眼科 ›› 2025, Vol. 34 ›› Issue (4): 272-278.doi: 10.13281/j.cnki.issn.1004-4469.2025.04.004

• 论著 • 上一篇    下一篇

PLGA负载丝裂霉素C纳米粒抑制青光眼术后纤维增生的安全性及治疗效果的体外研究

李涛1   赵玲2   曹会蓉3   杨雪1   熊思伦1   刘国刚4   唐娟1

  

  1. 1资阳市中心医院眼科(含重点实验室),四川资阳 641300; 2四川省资阳市乐至县人民医院眼科,四川资阳 641300;3简阳市中医医院外二科,四川简阳 641400;4资阳市中心医院皮肤科,四川资阳 641300
  • 收稿日期:2024-05-27 出版日期:2025-07-25 发布日期:2025-07-13
  • 通讯作者: 唐娟, Email: 874548166@qq.com
  • 基金资助:
    2024年度四川省医学会医学科研项目和青年创新项目(Q2024062);2024年度四川省医疗卫生与健康促进会科研项目(KY2024QN0082)

Safety and efficacy evaluation of poly lactic-co-glycolic acid loaded mitomycin nanoparticles in inhibiting postoperative fiber proliferation in glaucoma surgery in vitro research 

Li Tao1, Zhao Ling2, Cao Huirong3, Yang Xue1, Xiong Silun1, Liu Guogang4, Tang Juan1   

  1. 1 Department of Ophthalmology (Key Laboratory), Ziyang Central Hospital, Ziyang Sichuan 641300, China; 
    2 Department of Ophthalmology, Lezhi County People's Hospital, Ziyang Sichuan 641300, China; 3 Department of External Medicine, Jianyang Chinese Medicine Hospital, Jianyang Sichuan 641400, China; 4 Department of Dermatology, Ziyang Central Hospital, Ziyang Sichuan 641300, China
  • Received:2024-05-27 Online:2025-07-25 Published:2025-07-13
  • Contact: Tang Juan, Email: 874548166@qq.com
  • Supported by:
    Medical Research Projects and Youth Innovation Projects of Sichuan Medical Association in 2024(Q2024062); Research Project of Sichuan Medical and Health Promotion Association in 2024 (KY2024QN0082)

摘要:  目的  制备一种以聚乳酸-羟基乙酸共聚物(PLGA)为载体,丝裂霉素C(MMC)搭载于PLGA的纳米药物MMC-ATS-@PLGA,并从体外实验角度分析该纳米药物对于青光眼术后抑制纤维增生的生物安全性和抗炎效果。设计  实验研究。研究对象  兔结膜成纤维细胞(RCF)。方法  采用薄膜分散-水化超声法制备纳米药物MMC-ATS-@PLGA。检测MMC-ATS-@PLGA物理和化学性质,通过CCK-8和Cam PI细胞活/死染色法评估MMC-ATS-@PLGA对RCF活性的影响,采用流式细胞术、细胞免疫荧光法、q-PCR等角度对比分析氟米龙滴眼液(FML)、MMC和MMC-ATS-@PLGA纳米粒在炎症化RCF细胞中体外抗炎效果。主要指标  物理和化学性质、细胞活性、抗炎效果。结果  MMC-ATS-@PLGA平均粒径和电位为(128.78±2.54)nm和(36.49±4.25)mV,其包封率和载药率分别为(78.49±2.75)% 和(30.86±1.84)%;在33℃(眼表温度)条件下,MMC-ATS-@PLGA纳米粒经过600 min累计释放可达(76.58±2.68)%。同时细胞形态学和流式细胞术结果显示,MMC-ATS-@PLGA可有效促进炎症化RCF细胞凋亡,细胞形态将变小,细胞核呈现固缩的表现。从细胞免疫荧光法和Q-PCR实验角度证实炎症化RCF细胞与FML、MMC和MMC-ATS-@PLGA共同孵育24小时后,炎性因子α-SMA、CTGF和 III型胶原纤维的表达强度呈逐渐下降趋势,其中MMC-ATS-@PLGA组的表达强度下降最为显著(P均<0.05)。结论  本研究成功合成一种抑制青光眼术后瘢痕增生的纳米药物MMC-ATS-@PLGA,该纳米药物细胞毒性明显降低,体外抗炎效果增强,为青光眼术后抑制纤维增生,提高手术成功率提供了一种新的治疗思路。

关键词:  青光眼;丝裂霉素C;聚乳酸-羟基乙酸共聚物, 纳米医学;抗炎

Abstract: Objective  To prepare a nano medicine(MMC-ATS-@PLGA) with poly lactic-co-glycolic acid (PLGA) as the carrier, mitomycin C (MMC) loading on the PLGA, and analyze the biological safety and anti-inflammatory effect of MMC-ATS-@PLGA on inhibiting the fiber proliferation after glaucoma surgery from an in vitro experimental perspective. Design  Experimental research. Participants  Rabbit conjunctival fibroblasts (RCF). Methods  The thin film dispersion hydration ultrasound method was used to prepare nano drug MMC-ATS-@PLGA. The physical and chemical properties of MMC-ATS-@PLGA were detected. The effect of MMC-ATS-@-PLGA on the activity of rabbit conjunctival fibroblasts (RCF)was evaluated using CCK-8 and Cam PI cell viability staining. The flow cytometry, cell immunofluorescence, q-PCR, and other methods from multiple perspectives were used to compare the anti-inflammatory effects of flumiolone eye drops (FML), MMC, and MMC-ATS-@PLGA nanoparticles on inflamed RCF cells in vitro research. Main Outcome Measures  Physical and chemical properties, RCF activity, anti-inflammatory effects. Results  The average particle size and zeta potential of MMC-ATS-@PLGA are (128.78±2.54) nm and 36.49±4.25) mV, with encapsulation efficiency and drug loading rate of (78.49±2.75) % and (30.86±1.84) %, respectively. Under the condition of 33℃ (ocular surface temperature), the cumulative release of MMC-ATS-@PLGA nanoparticles can reach (76.58±2.68) % after 600 minutes. The cell morphology and flow cytometry results showed that MMC-ATS-@PLGA can effectively promote the apoptosis of inflammatory RCF cells, resulting in smaller cell morphology and a pyknotic appearance of the nucleus. Further research confirmed from the perspectives of cell immunofluorescence and Q-PCR experiments that after inflammatory RCF cells co-incubation with FML, MMC, and MMC-ATS-@PLGA for 24 hours, the expression intensity of α-SMA, CTGF, and type III collagen fiber showed a gradually decreasing trend, with the MMC-ATS-@PLGA group showing the most significant decrease , and the difference was statistically significant (all P<0.05). Conclusion  This study successfully synthesized a nanomedicine MMC-ATS-@PLGA that can inhibit the scar proliferation after glaucoma surgery. The cytotoxicity of this nano-drug was significantly reduced, and the anti-inflammatory effect in vitro was enhanced. This research provided a new treatment approach for anti-scar proliferation and improving surgical success rate after glaucoma surgery.

Key words:  Glaucoma, Mitomycin C, Poly lactic-co-glycolic acid, Nanomedicine, Anti-inflammation