Department of Medical Biophysics, University of Western Ontario, London, Ontario N6A 3K7, Canada.
The Athinoula A. Martinos Center for Biomedical Imaging, The Institute for Innovation in Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Charlestown, Massachusetts 02129, United States.
J Med Chem. 2023 May 25;66(10):6567-6576. doi: 10.1021/acs.jmedchem.2c01561. Epub 2023 May 9.
Five amphiphilic, anionic Mn(II) complexes were synthesized as contrast agents targeted to organic anion transporting polypeptide transporters (OATP) for liver magnetic resonance imaging (MRI). The Mn(II) complexes are synthesized in three steps, each from the commercially available -1,2-diaminocyclohexane-,,','-tetraacetic acid (CDTA) chelator, with -relaxivity of complexes ranging between 2.3 and 3.0 mM s in phosphate buffered saline at an applied field strength of 3.0 T. Pharmacokinetics were assessed in female BALB/c mice by acquiring -weighted images dynamically for 70 min after agent administration and determining contrast enhancement and washout in various organs. Uptake of Mn(II) complexes in human OATPs was investigated through in vitro assays using MDA-MB-231 cells engineered to express either OATP1B1 or OATP1B3 isoforms. Our study introduces a new class of Mn-based OATP-targeted contrast that can be broadly tuned via simple synthetic protocols.
五种两亲性、阴离子型 Mn(II) 配合物被合成出来,作为针对有机阴离子转运多肽转运体 (OATP) 的磁共振成像 (MRI) 对比剂。这些 Mn(II) 配合物通过三步合成,每一步均使用市售的 -1,2-二氨基环己烷-,,','-四乙酸 (CDTA) 螯合剂,在 3.0 T 的应用场强下,其弛豫率在磷酸盐缓冲盐水中的范围在 2.3 到 3.0 mM s 之间。通过在给药后 70 分钟内动态采集 -加权图像,并在各种器官中测定对比增强和洗脱,在雌性 BALB/c 小鼠中评估了这些 Mn(II) 配合物的药代动力学。通过使用表达 OATP1B1 或 OATP1B3 同工型的 MDA-MB-231 细胞进行的体外测定,研究了 Mn(II) 配合物在人 OATPs 中的摄取情况。我们的研究引入了一类新的基于 Mn 的 OATP 靶向对比剂,可通过简单的合成方案进行广泛调节。