首页> 外文期刊>Wound repair and regeneration: official publication of the Wound Healing Society [and] the European Tissue Repair Society >Topical application of a film-forming emulgel dressing that controls the release of stratifin and acetylsalicylic acid and improves/prevents hypertrophic scarring
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Topical application of a film-forming emulgel dressing that controls the release of stratifin and acetylsalicylic acid and improves/prevents hypertrophic scarring

机译:成膜emulgel局部应用控制释放stratifin敷料和乙酰水杨酸,改善/阻止肥厚性疤痕

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摘要

Here, we evaluate the efficacy of an emulgel dressing to control the release of an antifibrogenic factor, stratifin (SFN), along with an anti-inflammatory drug, acetylsalicylic acid (ASA), to be used as a wound dressing with hypertrophic scar reducing features. Emulgel dressings were prepared by dispersing positively charged submicron vesicles in carboxymethyl cellulose gel. Release kinetics of SFN/ASA and toxicity for primary skin cells were assessed in vitro. Antifibrogenic efficacy of medicated emulgel dressings was tested on a rabbit ear fibrotic model. Following topical application on the wounds, emulgels formed an occlusive film and controlled the release of SFN and ASA for 7 and 24 hours, respectively. Wounds treated with SFN/ASA-containing emulgel dressings showed an 80% reduction in scar elevation compared with untreated controls. Topical formulations were nontoxic for cultured human keratinocytes and fibroblasts. Inflammation was significantly controlled in treated wounds, as shown by a reduced number of infiltrated CD3+ T cells (p 0.001) and macrophages. SFN/ASA-treated wounds showed a significantly higher (p 0.001) expression of matrix metalloproteinase-1, resulting in reduced collagen deposition and less scarring. Film-forming emulgel dressings that control the release of antifibrogenic and anti-inflammatory factors provide an excellent treatment option for postburn hypertrophic scar management.
机译:在这里,我们评估emulgel的功效酱来控制的释放antifibrogenic因素,stratifin (SFN)乙酰水杨酸的抗炎药物酸(ASA),作为伤口敷料肥厚性疤痕减少功能。敷料被分散积极准备亚微米囊泡在羧甲基纤维素凝胶。为原发性皮肤细胞毒性进行评估体外。兔耳emulgel酱进行了测试纤维化的模型。伤口,emulgels形成一个闭塞的电影控制SFN的释放,为7和亚撒分别为24小时。SFN / ASA-containing emulgel敷料显示海拔相比减少80%的疤痕未经处理的控制。人工培养的角质细胞和无毒的成纤维细胞。控制在治疗伤口,如图所示渗透CD3 + T细胞的数量减少(p& 伤口显示显著提高(p & 0.001)的矩阵metalloproteinase-1的表达,导致减少胶原蛋白沉积和更少疤痕。控制释放antifibrogenic和抗炎因子提供了一个很好的治疗选择postburn肥厚性疤痕管理。

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