Chitosan as a Templating Agent of Calcium Phosphate Crystalline Phases in Biomimetic Mineralization: Theoretical and Experimental Studies

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY ACS Applied Materials & Interfaces Pub Date : 2024-11-11 DOI:10.1021/acsami.4c11887
Krzysztof Stafin, Paweł Śliwa, Marek Pia̧tkowski, Dalibor Matýsek
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Abstract

Highlighting the essential role of chitosan (CS), known for its biocompatibility, biodegradability, and ability to promote cell adhesion and proliferation, this study explores its utility in modulating the biomimetic mineralization of calcium phosphate (CaP). This approach holds promise for developing biomaterials suitable for bone regeneration. However, the interactions between the CS surface and in situ precipitated CaP still require further exploration. In the theoretical section, molecular dynamics (MD) simulations demonstrate that, at an appropriate pH level during the prenucleation stage, calcium ions (Ca2+) and hydrogen phosphate ions (HPO42–) form Posner-like clusters. Additionally, the interaction between these clusters and the CS molecule enhances system stability. Together, these phenomena facilitate the transition to subsequent heterogeneous nucleation on the surface of the organic matrix, which is a more controlled process than homogeneous nucleation in solution. Dynamic simulation results suggest that CS acts as a stabilizing matrix at pH 8.0 during biomimetic mineralization. In the experimental section, the effects of pH and the molecular weight of CS were investigated, with a focus on their impact on the crystal structure of the resulting material. X-ray diffraction and scanning electron microscopy analyses reveal that, under conditions of approximately pH 8.0 and a CS molecular weight of 20 000 g/mol, and controlled ion concentration, ultrasound radiation, and temperature, the dominant CaP phases in the material are carbonate-doped hydroxyapatite (CHA) and octacalcium phosphate (OCP). These findings suggest that CS, when adjusted for molecular weight and pH, facilitates the formation of CaP crystal phases that closely resemble the natural inorganic composition of bone, highlighting its protective and regulatory roles in the growth and maturation of crystals during mineralization. The theoretical predictions and experimental outcomes confirm the crucial role of CS as a templating agent, enabling the development of a biomimetic mineralization pathway. CS’s ability to guide this process may prove valuable in the design of materials for bone tissue engineering, particularly in developing effective materials for bone tissue healing and regeneration.

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壳聚糖作为仿生矿化中磷酸钙晶相的模板剂:理论与实验研究
壳聚糖(CS)以其生物相容性、生物可降解性以及促进细胞粘附和增殖的能力而著称,本研究强调了壳聚糖在调节磷酸钙(CaP)生物仿生矿化过程中的重要作用。这种方法有望开发出适用于骨再生的生物材料。然而,CS 表面与原位沉淀的 CaP 之间的相互作用仍需进一步探索。在理论部分,分子动力学(MD)模拟证明,在成核前阶段的适当 pH 值下,钙离子(Ca2+)和磷酸氢根离子(HPO42-)会形成类似波斯纳的簇。此外,这些团簇与 CS 分子之间的相互作用增强了系统的稳定性。这些现象共同促进了有机基质表面向随后的异质成核过渡,与溶液中的均匀成核相比,异质成核是一个更可控的过程。动态模拟结果表明,在 pH 值为 8.0 的条件下,CS 在仿生矿化过程中起到了稳定基质的作用。在实验部分,研究了 pH 值和 CS 分子量的影响,重点是它们对所得材料晶体结构的影响。X 射线衍射和扫描电子显微镜分析表明,在 pH 值约为 8.0、CS 分子量为 20 000 克/摩尔、离子浓度、超声辐射和温度受控的条件下,材料中的主要 CaP 相为碳酸盐掺杂的羟基磷灰石(CHA)和磷酸八钙(OCP)。这些研究结果表明,CS 在调节分子量和 pH 值后,能促进 CaP 晶体相的形成,这些晶体相与骨骼的天然无机组成非常相似,突出了 CS 在矿化过程中晶体生长和成熟过程中的保护和调节作用。理论预测和实验结果证实了希尔思作为模板剂的关键作用,使生物仿生矿化途径得以发展。希尔思引导这一过程的能力可能会被证明在骨组织工程材料的设计中很有价值,特别是在开发骨组织愈合和再生的有效材料方面。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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