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A Review of Currently Available Fenofibrate and Fenofibric Acid Formulations

机译:当前可用的非诺贝特和非纤维酸制剂的综述

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摘要

Fenofibrate is a third-generation fibric acid derivative indicated as a monotherapy to reduce elevated low-density lipoprotein cholesterol, total cholesterol, triglycerides, and apolipoprotein B; to increase high-density lipoprotein cholesterol in patients with primary hyperlipidemia or mixed dyslipidemia; and to reduce triglycerides in patients with severe hypertriglyceridemia. In this review, the key characteristics of available fenofibrate formulations are examined. A literature search was conducted, focusing on comparative studies examining bioavailability, food effects, absorption, and lipid efficacy. Fenofibrate is highly lipophilic, virtually insoluble in water, and poorly absorbed. Coadministration with meals was necessary to maximize bioavailability of early formulations. Micronized and nanoparticle formulations of fenofibrate with reduced particle sizes were developed, resulting in greater solubility, improved bioavailability, and in some cases, the ability to be given irrespective of food. A recently introduced hydrophilic choline salt of fenofibric acid also can be taken without regard to meals, is absorbed throughout the gastrointestinal tract, has the highest bioavailability among marketed formulations, and is approved for coadministration with a statin. Differences in bioavailability of fenofibrate formulations have resulted in low-dose (40 - 67) mg and standard-dose (120 - 200 mg) formulations. Different formulations are not equivalent on a milligram-to-milligram basis. In order to prevent medication errors, resulting in underdosing or overdosing with attendant consequences, it is important for healthcare providers to recognize that the formulations of fenofibrate and fenofibric acid that are currently available vary substantially in relation to food effect, equivalency on a milligram-to-milligram basis, and indication to be coadministered with a statin.
机译:非诺贝特是第三代纤维状酸衍生物,可通过单一疗法降低低密度脂蛋白胆固醇,总胆固醇,甘油三酸酯和载脂蛋白B的水平。增加原发性高脂血症或混合血脂异常患者的高密度脂蛋白胆固醇;并降低重症高甘油三酯血症患者的甘油三酸酯。在这篇综述中,研究了可用的非诺贝特制剂的关键特性。进行了文献检索,重点是检查生物利用度,食物效果,吸收和脂质功效的比较研究。非诺贝特具有很高的亲脂性,几乎不溶于水,吸收差。与膳食共同给药对于最大化早期制剂的生物利用度是必要的。开发了具有减小的粒径的非诺贝特的微粉化和纳米颗粒制剂,从而产生了更高的溶解度,更高的生物利用度,并且在某些情况下,无论食物如何,都具有给药的能力。也可以不考虑进餐而服用最近引入的非诺贝特酸亲水性胆碱盐,在胃肠道中吸收,在市售制剂中具有最高的生物利用度,并被批准与他汀类药物共同给药。非诺贝特制剂的生物利用度差异导致低剂量(40-67)mg和标准剂量(120-200 mg)制剂。在毫克对毫克的基础上,不同的配方并不等效。为了防止用药错误,导致用药过量或过量,随之而来的后果是重要的,对于医疗保健提供者来说,认识到目前可用的非诺贝特和非诺贝特酸的配方在食品效果,毫克当量至-毫克级,并与他汀类药物共同给药的适应症。

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