Department of Functional Materials in Medicine and Dentistry, University of Würzburg, D-97070 Würzburg, Germany.
Acta Biomater. 2013 Dec;9(12):9558-67. doi: 10.1016/j.actbio.2013.08.009. Epub 2013 Aug 14.
Current developments in calcium phosphate cement (CPC) technology concern the use of ready-to-use injectable cement pastes by dispersing the cement powder in a water-miscible solvent, such that, after injection into the physiological environment, setting of cements occurs by diffusion of water into the cement paste. It has also been demonstrated recently that the combination of a water-immiscible carrier liquid combined with suitable surfactants facilitates a discontinuous liquid exchange in CPC, enabling the cement setting reaction to take place. This paper reports on the use of these novel cement paste formulations as a controlled release system of antibiotics (gentamicin, vancomycin). Cement pastes were applied either as a one-component material, in which the solid drugs were physically dispersed, or as a two-component system, where the drugs were dissolved in an aqueous phase that was homogeneously mixed with the cement paste using a static mixing device during injection. Drug release profiles of both antibiotics from pre-mixed one- and two-component cements were characterized by an initial burst release of ∼7-28%, followed by a typical square root of time release kinetic for vancomycin. Gentamicin release rates also decreased during the first days of the release study, but after ∼1 week, the release rates were more or less constant over a period of several weeks. This anomalous release kinetic was attributed to participation of the sulfate counter ion in the cement setting reaction altering the drug solubility. The drug-loaded cement pastes showed high antimicrobial potency against Staphylococcus aureus in an agar diffusion test regime, while other cement properties such as mechanical performance or phase composition after setting were only marginally affected.
目前磷酸钙水泥(CPC)技术的发展涉及到使用即用型可注射水泥糊剂,即将水泥粉末分散在水溶性溶剂中,这样,在注入生理环境后,水泥通过水扩散到水泥糊中发生凝固。最近也证明,将不混水的载体液体与合适的表面活性剂结合,可以促进 CPC 中的不连续液体交换,从而使水泥凝固反应发生。本文报告了这些新型水泥糊剂作为抗生素(庆大霉素、万古霉素)的控释系统的用途。水泥糊可以作为单一组分材料使用,其中固体药物被物理分散,也可以作为双组分系统使用,药物溶解在水相中,在注射过程中使用静态混合装置将水相均匀混合到水泥糊中。预混合的单组分和双组分水泥中两种抗生素的药物释放曲线表现出约 7-28%的初始突释,随后是万古霉素的典型平方根时间释放动力学。庆大霉素的释放速率在释放研究的最初几天也有所下降,但在大约 1 周后,释放速率在数周的时间内或多或少保持恒定。这种异常的释放动力学归因于硫酸盐抗衡离子参与水泥凝固反应改变了药物的溶解度。载药水泥糊在琼脂扩散试验中对金黄色葡萄球菌表现出很高的抗菌效力,而其他水泥性能,如凝固后的机械性能或相组成,仅受到轻微影响。