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羧酸加速酸性环境介导的纳米氧化铈的溶解。

Carboxylic acids accelerate acidic environment-mediated nanoceria dissolution.

机构信息

a Department of Pharmaceutical Sciences , University of Kentucky , Lexington , KY , USA.

b Department of Chemical & Materials Engineering , University of Kentucky , Lexington , KY , USA.

出版信息

Nanotoxicology. 2019 May;13(4):455-475. doi: 10.1080/17435390.2018.1553251. Epub 2019 Feb 7.

Abstract

Ligands that accelerate nanoceria dissolution may greatly affect its fate and effects. This project assessed the carboxylic acid contribution to nanoceria dissolution in aqueous, acidic environments. Nanoceria has commercial and potential therapeutic and energy storage applications. It biotransforms . Citric acid stabilizes nanoceria during synthesis and in aqueous dispersions. In this study, citrate-stabilized nanoceria dispersions (∼4 nm average primary particle size) were loaded into dialysis cassettes whose membranes passed cerium salts but not nanoceria particles. The cassettes were immersed in iso-osmotic baths containing carboxylic acids at pH 4.5 and 37 °C, or other select agents. Cerium atom material balances were conducted for the cassette and bath by sampling of each chamber and cerium quantitation by ICP-MS. Samples were collected from the cassette for high-resolution transmission electron microscopy observation of nanoceria size. In carboxylic acid solutions, nanoceria dissolution increased bath cerium concentration to >96% of the cerium introduced as nanoceria into the cassette and decreased nanoceria primary particle size in the cassette. In solutions of citric, malic, and lactic acids and the ammonium ion ∼15 nm, ceria agglomerates persisted. In solutions of other carboxylic acids, some select nanoceria agglomerates grew to ∼1 micron. In carboxylic acid solutions, dissolution half-lives were 800-4000 h; in water and horseradish peroxidase they were ≥55,000 h. Extending these findings to and environmental systems, one expects acidic environments containing carboxylic acids to degrade nanoceria by dissolution; two examples would be phagolysosomes and in the plant rhizosphere.

摘要

加速纳米铈溶解的配体可能会极大地影响其命运和效应。本项目评估了羧酸在纳米铈在水相、酸性环境中的溶解作用。纳米铈具有商业和潜在的治疗和储能应用。它在生物转化过程中。柠檬酸在合成过程中和水分散体中稳定纳米铈。在这项研究中,将柠檬酸稳定的纳米铈分散体(平均初级粒径约为 4nm)装入透析盒中,其膜可以通过铈盐但不能通过纳米铈颗粒。将这些小室浸入含有羧酸的等渗浴中,在 pH 4.5 和 37°C 或其他选择的试剂中。通过对每个腔室进行取样和通过 ICP-MS 对铈进行定量,对小室和浴的铈原子物料平衡进行了研究。从小室中收集样品,用于高分辨率透射电子显微镜观察纳米铈的粒径。在羧酸溶液中,纳米铈的溶解增加了浴中铈的浓度,达到了作为纳米铈引入小室的铈的 96%以上,并减小了小室中纳米铈初级颗粒的尺寸。在柠檬酸、苹果酸和乳酸以及铵离子的溶液中,氧化铈团聚体仍然存在。在其他羧酸的溶液中,一些选择的纳米铈团聚体生长到约 1 微米。在羧酸溶液中,溶解半衰期为 800-4000 小时;在水中和辣根过氧化物酶中,半衰期大于 55000 小时。将这些发现扩展到 和环境系统中,可以预期含有羧酸的酸性环境会通过溶解来降解纳米铈;两个例子是吞噬溶酶体和植物根际。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acbb/6609459/49aa43114cee/nihms-1520195-f0001.jpg

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