Institute of Biotechnology, Zurich University of Applied Sciences, Grueental, Waedenswil CH-8820, Switzerland.
J Biomed Mater Res B Appl Biomater. 2010 Feb;92(2):341-52. doi: 10.1002/jbm.b.31520.
For use in the prevention of bone infections, a novel controlled release system composed of beta-tricalcium phosphate (TCP) granules with biodegradable coatings incorporating the antibiotic drug tetracycline (TC) was developed. Six formulations using poly(D,L-lactide) and poly(D,L-lactide-co-glycolide) as coating materials to incorporate TC were prepared and tested in vitro and in vivo. Release of TC from TCP composites was dependent on the biodegradability of the used polymers and on physical-chemical interactions of TC with the polymer materials. Three characteristic release profiles were obtained: slow release lasting up to 67 days, intermediate release with 60% of the total dose released up to day 20, and fast release with a high initial burst and 90% of TC released within 4 days. Even though TC decomposition products had formed during in vitro release, no cytotoxic effects on osteoblast-like cells were observed. The biological activity of TC after incorporation into PL(G)A films was confirmed using a TC-repressible promoter system in genetically engineered Chinese Hamster Ovary (CHO) cells. TC-loaded TCP composites implanted in ovine cancellous bone defects showed good biocompatibility and new bone formation in the histological evaluation. No differences in the cellular reactions were seen between antibiotic-loaded composites and the control group. These experimental results indicate the potential of coated TCP composites to be used as local carrier system for controlled TC delivery with different release kinetics and good in vitro and in vivo biocompatibility.
为了预防骨感染,开发了一种新型的控释系统,该系统由β-磷酸三钙(TCP)颗粒组成,具有可生物降解的涂层,其中包含抗生素药物四环素(TC)。使用聚(D,L-丙交酯)和聚(D,L-丙交酯-共-乙交酯)作为涂层材料,制备了 6 种用于包埋 TC 的配方,并进行了体外和体内测试。TC 从 TCP 复合材料中的释放取决于所用聚合物的生物降解性以及 TC 与聚合物材料的物理化学相互作用。得到了三种特征释放曲线:持续长达 67 天的缓慢释放,60%的总剂量在 20 天内释放的中等释放,以及具有高初始突释和 90%TC 在 4 天内释放的快速释放。尽管在体外释放过程中形成了 TC 分解产物,但在成骨样细胞上没有观察到细胞毒性作用。使用基因工程中国仓鼠卵巢(CHO)细胞中的 TC 抑制性启动子系统证实了 TC 掺入 PL(G)A 薄膜后的生物活性。在绵羊松质骨缺损中植入的载 TC TCP 复合材料具有良好的生物相容性和组织学评估中的新骨形成。在细胞反应方面,载抗生素复合材料与对照组之间没有差异。这些实验结果表明,涂层 TCP 复合材料具有作为局部载体系统的潜力,可用于控制 TC 释放,具有不同的释放动力学和良好的体外和体内生物相容性。