4.8 Article

Controlled Osteogenic Differentiation of Human Mesenchymal Stem Cells Using Dexamethasone-Loaded Light-Responsive Microgels

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 6, 页码 7051-7059

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c17664

关键词

human mesenchymal stem cells; osteogenic differentiation; dexamethasone-loaded light-responsive microgels; controlled and triggered dexamethasone release; bone tissue engineering

资金

  1. University of Alberta (the Department of Chemistry)
  2. University of Alberta (Faculty of Science)
  3. Natural Sciences and Engineering Research Council of Canada (NSERC)
  4. Canada Foundation for Innovation (CFI)
  5. Alberta Advanced Education & Technology Small Equipment Grants Program (AET/SEGP)
  6. Grand Challenges Canada
  7. Alberta Innovates Technology Futures
  8. NSERC CREATE Advanced Protein Engineering Training, Internships, Courses, and Exhibition (APRENTICE) program

向作者/读者索取更多资源

The study involved the development of light-responsive microgels capable of loading and releasing DEX in a light-triggered manner to induce hMSC differentiation into osteoblasts. The microgels showed no cytotoxicity towards hMSCs and may have potential applications in niche clinical treatments such as bone tissue repair.
Human mesenchymal stem cells (hMSCs), which have the ability to differentiate into osteoblasts, show promise for bone tissue engineering and bone defect treatment. While there are a number of approaches currently available to accomplish this, e.g., utilizing biodegradable materials loaded with the synthetic glucocorticoid osteogenic inducer dexamethasone (DEX), there are still many disadvantages with the current technologies. Here, we generated light-responsive microgels that we showed are capable of loading and releasing DEX in a light-triggered fashion, with the released DEX being able to induce hMSC differentiation into osteoblasts. Specifically, light-responsive poly(N-isopropylacrylamide-co-nitrobenzyl methacrylate) (pNIPAm-co-NBMA) microgels were synthesized via free radical precipitation polymerization and their size, morphology, and chemical composition were characterized. We then went on to show that the microgels could be loaded with DEX (via what we think are hydrophobic interactions) and released upon exposure to UV light. We went on to show that the DEX released from the microgels was still capable of inducing osteogenic differentiation of hMSCs using an alamarBlue assay and normalized alkaline phosphatase (ALP) activity assay. We also investigated how hMSC differentiation was impacted by intermittent DEX released from UV-exposed microgels. Finally, we confirmed that the microgels themselves were not cytotoxic to hMSCs. Taken together, the DEX-loaded light-responsive microgels reported here may find a use for niche clinical applications, e.g., bone tissue repair.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据