Department of Biomedical Engineering, Feinberg School of Medicine , Northwestern University , Chicago , Illinois 60611 , United States.
Departments of Chemistry, Molecular Biosciences, Neurobiology, and Radiology , Northwestern University , Evanston , Illinois 60208 , United States.
Bioconjug Chem. 2019 Nov 20;30(11):2947-2957. doi: 10.1021/acs.bioconjchem.9b00640. Epub 2019 Oct 22.
ProGlo is an efficient steroid receptor-targeted magnetic resonance (MR) imaging contrast agent (CA). It has been shown to bind to the progesterone receptor (PR) and produce enhanced image contrast in PR-positive cells and tissues and . However, the hydrophobicity of the steroid targeting domain of ProGlo (logP = 1.4) limits its formulation and delivery at clinically relevant doses. In this work, a hydrophobic moiety was utilized to drive efficient adsorption onto nanodiamond (ND) clusters to form a water-soluble nanoconstruct (logP = -2.4) with 80% release in 8 h under biological conditions. In cell culture, the ND-ProGlo construct delivered increased concentrations of ProGlo to target cells compared to ProGlo alone. Importantly, these results were accomplished without the use of solvents such as DMSO, providing a significant advance toward formulating ProGlo for translational applications. Biodistribution studies confirm the delivery of ProGlo to PR(+) tissues with enhanced efficacy over untargeted controls. These results demonstrate the potential for a noncovalent ND-CA construct as a general strategy for solubilizing and delivering hydrophobic targeted MR CAs.
ProGlo 是一种高效的类固醇受体靶向磁共振(MR)成像对比剂(CA)。已证明它可以与孕激素受体(PR)结合,并在 PR 阳性细胞和组织中产生增强的图像对比效果。然而,ProGlo 的类固醇靶向结构域的疏水性(logP = 1.4)限制了其在临床相关剂量下的制剂和输送。在这项工作中,利用疏水性部分将其有效吸附到纳米金刚石(ND)簇上,形成一种水溶性纳米结构(logP = -2.4),在生物条件下 8 小时内 80%释放。在细胞培养中,与单独的 ProGlo 相比,ND-ProGlo 构建体将更多浓度的 ProGlo 递送到靶细胞。重要的是,这些结果是在不使用 DMSO 等溶剂的情况下实现的,这为 ProGlo 的转化应用提供了一个重大进展。生物分布研究证实,与未靶向对照相比,ProGlo 递送至 PR(+)组织的疗效增强。这些结果表明,非共价 ND-CA 构建体作为一种溶解和输送疏水性靶向 MR CA 的通用策略具有潜力。