在生物液体中制备具有暴露活性晶面的磷酸八钙薄膜

IF 5.5 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
Yanni Zhou, Zizhen Liu, Daichi Noda, Iori Yamada, Motohiro Tagaya
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引用次数: 0

摘要

磷酸八钙(OCP)由于具有较高的骨亲和力而被用作骨替代材料。然而,亲和性的机制尚未明确。由于OCP的100晶面与成骨过程中的生物反应密切相关,因此将OCP的100晶面暴露于生物液中以精确测量其界面反应具有重要意义。本研究将OCP板状晶体以单颗粒沉积的形式固定在导电衬底上,制备出具有100个晶面的薄膜。然后,通过形成薄膜的方式暴露100个晶面,增强OCP晶体中水化层的特性,发现其生物反应性与水化层在生物流体中的溶胀和溶解有关。具体来说,OCP晶体通过电泳沉积(OCP/Au-1)沉积在金传感器上。结果表明,通过电泳,OCP片状晶体被选择性地沉积在金传感器上。随后发现,OCP/Au-1的超声作用可在金传感器上形成单颗粒厚度的OCP晶体薄膜(m-OCP/Au-1),暴露出100个晶面。此外,m-OCP/Au-1的FT-IR光谱显示,水化层中磷酸离子的结构在超声作用下发生了重排,导致层状纳米结构受到调控,提高了结晶度。此外,m-OCP/Au-1的XPS光谱表明,水化层中的磷酸氢离子暴露在最表层的100晶面上。制备的m-OCP/Au-1在柠檬酸缓冲液中表现稳定,而在磷酸盐缓冲液中表现出很高的反应活性,溶胀后水化层逐渐溶解,用QCM-D技术测定。因此,本研究发现,由于水化层暴露增强,OCP晶体薄膜具有更高的表面反应性,这被认为是其促进骨再生作用(即更高的骨亲和力)的原因。本研究制备的膜在胃酸pH下稳定,在中性pH下溶解,可作为口服药物载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation of Octacalcium Phosphate Thin Film with Exposing Reactive Crystalline Plane in Biological Fluid.

Octacalcium phosphate (OCP) has been used as a bone replacement material due to its higher bone affinity. However, the mechanism of affinity has not been clarified. Since the 100 crystalline plane of OCP is closely involved in the biological reactions during osteogenesis, it is important to expose the 100 crystalline plane of OCP to the biological fluid to precisely measure the interfacial reactions. In this study, the OCP plate-like crystals were fixed on a conductive substrate in the form of single-particle deposition, and the thin films with exposing 100 crystalline planes were fabricated. Then, the characteristics of hydration layers in the OCP crystals were enhanced by the exposure of 100 crystalline planes through the thin film formation, and the bioreactivity was found to be associated with the swelling and dissolution of the hydration layer in the biological fluid. Specifically, the OCP crystals were deposited on the gold sensor by electrophoretic deposition (OCP/Au-1). The results showed that the OCP plate-like crystals were selectively deposited on the gold sensor by electrophoresis. Subsequently, it was found that the ultrasonication of OCP/Au-1 resulted in the formation of an OCP crystalline thin film (m-OCP/Au-1) with the single-particle thickness on the gold sensor with exposing 100 crystalline planes. Moreover, the FT-IR spectra of m-OCP/Au-1 showed that the structure of the phosphate ions was rearranged by ultrasonication in the hydration layer, resulting in the regulation of the layered nanostructures, promoting higher crystallinity. Furthermore, the XPS spectra of m-OCP/Au-1 indicated that the hydrogen phosphate ions in the hydration layer were exposed on the 100 crystalline plane of the topmost surface. The prepared m-OCP/Au-1 was stable in citrate buffer, whereas it showed very high reactivity in phosphate buffer as the hydration layer gradually dissolved after the swelling, which was measured by the QCM-D technique. Therefore, the OCP crystalline thin films in this study were found to have higher surface reactivity due to the enhanced exposure of the hydration layer, which is assumed to be the cause of their bone-regeneration-promoting effect (i.e., higher bone affinity). The films in this study were stable at gastric acid pH and dissolved at neutral pH, which could make them useful as the orally administered drug carrier.

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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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