首页> 美国卫生研究院文献>International Journal of Nanomedicine >A blue fluorescent labeling technique utilizing micro- and nanoparticles for tracking in LIVE/DEAD® stained pathogenic biofilms of Staphylococcus aureus and Burkholderia cepacia
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A blue fluorescent labeling technique utilizing micro- and nanoparticles for tracking in LIVE/DEAD® stained pathogenic biofilms of Staphylococcus aureus and Burkholderia cepacia

机译:一种蓝色荧光标记技术,利用微米和纳米颗粒跟踪金黄色葡萄球菌和洋葱伯克霍尔德菌的LIVE /DEAD®染色病原生物膜

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摘要

Strategies that target and treat biofilms are widely applied to bacterial cultures using popular live/dead staining techniques with mostly red or green fluorescent markers (eg, with SYTO® 9, propidium iodide, fluorescein). Therefore, visualizing drugs or micro- and nanoparticulate delivery systems to analyze their distribution and effects in biofilms requires a third fluorescent dye that does not interfere with the properties of the live/dead markers. The present study establishes and evaluates a model for tracking polymeric particles in fluorescently stained biological material. To this end, poly(d,l-lactide-co-glycolide) (PLGA)-based micro- and nanoparticles were used as well-established model systems, which, because of their favorable safety profiles, are expected to play important future roles with regard to drug delivery via inhalation. PLGA was covalently and stably labeled with 7-amino-4-methyl-3-coumarinylacetic acid (AMCA), after which blue fluorescent poly(ethylene glycol)-block-PLGA (PEG-PLGA) particles were prepared using a mixture of fluorescent AMCA-PLGA and PEG-PLGA. Because chitosan is known to reduce negative surface charge, blue fluorescent PEG-PLGA-particles with chitosan were also prepared. These micro- and nanoparticles were physicochemically characterized and could be clearly distinguished from live/dead stained bacteria in biofilms using confocal laser scanning microscopy.
机译:使用流行的活/死染色技术,以红色或绿色荧光标记(例如,使用SYTO ® 9,碘化丙锭,荧光素)流行的活/死染色技术,将靶向和处理生物膜的策略广泛应用于细菌培养。因此,可视化药物或微颗粒和纳米颗粒递送系统以分析其在生物膜中的分布和作用需要第三种荧光染料,该染料不会干扰活/死标记的特性。本研究建立并评估了一种模型,用于跟踪荧光染色的生物材料中的聚合物颗粒。为此,基于聚(d,l-丙交酯-乙交酯)(PLGA)的微米和纳米颗粒被用作公认的模型系统,由于其良好的安全性,有望在未来起重要作用关于通过吸入给药。用7-氨基-4-甲基-3-香豆基乙酸(AMCA)共价和稳定地标记PLGA,然后使用荧光AMCA的混合物制备蓝色荧光聚(乙二醇)-嵌段-PLGA(PEG-PLGA)颗粒-PLGA和PEG-PLGA。因为已知壳聚糖可减少负表面电荷,所以还制备了带有壳聚糖的蓝色荧光PEG-PLGA颗粒。这些微颗粒和纳米颗粒具有物理化学特征,可以使用共聚焦激光扫描显微镜与生物膜中的活/死染色细菌区分开。

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