壳聚糖
生物相容性
透皮
破骨细胞
药物输送
材料科学
药品
明胶
间充质干细胞
生物医学工程
药理学
化学
纳米技术
医学
生物化学
体外
病理
冶金
作者
Simindokht Afra,Marcus Koch,Joanna Żur-Pińska,Maryam Dolatshahi,Ahmad Reza Bahrami,Julien Es Sayed,Ali Moradi,Maryam Moghaddam Matin,Małgorzata K. Włodarczyk‐Biegun
标识
DOI:10.1016/j.carpta.2023.100418
摘要
Osteoporosis is a silent bone disease and a growing health issue. Despite recent progress in diagnosis and treatment, effective therapeutic strategies are still needed. One of the possible solutions is the implantation of engineered drug-releasing scaffolds at the disease site. To boost this approach further, we aimed to develop printable materials (the inks) for the construction of patient-specific 3D scaffolds with drug-release capability. The inks were composed of chitosan – a natural osteoinductive polysaccharide, nanohydroxyapatite – a natural bone matrix ingredient improving mechanical properties, sodium alendronate – a bioactive drug, and hydroxyethyl-cellulose – a filler improving printability. Printed scaffolds were crosslinked with citric acid or KOH. After coating with collagen and gelatin, they demonstrated biocompatibility with the adipose-derived mesenchymal stem cells and MG-63 cell line. They also showed a sustained release of alendronate for 50 days, causing a significant reduction in the expression of the osteoclast-specific gene markers that indicated the osteoclast-inhibiting capacities of these coated scaffolds. This work demonstrates the potential of developed printable materials to find applications as cell and drug carriers for the treatment of osteoporosis.
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