| Literature DB >> 33071712 |
KangJu Lee1, Yumeng Xue1, Junmin Lee1, Han-Jun Kim1, Yaowen Liu2, Peyton Tebon1, Einollah Sarikhani1, Wujin Sun1, Shiming Zhang1, Reihaneh Haghniaz1, Betül Çelebi-Saltik1, Xingwu Zhou1, Serge Ostrovidov1, Samad Ahadian1, Nureddin Ashammakhi1, Mehmet R Dokmeci1, Ali Khademhosseini1.
Abstract
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 in vitro and the regenerative efficacy of the d-HMND was demonstrated in vivo using a mouse skin wound model.Entities:
Keywords: GelMA hydrogel; biodegradable polymer; mesenchymal stem cell; microneedle; regenerative therapy
Year: 2020 PMID: 33071712 PMCID: PMC7567343 DOI: 10.1002/adfm.202000086
Source DB: PubMed Journal: Adv Funct Mater ISSN: 1616-301X Impact factor: 18.808