脱盐
化学
基质(化学分析)
醋酸
Ⅰ型胶原
骨灰
傅里叶变换红外光谱
溶解度
色谱法
核化学
生物化学
化学工程
材料科学
有机化学
钙
医学
搪瓷漆
病理
工程类
复合材料
作者
Vanessa Ricas Biancardi,Marcos Vinícius Ferreira Silva,Antônio Renato Bigansolli,Karine Moura de Freitas,Everaldo Zonta,Maria Ivone Martins Jacintho Barbosa,Louise Emy Kurozawa,José Lucena Barbosa
标识
DOI:10.1111/1750-3841.16954
摘要
Abstract Bovine bone is an animal‐origin matrix rich in type I collagen (COL I) and it necessitates prior demineralization and makes COL I available. This study investigated the ossein–hydroxyapatite physicochemical properties evaluation as a result of processing and solubilization by acids and revealed the bone matrix demineralization and making COL I available. The tibia residue from bovine sources was processed, ground, and transformed into bone matrix powder. The bone matrix was solubilized in acetic acid followed by lactic acid. The bone matrix was evaluated as a result of processing and solubilization by acids: ossein and hydroxyapatite percentages by nitrogen and ash content, mineral content, particle size distribution, Fourier‐transformation infrared spectroscopy, x‐ray diffraction, and scanning electron microscope. For the obtained residual extracts, pH and mineral content were evaluated. The solubilization by acids affected the ossein–hydroxyapatite physicochemical properties, and the bone matrix solubilized by acetic and lactic acid showed the preservation of the ossein alongside the loss of hydroxyapatite. The processing and the solubilization by acids were revealed to be a alternative to bone matrix demineralization and enabling the accessibility of bone COL I. Practical Application Bovine bone is an abundant type I collagen source, but processing maneuvers and demineralization effect present limitations due to the rigidity of the structural components. Exploring methodologies to process and demineralize will allow type I collagen to be obtained from the bone source, and direct and amplify the potentialities in the chemical and food industries. The research focused on bone sources and collagen availability holds paramount significance, and promotes repurposing agribusiness residues and development of protein–base products.
科研通智能强力驱动
Strongly Powered by AbleSci AI