Department of Chemistry, Wayne State University, 5101 Cass Avenue, Detroit, MI, 48202, USA.
Department of Integrative Physiology, Baylor College of Medicine, Houston, TX, 77030, USA.
Adv Healthc Mater. 2023 Jul;12(19):e2203209. doi: 10.1002/adhm.202203209. Epub 2023 Mar 24.
Radiographic mapping of hypoxia is needed to study a wide range of diseases. Complexes of Eu(II) are a promising class of molecules to fit this need, but they are generally limited by their rapid oxidation rates in vivo. Here, a perfluorocarbon-nanoemulsion perfused with N , forms an interface with aqueous layers to hinder oxidation of a new perfluorocarbon-soluble complex of Eu(II). Conversion of the perfluorocarbon solution of Eu(II) into nanoemulsions results in observable differences between reduced and oxidized forms by magnetic resonance imaging both in vitro and in vivo. Oxidation in vivo occurrs over a period of ≈30 min compared to <5 min for a comparable Eu(II)-containing complex without nanoparticle interfaces. These results represent a critical step toward delivery of Eu(II)-containing complexes in vivo for the study of hypoxia.
缺氧的放射图测绘对于研究广泛的疾病是必要的。Eu(II) 配合物是满足这一需求的一类很有前途的分子,但它们通常受到体内快速氧化速率的限制。在这里,用 N 灌注的全氟碳纳米乳液与水层形成界面,以阻止新的全氟碳可溶性 Eu(II) 配合物的氧化。将 Eu(II) 的全氟碳溶液转化为纳米乳液,通过体外和体内磁共振成像观察到还原和氧化形式之间的可观察到的差异。与没有纳米颗粒界面的类似的含 Eu(II) 配合物相比,体内氧化发生在 ≈30 分钟左右,而不是 <5 分钟。这些结果代表了在体内输送含 Eu(II) 配合物以研究缺氧的重要一步。