Department of Chemistry "Ugo Schiff", Università degli Studi di Firenze, via della Lastruccia 3-13, 50019 Sesto Fiorentino, Firenze, Italy.
Department of Cancer Systems Imaging, Division of Diagnostic Imaging, The University of Texas MD Anderson Cancer Center, 1881 East Road, 77054 Houston, TX, USA.
J Mater Chem B. 2019 Apr 28;7(16):2678-2687. doi: 10.1039/C8TB03299H. Epub 2019 Mar 12.
A drug delivery system (DDS) for combined therapy, based on a short oxidized multiwalled carbon nanotube, is reported. It was prepared exploiting a synthetic approach which allowed loading of two drugs, doxorubicin and metformin, the targeting agent biotin and a radiolabeling tag, to enable labeling with Ga-68 or Cu-64 in order to perform an extensive biodistribution study by PET/CT. The DDS biodistribution profile changes with different administration methods. Once administered at therapeutic doses, the DDS showed a marginal beneficial effect on 4T1 tumor bearing mice, a syngeneic and orthotopic model of triple negative breast cancer, with survival extended by 1 week and 2 days in 20% of the mice. This is encouraging given the aggressiveness of the 4T1 tumor. Furthermore our DDS was well tolerated, ruling out concerns regarding the toxicity of carbon nanotubes.
一种基于短氧化多壁碳纳米管的联合治疗药物输送系统(DDS)被报道。它是通过一种合成方法制备的,该方法允许加载两种药物,阿霉素和二甲双胍,靶向剂生物素和放射性标记物,以便用 Ga-68 或 Cu-64 进行标记,从而通过 PET/CT 进行广泛的生物分布研究。DDS 的生物分布特征随不同的给药方式而变化。一旦以治疗剂量给药,DDS 对 4T1 荷瘤小鼠(三阴性乳腺癌的同基因和原位模型)表现出轻微的有益作用,其中 20%的小鼠的存活期延长了 1 周零 2 天。考虑到 4T1 肿瘤的侵袭性,这是令人鼓舞的。此外,我们的 DDS 耐受性良好,排除了对碳纳米管毒性的担忧。