Institute for Advanced Ceramics, State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150001, PR China; Bio-acoustic MEMS in Medicine Laboratory, Department of Medicine, Division of Biomedical Engineering, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Institute for Advanced Ceramics, State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin 150001, PR China.
Acta Biomater. 2015 Aug;22:59-69. doi: 10.1016/j.actbio.2015.04.026. Epub 2015 Apr 25.
Natural and biodegradable chitosan with unique amino groups has found widespread applications in tissue engineering and drug delivery. However, its applications have been limited by the poor solubility of native chitosan in neutral pH solution, which subsequently fails to achieve cell-laden hydrogel at physiological pH. To address this, we incorporated UV crosslinking ability in chitosan, allowing fabrication of patterned cell-laden and rapid transdermal curing hydrogel in vivo. The hydrosoluble, UV crosslinkable and injectable N-methacryloyl chitosan (N-MAC) was synthesized via single-step chemoselective N-acylation reaction, which simultaneously endowed chitosan with well solubility in neutral pH solution, UV crosslinkable ability and injectability. The solubility of N-MAC in neutral pH solution increased 2.21-fold with substitution degree increasing from 10.9% to 28.4%. The N-MAC allowed fabrication of cell-laden microgels with on-demand patterns via photolithography, and the cell viability in N-MAC hydrogel maintained 96.3 ± 1.3% N-MAC allowed rapid transdermal curing hydrogel in vivo within 60s through minimally invasive clinical surgery. Histological analysis revealed that low-dose UV irradiation hardly induced skin injury and acute inflammatory response disappeared after 7 days. N-MAC would allow rapid, robust and cost-effective fabrication of patterned cell-laden polysaccharide microgels with unique amino groups serving as building blocks for tissue engineering and rapid transdermal curing hydrogel in vivo for localized and sustained protein delivery.
具有独特氨基的天然可生物降解壳聚糖在组织工程和药物输送中得到了广泛的应用。然而,其应用受到了天然壳聚糖在中性 pH 溶液中溶解度差的限制,这使得它无法在生理 pH 下实现细胞负载水凝胶。为了解决这个问题,我们在壳聚糖中加入了紫外光交联能力,从而能够在生理条件下制造图案化的细胞负载和快速经皮固化水凝胶。通过一步化学选择性 N-酰化反应合成了水溶性、紫外光交联和可注射的 N-丙烯酰壳聚糖(N-MAC),这同时赋予了壳聚糖在中性 pH 溶液中的良好溶解性、紫外光交联能力和可注射性。N-MAC 在中性 pH 溶液中的溶解度随着取代度从 10.9%增加到 28.4%而增加了 2.21 倍。N-MAC 允许通过光刻法制造按需图案的细胞负载微凝胶,并且 N-MAC 水凝胶中的细胞活力保持在 96.3±1.3%。N-MAC 允许通过微创临床手术在体内 60s 内快速经皮固化水凝胶。组织学分析显示,低剂量的紫外线照射几乎不会引起皮肤损伤,并且 7 天后急性炎症反应消失。N-MAC 将允许快速、稳健和具有成本效益的制造具有独特氨基的图案化细胞负载多糖微凝胶,这些氨基可以作为组织工程的构建块,并在体内快速经皮固化水凝胶,用于局部和持续的蛋白质输送。