Han Yuemei, Wang Jiahao, Chen Hao, Lin Quankui
National Engineering Research Center of Ophthalmology and Optometry, School of Biomedical Engineering, School of Ophthalmology and Optometry, Eye Hospital, Wenzhou Medical University, Wenzhou 325027, China.
Regen Biomater. 2025 Jul 28;12:rbaf077. doi: 10.1093/rb/rbaf077. eCollection 2025.
Intraocular lens (IOL) is a crucial implant for cataract therapy. Posterior capsule opacification (PCO) is the most common postoperative complication after IOL implantation, which is the abnormal hyperplasia of the residual lens epithelial cells (LECs) after IOL implantation in cataract surgery. It is reported that the cellular microenvironment in the lens capsule changes after surgery, such as the elevated secretion of matrix metalloproteinases (MMPs) and a decrease in pH due to undesired cell proliferation. In this study, MMP-2 and pH-triggered drug delivery polysaccharide multilayer coating was designed and introduced onto the IOL surface for obtaining the cellular microenvironment-sensitive drug-eluting intraocular implant. The methacrylated heparin (HEP-MA) was synthesized and used to layer-by-layer self-assemble with the doxorubicin-loaded chitosan nanoparticles on the IOL surface. The matrix metalloproteinase-2 (MMP-2) sensitive peptide with cysteine contained in both ends (GCRD-GPQGIWGQ-DRCG) was then used to crosslink the polysaccharide multilayer via the Michael addition reaction between sulfhydryl group in cysteines and double bonds in methacrylate groups. The multilayer construction and subsequent cross-linking were validated through ultraviolet-visible spectrophotometer (UV-Vis) and Fourier transform infrared spectroscopy (FTIR). After modification, the IOL material surface becomes more hydrophilic while the optical properties were well maintained. The MMP-2 and pH-sensitive drug sustained-release coating were successfully obtained on the IOL surface via such design. The enzyme-triggered cell proliferation inhibition was realized in the experiments. In an animal model, significant up-regulation of MMP-2 was observed in the aqueous humor after cataract surgery. The multi-functionalized polysaccharide-coated IOL implanted in the animal eye via cataract surgery effectively inhibits PCO formation while it keeps good biosafety.
人工晶状体(IOL)是白内障治疗的关键植入物。后囊膜混浊(PCO)是IOL植入术后最常见的并发症,它是白内障手术中IOL植入后残留晶状体上皮细胞(LECs)的异常增生。据报道,手术后晶状体囊膜内的细胞微环境发生变化,如基质金属蛋白酶(MMPs)分泌增加以及由于不必要的细胞增殖导致pH值降低。在本研究中,设计了MMP - 2和pH触发的药物递送多糖多层涂层,并将其引入到IOL表面,以获得细胞微环境敏感的药物洗脱眼内植入物。合成了甲基丙烯酸化肝素(HEP - MA),并用于与负载阿霉素的壳聚糖纳米颗粒在IOL表面进行逐层自组装。然后使用两端含有半胱氨酸的基质金属蛋白酶 - 2(MMP - 2)敏感肽,通过半胱氨酸中的巯基与甲基丙烯酸酯基团中的双键之间的迈克尔加成反应交联多糖多层膜。通过紫外 - 可见分光光度计(UV - Vis)和傅里叶变换红外光谱(FTIR)验证了多层结构及随后的交联。修饰后,IOL材料表面变得更亲水,同时光学性能得到良好保持。通过这种设计在IOL表面成功获得了MMP - 2和pH敏感的药物缓释涂层。在实验中实现了酶触发的细胞增殖抑制。在动物模型中,白内障手术后房水中观察到MMP - 2显著上调。通过白内障手术植入动物眼中的多功能多糖涂层IOL有效抑制了PCO的形成,同时保持了良好的生物安全性。