Sakagami Masahiro, Kinoshita Wataru, Sakon Kiyoyuki, Makino Yuji
DDS Research Laboratories, Teijin Ltd., Asahigaoka, Hino, 191-8512, Tokyo, Japan.
Arch Toxicol. 2003 Jun;77(6):321-9. doi: 10.1007/s00204-003-0450-2. Epub 2003 Mar 15.
Because absorption takes place from multiple sites of aerosol deposition, it is generally difficult to interpret systemic levels following nose-only inhalation in laboratory rodents. Therefore, this study attempted to determine the fractional contribution of lung, nasal and gastrointestinal (GI) absorption to the observed systemic level following nose-only aerosol exposure in rats using fluorescein as a model powder solute. Rats were treated orally with vehicle or activated charcoal, the latter diminishing GI absorption of fluorescein, and were subsequently nose-only exposed to 3.7- micro m fluorescein aerosols at 25.2 micro g/l(air) for 10 min. While fluorescein similarly disappeared from the lung at a half-life of 0.23 hr, its plasma concentrations in the charcoal-treated group were significantly lower than those in the charcoal-untreated (vehicle) group. This suggests that significant portions of fluorescein were transported by nasopharyngeal and tracheobronchial mucociliary clearances following aerosol exposure and were absorbed from the GI tract. Despite the lack of GI absorption in the charcoal-treated animals, it was estimated that this nose-only exposure of fluorescein allowed 25.7 and 82.5 micro g/kg of simultaneous lung and nasal deposition, respectively, followed by their absorption composing the observed systemic level in this group (AUC(0- infinity ) 137.49 ng/ml h). Thus, assuming linear pharmacokinetics of fluorescein, the extent of absorption (AUC(0- infinity )) due to such nasal deposit (82.5 micro g/kg) was estimated to be 47.00 ng/ml h using the AUC(0- infinity ) obtained in an independent study of intranasal powder insufflation at 34.5 micro g/kg in the charcoal-treated rats (AUC(0- infinity ) 19.66 ng/ml h). As a result, the AUC(0- infinity ) due to 25.7 micro g/kg of the lung deposit was deconvoluted to be 90.49 ng/ml h and finally, the absolute bioavailability (F%) of the "lung-region-specific" deposition and absorption of fluorescein was estimated to be 55.0%. It is observed therefore, that lung, nasal and GI absorption accounted for 24.2, 12.5 and 63.3% of the total fluorescein absorption, respectively, following nose-only exposure of 3.7- micro m aerosols. This study addresses the common methodological insufficiency of nose-only inhalation studies in rodents, which have been neglected in most cases, and provides the appropriate kinetic interpretation for their observed systemic level.
由于气溶胶沉积的多个部位均可发生吸收,因此通常难以解读实验室啮齿动物仅经鼻吸入后的全身水平。因此,本研究试图以荧光素作为模型粉末溶质,确定大鼠仅经鼻暴露于气溶胶后,肺、鼻和胃肠道(GI)吸收对所观察到的全身水平的相对贡献。给大鼠口服赋形剂或活性炭,后者可减少荧光素的胃肠道吸收,随后将大鼠仅经鼻暴露于浓度为25.2μg/l(空气)的3.7μm荧光素气溶胶中10分钟。虽然荧光素在肺中的消除半衰期同样为0.23小时,但其在活性炭处理组中的血浆浓度显著低于未处理(赋形剂)组。这表明气溶胶暴露后,荧光素的很大一部分通过鼻咽和气管支气管的黏液纤毛清除作用转运,并从胃肠道吸收。尽管活性炭处理的动物不存在胃肠道吸收,但据估计,仅经鼻暴露于荧光素后,分别有25.7和82.5μg/kg的荧光素同时沉积在肺和鼻中,随后它们的吸收构成了该组中观察到的全身水平(AUC(0-∞) 137.49 ng/ml·h)。因此,假设荧光素的药代动力学呈线性,根据在活性炭处理的大鼠中以34.5μg/kg进行鼻内粉末吹入的独立研究中获得的AUC(0-∞)(19.66 ng/ml·h),估计由这种鼻内沉积(82.5μg/kg)引起的吸收程度(AUC(0-∞))为47.00 ng/ml·h。结果,由25.7μg/kg的肺沉积引起的AUC(0-∞)经反卷积计算为90.49 ng/ml·h,最终,荧光素“肺区域特异性”沉积和吸收的绝对生物利用度(F%)估计为55.0%。因此可以观察到,仅经鼻暴露于3.7μm气溶胶后,肺、鼻和胃肠道吸收分别占荧光素总吸收的24.2%、12.5%和63.3%。本研究解决了啮齿动物仅经鼻吸入研究中常见的方法学不足问题,该问题在大多数情况下都被忽视了,并为所观察到的全身水平提供了适当的动力学解释。