Preparation, characterization, and in vitro/vivo evaluation of a multifunctional electrode coating for cochlear implants

被引:1
|
作者
Xu, Muqing [1 ,2 ]
Chen, Anning [1 ,2 ]
Chen, Dongxiu [1 ,2 ]
Wu, Shengquan [1 ]
Deng, Zhipeng [1 ]
Wen, Hang [1 ]
Zhong, Huiling [1 ]
Lu, Kejin [1 ]
Tang, Jie [1 ,2 ,3 ,4 ]
Ma, Dong [5 ]
Zhang, Hongzheng [1 ,2 ]
机构
[1] Southern Med Univ, Zhujiang Hosp, Dept Otolaryngol Head & Neck Surg, Guangzhou 510282, Peoples R China
[2] Southern Med Univ, Zhujiang Hosp, Ear Res Inst, Guangzhou 510282, Peoples R China
[3] Southern Med Univ, Sch Basic Med Sci, Dept Physiol, Guangzhou 510515, Peoples R China
[4] Southern Med Univ, Key Lab Mental Hlth, Minist Educ, Guangzhou 510515, Peoples R China
[5] Jinan Univ, Guangdong Prov Engn & Technol Res Ctr Drug Carrier, Key Lab Biomat Guangdong Higher Educ Inst, Dept Biomed Engn, Guangzhou 510632, Peoples R China
来源
BIOMATERIALS ADVANCES | 2024年 / 157卷
基金
中国国家自然科学基金;
关键词
Cochlear implantation; Electrode coating; Delivery system; Poly(trimethylene carbonate); Dexamethasone; DRUG-DELIVERY; DEXAMETHASONE; HEARING; NANOPARTICLES; SILICONE; RELEASE;
D O I
10.1016/j.bioadv.2023.213736
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Cochlear implantation (CI) is the primary intervention for patients with sensorineural hearing loss to restore their hearing. However, approximately 90 % of CI recipients experience unexpected fibrosis around the inserted electrode arrays due to acute and chronic inflammation. This fibrosis leads to progressive residual hearing loss. Addressing this complication is crucial for enhancing CI outcomes, yet an effective treatment has not yet been found. In this study, we developed a multifunctional dexamethasone (DXM)-loaded polytrimethylene carbonate (PTMC) electrode coating to mitigate inflammatory reactions and fibrosis after CI. This thin and flexible coating could preserve the mechanical performance of the electrode and reduce the implantation resistance for CI. The in vitro release studies demonstrated the DXM-PTMC coating's efficient drug loading and sustained release capa-bility over 90 days. DXM-PTMC also showed long-term stability, high biocompatibility, and effective anti-inflammatory effects in vitro and in vivo. Compared with the uncoated group, DXM-PTMC coating significantly inhibited the expression of inflammatory factors, such as NO, TNF-alpha, IL-1 beta, and IL-6. DXM-PTMC coating sup-pressed fibrosis in rat implantation models for 3 weeks by reducing both acute and chronic inflammation. Our findings suggest that DXM-PTMC coating is a novel strategy to improve the outcomes of CI.
引用
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页数:9
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