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Real-Time Monitoring of Pharmacokinetics of Antibiotics in Biofilms with Raman-Tagged Hyperspectral Stimulated Raman Scattering Microscopy

机译:拉曼标记的高光谱刺激拉曼散射显微镜实时监测生物膜中抗生素的药代动力学。

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摘要

Antibiotics resistance developed by biofilms has posed a clinical challenge in the effective treatment of bacterial infections. However, the resistance mechanisms have not been well understood due to a lack of suitable tools for dynamic observation of the interplay between antibiotics and biofilm. In this work, with the use of rapid hyperspectral stimulated Raman scattering microscopy associated with an aryl-alkyne-based Raman tag synthesized, we investigate dynamic interactions between vancomycin and Staphylococcus aureus (S. aureus) biofilm to gain new insights into the resistance mechanisms of the biofilm.>Methods: We utilize spectral focusing hyperspectral stimulated Raman scattering microscopy ensued with multivariate curve resolution analysis to spectrally decompose S. aureus biofilm into its major components (i.e., bacteria and extracellular polymeric substances). Concurrently, vancomycin is conjugated with aryl-alkyne Raman tag (Raman peak at 2218 cm-1) for in vivo tracking of its uptake into biofilm without tissue interference.>Results: We find that vancomycin penetration is a non-uniform diffusion process with penetration depths limited by the preferential affinity to the cell clusters. Semi-quantitative analysis shows that the majority of vancomycin binds to the bacteria, achieving intracellular concentrations of up to 4- to 10- fold higher than the administered dosage. The diffusion constant of ~3.16 µm2/min based on the diffusion and antibiotic binding equations is obtained that well accounts for the antibiotic penetration into the biofilm. SRS longitudinal monitoring of antibiotic effect on the growth of biofilms shows that the antibiotics can eradicate the upper layer of the biofilm exposed to sufficient dosages, while the lower layer of the biofilm at a sub-inhibitory dose remains viable, eventually re-growing to significant bio-volume.>Conclusion: The Raman-tagged hyperspectral SRS microscopy developed is a powerful imaging tool for dynamic monitoring of inhibitory effects of antibiotics on the growing biofilm in vivo, which would facilitate the formulation of new antibiotics for more effective treatments of bacterial infections in near future.
机译:由生物膜形成的抗生素抗性在有效治疗细菌感染方面提出了临床挑战。然而,由于缺乏动态观察抗生素和生物膜之间相互作用的合适工具,因此耐药机制尚未得到很好的理解。在这项工作中,利用快速的高光谱激发拉曼散射显微镜与合成的基于芳基炔烃的拉曼标签相关联,我们研究了万古霉素与金黄色葡萄球菌(金黄色葡萄球菌)生物膜之间的动态相互作用,从而获得了对新霉素抗性机制的新见解。 >方法:我们利用随后通过光谱聚焦的高光谱刺激拉曼散射显微镜和多变量曲线分辨率分析,将金黄色葡萄球菌生物膜光谱分解为主要成分(即细菌和细胞外聚合物)。同时,万古霉素与芳基炔烃拉曼标签(在2218 cm -1 上的拉曼峰)缀合,以在体内跟踪其对生物膜的吸收,而不受组织干扰。>结果:发现万古霉素的渗透是一个不均匀的扩散过程,其渗透深度受到对细胞簇的优先亲和力的限制。半定量分析表明,大多数万古霉素与细菌结合,使细胞内浓度比给药剂量高4至10倍。根据扩散和抗生素结合方程式得出的〜3.16 µm 2 / min的扩散常数很好地说明了抗生素渗透到生物膜中的原因。 SRS对抗生素对生物膜生长的影响的纵向监测表明,抗生素可以根除暴露于足够剂量的生物膜的上层,而亚抑制剂量的生物膜的下层仍然可行,并最终重新生长到显着水平>结论:开发的拉曼标记高光谱SRS显微镜是一种功能强大的成像工具,可动态监测抗生素对体内正在生长的生物膜的抑制作用,这将有助于开发新的抗生素在不久的将来更有效地治疗细菌感染。

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