Zeolitic Imidazolate Framework-8 Offers an Anti-Inflammatory and Antifungal Method in the Treatment of Aspergillus Fungal Keratitis in vitro and in vivo

被引:2
作者
Fu, Xueyun [1 ]
Tian, Xue [1 ]
Lin, Jing [1 ]
Wang, Qian [1 ]
Gu, Lingwen [1 ]
Wang, Ziyi [1 ]
Chi, Menghui [1 ]
Yu, Bing [1 ]
Feng, Zhuhui [1 ]
Liu, Wenyao [1 ]
Zhang, Lina [1 ]
Li, Cui [1 ]
Zhao, Guiqiu [1 ]
机构
[1] Qingdao Univ, Dept Ophthalmol, Affiliated Hosp, 16 Jiangsu Rd, Qingdao 266003, Shandong, Peoples R China
来源
INTERNATIONAL JOURNAL OF NANOMEDICINE | 2024年 / 19卷
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
fungal keratitis; MOFs; antifungal; anti-inflammatory; ZIF-8; METAL-ORGANIC-FRAMEWORK; ZIF-8; NANOPARTICLES; MACROPHAGES; FUSARIUM; BACTERIA; BIOFILM; RELEASE; CARRIER; SYSTEM;
D O I
10.2147/IJN.S480800
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Fungal keratitis is a serious blinding eye disease. Traditional drugs used to treat fungal keratitis commonly have the disadvantages of low bioavailability, poor dispersion, and limited permeability. Purpose: To develop a new method for the treatment of fungal keratitis with improved bioavailability, dispersion, and permeability. Methods: Zeolitic Imidazolate Framework-8 (ZIF-8) was formed by zinc ions and 2-methylimidazole linked by coordination bonds and characterized by Scanning electron microscopy (SEM), X-ray diffraction (XRD), and Zeta potential. The safety of ZIF-8 on HCECs and RAW 264.7 cells was detected by Cell Counting Kit-8 (CCK-8). Safety evaluation of ZIF-8 on mice corneal epithelium was conducted using the Draize corneal toxicity test. The effects of ZIF-8 on fungal growth, biofilm formation, and hyphae structure were detected by Minimal inhibit concentration (MIC), crystal violet staining, Propidium Iodide (PI) testing, and calcofluor white staining. The anti-inflammatory effects of ZIF-8 on RAW 246.7 cells were evaluated by Quantitative Real-Time PCR Experiments (qPCR) and Enzyme-linked immunosorbent assay (ELISA). Clinical score, Colony-Forming Units (CFU), Hematoxylin-eosin (HE) staining, and immunofluorescence were conducted to verify the therapeutic effect of ZIF-8 on C57BL/6 female mice with fungal keratitis. Results: In vitro, ZIF-8 showed outstanding antifungal effects, including inhibiting the growth of Aspergillus fumigatus over 90% at 64 mu g/mL, restraining the formation of biofilm, and destroying cell membranes. In vivo, treatment with ZIF-8 reduced corneal fungal load and mitigated neutrophil infiltration in fungal keratitis, which effectively reduced the severity of keratitis in mice and alleviated the infiltration of inflammatory factors in the mouse cornea. In addition, ZIF-8 reduces the inflammatory response by downregulating the expression of pro-inflammatory cytokines TNF-alpha, IL-6, and IL-1 beta after Aspergillus fumigatus infection in vivo and in vitro. Conclusion: ZIF-8 has a significant anti-inflammatory and antifungal effect, which provides a new solution for the treatment of fungal keratitis.
引用
收藏
页码:11163 / 11179
页数:17
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