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首页> 外文期刊>Journal of materials science >Amorphous calcium phosphate/urethane methacrylate resin composites. I. Physicochemical characterization
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Amorphous calcium phosphate/urethane methacrylate resin composites. I. Physicochemical characterization

机译:非晶态磷酸钙/氨基甲酸酯甲基丙烯酸酯树脂复合材料。一,理化特性

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摘要

Urethane dimethacrylate (UDMA), an oligo-meric poly(ethylene glycol) extended UDMA (PEG-U) and a blend of UDMA/PEG-U were chosen as model systems for introducing both hydrophobic and hydrophilic segments and a range of compliances in their derived polymers. Experimental composites based on these three resins with amorphous calcium phosphate (ACP) as the filler phase were polymerized and evaluated for mechanical strength and ion release profiles in different aqueous media. Strength of all composites decreased upon immersion in saline (pH = 7.4). Both polymer matrix composition and the pH of the liquid environment strongly affected the ion release kinetics. In saline, the UDMA/PEG-U composite showed a sustained release for at least 350 h. The initially high ion release of the PEG-U composites decreased after 72 h, seemingly due to the mineral re-deposition at the composite surface. Internal conversion from ACP to poorly crystallized apatite could be observed by X-ray diffraction. In various lactic acid (LA) environments (initial pH = 5.1) ion release kinetics was much more complex. In LA medium without thymol and/or carboxymethylcellulose, asrna result of unfavorable changes in the internal calcium/ phosphate ion stoichiometry, the ion release rate greatly increased but without observable conversion of ACP to apatite.
机译:选择氨基甲酸酯二甲基丙烯酸酯(UDMA),低聚聚(乙二醇)延伸的UDMA(PEG-U)和UDMA / PEG-U的混合物作为模型系统,以引入疏水和亲水链段以及它们的一系列相容性衍生的聚合物。将基于这三种树脂的实验复合材料与无定形磷酸钙(ACP)作为填充相进行聚合,并评估其在不同水性介质中的机械强度和离子释放曲线。浸入盐水(pH = 7.4)后,所有复合材料的强度都会降低。聚合物基质组成和液体环境的pH值都强烈影响离子释放动力学。在盐水中,UDMA / PEG-U复合材料显示持续释放至少350小时。 PEG-U复合材料最初的高离子释放在72小时后下降,这似乎是由于复合材料表面的矿物重新沉积所致。可以通过X射线衍射观察到从ACP内部转变为结晶性差的磷灰石。在各种乳酸(LA)环境中(初始pH = 5.1),离子释放动力学要复杂得多。在没有百里香酚和/或羧甲基纤维素的LA培养基中,内部钙/磷酸根离子化学计量比发生不利变化的结果是,离子释放速率大大提高,但没有观察到ACP向磷灰石的转化。

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  • 来源
    《Journal of materials science》 |2008年第2期|507-515|共9页
  • 作者单位

    Center for Devices and Radiological Health, Food and Drug Administration (FDA), Rockville, MD, USA;

    Center for Devices and Radiological Health, Food and Drug Administration (FDA), Rockville, MD, USA;

    Polymers Division, National Institute of Standards and Technology (NIST), Gaithersburg, MD, USA;

    Paffenbarger Research Center, American Dental Association Foundation (ADAF), Gaithersburg, MD 20899, USA;

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