Prokaryotic/eukaryotic co-culture as a model forin vitrofunctional validation of a dual and sequential drug delivery system with antimicrobial and bone regenerative features.

Miguel A Rodrigues, Giorgia Barbolini, Maria P Ferraz, João P Borges, José D Santos, Maria A Lopes
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Abstract

Bacteria-mammalian cell co-cultures can provide information on host-cell responses to biomaterials under bacterial challenge that is not available from separate monocultures. This study established a two-stage osteogenic cell-Staphylococcus aureusco-culture for assessment of a previously developed dual and sequential drug delivery system (DDS) designed to release gentamicin followed by alendronate. MG-63 cells were initially exposed toCFU/ml ofS. aureusfor different periods. An inoculum ofCFU/ml and a 2 h exposure were selected because MG-63 metabolic activity did not differ significantly from the monoculture control at this time point (p> 0.05). These conditions were subsequently transferred to primary human bone-marrow mesenchymal stromal cells. The DDS-containing co-culture exhibited an increasing resazurin signal over 16 d and maintained adherent cells with an organised F-actin cytoskeleton. On day 25, protein-normalised alkaline phosphatase activity was 40 mol µg-1protein in the DDS-containing co-culture, compared with 5 mol µg-1protein in the basal-medium control and 63 mol µg-1protein in the osteogenic-medium control. The model supports preliminary assessment of mammalian-cell compatibility and osteogenic-associated activity during sequential drug release under an initial bacterial challenge.

原核/真核生物共培养作为具有抗菌和骨再生功能的双重和顺序给药系统的体外功能验证模型。
细菌-哺乳动物细胞共培养可以提供宿主细胞在细菌攻击下对生物材料反应的信息,这是单独的单一培养所无法提供的。本研究建立了两阶段成骨细胞-金黄色葡萄球菌共培养,以评估先前开发的双重顺序给药系统,该系统旨在释放庆大霉素,然后是阿仑膦酸盐。MG-63细胞初始暴露于10^2“-”10^5CFU/mL金黄色葡萄球菌不同时期。选择10^2CFU/mL的接种量和2 h的暴露,因为MG-63的代谢活性在这个时间点与单培养对照没有显著差异(p > 0.05)。这些条件随后被转移到原代人骨髓间充质干细胞。含有dds的共培养在16天内显示出resazurin信号增加,并保持了有组织的f -肌动蛋白细胞骨架的贴壁细胞。在第25天,含有dds的共培养中,蛋白质正常化的ALP活性为40 mol/µg蛋白,而基础培养基对照组为5 mol/µg蛋白,成骨培养基对照组为63 mol/µg蛋白。该模型支持初步评估哺乳动物细胞相容性和成骨相关活性在初始细菌挑战下的顺序药物释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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