Derakhshandeh Hossein, Aghabaglou Fariba, McCarthy Alec, Mostafavi Azadeh, Wiseman Chris, Bonick Zack, Ghanavati Ian, Harris Seth, Kreikemeier-Bower Craig, Basri Seyed Masoud Moosavi, Rosenbohm Jordan, Yang Ruiguo, Mostafalu Pooria, Orgill Dennis, Tamayol Ali
Department of Mechanical and Materials Engineering, University of Nebraska, Lincoln, NE 68588, USA.
Veterinary Diagnostic Center, School of Veterinary Medicine and Biomedical Sciences, University of Nebraska-Lincoln Lincoln, NE 68583, USA.
Adv Funct Mater. 2020 Mar 24;30(13). doi: 10.1002/adfm.201905544. Epub 2020 Feb 13.
Chronic wounds are one of the most devastating complications of diabetes and are the leading cause of nontraumatic limb amputation. Despite the progress in identifying factors and promising in vitro results for the treatment of chronic wounds, their clinical translation is limited. Given the range of disruptive processes necessary for wound healing, different pharmacological agents are needed at different stages of tissue regeneration. This requires the development of wearable devices that can deliver agents to critical layers of the wound bed in a minimally invasive fashion. Here, for the first time, a programmable platform is engineered that is capable of actively delivering a variety of drugs with independent temporal profiles through miniaturized needles into deeper layers of the wound bed. The delivery of vascular endothelial growth factor (VEGF) through the miniaturized needle arrays demonstrates that, in addition to the selection of suitable therapeutics, the delivery method and their spatial distribution within the wound bed is equally important. Administration of VEGF to chronic dermal wounds of diabetic mice using the programmable platform shows a significant increase in wound closure, re-epithelialization, angiogenesis, and hair growth when compared to standard topical delivery of therapeutics.
慢性伤口是糖尿病最具破坏性的并发症之一,也是非创伤性肢体截肢的主要原因。尽管在确定慢性伤口治疗因素及取得有前景的体外实验结果方面取得了进展,但其临床转化仍然有限。鉴于伤口愈合所需的一系列破坏过程,在组织再生的不同阶段需要不同的药物制剂。这就需要开发可穿戴设备,能够以微创方式将药物递送至伤口床的关键层。在此,首次设计了一种可编程平台,该平台能够通过微型针头以独立的时间模式将多种药物主动递送至伤口床的更深层。通过微型针阵列递送血管内皮生长因子(VEGF)表明,除了选择合适的治疗方法外,递送方式及其在伤口床内的空间分布同样重要。与标准的局部治疗递送相比,使用可编程平台向糖尿病小鼠的慢性皮肤伤口施用VEGF显示伤口闭合、再上皮化、血管生成和毛发生长显著增加。