In Situ Synthesis and Characterizations of a Strontium-Substituted Dicalcium Phosphate Anhydrous/Hydroxyapatite Biphasic Whisker and Its Properties Evaluation.

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Weiye Du, Yunping Yang, Jinkun Liu, Yan Zhu, Tao Shen, Qinghua Chen, Toshiki Miyazaki
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Abstract

Dicalcium phosphate anhydrous (DCPA) presents good biomineralization ability, the strontium element is known for superior bone affinity, and a whisker possesses good mechanical strength; all these are beneficial for improving the drawbacks of hydroxyapatite (HAP) like weaker mechanical properties, poor biomineralization, and slower degradation/absorption. Therefore, a homogeneous precipitation was adopted to synthesize Sr-substituted and DCPA and HAP coexisting whiskers. The composition, structure, and morphology based on urea dosage and substitution content were characterized, and the roles of DCPA, Sr, and whisker shape were investigated. It turned out that Sr-DCPA/HAP biphasic products contained about 19% DCPA and 81% HAP, and both phases occupied the outer and inner parts of the whisker, respectively. Increasing the urea dosage made the morphology transform from a sea urchin shape to fiber clusters and then whiskers, while Sr substitution brought the whisker back to the porous microsphere shape. Only 5% of Sr content and 15 g of urea could maintain the whisker shape. Sr could promote the proliferation of MC3T3-E1 cells even at a higher extract concentration of 10 mg/mL. The cells stayed in a healthy state whether cocultured with the whisker or the microsphere. The unstable DCPA combined with the decreased crystallinity brought by Sr doping contributed to shortening the apatite deposition period to within 7 days. The whisker morphology enhanced the compressive strength of acrylic resin, and the apatite layer helped to reduce the strength loss during soaking. The Sr-DCPA/HAP biphasic whisker with enhanced overall properties possessed more promising potential for biomedical application.

锶取代的无水磷酸二钙/羟基磷灰石双相晶须的原位合成、表征及其性能评估
无水磷酸二钙(DCPA)具有良好的生物矿化能力,锶元素以其卓越的骨亲和性而著称,晶须具有良好的机械强度;所有这些都有利于改善羟基磷灰石(HAP)机械性能较弱、生物矿化能力较差、降解/吸收较慢等缺点。因此,我们采用均相沉淀法合成了锶取代和 DCPA 与 HAP 共存晶须。根据尿素用量和取代含量对晶须的组成、结构和形态进行了表征,并研究了 DCPA、Sr 和晶须形状的作用。结果表明,Sr-DCPA/HAP 双相产物中含有约 19% 的 DCPA 和 81% 的 HAP,两相分别占据晶须的外部和内部。增加尿素用量可使晶须的形态从海胆状转变为纤维簇状,然后再转变为晶须状,而 Sr 替代则可使晶须恢复为多孔微球状。只有 5%的硒含量和 15 克尿素才能保持晶须的形状。即使在 10 毫克/毫升的较高提取物浓度下,硒也能促进 MC3T3-E1 细胞的增殖。无论是与晶须还是微球共培养,细胞都能保持健康状态。不稳定的DCPA加上掺杂锶带来的结晶度降低,有助于将磷灰石沉积期缩短至7天内。晶须形态增强了丙烯酸树脂的抗压强度,而磷灰石层则有助于减少浸泡过程中的强度损失。整体性能增强的 Sr-DCPA/HAP 双相晶须在生物医学应用方面具有更大的潜力。
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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
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 Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring 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
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