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布地奈德泡沫剂在轻至中度活动性溃疡性结肠炎患者中的结肠扩散及血清药代动力学

Colonic spread and serum pharmacokinetics of budesonide foam in patients with mildly to moderately active ulcerative colitis.

作者信息

Brunner M, Vogelsang H, Greinwald R, Kletter K, Kvaternik H, Schrolnberger C, Eichler H-G, Brunner H, Dudczak R, Müller M

机构信息

Department of Clinical Pharmacology, Division of Clinical Pharmacokinetics, Medical University of Vienna, Vienna, Austria.

出版信息

Aliment Pharmacol Ther. 2005 Sep 1;22(5):463-70. doi: 10.1111/j.1365-2036.2005.02571.x.

Abstract

BACKGROUND

Local treatment with foams in patients suffering from ulcerative proctitis or proctosigmoiditis is considered a rational treatment option.

AIMS

To investigate colonic spread, safety, tolerability and acceptance of a newly developed budesonide foam formulation.

METHODS

Twelve patients (four females, eight males) with acute proctosigmoiditis or left-sided ulcerative colitis were rectally administered a single dose of [99Tcm]-labelled budesonide foam (Budenofalk; Dr Falk Pharma GmbH, Freiburg, Germany) containing 2 mg budesonide in 20 mL foam after diagnostic colonoscopy. Thereafter, the colonic spread was assessed by means of gamma-scintigraphy for 6 h. Serum samples were taken simultaneously.

RESULTS

Budesonide foam spread with a maximum between 11 and 40 cm, thus reaching the sigmoid colon in all patients. In some patients, the foam even extended into the distal third and the middle of the descending colon with maximum radioactivity at 4 h. Systemic budesonide absorption was rapid and pharmacokinetic data were comparable with published data on marketed budesonide enemas, with mean serum C(max) and AUC(0-8 h) values of 0.8 +/- 0.5 ng/mL and 3.7 +/- 1.9 ng h/mL, respectively. The new formulation was well accepted by all patients, who could retain the foam for at least 4 h.

CONCLUSIONS

In the majority of patients, budesonide foam effectively spread up to the left-sided colon and thus qualifies for the local treatment of proctosigmoiditis.

摘要

背景

对于患有溃疡性直肠炎或直肠乙状结肠炎的患者,使用泡沫剂进行局部治疗被认为是一种合理的治疗选择。

目的

研究一种新开发的布地奈德泡沫制剂在结肠内的扩散情况、安全性、耐受性及接受度。

方法

12例患者(4例女性,8例男性)患有急性直肠乙状结肠炎或左侧溃疡性结肠炎,在诊断性结肠镜检查后,经直肠给予单剂量含2mg布地奈德的20mL[99锝]标记布地奈德泡沫(布地奈德福可,德国弗赖堡法尔克制药有限公司)。此后,通过γ闪烁扫描术评估结肠内扩散情况,持续6小时。同时采集血清样本。

结果

布地奈德泡沫在11至40厘米处扩散范围最大,所有患者均到达乙状结肠。在一些患者中,泡沫甚至延伸至降结肠远段和中段,4小时时放射性最强。布地奈德的全身吸收迅速,药代动力学数据与已发表的市售布地奈德灌肠剂数据相当,平均血清C(max)和AUC(0 - 8小时)值分别为0.8±0.5ng/mL和3.7±1.9ng·h/mL。所有患者对新制剂接受度良好,均可将泡沫保留至少4小时。

结论

在大多数患者中,布地奈德泡沫可有效扩散至左侧结肠,因此有资格用于直肠乙状结肠炎的局部治疗。

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