Department of Biosystems & Biomaterials Science and Engineering, Seoul National University, Seoul 151-742, Republic of Korea.
Biomater Sci. 2018 Jan 30;6(2):364-371. doi: 10.1039/c7bm01061c.
Damage to the eardrum causes acute pain and can lead to chronic otitis media if it develops into chronic tympanic membrane (TM) perforations. Chronic TM perforations are usually treated with surgical methods such as tympanoplasty and myringoplasty. However, these surgeries are not only complicated and difficult but also cost a lot of money. Our research team developed chitosan patches (E-CPs) that release epidermal growth factor (EGF) as a patch therapy to replace surgical methods. However, there was a limitation in the healing ratio of the treatment compared to the surgical methods. In this study, we developed EGF and epidermal growth factor receptor (EGFR) gene-releasing polyethyleneimine (PEI)/chitosan patches (EErP-CPs) to increase the regeneration of TM perforations. The addition of PEI increased the adhesion and migration ability of TM cells on the patches. The simultaneous release of the EGF and the EGFR gene further enhanced TM cell proliferation, adhesion and migratory ability. It was confirmed that the EGF protein and EGFR gene were released for 30 days; however, EGF was released and increased TM cell viability almost immediately after treatment and EGFR took a minimum of 3 days before showing its effect on improved cell viability. It was also shown that EErP-CPs are more hydrophilic and have more positive charge than E-CP because of added amine groups from PEI. In conclusion, the developed EErP-CPs resulted in the improved healing of TM perforations and can potentially be applied to the regeneration of both chronic and acute tympanic membrane perforations.
鼓膜损伤会引起急性疼痛,如果发展为慢性鼓膜穿孔,可能导致慢性中耳炎。慢性鼓膜穿孔通常采用鼓室成形术和鼓膜成形术等手术方法治疗。然而,这些手术不仅复杂且困难,而且费用高昂。我们的研究团队开发了壳聚糖贴片(E-CPs),作为一种贴片疗法来释放表皮生长因子(EGF),以替代手术方法。然而,与手术方法相比,治疗的愈合率存在一定的局限性。在这项研究中,我们开发了释放表皮生长因子(EGF)和表皮生长因子受体(EGFR)基因的聚乙烯亚胺(PEI)/壳聚糖贴片(EErP-CPs),以增加鼓膜穿孔的再生。PEI 的添加提高了 TM 细胞在贴片上的黏附和迁移能力。EGF 和 EGFR 基因的同时释放进一步增强了 TM 细胞的增殖、黏附和迁移能力。研究证实,EGF 蛋白和 EGFR 基因可释放 30 天;然而,EGF 在治疗后几乎立即释放并增加 TM 细胞活力,而 EGFR 则需要至少 3 天才能显示其对提高细胞活力的作用。还表明,由于添加了来自 PEI 的胺基,EErP-CPs 比 E-CP 具有更高的亲水性和正电荷。总之,开发的 EErP-CPs 可改善鼓膜穿孔的愈合,并且可能潜在地应用于慢性和急性鼓膜穿孔的再生。