Thermosensitive Polyhedral Oligomeric Silsesquioxane Hybrid Hydrogel Enhances the Antibacterial Efficiency of Erythromycin in Bacterial Keratitis

Author:

Zheng Lan1,Chen Ying2,Han Yi13,Lin Jingwei1,Fan Kai2,Wang Mengyuan1,Teng Ting3,Yang Xiuqin2,Ke Lingjie2,Li Muyuan4,Guo Shujia1,Li Zibiao5,Wu Yunlong2,Li Cheng145ORCID

Affiliation:

1. Fujian Provincial Key Laboratory of Ophthalmology and Visual Science & Ocular Surface and Corneal Diseases, Eye Institute & Affiliated Xiamen Eye Center & Affiliated First Hospital, School of Medicine, Xiamen University, Xiamen 361102, PR China.

2. Fujian Provincial Key Laboratory of Innovative Drug Target Research and State Key Laboratory of Cellular Stress Biology, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, PR China.

3. Department of Ophthalmology, The First Affiliated Hospital of University of South China, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, PR China.

4. Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan 250117,Shandong Province, PR China.

5. Huaxia Eye Hospital of Quanzhou, Quanzhou, Fujian 362000, China.

Abstract

Bacterial keratitis is a serious ocular infection that can impair vision or even cause blindness. The clinical use of antibiotics is limited due to their low bioavailability and drug resistance. Hence, there is a need to develop a novel drug delivery system for this infectious disease. In this study, erythromycin (EM) was encapsulated into a bifunctional polyhedral oligomeric silsesquioxane (BPOSS) with the backbone of the poly-PEG/PPG urethane (BPEP) hydrogel with the aim of improving the drug efficiency in treating bacterial keratitis. A comprehensive characterization of the BPEP hydrogel was performed, and its biocompatibility was assessed. Furthermore, we carried out the evaluation of the antimicrobial effect of the BPEP-EM hydrogel in S. aureus keratitis using in vivo mouse model. The BPEP hydrogel exhibited self-assembling and thermogelling properties, which assisted the drug loading of drug EM and improved its water solubility. Furthermore, the BPEP hydrogel could effectively bind with mucin on the ocular surface, thereby markedly prolonging the ocular residence time of EM. In vivo testing confirmed that the BPEP-EM hydrogel exerted a potent therapeutic action in the mouse model of bacterial keratitis. In addition, the hydrogel also exhibited an excellent biocompatibility. Our findings demonstrate that the BPEP-EM hydrogel showed a superior therapeutic effect in bacterial keratitis and demonstrated its potential as an ophthalmic formulation.

Funder

The National Key R&D Program of China

the National Natural Science Foundation of China

Natural Science Foundation of Fujian Province of China

J01046), the Fundamental Research Funds for the Central Universities

the Huaxia Translational Medicine Fund for Young Scholars

Publisher

American Association for the Advancement of Science (AAAS)

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