Regnault William F, Icenogle Tonya B, Antonucci Joseph M, Skrtic Drago
Center for Devices and Radiological Health, Food and Drug Administration, Rockville, MD, USA.
J Mater Sci Mater Med. 2008 Feb;19(2):507-15. doi: 10.1007/s10856-007-3178-3. Epub 2007 Jul 10.
Urethane dimethacrylate (UDMA), an oligomeric 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, as a 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.
选择聚氨酯二甲基丙烯酸酯(UDMA)、一种低聚聚乙二醇扩链的UDMA(PEG-U)以及UDMA/PEG-U共混物作为模型体系,用于在其衍生聚合物中引入疏水和亲水链段以及一系列顺应性。以这三种树脂为基础、以无定形磷酸钙(ACP)为填充相的实验性复合材料进行了聚合,并评估了其在不同水性介质中的机械强度和离子释放曲线。所有复合材料在浸入盐水(pH = 7.4)后强度均下降。聚合物基体组成和液体环境的pH值都强烈影响离子释放动力学。在盐水中,UDMA/PEG-U复合材料显示出至少350小时的持续释放。PEG-U复合材料最初较高的离子释放在72小时后下降,这似乎是由于矿物在复合材料表面重新沉积。通过X射线衍射可以观察到ACP向结晶度较差的磷灰石的内部转变。在各种乳酸(LA)环境(初始pH = 5.1)中,离子释放动力学要复杂得多。在没有百里酚和/或羧甲基纤维素的LA介质中,由于内部钙/磷酸根离子化学计量比的不利变化,离子释放速率大幅增加,但没有观察到ACP向磷灰石的转变。