兼具自矿化与成骨诱导特性的六磷酸肌醇-锌水凝胶的制备及性能评价OA
Fabrication and evaluation of an inositol hexaphosphate-zinc hydrogel with dual capabilities of self-mineralization and osteoinduction
目的 构建一种负载六磷酸肌醇-锌的水凝胶,同时初步评估其在自矿化和成骨诱导方面的性能,为骨再生材料开发提供研究基础.方法 利用甲基丙烯酰氧乙基三甲基氯化铵(methacryloyloxyethyltrimeth-ylammonium chloride,DMC)和四臂聚乙二醇丙烯酸酯共聚形成水凝胶框架DF0,再依次借助静电作用和螯合作用负载六磷酸肌醇阴离子和锌离子.仅负载六磷酸肌醇阴离子的水凝胶被命名为DF1,同时负载六磷酸肌醇-锌的水凝胶被命名为DF2.通过扫描电镜(scanning electron microscope,SEM)、透射电镜(transmission elec-tron microscope,TEM)、能量色散X射线光谱仪(energy dispersive spectroscopy,EDS)、选区电子衍射(selected area electron diffraction,SAED)等手段表征DF0、DF1、DF2 水凝胶自矿化效果;借助死/活细胞染色、CCK-8实验测定DF0、DF1、DF2 水凝胶生物相容性;通过碱性磷酸酶(alkaline phosphatase,ALP)和茜素红S(alizarin red S,ARS)染色评估DF0、DF1、DF2 水凝胶对小鼠胚胎成骨细胞前体细胞(mouse embryonic osteoblast precursors,MC3T3-E1)的成骨诱导能力;在上述细胞实验中,均以普通培养基饲养的细胞作为对照组.结果 DF0、DF1、DF2水凝胶被成功合成,其中DF1、DF2可在6 d内产生明显的自矿化现象;TEM、EDS、SAED结果证实DF1组矿化产物为无定形磷酸钙,而DF2组产物为无定形磷酸锌钙;生物相容性实验结果显示,DF0、DF1、DF2水凝胶未对细胞存活及增殖产生影响;成骨诱导实验中,DF1组和DF2组的ALP及ARS染色都有所加深,其中DF2组两种染色结果最深.结论 本研究构建的六磷酸肌醇-锌水凝胶(DF2)可通过自矿化实现钙磷化合物生成,同时兼具良好的成骨诱导特性;这种生物相容性良好的双重促成骨水凝胶为骨再生提供了一种新的策略.
Objective To fabricate a hydrogel loaded with inositol hexaphosphate-zinc and preliminarily evaluate its performance in self-mineralization and osteoinduction,thereby providing a theoretical basis for the development of bone regeneration materials.Methods The hydrogel framework(designated DF0)was formed by copolymerizing meth-acryloyloxyethyltrimethylammonium chloride and four-armed poly(ethylene glycol)acrylate,followed by sequentially loading inositol hexaphosphate anions via electrostatic interaction and zinc ions via chelation.The hydrogel loaded only with inositol hexaphosphate anions was named DF1,while the co-loaded hydrogel was named DF2.The self-mineralization efficacy of the DF0,DF1 and DF2 hydrogels was characterized using scanning electron microscopy,trans-mission electron microscopy(TEM),energy dispersive spectroscopy(EDS),and selected area electron diffraction(SAED).The biocompatibility was assessed via live/dead cell staining and a CCK-8 assay.The osteoinductive capacity of the DF0,DF1 and DF2 hydrogels on MC3T3-E1 cells was assessed via alkaline phosphatase(ALP)and Alizarin Red S(ARS)staining.In the aforementioned cell experiments,cells cultured in standard medium served as the control group.Results The DF0,DF1,and DF2 hydrogels were successfully synthesized.Notably,DF1 and DF2 exhibited dis-tinct self-mineralization within 6 days.Results from TEM,EDS,and SAED confirmed that the mineralization products were amorphous calcium phosphate in group DF1,and amorphous calciumzinc phosphate in group DF2.Biocompatibility tests revealed that none of the hydrogels(DF0,DF1,and DF2)adversely affected cell viability or proliferation.In osteo-genic induction experiments,both ALP and ARS staining were intensified in the DF1 and DF2 groups,with the most pro-found staining observed in the DF2 group.Conclusion The developed inositol hexaphosphate-zinc hydrogel(DF2)dem-onstrates the dual capacity to generate calcium-phosphate compounds through self-mineralization while exhibiting excel-lent osteoinductive properties.This biocompatible,dual-promoting osteogenic hydrogel presents a novel strategy for bone regeneration.
刘鸣一;苗晓雨;蔡云帆;王妍;孙小棠;康靖蕊;赵耀;牛丽娜
口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)口颌系统重建与再生全国重点实验室,国家口腔疾病临床医学研究中心,陕西省口腔医学重点实验室,空军军医大学口腔医院修复科,陕西 西安(710032)
医药卫生
生物材料六磷酸肌醇天然化合物螯合作用锌离子自矿化成骨诱导水凝胶骨再生
biomaterialinositol hexaphosphatenatural compoundchelationzinc ionsself-mineralizationosteoinductionhydrogelbone regeneration
《口腔疾病防治》 2026 (1)
29-40,12
国家自然科学基金项目(82325012)中国博士后面上基金项目(2024M754272) This study was supported by the grants from National Natural Science Foundation of China(No.82325012)and the China Postdoctoral Science Foundation(No.2024M754272).
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