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健康日本男性受试者中食物对 ω-3 羧酸类药代动力学的影响:一项 I 期、随机、开放标签、三周期、交叉试验。

Effects of Food on the Pharmacokinetics of Omega-3-Carboxylic Acids in Healthy Japanese Male Subjects: A Phase I, Randomized, Open-label, Three-period, Crossover Trial.

机构信息

AstraZeneca KK.

AstraZeneca Gothenburg.

出版信息

J Atheroscler Thromb. 2017 Sep 1;24(9):980-987. doi: 10.5551/jat.38737. Epub 2017 Mar 24.

Abstract

AIMS

Omega-3-carboxylic acids (OM3-CA) contain omega-3 free fatty acids, such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), as carboxylic acids. Food intake is known to affect the bioavailability of ethyl ester fatty acid formulations. We conducted a phase I study to investigate the effects of the timing of OM3-CA administration relative to food intake on the pharmacokinetics of EPA and DHA.

METHODS

In this randomized, open-label, three-period crossover study, Japanese healthy male subjects were administered 4×1 g OM3-CA capsules with continued fasting, before a meal, or after a meal. All subjects fasted for ≥10 h prior to drug/meal administration. The primary objective was to examine the effect of meal timing on the pharmacokinetics of EPA and DHA after OM3-CA administration. The secondary objectives were to examine the safety and tolerability of OM3-CA.

RESULTS

A total of 42 Japanese subjects was enrolled in the study. The baseline-adjusted maximum concentration and area under the concentration-time curve from 0 to 72 h for EPA, DHA, and EPA +DHA were lower in the fasting and before meal conditions than in the after meal condition. The maximum total EPA, total DHA, and total EPA+DHA concentrations were reached later when administered in fasting conditions than in fed conditions, indicating slower absorption in fasting conditions. Diarrhea was reported by five, six, and no subjects in the fasting, before meal, and after meal conditions, respectively.

CONCLUSIONS

The timing of OM3-CA administration relative to food intake influences the systemic bioavailability of EPA and DHA in healthy Japanese male subjects.

TRIAL REGISTRATION

NCT02372344.

摘要

目的

ω-3 羧酸(OM3-CA)含有作为羧酸的 ω-3 游离脂肪酸,如二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)。已知食物摄入会影响乙酯脂肪酸制剂的生物利用度。我们进行了一项 I 期研究,以调查 OM3-CA 给药相对于食物摄入的时间对 EPA 和 DHA 药代动力学的影响。

方法

在这项随机、开放标签、三周期交叉研究中,日本健康男性受试者分别在禁食、餐前或餐后服用 4×1 g OM3-CA 胶囊。所有受试者在给药/餐前禁食至少 10 小时。主要目的是研究餐时对 OM3-CA 给药后 EPA 和 DHA 药代动力学的影响。次要目的是研究 OM3-CA 的安全性和耐受性。

结果

共有 42 名日本受试者入组该研究。与餐后条件相比,禁食和餐前条件下 EPA、DHA 和 EPA+DHA 的基线调整后最大浓度和 0 至 72 小时浓度-时间曲线下面积较低。在禁食条件下给予时,最大总 EPA、总 DHA 和总 EPA+DHA 浓度达到时间较晚,表明禁食条件下吸收较慢。在禁食、餐前和餐后条件下,分别有 5、6 和 0 名受试者报告腹泻。

结论

OM3-CA 给药相对于食物摄入的时间会影响健康日本男性受试者中 EPA 和 DHA 的全身生物利用度。

试验注册

NCT02372344。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4db6/5587524/f8aa95a89ad5/jat-24-980-g001.jpg

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