Qiu Yingshan, Liao Qiuying, Chow Michael Y T, Lam Jenny K W
Department of Pharmacology and Pharmacy, LKS Faculty of Medicine, The University of Hong Kong.
Department of Pharmacology and Pharmacy, LKS Faculty of Medicine, The University of Hong Kong; Advanced Drug Delivery Group, Sydney Pharmacy School, Faculty of Medicine and Health, The University of Sydney.
J Vis Exp. 2020 Jul 25(161). doi: 10.3791/61469.
In the development of inhalable dry powder formulations, it is essential to evaluate their biological activities in preclinical animal models. This paper introduces a noninvasive method of intratracheal delivery of dry powder formulation in mice. A dry powder loading device that consists of a 200 µL gel loading pipette tip connected to an 1 mL syringe via a three-way stopcock is presented. A small amount of dry powder (1-2 mg) is loaded into the pipette tip and dispersed by 0.6 mL of air in the syringe. Because pipette tips are disposable and inexpensive, different dry powder formulations can be loaded into different tips in advance. Various formulations can be evaluated in the same animal experiment without device cleaning and dose refilling, thereby saving time and eliminating the risk of cross-contamination from residual powder. The extent of powder dispersion can be inspected by the amount of powder remaining in the pipette tip. A protocol of intubation in mouse with a custom-made light source and a guiding cannula is included. Proper intubation is one of the key factors that influences the intratracheal delivery of dry powder formulation to the deep lung region of the mouse.
在可吸入干粉制剂的研发过程中,在临床前动物模型中评估其生物活性至关重要。本文介绍了一种在小鼠中进行气管内干粉制剂给药的非侵入性方法。提出了一种干粉装载装置,该装置由一个通过三通旋塞连接到1 mL注射器的200 μL凝胶装载移液器吸头组成。将少量干粉(1 - 2 mg)装入移液器吸头,并通过注射器中的0.6 mL空气进行分散。由于移液器吸头是一次性且价格低廉的,不同的干粉制剂可以预先装入不同的吸头中。在同一动物实验中可以评估各种制剂,而无需清洁装置和重新填充剂量,从而节省时间并消除残留粉末交叉污染的风险。粉末分散程度可以通过移液器吸头中残留的粉末量来检查。文中还包括了使用定制光源和引导套管对小鼠进行插管的方案。正确插管是影响干粉制剂向小鼠深部肺区域进行气管内给药的关键因素之一。