳米颗粒和微米颗粒是持续且大规模的(在欧洲,成年人每天接触10-10个颗粒)。这是否会产生影响尚不清楚,但空气传播颗粒暴露已确认的健康风险警示我们不能掉以轻心。口服暴露的小鼠模型将有助于识别风险,但迄今为止,缺乏与人类的相关性或验证。这项工作弥补了这一差距。它报告了:i)一种小鼠饮食,用不同浓度的常见饮食颗粒——食品级二氧化钛(fgTiO)进行了改良,fgTiO是一种多分散形式的添加剂,包含微米和纳米颗粒;ii)这些饮食将颗粒递送至肠道淋巴滤泡的基底细胞,这与在人类中“正常发生”的情况完全一致;iii)共聚焦反射显微镜是确定这一点的分析选择方法;iv)在长达18周的喂养过程中,喂食fgTiO的组与对照组之间在食物摄入量、体重增加和派尔集合淋巴结免疫细胞谱方面没有差异。这些发现为fgTiO风险评估提供了一种与人类相关且经过验证的口服给药方案,并为应用于纳米和微米颗粒的口服暴露研究提供了一个通用平台。