Department of Pharmaceutics, College of Pharmacy, Third Military Medical University (Army Medical University), Chongqing, 400038, China.
Department of Vascular Surgery, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, 430060, China.
Adv Mater. 2022 Nov;34(44):e2204455. doi: 10.1002/adma.202204455. Epub 2022 Oct 3.
Abdominal aortic aneurysm (AAA) remains a lethal aortic disease in the elderly. Currently, no effective drugs can be clinically applied to prevent the development of AAA. Herein, a "one stone for multiple birds" strategy for AAA therapy is reported. As a proof of concept, three bioactive conjugates are designed and synthesized, which can assemble into nanomicelles. Cellularly, these nanomicelles significantly inhibit migration and activation of inflammatory cells as well as protect vascular smooth muscle cells (VSMCs) from induced oxidative stress, calcification and apoptosis, with the best effect for nanomicelles (TPTN) derived from a conjugate defined as TPT. After intravenous delivery, TPTN efficiently accumulates in the aneurysmal tissue of AAA rats, showing notable distribution in neutrophils, macrophages and VSMCs, all relevant to AAA pathogenesis. Whereas three examined nanomicelles effectively delay expansion of AAA in rats, TPTN most potently prevents AAA growth by simultaneously normalizing the pro-inflammatory microenvironment and regulating multiple pathological cells. TPTN is effective even at 0.2 mg kg . Besides, TPTN can function as a bioactive nanoplatform for site-specifically delivering and triggerably releasing anti-aneurysmal drugs, affording synergistic therapeutic effects. Consequently, TPTN is a promising multi-bioactive nanotherapy and bioresponsive targeting delivery nanocarrier for effective therapy of AAA and other inflammatory vascular diseases.
腹主动脉瘤 (AAA) 仍然是老年人的一种致命性主动脉疾病。目前,临床上尚无有效的药物可用于预防 AAA 的发展。在此,报告了一种用于 AAA 治疗的“一石多鸟”策略。作为概念验证,设计并合成了三种具有生物活性的缀合物,它们可以组装成纳米胶束。在细胞水平上,这些纳米胶束能显著抑制炎症细胞的迁移和激活,并保护血管平滑肌细胞 (VSMCs) 免受诱导的氧化应激、钙化和凋亡,其中源自缀合物 TPT 的纳米胶束(TPTN)效果最佳。静脉给药后,TPTN 能有效地在 AAA 大鼠的动脉瘤组织中积累,在与 AAA 发病机制相关的中性粒细胞、巨噬细胞和 VSMCs 中均有显著分布。三种被检查的纳米胶束均能有效延缓大鼠 AAA 的扩张,而 TPTN 通过同时使促炎微环境正常化和调节多种病理细胞,最有效地防止 AAA 的生长。TPTN 在 0.2 mg/kg 的剂量下仍然有效。此外,TPTN 可用作生物活性纳米平台,用于特异性递药和触发释放抗动脉瘤药物,提供协同治疗效果。因此,TPTN 是一种有前途的多生物活性纳米疗法和响应性靶向递药纳米载体,可有效治疗 AAA 和其他炎症性血管疾病。