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DOI: 10.3791/65756-v
Sara E. Maloney1, Ian E. Stewart1, Jeffrey B. Mecham1, Mercedes Gonzalez-Juarrero2, Bernd Meibohm3, Anthony J. Hickey1
1Technology Advancement and Commercialization,RTI International, 2Mycobacteria Research Laboratories, Department of Microbiology, Immunology, and Pathology,Colorado State University, 3Department of Pharmaceutical Sciences, College of Pharmacy,University of Tennessee Health Science Center
Please note that some of the translations on this page are AI generated. Click here for the English version.
药物干粉开发需要可靠的 体内 测试,通常使用小鼠模型。用于准确和可重复地将干粉气溶胶输送给小鼠的设备技术受到限制。本研究介绍了用于小鼠相关剂量的肺部药物递送的一次性给药器,有助于初步的概念验证研究。
我们正在开发用于分枝杆菌疾病吸入治疗的新药和现有药物。我们的重点是治疗耐药微生物的新方法,确保使用干粉的安全性和有效性。干粉吸入器产品的初步临床前测试通常在小鼠模型中进行,然后再转移到更大的动物模型中。
这种方法的一个重大局限性是缺乏合适的设备技术,无法准确和可重复地将干粉输送给小动物。我们开发的一次性给药器易于制造,使其易于获得且具有成本效益,可用于小鼠的初步概念验证研究。一次性特性允许它们在动物手术室中使用,而无需担心清洁、重新填充和称量可重复使用设备的材料。
我们未来的工作将采用针对病原体的生物治疗部分,以避免对宿主产生任何影响。然后,这种方法可以针对患者进行定制,因为它具有病原体特异性。
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