Yu Tony, DeSantis Paul, Kim Seyong, Li Christopher Y, Marcolongo Michele
Department of Material Science and Engineering, Drexel University, Philadelphia, Pennsylvania, USA.
School of Biomedical Engineering, Science, and Health Systems, Drexel University, Philadelphia, Pennsylvania, USA.
J Biomed Mater Res A. 2025 Jul;113(7):e37955. doi: 10.1002/jbm.a.37955.
Synthetic polymeric bone grafts have emerged as a promising strategy for bone tissue engineering. Polycaprolactone (PCL) nanofiber shish kebab (NFSK) templates were fabricated as synthetic bone scaffolds via polymer crystallization of a block copolymer (BCP) of PCL-b-polyacrylic acid (PAA). The BCP-functionalized NSFKs provide a unique template that allows for the spatial and orientational control of the nanosized mineral crystals in the PAA anionic galleries, mimicking the molecular structure of bone. The objective of this study was to use this platform to design biomimetic bone templates by modifying the surface with biomimetic functional groups. As a result, chondroitin sulfate (CS) was conjugated onto the kebabs via 1-ethyl-3-(-3-dimethylaminopropyl) carbodiimide/N-hydroxysuccinimide (EDC/NHS) crosslinking of the CS terminal amine group and the PAA carboxylic acid group. Fourier-transform infrared spectroscopy (FTIR) and mass balance showed the formation of an amide bond and an increase in mass after conjugation. MC3T3 E1 pre-osteoblast cells were cultured on the CS-NFSK templates and showed that the presence of CS promoted alkaline phosphatase (ALP) activity and cell proliferation. Osteogenic gene expression, including RUNX2, ALP, COL1, and BGLAP, were upregulated in the CS-NFSK templates. For the first time, CS-NFSK was molecularly engineered to mimic the bone structure and matrix, showing promise as a biomimetic bone template.
合成聚合物骨移植材料已成为骨组织工程领域一种很有前景的策略。聚己内酯(PCL)纳米纤维串(NFSK)模板是通过PCL-b-聚丙烯酸(PAA)嵌段共聚物(BCP)的聚合物结晶制备而成的合成骨支架。经BCP功能化的NFSK提供了一个独特的模板,能够对PAA阴离子通道中的纳米级矿物晶体进行空间和取向控制,模仿了骨的分子结构。本研究的目的是利用该平台,通过用仿生功能基团修饰表面来设计仿生骨模板。结果,通过将硫酸软骨素(CS)的末端胺基与PAA羧酸基团进行1-乙基-3-(3-二甲基氨基丙基)碳二亚胺/ N-羟基琥珀酰亚胺(EDC / NHS)交联,将CS缀合到纤维串上。傅里叶变换红外光谱(FTIR)和质量平衡表明形成了酰胺键,并且缀合后质量增加。将MC3T3 E1前成骨细胞培养在CS-NFSK模板上,结果表明CS的存在促进了碱性磷酸酶(ALP)活性和细胞增殖。在CS-NFSK模板中,包括RUNX2、ALP、COL1和BGLAP在内的成骨基因表达上调。CS-NFSK首次经过分子工程设计以模仿骨结构和基质,显示出作为仿生骨模板的潜力。