Trivedi Poonam, Saloranta-Simell Tiina, Maver Uroš, Gradišnik Lidija, Prabhakar Neeraj, Smått Jan-Henrik, Mohan Tamilselvan, Gericke Martin, Heinze Thomas, Fardim Pedro
Laboratory of Fibre and Cellulose, Åbo Akademi University, 20500 Turku, Finland.
Johan Gadolin Process Chemistry Centre, Laboratory of Organic Chemistry, Åbo Akademi University, 20500 Turku, Finland.
Bioengineering (Basel). 2018 Jan 9;5(1):3. doi: 10.3390/bioengineering5010003.
Cytocompatible polysaccharide-based functional scaffolds are potential extracellular matrix candidates for soft and hard tissue engineering. This paper describes a facile approach to design cytocompatible, non-toxic, and multifunctional chitosan-cellulose based hydrogel beads utilising polysaccharide dissolution in sodium hydroxide-urea-water solvent system and coagulation under three different acidic conditions, namely 2 M acetic acid, 2 M hydrochloric acid, and 2 M sulfuric acid. The effect of coagulating medium on the final chemical composition of the hydrogel beads is investigated by spectroscopic techniques (ATR-FTIR, Raman, NMR), and elemental analysis. The beads coagulated in 2 M acetic acid displayed an unchanged chitosan composition with free amino groups, while the beads coagulated in 2 M hydrochloric and sulfuric acid showed protonation of amino groups and ionic interaction with the counterions. The ultrastructural morphological study of lyophilized beads showed that increased chitosan content enhanced the porosity of the hydrogel beads. Furthermore, cytocompatibility evaluation of the hydrogel beads with human breast adenocarcinoma cells (soft tissue) showed that the beads coagulated in 2 M acetic acid are the most suitable for this type of cells in comparison to other coagulating systems. The acetic acid fabricated hydrogel beads also support osteoblast growth and adhesion over 192 h. Thus, in future, these hydrogel beads can be tested in the in vitro studies related to breast cancer and for bone regeneration.
具有细胞相容性的多糖基功能支架是软组织和硬组织工程中潜在的细胞外基质候选材料。本文描述了一种简便的方法,利用多糖在氢氧化钠-尿素-水溶剂体系中的溶解以及在三种不同酸性条件(即2M乙酸、2M盐酸和2M硫酸)下的凝固,来设计具有细胞相容性、无毒且多功能的壳聚糖-纤维素基水凝胶珠。通过光谱技术(衰减全反射傅里叶变换红外光谱、拉曼光谱、核磁共振)和元素分析研究了凝固介质对水凝胶珠最终化学成分的影响。在2M乙酸中凝固的珠子显示出壳聚糖组成不变且带有游离氨基,而在2M盐酸和硫酸中凝固的珠子显示出氨基质子化以及与抗衡离子的离子相互作用。冻干珠子的超微结构形态学研究表明,壳聚糖含量的增加提高了水凝胶珠的孔隙率。此外,对水凝胶珠与人乳腺癌细胞(软组织)的细胞相容性评估表明,与其他凝固体系相比,在2M乙酸中凝固的珠子最适合这类细胞。乙酸制备的水凝胶珠在192小时内也支持成骨细胞的生长和黏附。因此,未来这些水凝胶珠可用于与乳腺癌相关的体外研究以及骨再生研究。