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一种新的乳酸镁二水合物延长释放胶囊在健康受试者中的绝对生物利用度和食物的影响。

The absolute bioavailability and the effect of food on a new magnesium lactate dihydrate extended-release caplet in healthy subjects.

机构信息

a QPS, LLC , Newark , DE , USA.

b Pharmalyte Solutions, LLC , Southlake , TX , USA.

出版信息

Drug Dev Ind Pharm. 2018 Sep;44(9):1481-1487. doi: 10.1080/03639045.2018.1464020. Epub 2018 Apr 25.

Abstract

OBJECTIVE

To assess the absolute bioavailability of 20 mEq magnesium lactate extended-release (ER) caplets and to assess the effect of food on the pharmacokinetics of these ER caplets.

SIGNIFICANCE

Magnesium in different salt forms is available as over-the-counter oral formulations. The absorption and bioavailability is highly affected by the water solubility of the salt form. A new ER caplet of 10 mEq strength of magnesium L-lactate dihydrate has been developed to increase the bioavailability of magnesium.

METHODS

An open label, single-dose, randomized, three-period, cross-over study in healthy adults was conducted with three treatments: (a) single oral dose of 20 mEq magnesium L-lactate dehydrate under fasting conditions, (b) single intravenous (IV) infusion of 20 mEq magnesium sulfate, and (c) single oral dose of 20 mEq magnesium L-lactate dehydrate under fed conditions. Urine and blood samples were collected for analysis of urinary and serum magnesium concentrations.

RESULTS

Absolute bioavailabilities of the caplets under fasted and fed conditions, compared to IV magnesium sulfate, were 20.26% (fasted) and 12.49% (fed) in serum, based on the geometric mean ratio (GMR) of the baseline-adjusted AUC, and 38.11% (fasted) and 40.99% (fed) in urine, based on the GMR of the baseline-adjusted Ae. Relative bioavailability of the caplets comparing the fed and fasted states was 61.67% in serum, based on the GMR of the baseline-adjusted AUC, and 107.57% in urine, based on the GMR of the baseline-adjusted Ae.

CONCLUSIONS

This new magnesium formulation has reasonable bioavailability and might be a valuable addition to the currently available magnesium oral products.

摘要

目的

评估 20mEq 乳酸镁缓释(ER)胶囊的绝对生物利用度,并评估食物对这些 ER 胶囊药代动力学的影响。

意义

不同盐形式的镁以非处方口服制剂形式存在。盐形式的水溶性高度影响镁的吸收和生物利用度。为提高镁的生物利用度,已开发出一种新的 10mEq 强度的 L-乳酸镁二水合物 ER 胶囊。

方法

一项在健康成年人中进行的开放标签、单剂量、随机、三周期、交叉研究,采用三种治疗方法:(a)空腹单次口服 20mEq 无水 L-乳酸镁,(b)单次静脉(IV)输注 20mEq 硫酸镁,(c)进食状态下单次口服 20mEq 无水 L-乳酸镁。收集尿液和血液样本,用于分析尿镁和血清镁浓度。

结果

基于基线校正 AUC 的几何均数比(GMR),胶囊在空腹和进食状态下的绝对生物利用度分别为血清中的 20.26%(空腹)和 12.49%(进食),以及尿液中的 38.11%(空腹)和 40.99%(进食),基于基线校正 Ae 的 GMR。胶囊在进食和空腹状态下的相对生物利用度分别为血清中的 61.67%(基于 AUC 的 GMR)和尿液中的 107.57%(基于 Ae 的 GMR)。

结论

这种新的镁制剂具有合理的生物利用度,可能是目前可用的镁口服产品的有价值补充。

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