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Rat model for chronic tympanic membrane perforation and the efficiency of chitosan patch scaffold for treatment

机译:慢性鼓膜膜穿孔的大鼠模型及壳聚糖贴片支架治疗的效率

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The common treatments of chronic otitis media (COM) are surgeries including myringoplasty or tympanoplasty. However, for some patients the risks, costs, and inconvenience of an operation are of significant concerns. Therefore, the development of a simple, effective, and inexpensive outpatient procedure has been needed as the substitute for surgical procedures. Unfortunately, however, reliable models for chronic tympanic membrane (TM) perforation have not yet been established until now. Many attempts have been made for manufacturing chronic TM perforations in animal models; an infolding technique in chinchillas (Amoils et al., 1992), local application of hydrocortisone (Spandow and Hellstrom, 1993), local application of mitomycin C in rats (Estrem and Batra, 1999), local application of mitomycin C and hydrocortisone (Cui et al., 2005), and local application of 5-fluorouracil (Cincik et al., 2005), etc. Several scaffolds, such as hydrogels or collagen, that could stimulate tympanic regeneration, guide eardrum growing, or replace the perforated defects, have recently been introduced for alternative methods of paper patches. However, all previous methods have disadvantages as well as advantages and limitations for clinical application in cases of chronic TM perforations. Chitosan has been suggested to have the proper characteristics as a scaffold for treatment of TM perforation (Kim et al., 2008). We previously showed that a chitosan patch scaffold (CPS) was more effective than spontaneous healing to repair acute and traumatic TM perforations (Kim et al., 2008). The objectives of this study were to develop animal models for chronic TM perforations which could be maintained for at least more than 8 weeks and to assessed the healing efficiency of CPS using animal models by comparing with paper patches.
机译:慢性上耳炎常见的常见治疗(COM)是包括灭弧剂或鼓膜形状的手术。但是,对于某些患者,运作的风险,成本和不便具有重要意义。因此,已经需要开发简单,有效和廉价的门诊过程作为外科手术的替代品。然而,迄今为止,尚未建立慢性鼓膜膜(TM)穿孔的可靠模型。在动物模型中制造慢性TM穿孔进行了许多尝试; Chinchillas(Amoots等,1992)中的一种肾上腺化技术,局部应用氢化体(Spandow和Hellstrom,1993),大鼠丝霉素C的局部应用(Estrem和Batra,1999),拟霉素C和氢化可源性的局部应用(Cui等人,2005),以及5-氟尿嘧啶的局部应用(Cincik等,2005)等。多种支架,如水凝胶或胶原蛋白,可以刺激鼓膜再生,导膜生长,或取代穿孔缺陷,最近被引入替代纸质补丁方法。然而,所有以前的方法都具有缺点以及在慢性TM穿孔的情况下的临床应用的优缺点。壳聚糖已经建议具有适当的特征作为用于治疗TM穿孔的支架(Kim等人,2008)。我们以前表明,壳聚糖贴片支架(CPS)比自发愈合更有效,以修复急性和创伤性TM穿孔(Kim等,2008)。本研究的目的是为慢性TM穿孔进行动物模型,其可以保持至少超过8周并通过与纸贴片进行比较来评估使用动物模型的CPS的愈合效率。

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