LAQV, REQUIMTE, Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira N.º 228, 4050-313, Porto, Portugal.
UCIBIO, REQUIMTE, Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050‑313, Porto, Portugal.
Arch Toxicol. 2023 Oct;97(10):2643-2657. doi: 10.1007/s00204-023-03558-5. Epub 2023 Aug 18.
Silver nanoparticles (AgNP) are among the most widely commercialized nanomaterials globally, with applications in medicine and the food industry. Consequently, the increased use of AgNP in the food industry has led to an unavoidable rise in human exposure to these nanoparticles. Their widespread use raises concerns about potential hazards to human health, specifically their intestinal pro-inflammatory effects. Thus, the main objective of this study was to evaluate the biological effects of two subacute doses of 5 nm polyvinylpyrrolidone (PVP)-AgNP in C57BL/6J mice. One mg/kg body weight or 10 mg/kg bw was provided once a day for 14 days, using a new technology (HaPILLness) that allows voluntary, stress-free, and accurate oral dosing. It was observed that after oral ingestion, while AgNP is biodistributed throughout the entire organism, most of the ingested dose is excreted in the feces. The passage and accumulation of AgNP throughout the intestine instigated a prominent inflammatory response, marked by significant histological, vascular, and cellular transformations. This response was driven by the activation of the nuclear factor-кB (NF-кB) inflammatory pathway, ultimately leading to the generation of multiple cytokines and chemokines.
银纳米粒子(AgNP)是全球商业化应用最广泛的纳米材料之一,在医学和食品工业中都有应用。因此,AgNP 在食品工业中的使用增加,导致人类不可避免地接触到这些纳米粒子。它们的广泛使用引起了对人类健康潜在危害的关注,特别是它们对肠道的促炎作用。因此,本研究的主要目的是评估两种亚急性剂量的 5nm 聚维酮(PVP)-AgNP 在 C57BL/6J 小鼠中的生物学效应。使用一种新技术(HaPILLness),每天一次给予 1mg/kg 体重或 10mg/kg bw,该技术允许自愿、无压力和精确的口服给药。结果表明,口服摄入后,AgNP 虽然在整个生物体中分布,但大部分摄入的剂量都在粪便中排出。AgNP 在整个肠道的通过和积累引发了明显的炎症反应,表现为显著的组织学、血管和细胞转化。这种反应是由核因子-кB(NF-кB)炎症途径的激活所驱动的,最终导致多种细胞因子和趋化因子的产生。