Soto-Montenegro M L, Conejero L, Vaquero J J, Baeza M L, Zubeldia J M, Desco M
Unidad de Medicina y Cirugía Experimental, Hospital General Universitario Gregorio Marañón, Dr. Esquerdo, 46, 28007, Madrid, Spain.
Mol Imaging Biol. 2009 Jul-Aug;11(4):263-8. doi: 10.1007/s11307-009-0199-y. Epub 2009 Apr 2.
Transnasal administration is one of the most common routes for allergen challenge in mouse models of airway diseases. Although this technique is widely used, neither the amount of allergen that reaches the lung nor its airway distribution has been well established. We used positron emission tomography (PET) and computed tomography (CT) to examine the anatomical distribution of a solution containing a tracer immediately after transnasal delivery and to determine the possible influence of age and administered volume.
Forty-six female BALB/c mice were divided into three groups according to instillation volume and age: (A) 15 microl, 8-10 weeks old (N = 10), (B) 30 microl, 8-10 weeks old (N = 20), and (C) 30 microl, 32 weeks old (N = 16). Anesthetized animals underwent a dynamic scan in a dedicated small-animal PET scanner immediately after transnasal administration of a solution containing (18)FDG. Regions of interest were used to obtain quantitative data. Animals were also imaged with a small-animal CT scanner to obtain complementary anatomical information.
Mean +/- SD (5.69 +/- 4.51%) of the solution administered reached the lungs in group A, 41.84 +/- 8.03% in group B, and 36.65 +/- 16.15% in group C. A comparable percentage was delivered to the left and right lungs in all the groups. Analysis of variance revealed a significant difference between the groups in the proportion of the solution that reached the lungs depending on the injection volume (P < 0.001), but not depending on animal age.
In this first report on quantitative imaging by PET and CT in small animals, we confirmed the suitability of the transnasal route with an instilled volume of 30 microl delivering fluids into the lower airways, although only about 40% of the dose reaches the lungs.
经鼻给药是气道疾病小鼠模型中变应原激发的最常用途径之一。尽管该技术被广泛应用,但到达肺部的变应原量及其在气道中的分布情况尚未完全明确。我们使用正电子发射断层扫描(PET)和计算机断层扫描(CT)来检查经鼻给药后含有示踪剂的溶液的解剖分布,并确定年龄和给药体积可能产生的影响。
46只雌性BALB/c小鼠根据滴注体积和年龄分为三组:(A)15微升,8 - 10周龄(N = 10),(B)30微升,8 - 10周龄(N = 20),以及(C)30微升,32周龄(N = 16)。麻醉后的动物在经鼻给予含有(18)FDG的溶液后,立即在专用的小动物PET扫描仪中进行动态扫描。使用感兴趣区域获取定量数据。动物还使用小动物CT扫描仪进行成像以获得补充的解剖学信息。
A组给药溶液平均±标准差(5.69±4.51%)到达肺部,B组为41.84±8.03%,C组为36.65±16.15%。所有组中输送到左肺和右肺的百分比相当。方差分析显示,根据注射体积,各组中到达肺部的溶液比例存在显著差异(P < 0.001),但与动物年龄无关。
在这份关于小动物PET和CT定量成像的首次报告中,我们证实了经鼻途径适合以30微升的滴注体积将液体输送到下呼吸道,尽管只有约40%的剂量到达肺部。