间充质干细胞
车辆段
材料科学
生物医学工程
再生(生物学)
干细胞
纳米技术
细胞生物学
医学
生物
病理
历史
考古
作者
KangJu Lee,Yumeng Xue,Junmin Lee,Han‐Jun Kim,Yaowen Liu,Peyton Tebon,Einollah Sarikhani,Wujin Sun,Shiming Zhang,Reihaneh Haghniaz,Betül Çelebi‐Saltik,Xingwu Zhou,Serge Ostrovidov,Samad Ahadian,Nureddin Ashammakhi,Mehmet R. Dokmeci,Ali Khademhosseini
标识
DOI:10.1002/adfm.202000086
摘要
Mesenchymal stem cells (MSCs) have been widely used for regenerative therapy. In most current clinical applications, MSCs are delivered by injection but face significant issues with cell viability and penetration into the target tissue due to a limited migration capacity. Some therapies have attempted to improve MSC stability by their encapsulation within biomaterials; however, these treatments still require an enormous number of cells to achieve therapeutic efficacy due to low efficiency. Additionally, while local injection allows for targeted delivery, injections with conventional syringes are highly invasive. Due to the challenges associated with stem cell delivery, a local and minimally invasive approach with high efficiency and improved cell viability is highly desired. In this study, we present a detachable hybrid microneedle depot (d-HMND) for cell delivery. Our system consists of an array of microneedles with an outer poly(lactic-co-glycolic) acid (PLGA) shell and an internal gelatin methacryloyl (GelMA)-MSC mixture (GMM). The GMM was characterized and optimized for cell viability and mechanical strength of the d-HMND required to penetrate mouse skin tissue was also determined. MSC viability and function within the d-HMND was characterized
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