鱼鳞废弃物制备磷酸钙生物材料的脱蛋白控制相选择:可持续增值方法

Mashrafi Bin Mobarak*, Shahriar Atik Fahim, Md Sohag Hossain, Fariha Chowdhury, Nazmul Islam Tanvir, Umme Sarmeen Akhtar and Samina Ahmed*, 
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引用次数: 0

摘要

渔业废物的可持续管理是一个日益受到关注的环境问题,鱼鳞是高价值生物材料的有希望的来源。采用不同的化学处理方法,选择性地合成了磷酸钙生物材料(CPBs)。单步酸(1 N HCl)或碱(1 N NaOH)脱蛋白,然后在1000℃下煅烧,得到含镁的β-磷酸三钙(β-TCP, whitlockite)相,通过x射线衍射(XRD)分析证实。相反,连续的酸碱处理导致形成高结晶的单斜羟基磷灰石(HAp)。详细的晶体学分析表明,与whitlockite相相比,HAp相具有更好的结晶度、更大的晶粒尺寸和更低的晶格应变。利用Scherrer方程对酸法、碱法和酸碱法制备的样品分别估计了52、48和118 nm的晶粒尺寸。x射线光电子能谱(XPS)的表面成分分析进一步证实了Mg在β-TCP晶格结构中的整合。在傅里叶变换红外光谱(FTIR)中,两相之间有明显的区别,其中β-TCP含有P2O74 -基团的条带,这是由于β-TCP从TCP和/或高温处理中不完全转化引起的。PO43 -拉曼带位置的差异和惠洛克相对称P-O拉伸带的分裂进一步突出了结构上的差异。透射电子显微镜(TEM)和场发射扫描电子显微镜(FESEM)的形态学表征表明,HAp相形成更细、更小、更均匀的颗粒。基于fesem的能量色散x射线光谱(EDX)分析显示,所有样品都是缺钙的,Ca/P比值(0.92-1.38)始终低于理论值。细胞活力研究表明,所有样品均具有良好的生物相容性(95%存活率)。从机理上讲,相的形成遵循ph依赖的离子动力学,其中单步处理增强了Mg的掺入并有利于β-TCP的形成,而顺序酸碱处理可能重新分配和稳定磷酸盐,促进HAp结晶。这种阶段选择方法提供了一种简单的废物来源途径,使CPBs适合各种生物医学和环境应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deproteinization Controlled Phase Selection in Calcium Phosphate Biomaterials Derived from Tenualosa ilisha Fish Scale Waste: A Sustainable Valorization Approach

Deproteinization Controlled Phase Selection in Calcium Phosphate Biomaterials Derived from Tenualosa ilisha Fish Scale Waste: A Sustainable Valorization Approach

The sustainable management of fishery waste is a growing environmental concern, with fish scales offering promising sources for high-value biomaterials. In this study, calcium phosphate biomaterials (CPBs) were selectively synthesized by varying the chemical treatment of Tenualosa ilisha fish scales. Single-step acid (1 N HCl) or base (1 N NaOH) deproteinization followed by calcination at 1000 °C yielded the magnesium-containing β-tricalcium phosphate (β-TCP, whitlockite) phase, confirmed through X-ray diffraction (XRD) analysis. In contrast, a sequential acid–base treatment led to the formation of highly crystalline monoclinic hydroxyapatite (HAp). Detailed crystallographic analysis revealed superior crystallinity, larger crystallite size, and lower lattice strain for the HAp phase compared to those of the whitlockite phase. Crystallite sizes of 52, 48, and 118 nm were estimated using the Scherrer equation for samples prepared by the acid, base, and acid–base methods, respectively. Surface compositional analysis by X-ray photoelectron spectroscopy (XPS) further corroborated the integration of Mg into the β-TCP lattice structure. A clear distinction was evident in the Fourier transform infrared spectroscopy (FTIR) spectra between the two phases, where β-TCP contained bands for the P2O74– group caused by incomplete transformation of β-TCP from TCP and/or high temperature treatment. Differences in PO43– Raman band positions and splitting of the symmetric P–O stretching band for the whitlockite phase further highlighted structural distinctions. Morphological characterization in terms of transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM) demonstrated finer, smaller, and more uniform particle formation for the HAp phase. FESEM-based energy dispersive X-ray spectroscopy (EDX) analysis revealed that all samples were Ca-deficient, with Ca/P ratios (0.92-1.38) consistently lower than theoretical values. Cell viability studies indicated excellent biocompatibility (>95% viability) in all samples. Mechanistically, the phase formation is proposed to follow pH-dependent ionic dynamics, where single-step treatment enhanced Mg incorporation and favors β-TCP formation, while sequential acid–base processing likely redistributes ions and stabilizes phosphate, promoting HAp crystallization. This phase-selective approach provides a simple, waste-derived pathway to tailor CPBs for diverse biomedical and environmental applications.

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