A methacrylated hyaluronic acid network reinforced Pluronic F-127 gel for treatment of bacterial keratitis

被引:6
|
作者
Wang, Anyang [1 ]
Dong, Lina [2 ]
Guo, Zhongwei [1 ,2 ]
Sun, Wei [1 ,2 ,3 ,4 ]
Mi, Shengli [1 ]
机构
[1] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Precis Med & Healthcare Res Ctr, Tsinghua Berkeley Shenzhen Inst, Shenzhen 518055, Peoples R China
[3] Tsinghua Univ, Dept Mech Engn & Mech, Beijing 100084, Peoples R China
[4] Drexel Univ, Dept Mech Engn, Philadelphia, PA 19104 USA
关键词
Pluronic F-127; hyaluronic acid (HA); ocular drug delivery; DRUG-DELIVERY; CONTROLLED-RELEASE; HYDROGELS; SYSTEMS; DISSOLUTION;
D O I
10.1088/1748-605X/ac6ea9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, we developed a novel in situ thermoresponsive gel by introducing crosslinked methacrylated hyaluronic acid (HA-MA) networks into Pluronic F-127 (PF-127) gel (HP gel) to achieve sustained levofloxacin (LFX) delivery in bacterial keratitis treatment. The interactions between PF-127 molecules and HA-MA networks were studied by scanning electron microscopy, rheology, dynamic light scattering, differential scanning calorimetry, and small angle x-ray scattering. The results showed that the HP gel exhibited a higher critical gelling temperature and lower viscosity than the PF-127 gel (P gel), and could form a uniform thin layer on the ocular surface. Moreover, the drug release profile and gel dissolution rate revealed that the HA-MA network could retard the diffusion and dissolution of drug molecules and prolong the drug release time, which corresponded to an enhanced antibacterial ability of the HP-LFX gel. Furthermore, the HP gel exhibited low cytotoxicity to human corneal epithelial cells. Finally, an in vivo pharmacodynamic study was conducted with rabbit keratitis models. An improved treatment efficacy was observed after application of the HP-LFX gels. This study highlights the potential of HP gels in ophthalmic drug delivery.
引用
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页数:15
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