Baek Seung-Woon, Kim Da-Seul, Song Duck Hyun, Lee Semi, Lee Jun-Kyu, Park So-Yeon, Kim Jun Hyuk, Kim Tae-Hyung, Park Chun Gwon, Han Dong Keun
Department of Biomedical Science, CHA University, 335 Pangyo-ro, Bundang-gu, Seongnam-si 13488, Republic of Korea.
Department of Biomedical Engineering, SKKU Institute for Convergence, Sungkyunkwan University (SKKU), 2066 Seobu-ro, Jangan-gu, Suwon-si 16419, Republic of Korea.
Pharmaceutics. 2022 Nov 30;14(12):2661. doi: 10.3390/pharmaceutics14122661.
The development of a biodegradable vascular scaffold (BVS) for the treatment of cardiovascular diseases (CVDs) still requires some improvement. Among them, re-endothelialization and anti-inflammation are clinically important to restore vascular function. In this study, we proposed a coating system to deliver hydrophilic bioactive agents to BVS using nanoemulsion and drop-casting methods. The poly(L-lactide) (PLLA) scaffold containing magnesium hydroxide (MH) was coated on the surface with bioactive molecules such as polydeoxyribonucleotide (PDRN), L-arginine (Arg, R), and mesenchymal stem cell-derived extracellular vesicles (EVs). PDRN upregulates the expression of VEGF as one of the A2A receptor agonists; and Arg, synthesized into nitric oxide by intracellular eNOS, induces endothelialization. In particular, EVs, which are composed of a lipid bilayer and transfer bioactive materials such as protein and nucleic acid, regulate homeostasis in blood vessels. Such a bioactive agent coating system and its PLLA composite suggest a new platform for the treatment of cardiovascular dysfunction.
用于治疗心血管疾病(CVD)的可生物降解血管支架(BVS)的开发仍需进一步改进。其中,再内皮化和抗炎对于恢复血管功能在临床上具有重要意义。在本研究中,我们提出了一种涂层系统,使用纳米乳液和滴铸法将亲水性生物活性剂递送至BVS。含有氢氧化镁(MH)的聚(L-丙交酯)(PLLA)支架表面涂覆有生物活性分子,如聚脱氧核糖核苷酸(PDRN)、L-精氨酸(Arg,R)和间充质干细胞衍生的细胞外囊泡(EVs)。PDRN作为A2A受体激动剂之一上调VEGF的表达;而Arg通过细胞内eNOS合成一氧化氮,诱导内皮化。特别是,由脂质双层组成并传递蛋白质和核酸等生物活性物质的EVs可调节血管内环境稳态。这种生物活性剂涂层系统及其PLLA复合材料为治疗心血管功能障碍提供了一个新平台。