Jiang Xue, Jin Yinli, Zeng Yongnian, Shi Peng, Li Wei
Department of Thyroid and Breast Surgery, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan, 430071, China.
Department of Biomedical Engineering, The City University of Hong Kong, Kowloon, Hong Kong SAR, 999077, China.
Small. 2024 Jul;20(29):e2310461. doi: 10.1002/smll.202310461. Epub 2024 Feb 23.
Bacteria-induced keratitis is a major cause of corneal blindness in both developed and developing countries. Instillation of antibiotic eyedrops is the most common management of bacterial keratitis but usually suffers from low bioavailability (i.e., <5%) and frequent administration, due to the existence of corneal epithelial barrier that prevents large and hydrophilic drug molecules from entering the cornea, and the tear film on corneal surface that rapidly washes drug away from the cornea. Here, a self-implantable core-shell microneedle (MN) patch with programmed drug release property to facilitate bacterial keratitis treatment is reported. The pH-responsive antimicrobial nanoparticles (NPs), Ag@ZIF-8, which are capable of producing antibacterial metal ions in the infected cornea and generating oxidative stress in bacteria, are loaded in the dissolvable core, while the anti-angiogenic drug, rapamycin (Rapa), is encapsulated in the biodegradable shell, thereby enabling rapid release of Ag@ZIF-8 NPs and sustained release of Rapa after corneal insertion. Owing to the programmed release feature, one single administration of the core-shell MN patch in a rat model of bacterial keratitis, can achieve satisfactory antimicrobial activity and superior anti-angiogenic and anti-inflammation effects as compared to daily topical eyedrops, indicating a great potential for the infectious keratitis therapy in clinics.
在发达国家和发展中国家,细菌感染性角膜炎都是导致角膜盲的主要原因。滴注抗生素眼药水是治疗细菌性角膜炎最常用的方法,但由于角膜上皮屏障的存在会阻止大分子和亲水性药物分子进入角膜,以及角膜表面的泪膜会迅速将药物从角膜冲走,该方法通常存在生物利用度低(即<5%)和给药频繁的问题。在此,报道了一种具有程序控释特性的可自植入核壳微针(MN)贴片,以促进细菌性角膜炎的治疗。pH响应性抗菌纳米颗粒(NPs)Ag@ZIF-8能够在感染的角膜中产生抗菌金属离子并在细菌中产生氧化应激,被装载在可溶解的内核中,而抗血管生成药物雷帕霉素(Rapa)则被包裹在可生物降解的外壳中,从而在角膜插入后实现Ag@ZIF-8 NPs的快速释放和Rapa的持续释放。由于具有程序控释特性,在细菌性角膜炎大鼠模型中单次给药核壳MN贴片,与每日局部滴眼相比,可实现令人满意的抗菌活性以及卓越的抗血管生成和抗炎效果,表明其在临床感染性角膜炎治疗中具有巨大潜力。