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Treatment of Francisella infections via PLGA- and lipid-based nanoparticle delivery of antibiotics in a zebrafish model

机译:Zebrafish模型中PLGA和脂质纳米粒子培养的抗生素递送Francisella感染

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摘要

We tested the efficiency of 2 different antibiotics, rifampicin and oxolinic acid, against an established infection caused by fish pathogen Francisella noatunensis ssp. orientalis (F.n.o.) in zebrafish. The drugs were tested in the free form as well as encapsulated into bio degradable nanoparticles, either polylactic-co-glycolic acid (PLGA) nanoparticles or nano structured lipid carriers. The most promising therapies were PLGA-rifampicin nanoparticles and free oxolinic acid; the PLGA nanoparticles significantly delayed embryo mortality while free oxolinic acid prevented it. Encapsulation of rifampicin in both PLGA and nanostructured lipid carriers enhanced its efficiency against F.n.o. infection relative to the free drug. We propose that the zebrafish model is a robust, rapid system for initial testing of different treatments of bacterial diseases important for aquaculture.
机译:我们测试了利福平和恶喹酸两种不同抗生素对由鱼类病原体诺阿通纳弗朗西斯菌ssp引起的已知感染的有效性。斑马鱼中的东方鱼。这些药物以游离形式进行测试,并封装在可生物降解的纳米颗粒中,如聚乳酸-羟基乙酸(PLGA)纳米颗粒或纳米结构脂质载体。最有希望的治疗方法是PLGA利福平纳米粒和游离恶喹酸;PLGA纳米粒显著延缓了胚胎死亡率,而游离恶喹酸则阻止了胚胎死亡率。与游离药物相比,在PLGA和纳米结构脂质载体中包裹利福平可提高其抵抗F.n.o.感染的效率。我们认为斑马鱼模型是一个健壮、快速的系统,用于初步测试对水产养殖重要的细菌疾病的不同治疗方法。

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