Im Changkeun, Kim Hyeongi, Zaheer Javeria, Kim Jung Young, Lee Yong-Jin, Kang Choong Mo, Kim Jin Su
Division of Applied RI, Korea Institute of Radiological and Medical Sciences, Seoul, Korea; and.
Radiological and Medico-Oncological Sciences, University of Science and Technology, Seoul, Korea.
J Nucl Med. 2022 Mar;63(3):461-467. doi: 10.2967/jnumed.120.256982. Epub 2021 Jul 2.
Plastics are used commonly in the world because of their convenience and cost effectiveness. Microplastics, an environmental threat and human health risk, are widely detected in food and consequently ingested. However, degraded plastics are found everywhere, creating an environmental threat and human health risk. Therefore, real-time monitoring of orally administered microplastics to trace them in the body is tremendously important. In this study, to visualize their absorption path, we labeled polystyrene with [Cu]Cu-DOTA. We prepared radiolabeled polystyrene with Cu. Afterward, [Cu]Cu-DOTA-polystyrene was orally administered to mice, and we evaluated its transit and absorption using PET imaging. The absorption path and distribution of [Cu]Cu-DOTA-polystyrene were determined using PET over 48 h. Ex vivo tissue radio-thin-layer chromatography (TLC) was used to demonstrate the existence of [Cu]Cu-DOTA-polystyrene in tissue. PET images demonstrated that [Cu]Cu-DOTA-polystyrene began to transit to the intestine within 1 h. Accumulation of [Cu]Cu-DOTA-polystyrene in the liver was also observed. The biodistribution of [Cu]Cu-DOTA-polystyrene confirmed the distribution of [Cu]Cu-DOTA-polystyrene observed on the PET images. Ex vivo radio-TLC demonstrated that the detected γ-rays originated from [Cu]Cu-DOTA-polystyrene. This study provided PET evidence of the existence and accumulation of microplastics in tissue and cross-confirmed the PET findings by ex vivo radio-TLC. This information may be used as the basis for future studies on the toxicity of microplastics.
由于其便利性和成本效益,塑料在全球被广泛使用。微塑料作为一种环境威胁和人类健康风险,在食品中被广泛检测到并因此被摄入。然而,降解塑料随处可见,构成了环境威胁和人类健康风险。因此,对口服微塑料进行实时监测以追踪其在体内的行踪极为重要。在本研究中,为了可视化它们的吸收路径,我们用[Cu]Cu-DOTA标记了聚苯乙烯。我们制备了含铜的放射性标记聚苯乙烯。之后,将[Cu]Cu-DOTA-聚苯乙烯口服给予小鼠,并使用正电子发射断层扫描(PET)成像评估其转运和吸收情况。在48小时内使用PET确定[Cu]Cu-DOTA-聚苯乙烯的吸收路径和分布。采用离体组织放射性薄层色谱法(TLC)来证明组织中存在[Cu]Cu-DOTA-聚苯乙烯。PET图像显示,[Cu]Cu-DOTA-聚苯乙烯在1小时内开始转运至肠道。还观察到[Cu]Cu-DOTA-聚苯乙烯在肝脏中蓄积。[Cu]Cu-DOTA-聚苯乙烯的生物分布证实了PET图像上观察到的[Cu]Cu-DOTA-聚苯乙烯的分布情况。离体放射性TLC表明,检测到的γ射线源自[Cu]Cu-DOTA-聚苯乙烯。本研究提供了微塑料在组织中存在和蓄积的PET证据,并通过离体放射性TLC对PET结果进行了交叉验证。这些信息可作为未来微塑料毒性研究的基础。