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自微乳给药系统制剂与标准 ω-3 酸乙酯产品对健康男性和女性空腹状态下二十碳五烯酸和二十二碳六烯酸生物利用度的影响:一项研究。

Effects of a Self-micro-emulsifying Delivery System Formulation Versus a Standard ω-3 Acid Ethyl Ester Product on the Bioavailability of Eicosapentaenoic Acid and Docosahexaenoic Acid: A Study in Healthy Men and Women in a Fasted State.

机构信息

Midwest Biomedical Research/MB Clinical Research, Glen Ellyn, IL, United States; Great Lakes Clinical Trials, Chicago, IL, United States.

Midwest Biomedical Research/MB Clinical Research, Glen Ellyn, IL, United States.

出版信息

Clin Ther. 2018 Dec;40(12):2065-2076. doi: 10.1016/j.clinthera.2018.10.014. Epub 2018 Nov 16.

Abstract

PURPOSE

Intakes of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) are associated with several potential health benefits, but standard ethyl ester (EE) formulations of these ω-3 fatty acids require the co-ingestion of fat for adequate absorption. The objective of this research was to assess the relative bioavailability of EPA and DHA administered in a proprietary self-micro-emulsifying delivery system (SMEDS) formulation compared with EPA and DHA in a standard ω-3 acid EE product in healthy men and women in a fasted state.

METHODS

This randomized crossover study investigated the bioavailability of 2 encapsulated formulations of EPA and DHA, a capsule containing 500 mg EPA + DHA administered in a SMEDS formulation (SMEDS treatment), and a capsule containing 840 mg EPA + DHA in a standard ω-3 acid EE formulation (EE treatment). Subjects consumed a single dose of their assigned capsule in a fasting state, and plasma was collected before and for 24 h after dosing. Subjects underwent a ≥14-day washout and were crossed over to the other treatment condition. Plasma concentrations of EPA, DHA, and EPA + DHA were assessed.

FINDINGS

Twenty-three subjects (11 women, 12 men; mean [SEM] age, 33.8 [2.1] years; and body mass index, 24.9 [0.7] kg/m) completed the trial. The baseline-adjusted, dose-normalized, arithmetic means (SD) of the incremental (i)-AUC for EPA + DHA were 543 (266) and 102 (88.2) h · μg/mL/g for the SMEDS and EE formulations, respectively (P < 0.001). The iAUC least-squares geometric mean ratio (90% CI) for SMEDS:standard EE was 475/58 = 8.2 (4.8-13.9), indicating markedly higher bioavailability of EPA + DHA with the SMEDS formulation compared to the standard EE formulation. This finding was also true for EPA (geometric mean ratio [90% CI], 18.2 [11.3-29.3]) and DHA (geometric mean ratio [90% CI], 4.5 [2.9-7.0]).

IMPLICATIONS

The SMEDS delivery system markedly enhanced appearance in plasma of EPA and DHA, compared to a standard EE formulation, when ingested in the fasting state. ClinicalTrials.gov identifier: NCT03443076.

摘要

目的

二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)的摄入量与多种潜在的健康益处有关,但这些 ω-3 脂肪酸的标准乙酯(EE)制剂需要摄入脂肪才能充分吸收。本研究的目的是评估在禁食状态下,以专有自微乳化给药系统(SMEDS)制剂形式给予 EPA 和 DHA 与以标准 ω-3 酸 EE 产品形式给予 EPA 和 DHA 的相对生物利用度,在健康男性和女性中。

方法

这项随机交叉研究调查了两种封装的 EPA 和 DHA 制剂的生物利用度,一种胶囊含有 500mg EPA+DHA,以 SMEDS 制剂形式给药(SMEDS 治疗),另一种胶囊含有 840mg EPA+DHA,以标准 ω-3 酸 EE 制剂形式给药(EE 治疗)。受试者在禁食状态下单次服用指定胶囊,在给药前和给药后 24 小时内采集血浆。受试者进行了至少 14 天的洗脱期,并交叉到另一种治疗条件。评估了 EPA、DHA 和 EPA+DHA 的血浆浓度。

结果

23 名受试者(11 名女性,12 名男性;平均[SEM]年龄 33.8[2.1]岁;体重指数 24.9[0.7]kg/m)完成了试验。SMEDS 和 EE 制剂的基线校正、剂量归一化、EPA+DHA 的增量(i)-AUC 的算术平均值(SD)分别为 543(266)和 102(88.2)h·μg/mL/g(P<0.001)。SMEDS:标准 EE 的 iAUC 最小二乘几何均数比值(90%CI)为 475/58=8.2(4.8-13.9),表明与标准 EE 制剂相比,SMEDS 制剂中 EPA+DHA 的生物利用度明显更高。这一发现也适用于 EPA(几何均数比值[90%CI],18.2[11.3-29.3])和 DHA(几何均数比值[90%CI],4.5[2.9-7.0])。

意义

与标准 EE 制剂相比,SMEDS 给药系统在禁食状态下摄入时,明显增加了 EPA 和 DHA 在血浆中的出现。临床试验.gov 标识符:NCT03443076。

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