Fabrication of carboxymethyl cellulose-based thermo-sensitive hydrogels and inhibition of corneal neovascularization

羧甲基纤维素 自愈水凝胶 角膜新生血管 新生血管 化学 生物相容性 药物输送 泊洛沙姆 角膜 药理学 生物医学工程 材料科学 高分子化学 眼科 血管生成 纳米技术 有机化学 医学 聚合物 癌症研究 共聚物
作者
Yongyan Yang,Weijin Nan,Ruiting Zhang,Sitong Shen,Meiliang Wu,Shuangling Zhong,Yan Zhang,Xuejun Cui
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:261: 129933-129933 被引量:9
标识
DOI:10.1016/j.ijbiomac.2024.129933
摘要

Corneal neovascularization (CNV) is a common multifactorial sequela of anterior corneal segment inflammation, which could lead to visual impairment and even blindness. The main treatments available are surgical sutures and invasive drug injections, which could cause serious ocular complications. To solve this problem, a thermo-sensitive drug-loaded hydrogel with high transparency was prepared in this study, which could achieve the sustained-release of drugs without affecting normal vision. In briefly, the thermo-sensitive hydrogel (PFNOCMC) was prepared from oxidized carboxymethyl cellulose (OCMC) and aminated poloxamer 407 (PF127-NH2). The results proved the PFNOCMC hydrogels possess high transparency, suitable gel temperature and time. In the CNV model, the PFNOCMC hydrogel loading bone morphogenetic protein 4 (BMP4) showed significant inhibition of CNV, this is due to the hydrogel allowed the drug to stay longer in the target area. The animal experiments on the ocular surface were carried out, which proved the hydrogel had excellent biocompatibility, and could realize the sustained-release of loaded drugs, and had a significant inhibitory effect on the neovascularization after ocular surface surgery. In conclusion, PFNOCMC hydrogels have great potential as sustained-release drug carriers in the biomedical field and provide a new minimally invasive option for the treatment of neovascular ocular diseases.
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