Department of Chemical & Biochemical Engineering, Missouri University of Science and Technology, Rolla, Missouri 65409-1230, United States.
ACS Appl Bio Mater. 2021 Sep 20;4(9):6874-6880. doi: 10.1021/acsabm.1c00585. Epub 2021 Aug 11.
Recently, metal-organic frameworks (MOFs) have been widely employed as potential drug-delivery platforms; however, most studies have focused on the initial aspects of material development and have made little progress toward using MOFs as a means of controlling the pharmacokinetic rate of drug delivery. Nevertheless, it was recently determined that MOFs with highly soluble metal centers impart faster pharmacokinetic properties, so it stands to reason that combining two MOFs with different metal center solubilities could be used to control the pharmacokinetic release rate. To this end, in this study we varied the ratio of Mg-MOF-74 and Zn-MOF-74 between 80:20, 60:40, 40:60, and 20:80 wt % Mg:Zn to control the pharmacokinetic release rate of 30 wt % curcumin. The drug loading was characterized by using Fourier transform infrared spectroscopy and N physisorption, where it was confirmed that curcumin was impregnated successfully. More importantly, the drug delivery experiments in phosphate buffered saline from 0 to 24 h at 37.4 °C revealed that increasing the Mg-MOF-74 concentration enhanced both the raw amount of curcumin delivered and the pharmacokinetic rate of drug delivery. Specifically looking at the rate of drug delivery, drug diffusion constants of 0.17, 0.23, 0.24, and 0.26 h were calculated for the 20:80, 40:60, 60:40, and 80:20 Mg-Zn-MOF-74 samples, respectively, which indicated the profound relationship between the Mg-MOF-74 loading and the rate of curcumin delivery. In this regard, this study successfully demonstrated a potential pathway of controlling the pharmacokinetic rate of drug release from MOFs which can be considered a promising advancement in pharmacological medicine.
最近,金属有机骨架(MOFs)已被广泛用作潜在的药物输送平台;然而,大多数研究都集中在材料开发的初始阶段,在利用 MOFs 控制药物输送的药代动力学速率方面几乎没有进展。然而,最近发现具有高可溶性金属中心的 MOFs 赋予更快的药代动力学特性,因此可以合理地认为将两种具有不同金属中心溶解度的 MOFs 结合使用可以控制药代动力学释放速率。为此,在本研究中,我们改变了 Mg-MOF-74 和 Zn-MOF-74 的比例为 80:20、60:40、40:60 和 20:80wt%Mg:Zn,以控制 30wt%姜黄素的药代动力学释放速率。通过傅里叶变换红外光谱和 N 物理吸附来表征药物负载,证实了姜黄素成功浸渍。更重要的是,在 37.4°C 的磷酸盐缓冲盐水中进行 0 至 24 小时的药物输送实验表明,增加 Mg-MOF-74 的浓度可同时提高姜黄素的初始递送量和药物输送的药代动力学速率。具体来看药物输送的速率,计算出 20:80、40:60、60:40 和 80:20Mg-Zn-MOF-74 样品的药物扩散常数分别为 0.17、0.23、0.24 和 0.26h,这表明了 Mg-MOF-74 负载与姜黄素递送速率之间的深刻关系。在这方面,本研究成功地证明了控制 MOFs 中药物释放的药代动力学速率的潜在途径,可以被认为是药理学医学中的一项有前途的进展。