Department of Surgery and Clinical Science, Yamaguchi University Graduate School of Medicine, Ube 755-8505, Japan.
Graduate School of Health and Welfare, Yamaguchi Prefectural University, Yamaguchi 753-8502, Japan.
Int J Mol Sci. 2020 Aug 2;21(15):5538. doi: 10.3390/ijms21155538.
Ongoing aortic wall degeneration and subsequent aneurysm exclusion failure are major concerns after an endovascular aneurysm repair with a stent-graft. An ideal solution would be a drug therapy that targets the aortic wall and inhibits wall degeneration. Here, we described a novel drug delivery system, which allowed repetitively charging a graft with therapeutic drugs and releasing them to the aortic wall in vivo. The system was composed of a targeted graft, which was labeled with a small target molecule, and the target-recognizing nanocarrier, which contained suitable drugs. We developed the targeted graft by decorating a biotinylated polyester graft with neutravidin. We created the target-recognizing nanocarrier by conjugating drug-containing liposomes with biotinylated bio-nanocapsules. We successfully demonstrated that the target-recognizing nanocarriers could bind to the targeted graft, both in vitro and in blood vessels of live mice. Moreover, the drug released from our drug delivery system reduced the expression of matrix metalloproteinase-9 in mouse aortas. Thus, this hybrid system represents a first step toward an adjuvant therapy that might improve the long-term outcome of endovascular aneurysm repair.
血管内动脉瘤修复后,主动脉壁持续退化和随后的动脉瘤排除失败是主要关注点。理想的解决方案是一种针对主动脉壁并抑制壁退化的药物治疗。在这里,我们描述了一种新型药物输送系统,该系统允许重复向移植物充电并将其在体内释放到主动脉壁。该系统由靶向移植物组成,该移植物用小分子靶向分子标记,而靶向识别纳米载体则包含合适的药物。我们通过用中性蛋白酶修饰生物素化聚酯移植物来开发靶向移植物。我们通过将含药脂质体与生物素化生物纳米胶囊缀合来制备靶向识别纳米载体。我们成功地证明了靶向识别纳米载体可以与靶向移植物结合,无论是在体外还是在活体小鼠的血管中。此外,我们的药物输送系统释放的药物降低了小鼠主动脉中基质金属蛋白酶-9的表达。因此,这种混合系统代表了一种辅助治疗的第一步,可能会改善血管内动脉瘤修复的长期效果。