Kim Dae-Hyun, Jang Eui Hwa, Lee Kang Ju, Lee Ji Yong, Park Seung Hyun, Seo Il Ho, Lee Kang Woog, Lee Seung Hyun, Ryu WonHyoung, Youn Young-Nam
Division of Cardiovascular Surgery, Severance Cardiovascular Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Sedaemun-gu, Seoul 03722, Korea.
School of Mechanical Engineering, Yonsei University, 50 Yonsei-ro, Sedaemun-gu, Seoul 03722, Korea.
Polymers (Basel). 2017 Feb 8;9(2):56. doi: 10.3390/polym9020056.
Restenosis at a vascular anastomosis site is a major cause of graft failure and is difficult to prevent by conventional treatment. Perivascular drug delivery has advantages as drugs can be diffused to tunica media and subintima while minimizing the direct effect on endothelium. This in vivo study investigated the comparative effectiveness of paclitaxel, sirolimus, and sunitinib using a perivascular biodegradable microneedle cuff. A total of 31 New Zealand white rabbits were used. Rhodamine was used to visualize drug distribution ( = 3). Sirolimus- ( = 7), sunitinib- ( = 7), and paclitaxel-loaded ( = 7) microneedle cuffs were placed at balloon-injured abdominal aortae and compared to drug-free cuffs ( = 7). Basic histological structures were not affected by microneedle devices, and vascular wall thickness of the device-only group was similar to that of normal artery. Quantitative analysis revealed significantly decreased neointima formation in all drug-treated groups ( < 0.001). However, the tunica media layer of the paclitaxel-treated group was significantly thinner than that of other groups and also showed the highest apoptotic ratio ( < 0.001). Proliferating cell nuclear antigen (PCNA)-positive cells were significantly reduced in all drug-treated groups. Sirolimus or sunitinib appeared to be more appropriate for microneedle devices capable of slow drug release because vascular wall thickness was minimally affected.
血管吻合部位的再狭窄是移植物失败的主要原因,并且难以通过传统治疗方法预防。血管周围给药具有优势,因为药物可以扩散到中膜和内膜下层,同时将对内皮的直接影响降至最低。这项体内研究使用血管周围可生物降解微针套研究了紫杉醇、西罗莫司和舒尼替尼的相对有效性。总共使用了31只新西兰白兔。使用罗丹明来观察药物分布( = 3)。将负载西罗莫司( = 7)、舒尼替尼( = 7)和紫杉醇( = 7)的微针套置于球囊损伤的腹主动脉处,并与无药微针套( = 7)进行比较。基本组织学结构未受微针装置影响,仅放置微针装置组的血管壁厚度与正常动脉相似。定量分析显示,所有药物治疗组的新生内膜形成均显著减少( < 0.001)。然而,紫杉醇治疗组的中膜层明显比其他组薄,并且凋亡率也最高( < 0.001)。所有药物治疗组中增殖细胞核抗原(PCNA)阳性细胞均显著减少。西罗莫司或舒尼替尼似乎更适合能够缓慢释放药物的微针装置,因为血管壁厚度受影响最小。