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首页> 外文期刊>Journal of biomaterials science >Development of cultured dermal substitute composed of hyaluronic acid and collagen spongy sheet containing fibroblasts and epidermal growth factor
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Development of cultured dermal substitute composed of hyaluronic acid and collagen spongy sheet containing fibroblasts and epidermal growth factor

机译:由透明质酸和含有成纤维细胞和表皮生长因子的胶原蛋白海绵片组成的真皮替代培养物的开发

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摘要

The present study aimed to develop a two-layered cultured dermal substitute (CDS). The upper layer is a hyaluronic acid (HA) and collagen (Col) spongy sheet with or without epidermal growth factor (EGF). The lower layer is a HA spongy sheet and Col gel containing fibroblasts. The CDS is prepared in serum-free medium, followed by placing on the wound surface. Corresponding to clinical application, CDS was incubated in serum-free medium for a period of 1, 3 or 5 days, followed by placing onto the air and culture medium interface (wound surface model), and culture for 6 days using conventional culture medium supplemented with serum. Metabolic activity and cytokine production were considerably higher in EGF-incorporating CDS, as compared with EGF-free CDS. Metabolic activity of EGF-incorporating CDS was maintained for a period of 3 days, but decreased slightly after 5 days. EGF-incorporating CDS is able to effectively stimulate fibroblasts within CDS to release increased amounts of vascular endothelial growth factor and hepatocyte growth factor, which are essential for wound healing. CDS is promising for wound therapy, because there is no risk of cellular damage caused by cryopreservation, thawing and rinsing processes. The critical issue is how to reduce the cellular damage during a prolonged period of incubation in serum-free medium. EGF-incorporating CDS can be used after a period of 3-5 days incubation in serum-free medium. This period is sufficient for transport of CDS from manufacturing facilities to hospitals.
机译:本研究旨在开发两层培养的真皮替代品(CDS)。上层是带有或不带有表皮生长因子(EGF)的透明质酸(HA)和胶原蛋白(Col)海绵片。下层是HA海绵片和含有成纤维细胞的Col凝胶。在无血清培养基中制备CDS,然后将其置于伤口表面。根据临床应用,将CDS在无血清培养基中孵育1、3或5天,然后放置在空气和培养基界面(伤口表面模型)上,并使用添加了常规培养基的培养基培养6天与血清。与不含EGF的CDS相比,掺有EGF的CDS的代谢活性和细胞因子产生要高得多。掺有EGF的CDS的代谢活性维持3天,但5天后略有下降。整合有EGF的CDS能够有效刺激CDS中的成纤维细胞释放出增加量的血管内皮生长因子和肝细胞生长因子,这对于伤口愈合至关重要。 CDS有望用于伤口治疗,因为不存在因冷冻保存,解冻和冲洗过程而造成细胞损伤的风险。关键问题是如何在无血清培养基中长时间孵育期间减少细胞损伤。在无血清培养基中孵育3-5天后,可以使用掺有EGF的CDS。此期间足以将CDS从制造设施运输到医院。

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