Matrix metalloproteinase-2 and pH-responsive drug eluting multilayer as intraocular lens coating to improve the posterior capsule opacification inhibition.

IF 8.1 1区 医学 Q1 MATERIALS SCIENCE, BIOMATERIALS
Regenerative Biomaterials Pub Date : 2025-07-28 eCollection Date: 2025-01-01 DOI:10.1093/rb/rbaf077
Yuemei Han, Jiahao Wang, Hao Chen, Quankui Lin
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Abstract

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 in vitro 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 in vivo biosafety.

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基质金属蛋白酶-2和ph反应性药物洗脱多层作为人工晶状体涂层改善后囊膜混浊抑制作用。
人工晶状体(IOL)是白内障治疗的重要植入物。后囊膜混浊(Posterior capsule opacification, PCO)是人工晶状体植入术后最常见的术后并发症,是白内障人工晶状体植入术后残留晶状体上皮细胞(lens epithelial cells, LECs)异常增生。据报道,手术后晶状体囊内的细胞微环境发生变化,如基质金属蛋白酶(MMPs)分泌升高,pH值因不希望的细胞增殖而降低。本研究设计了MMP-2和ph触发的给药多糖多层涂层,并将其引入IOL表面,获得细胞微环境敏感的药物洗脱眼内植入物。合成甲基丙烯酸化肝素(HEP-MA),并将其与负载阿霉素的壳聚糖纳米颗粒在人工晶状体表面逐层自组装。然后利用两端含半胱氨酸的基质金属蛋白酶-2 (MMP-2)敏感肽(GCRD-GPQGIWGQ-DRCG)通过半胱氨酸巯基与甲基丙烯酸酯基团双键之间的Michael加成反应将多糖多层交联。通过紫外-可见分光光度计(UV-Vis)和傅里叶变换红外光谱(FTIR)验证了多层结构和随后的交联。改性后的IOL材料表面亲水性增强,光学性能保持良好。通过该设计,成功地在IOL表面获得了MMP-2和ph敏感的药物缓释涂层。体外实验实现了酶促细胞增殖抑制。在动物模型中,观察到白内障术后房水中MMP-2的显著上调。通过白内障手术植入动物眼内的多功能多糖包被IOL可有效抑制PCO的形成,同时保持良好的体内生物安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Regenerative Biomaterials
Regenerative Biomaterials Materials Science-Biomaterials
CiteScore
7.90
自引率
16.40%
发文量
92
审稿时长
10 weeks
期刊介绍: Regenerative Biomaterials is an international, interdisciplinary, peer-reviewed journal publishing the latest advances in biomaterials and regenerative medicine. The journal provides a forum for the publication of original research papers, reviews, clinical case reports, and commentaries on the topics relevant to the development of advanced regenerative biomaterials concerning novel regenerative technologies and therapeutic approaches for the regeneration and repair of damaged tissues and organs. The interactions of biomaterials with cells and tissue, especially with stem cells, will be of particular focus.
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