Miniaturized Needle Array‐Mediated Drug Delivery Accelerates Wound Healing

伤口愈合 药物输送 血管生成 医学 药理学 体内 生物医学工程 血管内皮生长因子 药品 材料科学 血管内皮生长因子受体 外科 癌症研究 纳米技术 生物 生物技术
作者
Mohamadmahdi Samandari,Fariba Aghabaglou,Kristo Nuutila,Hossein Derakhshandeh,Lei Zhang,Yori Endo,Seth Harris,Lindsay Barnum,Craig Kreikemeier‐Bower,Elmira Arab‐Tehrany,Nicholas A. Peppas,Indranil Sinha,Ali Tamayol
出处
期刊:Advanced Healthcare Materials [Wiley]
卷期号:10 (8): e2001800-e2001800 被引量:44
标识
DOI:10.1002/adhm.202001800
摘要

Abstract A major impediment preventing normal wound healing is insufficient vascularization, which causes hypoxia, poor metabolic support, and dysregulated physiological responses to injury. To combat this, the delivery of angiogenic factors, such as vascular endothelial growth factor (VEGF), has been shown to provide modest improvement in wound healing. Here, the importance of specialty delivery systems is explored in controlling wound bed drug distribution and consequently improving healing rate and quality. Two intradermal drug delivery systems, miniaturized needle arrays (MNAs) and liquid jet injectors (LJIs), are evaluated to compare effective VEGF delivery into the wound bed. The administered drug's penetration depth and distribution in tissue are significantly different between the two technologies. These systems' capability for efficient drug delivery is first confirmed in vitro and then assessed in vivo. While topical administration of VEGF shows limited effectiveness, intradermal delivery of VEGF in a diabetic murine model accelerates wound healing. To evaluate the translational feasibility of the strategy, the benefits of VEGF delivery using MNAs are assessed in a porcine model. The results demonstrate enhanced angiogenesis, reduced wound contraction, and increased regeneration. These findings show the importance of both therapeutics and delivery strategy in wound healing.
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