Li Tao, Tang Juan, Li Changfen, Liu Guogang, Li Ying, Guo Shanlan, Fang Qilin, Li Jing, Qi Xing, Liu Xingde, Du Juan, Zhang Dan, Xiong Silun, Li Jiaqian, Tan Yueyue, Li Biao, Dai Chuanqiang, Zhang Qinqin, Li Jiaman, Wu Xiaoli
Department of Ophthalmology, Zi Yang Central Hospital, Sichuan, China.
Department of Ophthalmology, Key Laboratory of Ophthalmology, Zi Yang Central Hospital, Sichuan, China.
Ann Med. 2025 Dec;57(1):2436458. doi: 10.1080/07853890.2024.2436458. Epub 2024 Dec 5.
To prepare a polyglycolic acid-loaded mitomycin drug (MMC-ATS-@PLGA) to inhibit scar proliferation after glaucoma filtering surgery (GFS) an anti-inflammatory mechanism that minimally affected intraocular pressure, which provided another therapeutic strategy for this disease.
We first detected the physicochemical properties of MMC-ATS-@PLGA. Next, we tested the biosafety of MMC-ATS-@PLGA and . Then, we assessed the therapeutic effects of MMC-ATS-@PLGA by laboratory and clinical examinations.
In this study, we synthesized a new type of nanomedicine (MMC-ATS-@PLGA) with good stability and biocompatibility for inhibiting scar proliferation after GFS. The break-up time (BUT), Schimer test and intraocular pressure changes in GFS rabbits before and after treatment with MMC-ATS-@PLGA were not significantly different. Three weeks after GFS, the MMC-ATS-@PLGA group displayed significant decreases in nuclear volume, corneal cell oedema, type I and III collagen fibre expression, normal organelle morphology and collagen fibre arrangement. Compared with those in the FML and MMC groups, the α-SMA, CTGF and type III collagen fibres in the MMC-ATS-@PLGA group decreased more significantly, indicating that MMC-ATS-@PLGA can effectively inhibit the expression of these inflammatory factors during the inhibition of scar proliferation after GFS.
We successfully synthesized MMC-ATS-@PLGA, which could effectively inhibit scar proliferation after GFS anti-inflammatory effects but had little effect on intraocular pressure. This new type of nanomedicine has good biosafety and stability and is worthy of further exploration in clinical practice.
制备载有丝裂霉素的聚乙醇酸药物(MMC-ATS-@PLGA),以抑制青光眼滤过手术后(GFS)的瘢痕增殖,其抗炎机制对眼压影响极小,为该疾病提供了另一种治疗策略。
我们首先检测了MMC-ATS-@PLGA的理化性质。接下来,我们测试了MMC-ATS-@PLGA的生物安全性。然后,我们通过实验室和临床检查评估了MMC-ATS-@PLGA的治疗效果。
在本研究中,我们合成了一种新型纳米药物(MMC-ATS-@PLGA),它具有良好的稳定性和生物相容性,可抑制GFS后的瘢痕增殖。MMC-ATS-@PLGA治疗前后GFS兔的泪膜破裂时间(BUT)、泪液分泌试验和眼压变化无显著差异。GFS三周后,MMC-ATS-@PLGA组的细胞核体积、角膜细胞水肿、I型和III型胶原纤维表达显著降低,细胞器形态和胶原纤维排列正常。与氟米龙(FML)和丝裂霉素(MMC)组相比,MMC-ATS-@PLGA组的α-平滑肌肌动蛋白(α-SMA)、结缔组织生长因子(CTGF)和III型胶原纤维下降更显著,表明MMC-ATS-@PLGA在抑制GFS后瘢痕增殖过程中能有效抑制这些炎症因子的表达。
我们成功合成了MMC-ATS-@PLGA,它能有效抑制GFS后的瘢痕增殖,具有抗炎作用,但对眼压影响较小。这种新型纳米药物具有良好的生物安全性和稳定性,值得在临床实践中进一步探索。