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使用或不使用储物罐吸入环索奈德时,哮喘儿童稳态药代动力学参数的相似结果。

Similar Results in Children with Asthma for Steady State Pharmacokinetic Parameters of Ciclesonide Inhaled with or without Spacer.

作者信息

Boss H, Minic P, Nave R

机构信息

Nycomed GmbH, Byk Gulden Str. 2, 78467 Konstanz, Germany.

出版信息

Clin Med Insights Pediatr. 2010 May 5;4:1-10. doi: 10.4137/cmped.s4311. Print 2010.

Abstract

BACKGROUND

Ciclesonide is an inhaled corticosteroid administered by a metered dose inhaler (MDI) to treat bronchial asthma. After inhalation, the inactive ciclesonide is converted by esterases in the airways to active metabolite desisobutyryl-ciclesonide (des-CIC).

AIM

To compare the pharmacokinetic (PK) parameters of des-CIC in children after administration of therapeutic dose of ciclesonide with and without spacer (AeroChamber Plus(™)).

METHODS

Open-label, 3 period, cross over, repeated dose, PK study in 37 children with mild to moderate stable asthma (age: 6-11 y; body weight: 20-53 kg). During each 7-day treatment period, ciclesonide was inhaled once in the morning: A) 160 μg MDI with spacer, B) 80 μg MDI with spacer, and C) 160 μg MDI without spacer. Serum PK parameters of ciclesonide and des-CIC were determined on Day 7 of each period. The primary PK parameters were the AUCτ and Cmax for des-CIC.

RESULTS

Inhaling ciclesonide with spacer led to a dose proportional systemic exposure (AUCτ) of des-CIC (0.316 μgh/L for 80 μg and 0.663 μgh/L for 160 μg). The dose-normalized systemic exposure for des-CIC (based on AUCτ) was 27% higher after inhalation of ciclesonide 80 μg or 160 μg with spacer than without spacer; the corresponding Cmax values for des-CIC were, respectively, 63% and 55% higher with spacer. No clinically relevant abnormalities or adverse drug reactions were observed.

CONCLUSIONS

Inhalation of therapeutic ciclesonide dose with spacer led to a slight increase in the systemic exposure of des-CIC, which does not warrant dose adjustment.

摘要

背景

环索奈德是一种通过定量吸入器(MDI)给药用于治疗支气管哮喘的吸入性糖皮质激素。吸入后,无活性的环索奈德在气道中被酯酶转化为活性代谢物去异丁酰基 - 环索奈德(des - CIC)。

目的

比较在有和没有储雾罐(AeroChamber Plus(™))的情况下,给予治疗剂量环索奈德后儿童体内des - CIC的药代动力学(PK)参数。

方法

对37名轻度至中度稳定哮喘儿童(年龄:6 - 11岁;体重:20 - 53 kg)进行开放标签、3期、交叉、重复剂量的PK研究。在每个7天的治疗期内,环索奈德于早晨吸入一次:A)160μg MDI搭配储雾罐,B)80μg MDI搭配储雾罐,C)160μg MDI不搭配储雾罐。在每个时期的第7天测定环索奈德和des - CIC的血清PK参数。主要PK参数为des - CIC的AUCτ和Cmax。

结果

搭配储雾罐吸入环索奈德导致des - CIC的全身暴露量(AUCτ)呈剂量比例关系(80μg时为0.316μgh/L,160μg时为0.663μgh/L)。吸入80μg或160μg环索奈德搭配储雾罐后,des - CIC的剂量标准化全身暴露量(基于AUCτ)比不搭配储雾罐时高27%;des - CIC相应的Cmax值搭配储雾罐时分别高63%和55%。未观察到临床相关异常或药物不良反应。

结论

搭配储雾罐吸入治疗剂量的环索奈德会导致des - CIC的全身暴露量略有增加,但这不值得调整剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff74/3666986/bfc78d8e1ce8/cmped-4-2010-001f1.jpg

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