Weßollek Katharina, Marquardt Yvonne, Wagner-Schiffler Sylvia, Baron Jens Malte, Huth Sebastian
Department of Dermatology and Allergology, University Hospital RWTH Aachen, Aachen, Germany.
Praxis für Dermatologie, Aachen, Germany.
Clin Cosmet Investig Dermatol. 2023 Jun 14;16:1533-1538. doi: 10.2147/CCID.S409310. eCollection 2023.
In vitro study on the molecular effects of post-treatment after micro-needling applications with a dexpanthenol-containing ointment (DCO) using 3D skin models.
In this in vitro study, full-thickness human 3D skin models were treated with a micro-needling device according to its clinical application. For post-treatment, some of the models were additionally treated with a dexpanthenol-containing ointment (DCO). Histological samples were taken at 0, 24 and 48 hours. Gene expression analysis was performed after 24 hours.
Histological examination showed that DCO post-treated 3D skin models revealed a completed wound closure 24 hours after the micro-needling procedure. In contrast, DCO-untreated models still clearly exhibited the micro-needling lesions after the same period of time. After 48 hours, all models revealed a completed wound healing. In skin models that received micro-needling but no post-treatment with DCO, microarray analysis identified an upregulation of proinflammatory cytokines and chemokines and a downregulation of skin barrier and differentiation markers. In contrast, post-treatment with DCO leads to accelerated wound healing without affecting the initial inflammatory response caused by micro-needling, which leads to the subsequent collagen expression. This data was supported by qRT-PCR analyses.
Post-treatment with DCO accelerates epidermal wound healing after micro-needling of 3D skin models without impairing the immunostimulatory properties of micro-needling. These findings can help to optimise the aftercare routine after micro-needling procedures and to shorten the downtime for the patient after treatment.
使用含泛醇的软膏(DCO)对微针治疗后的分子效应进行体外研究,采用3D皮肤模型。
在这项体外研究中,根据临床应用,使用微针装置对全层人3D皮肤模型进行治疗。对于后续治疗,部分模型额外使用含泛醇的软膏(DCO)进行处理。在0、24和48小时采集组织学样本。24小时后进行基因表达分析。
组织学检查显示,DCO处理后的3D皮肤模型在微针治疗24小时后伤口完全闭合。相比之下,未用DCO处理的模型在同一时间段仍明显可见微针损伤。48小时后,所有模型均显示伤口完全愈合。在接受微针治疗但未用DCO进行后续治疗的皮肤模型中,微阵列分析发现促炎细胞因子和趋化因子上调,皮肤屏障和分化标志物下调。相比之下,用DCO进行后续治疗可加速伤口愈合,且不影响微针引起的初始炎症反应,进而促进随后的胶原蛋白表达。定量逆转录聚合酶链反应(qRT-PCR)分析支持了该数据。
用DCO进行后续治疗可加速3D皮肤模型微针治疗后的表皮伤口愈合,且不损害微针的免疫刺激特性。这些发现有助于优化微针治疗后的护理程序,并缩短患者治疗后的恢复时间。