{"title":"用于注射矿化纤维组织类似物的分层胶原蛋白/patite 共组装。","authors":"Milena Lama, Marion Merle, Elora Bessot, Camila Bussola Tovani, Guillaume Laurent, Nicole Bouland, Halima Kerdjoudj, Thierry Azaïs, Guylaine Ducouret, Tissiana Bortolotto, Nadine Nassif","doi":"10.1021/acsbiomaterials.4c02115","DOIUrl":null,"url":null,"abstract":"<p><p>Mineralized biological tissues rich in type I collagen (e.g., bone and dentin) exhibit complex anisotropic suprafibrillar organizations in which the organic and inorganic moieties are intimately coassembled over several length scales. Above a critical size, a defect in such tissue cannot be self-repaired. Biomimetic materials with a composition and microstructure similar to that of bone have been shown to favorably influence bone regeneration. This highlights the value of developing a similar formulation in an injectable form to enable minimally invasive techniques. Here, we report on the fabrication and application potential of an injectable collagen/CHA (carbonated hydroxyapatite) cell-free hydrogel. The organic part consists of spray-dried nondenatured and dense collagen microparticles, while the inorganic part consists of biomimetic apatite mineral. By mixing both powders at desired tissue-like ratios with an aqueous solvent in one step, spontaneous co-self-assembly occurs, leading to the formation of a mineralized matrix with suprafibrillar tissue-like features thanks to the induced liquid crystalline properties of collagen on one hand and apatite on the other hand. When injected into soft tissue, the mineralized collagen hydrogel free of chemical cross-linking agents exhibits suitable cohesion and is biocompatible. Preliminary in vitro tests in a tooth cavity model show its integration onto dentin with a biomimetic interface. 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引用次数: 0
摘要
富含 I 型胶原蛋白的矿化生物组织(如骨骼和牙本质)呈现出复杂的各向异性超纤维组织,其中有机和无机分子在多个长度尺度上紧密地组装在一起。超过临界尺寸,此类组织的缺陷就无法自我修复。事实证明,具有与骨骼相似的成分和微观结构的仿生材料可对骨骼再生产生有利影响。这凸显了开发可注射形式的类似配方以实现微创技术的价值。在此,我们报告了一种可注射的胶原蛋白/CHA(碳化羟基磷灰石)无细胞水凝胶的制造和应用潜力。有机部分由喷雾干燥的非变性致密胶原蛋白微粒组成,无机部分由仿生磷灰石矿物组成。将这两种粉末按所需的组织样比例与水性溶剂混合后,一方面胶原蛋白具有诱导液晶特性,另一方面磷灰石具有诱导液晶特性,从而发生自发的共自组装,形成具有超纤维组织样特征的矿化基质。注入软组织后,不含化学交联剂的矿化胶原水凝胶会表现出适当的内聚力和生物相容性。在牙洞模型中进行的初步体外测试表明,这种水凝胶能与牙本质结合,形成仿生界面。根据这些结果,这种多功能可注射矿化胶原水凝胶有望成为骨组织修复的生物材料和生物打印应用的矿化组织墨水。
Hierarchical Collagen/Apatite Co-assembly for Injection of Mineralized Fibrillar Tissue Analogues.
Mineralized biological tissues rich in type I collagen (e.g., bone and dentin) exhibit complex anisotropic suprafibrillar organizations in which the organic and inorganic moieties are intimately coassembled over several length scales. Above a critical size, a defect in such tissue cannot be self-repaired. Biomimetic materials with a composition and microstructure similar to that of bone have been shown to favorably influence bone regeneration. This highlights the value of developing a similar formulation in an injectable form to enable minimally invasive techniques. Here, we report on the fabrication and application potential of an injectable collagen/CHA (carbonated hydroxyapatite) cell-free hydrogel. The organic part consists of spray-dried nondenatured and dense collagen microparticles, while the inorganic part consists of biomimetic apatite mineral. By mixing both powders at desired tissue-like ratios with an aqueous solvent in one step, spontaneous co-self-assembly occurs, leading to the formation of a mineralized matrix with suprafibrillar tissue-like features thanks to the induced liquid crystalline properties of collagen on one hand and apatite on the other hand. When injected into soft tissue, the mineralized collagen hydrogel free of chemical cross-linking agents exhibits suitable cohesion and is biocompatible. Preliminary in vitro tests in a tooth cavity model show its integration onto dentin with a biomimetic interface. Based on the results, this versatile injectable mineralized collagen hydrogel shows promising potential as a biomaterial for bone tissue repair and mineralized tissue-like ink for bioprinting applications.
期刊介绍:
ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics:
Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology
Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions
Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis
Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering
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Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration
Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials
Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture