A Collagen Membrane Pretreated with Citrate Promotes Collagen Mineralization and Bone Regeneration.

IF 5.2 3区 医学 Q1 ENGINEERING, BIOMEDICAL
Qi Zhang, Yewen Zhong, Xinlin He, Sui Mai
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Abstract

Purpose: Collagen membranes with biomimetic mineralization are emerging as promising materials for bone regeneration, owing to their high biocompatibility. In this study, we developed a biogenic collagen membrane by combining citrate (C) pretreatment and carboxymethyl chitosan (CMC)-mediated mineralization and further evaluated its bone healing potential. Methods: C-CMC collagen membranes were prepared by lyophilization. The mineral composition and content were tested through X-ray diffraction (XRD), Fourier transform infrared (FTIR), and thermogravimetric analysis (TGA). The micromorphology was observed using transmission electron microscopy (TEM), scanning electron microscopy (SEM), and scanning probe microscopy (SPM). Physical and mechanical properties, including the swelling rate, porosity, hydrophilicity, tensile strength, Young's modulus, degradation, and barrier function, were also evaluated. Bone mesenchymal stem cells (BMSCs) were cultured in vitro to observe their behavior. An in vivo critical-size rat calvarial defect model was used to validate the effects of the membrane on bone regeneration. Results: The C-CMC collagen membrane was successfully synthesized as a collagen-hydroxyapatite complex with intrafibrillar mineralization, exhibiting improved mechanical properties and an optimal swelling rate, porosity, hydrophilicity, and degradation rate. Additionally, the C-CMC collagen membrane promoted BMSC proliferation, adhesion, and osteogenesis while preventing epithelial cell infiltration. In vivo experiments indicated that C-CMC collagen membranes significantly stimulated bone regeneration without causing systemic toxicity. Conclusions: Our findings suggest that the C-CMC collagen membrane possesses satisfactory physical and mechanical properties, along with good biocompatibility and efficacy in bone defect regeneration, making it a potential candidate for a bioactive guided bone regeneration membrane in clinical applications.

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柠檬酸预处理胶原膜促进胶原矿化和骨再生。
目的:具有仿生矿化的胶原膜具有较高的生物相容性,是一种很有前途的骨再生材料。本研究采用柠檬酸盐(C)预处理和羧甲基壳聚糖(CMC)介导矿化相结合的方法制备生物源性胶原膜,并进一步评价其骨愈合潜力。方法:采用冻干法制备C-CMC胶原膜。通过x射线衍射(XRD)、红外傅立叶变换(FTIR)和热重分析(TGA)测定了矿物组成和含量。采用透射电子显微镜(TEM)、扫描电子显微镜(SEM)和扫描探针显微镜(SPM)观察微形貌。物理和机械性能,包括膨胀率,孔隙率,亲水性,抗拉强度,杨氏模量,降解和屏障功能,也进行了评估。体外培养骨间充质干细胞(BMSCs),观察其行为。用体内大鼠颅骨缺损模型验证了该膜对骨再生的作用。结果:C-CMC胶原膜成功合成为胶原-羟基磷灰石复合物,具有纤维内矿化,具有较好的力学性能和最佳的溶胀率、孔隙率、亲水性和降解率。此外,C-CMC胶原膜促进骨髓间充质干细胞增殖、粘附和成骨,同时阻止上皮细胞浸润。体内实验表明,C-CMC胶原膜可显著促进骨再生,但不会引起全身毒性。结论:C-CMC胶原膜具有良好的物理力学性能,具有良好的生物相容性和骨缺损再生效果,是临床应用的生物活性引导骨再生膜的潜在候选材料。
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来源期刊
Journal of Functional Biomaterials
Journal of Functional Biomaterials Engineering-Biomedical Engineering
CiteScore
4.60
自引率
4.20%
发文量
226
审稿时长
11 weeks
期刊介绍: Journal of Functional Biomaterials (JFB, ISSN 2079-4983) is an international and interdisciplinary scientific journal that publishes regular research papers (articles), reviews and short communications about applications of materials for biomedical use. JFB covers subjects from chemistry, pharmacy, biology, physics over to engineering. The journal focuses on the preparation, performance and use of functional biomaterials in biomedical devices and their behaviour in physiological environments. Our aim is to encourage scientists to publish their results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Several topical special issues will be published. Scope: adhesion, adsorption, biocompatibility, biohybrid materials, bio-inert materials, biomaterials, biomedical devices, biomimetic materials, bone repair, cardiovascular devices, ceramics, composite materials, dental implants, dental materials, drug delivery systems, functional biopolymers, glasses, hyper branched polymers, molecularly imprinted polymers (MIPs), nanomedicine, nanoparticles, nanotechnology, natural materials, self-assembly smart materials, stimuli responsive materials, surface modification, tissue devices, tissue engineering, tissue-derived materials, urological devices.
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