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A facile and efficient approach for hypertrophic scar therapyviaDNA-based transdermal drug delivery

机译:肥厚性的简单和有效的方法疤痕therapyviaDNA-based皮肤药交付

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The transdermal drug delivery approach has been considered a potential therapy for human hypertrophic scars (HSs) instead of current uncomfortable surgical excision, local injection and laser therapy. However, a facile and efficient drug delivery method is urgently needed to overcome the skin barrier of transdermal administration. Herein, we employed a DNA-Fe nanoparticle delivery systemviaFe ion driven self-assembly to satisfy the requirement of transdermal administration for HS therapy. Doxorubicin hydrochloride (DOX) as one of the widely used anticancer drugs was employed to treat the hyperplasia of abnormal skin fibrous tissue. Bothin vitroandin vivoexperiments of the DOX loaded DNA-Fe nanoparticles (DOX@DNA-Fe NPs) were performed to demonstrate the penetration ability, rapid drug release, and scar-inhibiting effects. This facile and efficient approach for HS therapyviaa DNA-based transdermal drug delivery system may provide more possibilities for the development of transdermal administration.
机译:透皮给药的方法被认为是一个潜在的治疗人类肥厚性疤痕(HSs)而不是电流不舒服的手术切除,局部注射和激光治疗。有效的药物输送方法是急需的为了克服皮肤的皮肤屏障管理。纳米颗粒交付systemviaFe离子驱动的自组装满足的要求皮肤管理HS疗法。盐酸阿霉素(阿霉素)之一广泛使用的抗癌药物来治疗皮肤纤维异常增生组织。阿霉素加载DNA-Fe纳米颗粒(DOX@DNA-Fe NPs)进行演示渗透能力,快速药物释放和scar-inhibiting效果。HS therapyviaa dna经皮肤药物交付系统可能提供更多的可能性对皮肤的发展管理。

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