Department of Oral and Craniofacial Health Sciences, College of Dental Medicine, University of Sharjah, Sharjah 27272, United Arab Emirates.
Research Institute of Medical and Health Sciences, University of Sharjah, Sharjah 27272, United Arab Emirates.
Int J Nanomedicine. 2020 Oct 12;15:7775-7789. doi: 10.2147/IJN.S274418. eCollection 2020.
Several scaffolds and cell sources are being investigated for cartilage regeneration. The aim of the study was to prepare nanocellulose-based thermosensitive injectable hydrogel scaffolds and assess their potential as 3D scaffolds allowing the chondrogenic differentiation of embedded human dental pulp stem and progenitor cells (hDPSCs).
The hydrogel-forming solutions were prepared by adding β-glycerophosphate (GP) to chitosan (CS) at different ratios. Nanocellulose (NC) suspension was produced from hemp hurd then added dropwise to the CS/GP mixture. In vitro characterization of the prepared hydrogels involved optimizing gelation and degradation time, mass-swelling ratio, and rheological properties. The hydrogel with optimal characteristics, NC-CS/GP-21, was selected for further investigation including assessment of biocompatibility. The chondrogenesis ability of hDPSCs embedded in NC-CS/GP-21 hydrogel was investigated in vitro and compared to that of bone marrow-derived mesenchymal stem cells (BMSCs), then was confirmed in vivo in 12 adult Sprague Dawley rats.
The selected hydrogel showed stability in culture media, had a gelation time of 2.8 minutes, showed a highly porous microstructure by scanning electron microscope, and was morphologically intact in vivo for 14 days after injection. Histological and immunohistochemical analyses and real-time PCR confirmed the chondrogenesis ability of hDPSCs embedded in NC-CS/GP-21 hydrogel.
Our results suggest that nanocellulose-chitosan thermosensitive hydrogel is a biocompatible, injectable, mechanically stable and slowly degradable scaffold. hDPSCs embedded in NC-CS/GP-21 hydrogel is a promising, minimally invasive, stem cell-based strategy for cartilage regeneration.
有几种支架和细胞来源正在被研究用于软骨再生。本研究的目的是制备基于纳米纤维素的温敏型可注射水凝胶支架,并评估其作为允许嵌入的人牙髓干细胞和祖细胞(hDPSCs)软骨分化的 3D 支架的潜力。
通过将β-甘油磷酸酯(GP)以不同比例添加到壳聚糖(CS)中来制备水凝胶形成溶液。纳米纤维素(NC)悬浮液是由麻纤维制成的,然后将其逐滴添加到 CS/GP 混合物中。对制备的水凝胶进行体外特性分析,包括优化凝胶和降解时间、质量溶胀比和流变性能。选择具有最佳特性的水凝胶,NC-CS/GP-21,用于进一步研究,包括评估生物相容性。将 hDPSCs 嵌入 NC-CS/GP-21 水凝胶中的软骨形成能力进行了体外研究,并与骨髓间充质干细胞(BMSCs)进行了比较,然后在 12 只成年 Sprague Dawley 大鼠体内进行了确认。
所选水凝胶在培养基中稳定,凝胶时间为 2.8 分钟,扫描电子显微镜显示具有高度多孔的微观结构,并且在注射后 14 天内在体内形态完整。组织学和免疫组织化学分析和实时 PCR 证实了 hDPSCs 嵌入 NC-CS/GP-21 水凝胶中的软骨形成能力。
我们的结果表明,纳米纤维素-壳聚糖温敏水凝胶是一种生物相容、可注射、机械稳定和缓慢降解的支架。hDPSCs 嵌入 NC-CS/GP-21 水凝胶是一种有前途的、微创、基于干细胞的软骨再生策略。