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Optimized Aerosol Delivery to a Mechanically Ventilated Rodent

机译:优化了向机械通风的啮齿动物的气溶胶输送

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Background: Aerosol delivery through an endotracheal tube during mechanical ventilation of small animals, simulating neonates and small infants, has shown to be influenced by a variety of factors including aerosol generator type, droplet/particle size, ventilator circuitry and ventilation regime. A review of the literature indicates that reported aerosol deposition rates in rodents are quite low, with lung deposition in anesthetized, mechanically ventilated rats reported to be approx3.9 and approx8% in anesthetized, spontaneously breathing rats. The optimization of aerosol delivery to both in vitro and in vivo models of anesthetized mechanically ventilated rodents is described in this study. Methods: Characterization and optimization of the in vitro system performance relied on gravimetric analysis, laser diffraction droplet sizing, and spectrophotometric analysis of drug mass on inspiratory filters. The optimized setup was subsequently employed in vivo to determine deposition of a tracer aerosol in the rat lung. Results: In vitro testing confirmed that droplet size, ventilation regimen, breath actuation setting, and the inclusion of a drug recycling step had the greatest effect on inhaled mass. During testing, improvements of up to 41% were seen in inhaled mass values between runs with the addition of a recycling step. The negative effects of the aerosolization process on albuterol sulphate were minimal. In vitro deposition rates of 29.95 +- 1.54% of the original dose were recorded (n = 3). In vivo deposition rates of Evans blue were highly comparable (30.88 +- 5.73%) (n = 6). Intratracheal instillation of the tracer dye resulted in deposition of 87.34 +- 6.23% of the original dose. Conclusions: This optimized experimental setup allows for greater inhaled mass than previously reported. The addition of a recycling step may prove to be a significant improvement in achieving higher deposition in mechanically ventilated lungs; however, the suitability of the test agent for repeated nebulization needs assessment.
机译:背景:在模拟模拟动物和婴儿的小型动物的机械通气过程中,通过气管插管的气溶胶输送受到多种因素的影响,包括气溶胶发生器的类型,液滴/颗粒大小,呼吸机回路和通风方式。文献综述表明,在啮齿动物中报告的气溶胶沉积速率非常低,据报告,在麻醉的,机械通气的大鼠中,肺沉积约为3.9,在自发呼吸的大鼠中约为8%。在这项研究中描述了将气雾剂递送至麻醉的机械通气啮齿动物的体外和体内模型的优化。方法:依靠重量分析,激光衍射滴定径和吸气过滤器上药物质量的分光光度分析来表征和优化体外系统性能。随后将优化的装置用于体内以确定示踪气溶胶在大鼠肺中的沉积。结果:体外测试证实,液滴大小,通气方案,呼吸启动设置以及包括药物回收步骤对吸入质量的影响最大。在测试过程中,运行之间增加了再循环步骤,吸入质量值提高了41%。雾化过程对硫酸沙丁胺醇的负面影响很小。记录的体外沉积率为原始剂量的29.95±1.54%(n = 3)。伊文思蓝的体内沉积率具有高度可比性(30.88±5.73%)(n = 6)。气管内注入示踪染料导致原始剂量的87.34±6.23%沉积。结论:这种优化的实验装置比以前报道的吸入量更大。在机械通气的肺中,增加再循环步骤可证明是实现更高沉积水平的重大改进。但是,需要评估测试剂是否适合重复雾化。

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