Chen Du, Song Tiantian, Liu Yi, Wang Ying, Qin Boyang, Zhang Qingyi, Hu Weipeng, Zhou Xiqiao, Qi Rong
Department of Pharmacology, School of Basic Medical Sciences, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing, 100191, China.
State Key Laboratory of Vascular Homeostasis and Remodeling. NHC Key Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Beijing Key Laboratory of Molecular Pharmaceutics and New Drug Delivery Systems, State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, 100191, China.
Adv Healthc Mater. 2025 Apr;14(11):e2402497. doi: 10.1002/adhm.202402497. Epub 2024 Dec 20.
Endovascular aneurysm repair (EVAR) plays a crucial role in the treatment of abdominal aortic aneurysm (AAA) in the clinic, but the aneurysm remains in the patient's body after surgery, continuing to pose a risk of progression. Cycloastragenol (CAG) is proven to be an effective anti-AAA drug, and its vascular protective effects can be further improved when the hydrophobic CAG is encapsulated into nano-sized formulations to enhance its bioavailability. In this context, this study developed an extravascular patch hydrogel loaded with CAG nanostructured lipid carriers and a hydrophilic drug of doxycycline hydrochloride (DOX). The extravascular patch delivered onto the mouse abdominal aortas can promote local permeation of hydrophilic/hydrophobic drugs at the vessel sites and provide effective vascular protection against AAA injury induced by elastase. This study introduces a novel and promising approach for AAA treatment, which can serve as a supplementary strategy after EVAR surgery.
血管内动脉瘤修复术(EVAR)在临床上对腹主动脉瘤(AAA)的治疗起着关键作用,但术后动脉瘤仍留在患者体内,持续存在进展风险。环黄芪醇(CAG)被证明是一种有效的抗AAA药物,当疏水性CAG被包裹成纳米制剂以提高其生物利用度时,其血管保护作用可进一步增强。在此背景下,本研究开发了一种负载CAG纳米结构脂质载体和盐酸多西环素(DOX)亲水性药物的血管外贴片水凝胶。敷贴在小鼠腹主动脉上的血管外贴片可促进亲水性/疏水性药物在血管部位的局部渗透,并有效保护血管免受弹性蛋白酶诱导的AAA损伤。本研究介绍了一种新颖且有前景的AAA治疗方法,可作为EVAR手术后的补充策略。