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碘化非离子二聚体造影剂碘克沙醇340注射液在健康人体受试者中的药代动力学特征、耐受性和安全性。

The pharmacokinetic profile, tolerability and safety of the iodinated, non-ionic, dimeric contrast medium Iosimenol 340 injection in healthy human subjects.

作者信息

Meurer Karoline, Kelsch Bettina, Hogstrom Barry

机构信息

Otsuka Novel Products GmbH, Munich, Germany, Germany

Department of Radiology, Charité, Humboldt University, Berlin, Germany.

出版信息

Acta Radiol. 2015 May;56(5):581-6. doi: 10.1177/0284185114534414. Epub 2014 Jun 3.

Abstract

BACKGROUND

Iosimenol 340 injection is a new isotonic iodinated contrast medium for X-ray angiography.

PURPOSE

To investigate the pharmacokinetics and biotransformation, tolerability, and safety of Iosimenol 340 in healthy human subjects.

MATERIAL AND METHODS

Twenty-four subjects were enrolled and randomized to receive either Iosimenol 340 (0.5, 1.5 or 3.0 mL/kg) or placebo (0.9% saline). In each dosing group, six subjects received Iosimenol 340 and two subjects received placebo. Safety was assessed by physical examination, vital signs, electrocardiography, and laboratory tests. Adverse events were recorded throughout the study up to 14 days after dosing. Blood samples were collected from 10 min before until 48 h after the start of dosing and urine samples were collected from 15 min before until 96 h after the start of dosing. Iosimenol was quantified in plasma and urine by measuring iodine concentrations with X-ray fluorescence. High-performance liquid chromatography was used to assess iosimenol biotransformation.

RESULTS

Mean half-lives (mean ± standard deviation [SD]) of iosimenol were 0.17 ± 0.08 h (10.2 ± 4.8 min) and 2.01 ± 0.32 h for distribution and terminal elimination phases, respectively. The apparent volume of distribution was 0.27 ± 0.05 L/kg, indicating distribution to the extracellular fluid volume. Iosimenol was excreted within 24 h without any sign of metabolic transformation. Thirty-two adverse events were observed in 14 subjects. All were mild or moderate, and were transient in nature.

CONCLUSION

Iosimenol was not metabolized, had a distribution volume corresponding to the extracellular space, and was rapidly excreted through the kidneys by glomerular filtration. The area under the plasma concentration curve and the peak plasma concentration was proportional to dose, while clearance was independent of dose. Iosimenol 340 was well tolerated.

摘要

背景

碘西门醇340注射液是一种用于X射线血管造影的新型等渗碘化造影剂。

目的

研究碘西门醇340在健康人体受试者中的药代动力学、生物转化、耐受性和安全性。

材料与方法

招募24名受试者并随机分为两组,分别接受碘西门醇340(0.5、1.5或3.0 mL/kg)或安慰剂(0.9%生理盐水)。在每个给药组中,6名受试者接受碘西门醇340,2名受试者接受安慰剂。通过体格检查、生命体征、心电图和实验室检查评估安全性。在整个研究过程中记录给药后长达14天的不良事件。给药开始前10分钟至给药后48小时采集血样,给药开始前15分钟至给药后96小时采集尿样。通过用X射线荧光测量碘浓度对血浆和尿液中的碘西门醇进行定量。采用高效液相色谱法评估碘西门醇的生物转化。

结果

碘西门醇分布相和终末消除相的平均半衰期(平均值±标准差[SD])分别为0.17±0.08小时(10.2±4.8分钟)和2.01±0.32小时。表观分布容积为0.27±0.05 L/kg,表明分布至细胞外液容积。碘西门醇在24小时内排出,无任何代谢转化迹象。14名受试者观察到32例不良事件。均为轻度或中度,且为一过性。

结论

碘西门醇未被代谢,分布容积与细胞外间隙相对应,通过肾小球滤过经肾脏快速排泄。血浆浓度曲线下面积和血浆峰浓度与剂量成正比,而清除率与剂量无关。碘西门醇340耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/440c/4396406/6e88a2d0308e/10.1177_0284185114534414-fig1.jpg

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